Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4670 |
| ensemblid | ENSG00000099783.13 |
| hgncid | 5046 |
| symbol | HNRNPM |
| name | heterogeneous nuclear ribonucleoprotein M |
| refseq_nuc | NM_005968.5 |
| refseq_prot | NP_005959.2 |
| ensembl_nuc | ENST00000325495.9 |
| ensembl_prot | ENSP00000325376.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 8444975 |
| end | 8489114 |
| strand | + |
| ver | v1.2 |
| region | chr19:8444975-8489114 |
| region5000 | chr19:8439975-8494114 |
| regionname0 | HNRNPM_chr19_8444975_8489114 |
| regionname5000 | HNRNPM_chr19_8439975_8494114 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 730 | 355 | 90 | 66 | 132 | 18 | 47 | 106 | HNRNPM_chr19_8439975_8494114 | HNRNPM | MAAGV others(725): Show |
chr19 | 8439975 | 8494114 |
| a0002 | 0/0 | 726 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | MAAGV others(721): Show |
chr19 | 8439975 | 8494114 |
| a0003 | 0/0 | 730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | MAAGV others(725): Show |
chr19 | 8439975 | 8494114 |
| a0004 | 0/0 | 730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | MAAGV others(725): Show |
chr19 | 8439975 | 8494114 |
| a0005 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | MAAGV others(725): Show |
chr19 | 8439975 | 8494114 |
| a0006 | 0/0 | 523 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | MAAGV others(518): Show |
chr19 | 8439975 | 8494114 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2190 | 286 | 47 | 59 | 121 | 15 | 44 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0002 | 1/0 | 2190 | 39 | 33 | 2 | 1 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0003 | 0/0 | 2190 | 15 | 0 | 5 | 6 | 3 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0004 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0005 | 0/0 | 2190 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0006 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0007 | 0/0 | 2190 | 2 | 1 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0008 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0011 | 0/1 | 2190 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0013 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0001c0014 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0002c0012 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2173): Show |
chr19 | 8439975 | 8494114 | ||
| a0003c0009 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0004c0010 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0005c0016 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2185): Show |
chr19 | 8439975 | 8494114 | ||
| a0006c0015 | 0/0 | 2180 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ATGGC others(2175): Show |
chr19 | 8439975 | 8494114 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2477 | 286 | 47 | 59 | 121 | 15 | 44 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0002t0001 | 1/0 | 2477 | 39 | 33 | 2 | 1 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0003t0001 | 0/0 | 2477 | 15 | 0 | 5 | 6 | 3 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0004t0001 | 0/0 | 2477 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0005t0001 | 0/0 | 2477 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0006t0001 | 0/0 | 2477 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0007t0001 | 0/0 | 2477 | 2 | 1 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0008t0001 | 0/0 | 2477 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0011t0001 | 0/1 | 2477 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0013t0001 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0001c0014t0001 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0002c0012t0001 | 0/0 | 2465 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2460): Show |
chr19 | 8439975 | 8494114 |
| a0003c0009t0001 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0004c0010t0001 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0005c0016t0001 | 0/0 | 2477 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2472): Show |
chr19 | 8439975 | 8494114 |
| a0006c0015t0001 | 0/0 | 2467 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | ACACA others(2462): Show |
chr19 | 8439975 | 8494114 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0023 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0007t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0008t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0008t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0011t0001g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0013t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0001c0014t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0002c0012t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0003c0009t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0004c0010t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0005c0016t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| a0006c0015t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0138 | EUR | GBR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | FIN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0255 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0252 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0158 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0313 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0156 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0139 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0117 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0154 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0312 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0157 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02145 | hp2 | a0001 | c0008 | t0001 | g0028 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0318 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02280 | hp1 | a0001 | c0008 | t0001 | g0027 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02683 | hp2 | a0002 | c0012 | t0001 | g0065 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02717 | hp1 | a0001 | c0006 | t0001 | g0267 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0303 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0320 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0295 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0300 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02976 | hp2 | a0001 | c0013 | t0001 | g0026 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0316 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03098 | hp1 | a0003 | c0009 | t0001 | g0078 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0259 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0319 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03486 | hp2 | a0001 | c0014 | t0001 | g0310 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0142 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03516 | hp2 | a0004 | c0010 | t0001 | g0298 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0307 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0025 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18950 | hp2 | a0001 | c0007 | t0001 | g0149 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18973 | hp1 | a0005 | c0016 | t0001 | g0098 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18985 | hp2 | a0001 | c0005 | t0001 | g0068 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19000 | hp2 | a0001 | c0005 | t0001 | g0063 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0260 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19060 | hp2 | a0001 | c0005 | t0001 | g0066 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19089 | hp1 | a0006 | c0015 | t0001 | g0070 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0317 | AFR | ASW | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0155 | EUR | TSI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | GIH | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | GIH | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02109 | hp2 | a0001 | c0007 | t0001 | g0166 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0261 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0308 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0265 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0315 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | USA | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0309 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| homoSapiens | chm13v2 | a0001 | c0011 | t0001 | g0280 | REF | REF | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0023 | REF | REF | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8445105 | C | T | 1 | a0005 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.107C>T | p.Pro36Leu | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/16 | 131/2477 | 107/2193 | 36/730 | chr19 | 8445105 | |||
| chr19:8473704 | G | A | 1 | a0003 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1038G>A | p.Met346Ile | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/16 | 1062/2477 | 1038/2193 | 346/730 | chr19 | 8473704 | |||
| chr19:8483168 | TAATGCAC others(3): Show |
T | 1 | a0006 | 1 | NA19089.hp1 | frameshift_variant | HIGH | c.1133_1142delATGCAC others(4): Show |
p.Asn378fs | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/16 | 1157/2477 | 1133/2193 | 378/730 | INFO_REALIGN_3_PRIME | chr19 | 8483168 | ||
| chr19:8485893 | G | A | 1 | a0004 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1465G>A | p.Gly489Ser | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1489/2477 | 1465/2193 | 489/730 | chr19 | 8485893 | |||
| chr19:8486200 | GCATGGGC others(5): Show |
G | 1 | a0002 | 1 | HG02683.hp2 | disruptive_inframe_deletion | MODERATE | c.1782_1793delTGCCAT others(6): Show |
p.Ala595_Pro598del | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1806/2477 | 1782/2193 | 594/730 | INFO_REALIGN_3_PRIME | chr19 | 8486200 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8474177 | G | A | 1 | a0001c0006 | 2 | HG02717.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.1053G>A | p.Gly351Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/16 | 1077/2477 | 1053/2193 | 351/730 | chr19 | 8474177 | |||
| chr19:8485688 | C | T | 1 | a0001c0014 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1260C>T | p.Gly420Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1284/2477 | 1260/2193 | 420/730 | chr19 | 8485688 | |||
| chr19:8485805 | G | A | 1 | a0001c0007 | 2 | HG02109.hp2 NA18950.hp2 |
synonymous_variant | LOW | c.1377G>A | p.Pro459Pro | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1401/2477 | 1377/2193 | 459/730 | chr19 | 8485805 | |||
| chr19:8486066 | C | T | 1 | a0001c0013 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1638C>T | p.Pro546Pro | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1662/2477 | 1638/2193 | 546/730 | chr19 | 8486066 | |||
| chr19:8486087 | C | T | 1 | a0001c0008 | 2 | HG02145.hp2 HG02280.hp1 |
synonymous_variant | LOW | c.1659C>T | p.Thr553Thr | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1683/2477 | 1659/2193 | 553/730 | chr19 | 8486087 | |||
| chr19:8486144 | C | T | 1 | a0001c0005 | 3 | NA18985.hp2 NA19000.hp2 NA19060.hp2 |
synonymous_variant | LOW | c.1716C>T | p.Gly572Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1740/2477 | 1716/2193 | 572/730 | chr19 | 8486144 | |||
| chr19:8486210 | T | C | 12 | a0001c0001 a0001c0002 a0001c0003 others(9): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
synonymous_variant | LOW | c.1782T>C | p.Pro594Pro | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1806/2477 | 1782/2193 | 594/730 | chr19 | 8486210 | |||
| chr19:8486228 | G | T | 1 | a0001c0003 | 15 | HG00140.hp2 HG00544.hp1 HG00673.hp1 others(12): Show |
synonymous_variant | LOW | c.1800G>T | p.Leu600Leu | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1824/2477 | 1800/2193 | 600/730 | chr19 | 8486228 | |||
| chr19:8486231 | C | T | 1 | a0001c0004 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.1803C>T | p.Gly601Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1827/2477 | 1803/2193 | 601/730 | chr19 | 8486231 | |||
| chr19:8488746 | C | T | 13 | a0001c0001 a0001c0003 a0001c0004 others(10): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
synonymous_variant | LOW | c.2085C>T | p.Gly695Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 16/16 | 2109/2477 | 2085/2193 | 695/730 | chr19 | 8488746 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8445260 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.113+149T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445260 | |||||||
| chr19:8445332 | T | TC | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG00323.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.113+222dupC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8445332 | ||||||
| chr19:8445339 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01952.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.113+228C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445339 | |||||||
| chr19:8445347 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0273 a0001c0001t0001g0274 |
4 | HG01981.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+236C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445347 | |||||||
| chr19:8445492 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.113+381C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445492 | |||||||
| chr19:8445515 | C | T | 2 | a0001c0002t0001g0320 a0001c0002t0001g0321 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.113+404C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445515 | |||||||
| chr19:8445529 | G | T | 20 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(17): Show |
20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.113+418G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445529 | |||||||
| chr19:8445542 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.113+431A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445542 | |||||||
| chr19:8445593 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.113+482C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445593 | |||||||
| chr19:8445642 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.113+531C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445642 | |||||||
| chr19:8445657 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0263 a0001c0001t0001g0264 others(8): Show |
13 | HG00323.hp1 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.113+546C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445657 | |||||||
| chr19:8445740 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.113+629C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445740 | |||||||
| chr19:8446042 | CACTT | C | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.113+933_113+936del others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8446042 | ||||||
| chr19:8446134 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.113+1023T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446134 | |||||||
| chr19:8446250 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.113+1139T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446250 | |||||||
| chr19:8446280 | A | G | 2 | a0001c0002t0001g0318 a0001c0002t0001g0319 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113+1169A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446280 | |||||||
| chr19:8446288 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.113+1177G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446288 | |||||||
| chr19:8446320 | C | T | 4 | a0001c0001t0001g0258 a0001c0004t0001g0259 a0001c0004t0001g0260 others(1): Show |
4 | HG02559.hp1 HG02738.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+1209C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446320 | |||||||
| chr19:8446403 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.113+1292A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446403 | |||||||
| chr19:8446441 | C | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.113+1330C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446441 | |||||||
| chr19:8446460 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+1349G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446460 | |||||||
| chr19:8446528 | G | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.113+1417G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446528 | |||||||
| chr19:8446872 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.113+1761A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446872 | |||||||
| chr19:8447005 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.113+1894T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447005 | |||||||
| chr19:8447234 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.113+2123A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447234 | |||||||
| chr19:8447243 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.113+2132A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447243 | |||||||
| chr19:8447260 | C | CT | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.113+2165dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8447260 | ||||||
| chr19:8447260 | C | CTT | 28 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(25): Show |
28 | HG00544.hp2 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.113+2164_113+2165d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8447260 | ||||||
| chr19:8447260 | C | CTTT | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(182): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.113+2163_113+2165d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8447260 | ||||||
| chr19:8447260 | C | CTTTT | 7 | a0001c0001t0001g0021 a0001c0001t0001g0253 a0001c0001t0001g0254 others(4): Show |
8 | HG00544.hp1 HG01891.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.113+2162_113+2165d others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8447260 | ||||||
| chr19:8447417 | A | G | 1 | a0001c0002t0001g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113+2306A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447417 | |||||||
| chr19:8447444 | A | T | 20 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(17): Show |
20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.113+2333A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447444 | |||||||
| chr19:8447503 | G | T | 1 | a0001c0002t0001g0316 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.113+2392G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447503 | |||||||
| chr19:8447518 | A | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG01109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.113+2407A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447518 | |||||||
| chr19:8447647 | G | A | 3 | a0001c0004t0001g0259 a0001c0004t0001g0260 a0001c0004t0001g0261 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.113+2536G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447647 | |||||||
| chr19:8447955 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
7 | HG02071.hp1 HG02135.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.113+2844G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447955 | |||||||
| chr19:8448025 | T | TCAAA | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+2930_113+2933d others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8448025 | ||||||
| chr19:8448056 | T | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(80): Show |
94 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.113+2945T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448056 | |||||||
| chr19:8448412 | T | A | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.113+3301T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448412 | |||||||
| chr19:8448452 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.113+3341A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448452 | |||||||
| chr19:8448473 | A | AT | 8 | a0001c0001t0001g0013 a0001c0001t0001g0159 a0001c0001t0001g0160 others(5): Show |
9 | HG02080.hp1 HG02129.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.113+3377dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8448473 | ||||||
| chr19:8448473 | AT | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(71): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.113+3377delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8448473 | ||||||
| chr19:8448509 | T | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.113+3398T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448509 | |||||||
| chr19:8448546 | C | T | 5 | a0001c0003t0001g0154 a0001c0003t0001g0155 a0001c0003t0001g0156 others(2): Show |
5 | HG01081.hp1 HG01243.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+3435C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448546 | |||||||
| chr19:8448576 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+3465C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448576 | |||||||
| chr19:8448607 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+3496A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448607 | |||||||
| chr19:8448622 | C | T | 10 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
10 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.113+3511C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448622 | |||||||
| chr19:8448651 | T | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(9): Show |
14 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.113+3540T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448651 | |||||||
| chr19:8448656 | T | C | 1 | a0001c0002t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.113+3545T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448656 | |||||||
| chr19:8448784 | C | T | 1 | a0004c0010t0001g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.113+3673C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448784 | |||||||
| chr19:8448918 | G | A | 20 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(17): Show |
20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.113+3807G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448918 | |||||||
| chr19:8448918 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.113+3807G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448918 | |||||||
| chr19:8448942 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.113+3831C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448942 | |||||||
| chr19:8449010 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.113+3899A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449010 | |||||||
| chr19:8449294 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(3): Show |
8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+4183G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449294 | |||||||
| chr19:8449313 | T | A | 4 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0320 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+4202T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449313 | |||||||
| chr19:8449509 | T | C | 1 | a0005c0016t0001g0098 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.113+4398T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449509 | |||||||
| chr19:8449526 | GCTAAGAG others(300): Show |
G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.113+4431_113+4737d others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8449526 | ||||||
| chr19:8449537 | C | CT | 19 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(16): Show |
19 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.113+4442dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8449537 | ||||||
| chr19:8449911 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.113+4800C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449911 | |||||||
| chr19:8449923 | C | A | 1 | a0001c0013t0001g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.113+4812C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449923 | |||||||
| chr19:8450105 | T | A | 1 | a0001c0001t0001g0034 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.113+4994T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450105 | |||||||
| chr19:8450182 | TTA | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+5076_113+5077d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450182 | ||||||
| chr19:8450276 | T | C | 2 | a0001c0008t0001g0027 a0001c0008t0001g0028 |
2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.114-5129T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450276 | |||||||
| chr19:8450400 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG00323.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.114-5005A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450400 | |||||||
| chr19:8450459 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.114-4946T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450459 | |||||||
| chr19:8450491 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.114-4914A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450491 | |||||||
| chr19:8450593 | T | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.114-4812T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450593 | |||||||
| chr19:8450689 | G | A | 1 | a0001c0002t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114-4716G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450689 | |||||||
| chr19:8450711 | A | AATT | 16 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 others(13): Show |
18 | HG00323.hp1 HG01109.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-4678_114-4676d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450711 | ||||||
| chr19:8450727 | A | AT | 12 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0069 others(9): Show |
12 | HG00438.hp1 HG03195.hp1 HG03490.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-4664dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450727 | ||||||
| chr19:8450727 | A | ATT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(20): Show |
25 | HG00741.hp1 HG01169.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.114-4665_114-4664d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450727 | ||||||
| chr19:8450727 | A | T | 2 | a0001c0001t0001g0222 a0001c0002t0001g0295 |
2 | HG02922.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.114-4678A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450727 | |||||||
| chr19:8450728 | T | TTA | 75 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(72): Show |
84 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.114-4676_114-4675i others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450728 | ||||||
| chr19:8450729 | T | TA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.114-4676_114-4675i others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450729 | |||||||
| chr19:8450729 | T | TATTA | 4 | a0001c0001t0001g0007 a0001c0008t0001g0027 a0001c0008t0001g0028 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-4676_114-4675i others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450729 | |||||||
| chr19:8450729 | T | TATTATTA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(80): Show |
93 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.114-4676_114-4675i others(9): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450729 | |||||||
| chr19:8450729 | T | TATTATTA others(3): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0144 |
3 | HG00639.hp2 NA19081.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.114-4676_114-4675i others(12): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450729 | |||||||
| chr19:8450730 | T | A | 26 | a0001c0001t0001g0035 a0001c0001t0001g0087 a0001c0001t0001g0088 others(23): Show |
26 | HG01109.hp2 HG01516.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.114-4675T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450730 | |||||||
| chr19:8450731 | T | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.114-4674T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450731 | |||||||
| chr19:8450732 | T | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
111 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.114-4673T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450732 | |||||||
| chr19:8450733 | T | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | HG02486.hp1 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.114-4672T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450733 | |||||||
| chr19:8450735 | T | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(87): Show |
102 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.114-4670T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450735 | |||||||
| chr19:8450744 | G | T | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0285 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-4661G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450744 | |||||||
| chr19:8450778 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.114-4627G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450778 | |||||||
| chr19:8450792 | T | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(106): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.114-4613T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450792 | |||||||
| chr19:8450855 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.114-4550G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450855 | |||||||
| chr19:8450891 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.114-4514G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450891 | |||||||
| chr19:8450928 | C | T | 1 | a0001c0003t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.114-4477C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450928 | |||||||
| chr19:8450932 | G | T | 1 | a0001c0001t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.114-4473G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450932 | |||||||
| chr19:8451095 | C | T | 2 | a0001c0001t0001g0079 a0003c0009t0001g0078 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.114-4310C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451095 | |||||||
| chr19:8451126 | C | T | 2 | a0001c0008t0001g0027 a0001c0008t0001g0028 |
2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.114-4279C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451126 | |||||||
| chr19:8451142 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.114-4263G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451142 | |||||||
| chr19:8451182 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.114-4223C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451182 | |||||||
| chr19:8451299 | C | T | 2 | a0001c0001t0001g0079 a0003c0009t0001g0078 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.114-4106C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451299 | |||||||
| chr19:8451394 | A | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.114-4011A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451394 | |||||||
| chr19:8451413 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.114-3992C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451413 | |||||||
| chr19:8451463 | T | TA | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-3935dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8451463 | ||||||
| chr19:8451527 | CTCCCCT | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(109): Show |
126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.114-3861_114-3856d others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8451527 | ||||||
| chr19:8451571 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.114-3834C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451571 | |||||||
| chr19:8451789 | C | T | 3 | a0001c0004t0001g0259 a0001c0004t0001g0260 a0001c0004t0001g0261 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114-3616C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451789 | |||||||
| chr19:8451793 | A | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.114-3612A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451793 | |||||||
| chr19:8451850 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.114-3555G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451850 | |||||||
| chr19:8451890 | A | G | 1 | a0001c0002t0001g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.114-3515A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451890 | |||||||
| chr19:8452130 | A | G | 20 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(17): Show |
20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-3275A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452130 | |||||||
| chr19:8452165 | A | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-3240A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452165 | |||||||
| chr19:8452274 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(98): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.114-3131C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452274 | |||||||
| chr19:8452327 | C | T | 1 | a0006c0015t0001g0070 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.114-3078C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452327 | |||||||
| chr19:8452328 | A | C | 1 | a0006c0015t0001g0070 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.114-3077A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452328 | |||||||
| chr19:8452429 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.114-2976G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452429 | |||||||
| chr19:8452502 | C | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.114-2903C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452502 | |||||||
| chr19:8452802 | G | A | 7 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.114-2603G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452802 | |||||||
| chr19:8452891 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-2514A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452891 | |||||||
| chr19:8452921 | A | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(106): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.114-2484A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452921 | |||||||
| chr19:8453376 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG01070.hp1 HG01978.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.114-2029A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453376 | |||||||
| chr19:8453500 | C | T | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-1905C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453500 | |||||||
| chr19:8453512 | A | G | 3 | a0001c0004t0001g0259 a0001c0004t0001g0260 a0001c0004t0001g0261 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114-1893A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453512 | |||||||
| chr19:8453531 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.114-1874G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453531 | |||||||
| chr19:8453588 | G | GT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0064 others(18): Show |
23 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.114-1809dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8453588 | ||||||
| chr19:8453660 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA18948.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.114-1745C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453660 | |||||||
| chr19:8453738 | T | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.114-1667T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453738 | |||||||
| chr19:8453774 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.114-1631C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453774 | |||||||
| chr19:8453994 | C | T | 1 | a0001c0002t0001g0296 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.114-1411C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453994 | |||||||
| chr19:8454016 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.114-1389C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454016 | |||||||
| chr19:8454080 | AT | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-1320delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454080 | ||||||
| chr19:8454082 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-1323T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454082 | |||||||
| chr19:8454102 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.114-1303A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454102 | |||||||
| chr19:8454135 | T | G | 1 | a0001c0001t0001g0178 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.114-1270T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454135 | |||||||
| chr19:8454164 | A | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-1241A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454164 | |||||||
| chr19:8454339 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.114-1066A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454339 | |||||||
| chr19:8454433 | AT | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0036 others(2): Show |
7 | HG01099.hp2 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.114-971delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454433 | |||||||
| chr19:8454492 | G | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.114-913G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454492 | |||||||
| chr19:8454557 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.114-848C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454557 | |||||||
| chr19:8454673 | G | GC | 91 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(88): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.114-721dupC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454673 | ||||||
| chr19:8454673 | G | GCC | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(44): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.114-722_114-721dup others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454673 | ||||||
| chr19:8454683 | C | CT | 4 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0006t0001g0265 others(1): Show |
5 | HG02717.hp1 HG02809.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-722_114-721ins others(1): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454683 | |||||||
| chr19:8454684 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(3): Show |
7 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.114-721C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454684 | |||||||
| chr19:8454684 | CT | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0089 others(6): Show |
9 | HG01074.hp1 HG02615.hp1 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-710delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454684 | ||||||
| chr19:8454684 | CTT | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(86): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.114-711_114-710del others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454684 | ||||||
| chr19:8454685 | T | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0194 a0001c0001t0001g0206 others(5): Show |
8 | HG00735.hp2 HG01106.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-720T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454685 | |||||||
| chr19:8454686 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0089 others(7): Show |
10 | HG01074.hp1 HG02615.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-719T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454686 | |||||||
| chr19:8454687 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.114-718T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454687 | |||||||
| chr19:8454743 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-662A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454743 | |||||||
| chr19:8454843 | G | C | 1 | a0001c0013t0001g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114-562G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454843 | |||||||
| chr19:8455004 | C | T | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0285 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-401C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455004 | |||||||
| chr19:8455021 | C | G | 1 | a0001c0002t0001g0316 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.114-384C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455021 | |||||||
| chr19:8455082 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.114-323C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455082 | |||||||
| chr19:8455106 | C | G | 1 | a0004c0010t0001g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.114-299C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455106 | |||||||
| chr19:8455153 | T | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(100): Show |
115 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.114-252T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455153 | |||||||
| chr19:8455156 | T | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.114-249T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455156 | |||||||
| chr19:8455165 | T | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.114-240T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455165 | |||||||
| chr19:8455217 | A | G | 1 | a0001c0007t0001g0149 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.114-188A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455217 | |||||||
| chr19:8455298 | A | C | 1 | a0001c0002t0001g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.114-107A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455298 | |||||||
| chr19:8455361 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.114-44G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455361 | |||||||
| chr19:8455661 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.283+87A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8455661 | |||||||
| chr19:8455725 | G | GT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0085 others(4): Show |
8 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+163dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455725 | ||||||
| chr19:8455745 | G | GT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(91): Show |
107 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+181dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455745 | ||||||
| chr19:8455746 | TTTTTTTT others(3): Show |
T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG01109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.283+177_283+186del others(10): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455746 | ||||||
| chr19:8455750 | T | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.283+176T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8455750 | |||||||
| chr19:8455751 | T | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0277 others(4): Show |
9 | HG00323.hp1 HG02055.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+177T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8455751 | |||||||
| chr19:8455944 | C | CT | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.283+386dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455944 | ||||||
| chr19:8455944 | C | CTT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0102 others(17): Show |
22 | HG01109.hp2 HG01169.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.283+385_283+386dup others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455944 | ||||||
| chr19:8455944 | C | CTTT | 61 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(58): Show |
71 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.283+384_283+386dup others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455944 | ||||||
| chr19:8456203 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+629A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456203 | |||||||
| chr19:8456296 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.283+722C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456296 | |||||||
| chr19:8456316 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.283+742C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456316 | |||||||
| chr19:8456338 | G | A | 1 | a0001c0002t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.283+764G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456338 | |||||||
| chr19:8456474 | C | T | 7 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+900C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456474 | |||||||
| chr19:8456651 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.283+1077C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456651 | |||||||
| chr19:8456932 | A | G | 1 | a0001c0002t0001g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.283+1358A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456932 | |||||||
| chr19:8457214 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.283+1640G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8457214 | |||||||
| chr19:8457705 | A | G | 1 | a0001c0002t0001g0302 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283+2131A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8457705 | |||||||
| chr19:8457994 | G | T | 1 | a0001c0002t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.283+2420G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8457994 | |||||||
| chr19:8458119 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.283+2545T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458119 | |||||||
| chr19:8458122 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(83): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.283+2548T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458122 | |||||||
| chr19:8458132 | T | C | 1 | a0001c0002t0001g0296 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283+2558T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458132 | |||||||
| chr19:8458137 | C | CG | 16 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(13): Show |
16 | HG01168.hp2 HG01934.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+2569dupG | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8458137 | ||||||
| chr19:8458138 | G | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG02559.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+2564G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458138 | |||||||
| chr19:8458242 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0106 a0001c0001t0001g0159 |
4 | HG03017.hp2 HG04184.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+2668T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458242 | |||||||
| chr19:8458266 | A | C | 2 | a0001c0002t0001g0305 a0001c0002t0001g0306 |
2 | HG02135.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.283+2692A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458266 | |||||||
| chr19:8458324 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+2750C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458324 | |||||||
| chr19:8458325 | C | G | 1 | a0001c0001t0001g0234 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.283+2751C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458325 | |||||||
| chr19:8458529 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.283+2955C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458529 | |||||||
| chr19:8458728 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.283+3154C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458728 | |||||||
| chr19:8458749 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.283+3175A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458749 | |||||||
| chr19:8458963 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG00323.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.283+3389G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458963 | |||||||
| chr19:8459085 | C | A | 1 | a0001c0001t0001g0021 | 2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.284-3444C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459085 | |||||||
| chr19:8459085 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-3444C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459085 | |||||||
| chr19:8459118 | G | A | 7 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-3411G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459118 | |||||||
| chr19:8459265 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-3264T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459265 | |||||||
| chr19:8459270 | A | G | 5 | a0001c0001t0001g0223 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | NA18957.hp1 NA18975.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-3259A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459270 | |||||||
| chr19:8459308 | C | T | 1 | a0001c0002t0001g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.284-3221C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459308 | |||||||
| chr19:8459368 | C | CGTG | 3 | a0001c0002t0001g0024 a0001c0002t0001g0288 a0001c0002t0001g0289 |
4 | HG02809.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-3159_284-3157d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8459368 | ||||||
| chr19:8459384 | T | C | 1 | a0002c0012t0001g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.284-3145T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459384 | |||||||
| chr19:8459571 | A | G | 1 | a0001c0005t0001g0068 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.284-2958A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459571 | |||||||
| chr19:8459690 | A | G | 1 | a0001c0002t0001g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.284-2839A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459690 | |||||||
| chr19:8459717 | G | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-2812G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459717 | |||||||
| chr19:8459754 | G | A | 4 | a0001c0005t0001g0063 a0001c0005t0001g0066 a0001c0005t0001g0068 others(1): Show |
4 | NA18985.hp2 NA19000.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-2775G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459754 | |||||||
| chr19:8459801 | T | G | 8 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0165 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-2728T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459801 | |||||||
| chr19:8459842 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.284-2687T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459842 | |||||||
| chr19:8459877 | A | G | 1 | a0001c0001t0001g0007 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.284-2652A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459877 | |||||||
| chr19:8459970 | A | C | 1 | a0001c0013t0001g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.284-2559A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459970 | |||||||
| chr19:8460088 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.284-2441T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460088 | |||||||
| chr19:8460420 | T | C | 4 | a0001c0003t0001g0020 a0001c0003t0001g0251 a0001c0003t0001g0252 others(1): Show |
5 | HG00544.hp1 HG00673.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-2109T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460420 | |||||||
| chr19:8460550 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | HG02486.hp1 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-1979C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460550 | |||||||
| chr19:8460711 | C | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.284-1818C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460711 | |||||||
| chr19:8460756 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0054 others(2): Show |
6 | HG00733.hp1 HG00741.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-1773G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460756 | |||||||
| chr19:8460844 | CTA | C | 4 | a0001c0002t0001g0303 a0001c0002t0001g0304 a0001c0002t0001g0305 others(1): Show |
4 | HG02135.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-1683_284-1682d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8460844 | ||||||
| chr19:8460864 | AGTG | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG01074.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.284-1663_284-1661d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8460864 | ||||||
| chr19:8460953 | G | A | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-1576G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460953 | |||||||
| chr19:8460967 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.284-1562T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460967 | |||||||
| chr19:8460987 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.284-1542G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460987 | |||||||
| chr19:8460994 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-1535A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460994 | |||||||
| chr19:8461103 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-1426G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461103 | |||||||
| chr19:8461113 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.284-1416C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461113 | |||||||
| chr19:8461178 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.284-1351C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461178 | |||||||
| chr19:8461245 | G | A | 3 | a0001c0004t0001g0259 a0001c0004t0001g0260 a0001c0004t0001g0261 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.284-1284G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461245 | |||||||
| chr19:8461253 | G | C | 10 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
10 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-1276G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461253 | |||||||
| chr19:8461561 | C | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.284-968C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461561 | |||||||
| chr19:8461575 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-954T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461575 | |||||||
| chr19:8461752 | AAGCGGC | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.284-775_284-770del others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8461752 | ||||||
| chr19:8461830 | C | G | 4 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0320 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-699C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461830 | |||||||
| chr19:8461938 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0054 others(2): Show |
6 | HG00733.hp1 HG00741.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-591A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461938 | |||||||
| chr19:8462020 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-509G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8462020 | |||||||
| chr19:8463036 | T | C | 1 | a0001c0002t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.336+455T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463036 | |||||||
| chr19:8463171 | G | A | 1 | a0001c0002t0001g0313 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.337-326G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463171 | |||||||
| chr19:8463393 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(83): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.337-104A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463393 | |||||||
| chr19:8463420 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.337-77T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463420 | |||||||
| chr19:8463426 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.337-71A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463426 | |||||||
| chr19:8463755 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.438+69A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8463755 | |||||||
| chr19:8463950 | C | G | 1 | a0001c0008t0001g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.438+264C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8463950 | |||||||
| chr19:8464054 | G | T | 2 | a0001c0002t0001g0293 a0001c0002t0001g0294 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.438+368G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464054 | |||||||
| chr19:8464090 | C | G | 1 | a0001c0001t0001g0277 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.438+404C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464090 | |||||||
| chr19:8464219 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.438+533C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464219 | |||||||
| chr19:8464228 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0107 |
2 | HG02615.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.438+542G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464228 | |||||||
| chr19:8464248 | TA | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.438+569delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr19 | 8464248 | ||||||
| chr19:8464316 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.438+630C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464316 | |||||||
| chr19:8464349 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0099 |
2 | NA18951.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.438+663C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464349 | |||||||
| chr19:8464362 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | NA19004.hp2 NA19086.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.438+676C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464362 | |||||||
| chr19:8464524 | C | T | 1 | a0001c0002t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.439-800C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464524 | |||||||
| chr19:8464563 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(54): Show |
67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.439-761C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464563 | |||||||
| chr19:8464574 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.439-750G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464574 | |||||||
| chr19:8464618 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.439-706G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464618 | |||||||
| chr19:8464686 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.439-638A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464686 | |||||||
| chr19:8464822 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.439-502G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464822 | |||||||
| chr19:8464880 | G | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0036 others(2): Show |
7 | HG01099.hp2 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.439-444G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464880 | |||||||
| chr19:8464912 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | HG02486.hp1 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.439-412T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464912 | |||||||
| chr19:8464959 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(3): Show |
8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.439-365C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464959 | |||||||
| chr19:8465003 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(83): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.439-321A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465003 | |||||||
| chr19:8465072 | C | T | 3 | a0001c0004t0001g0259 a0001c0004t0001g0260 a0001c0004t0001g0261 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.439-252C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465072 | |||||||
| chr19:8465165 | C | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.439-159C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465165 | |||||||
| chr19:8465189 | T | C | 16 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(13): Show |
16 | HG01168.hp2 HG01934.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.439-135T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465189 | |||||||
| chr19:8465207 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.439-117G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465207 | |||||||
| chr19:8465246 | A | C | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.439-78A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465246 | |||||||
| chr19:8465701 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.630+186C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465701 | |||||||
| chr19:8465701 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.630+186C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465701 | |||||||
| chr19:8465747 | G | A | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.630+232G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465747 | |||||||
| chr19:8465813 | T | C | 20 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(17): Show |
20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.630+298T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465813 | |||||||
| chr19:8465817 | C | T | 5 | a0001c0002t0001g0311 a0001c0002t0001g0312 a0001c0002t0001g0315 others(2): Show |
5 | HG01934.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+302C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465817 | |||||||
| chr19:8465945 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.631-290C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465945 | |||||||
| chr19:8465999 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.631-236A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465999 | |||||||
| chr19:8466472 | G | GACTGTGT others(6): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0049 a0001c0001t0001g0056 |
4 | HG01071.hp2 HG01256.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+86_784+98dupCT others(11): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466472 | ||||||
| chr19:8466594 | A | G | 1 | a0001c0002t0001g0305 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.784+206A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8466594 | |||||||
| chr19:8466828 | C | CA | 6 | a0001c0001t0001g0007 a0001c0001t0001g0271 a0001c0001t0001g0299 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+464dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | C | CAA | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
56 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.784+463_784+464dup others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | C | CAAA | 56 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(53): Show |
59 | HG00423.hp1 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.784+462_784+464dup others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | C | CAAAA | 12 | a0001c0001t0001g0075 a0001c0001t0001g0140 a0001c0001t0001g0141 others(9): Show |
12 | HG01070.hp1 HG01175.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.784+461_784+464dup others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | C | CAAAAA | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(46): Show |
59 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.784+460_784+464dup others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | C | CAAAAAA | 24 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0111 others(21): Show |
25 | HG00438.hp2 HG01081.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.784+459_784+464dup others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | C | CAAAAAAA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
7 | HG01106.hp1 HG01192.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.784+458_784+464dup others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | CA | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0057 others(14): Show |
17 | HG00280.hp1 HG01192.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.784+464delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | CAA | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.784+463_784+464del others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466828 | CAAA | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(7): Show |
10 | HG00323.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+462_784+464del others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | ||||||
| chr19:8466890 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784+502A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8466890 | |||||||
| chr19:8466917 | T | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.784+529T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8466917 | |||||||
| chr19:8466983 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.785-552G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8466983 | |||||||
| chr19:8467076 | GA | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(105): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.785-457delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8467076 | ||||||
| chr19:8467088 | TCTC | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.785-444_785-442del others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8467088 | ||||||
| chr19:8467335 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(105): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.785-200G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8467335 | |||||||
| chr19:8467356 | G | A | 3 | a0001c0004t0001g0259 a0001c0004t0001g0260 a0001c0004t0001g0261 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.785-179G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8467356 | |||||||
| chr19:8467390 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.785-145G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8467390 | |||||||
| chr19:8467603 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.834+19T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467603 | |||||||
| chr19:8467634 | A | G | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0285 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+50A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467634 | |||||||
| chr19:8467817 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(105): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.834+233C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467817 | |||||||
| chr19:8467823 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(66): Show |
80 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.834+239G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467823 | |||||||
| chr19:8467830 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.834+246G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467830 | |||||||
| chr19:8467885 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.834+301G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467885 | |||||||
| chr19:8467982 | G | A | 3 | a0001c0004t0001g0259 a0001c0004t0001g0260 a0001c0004t0001g0261 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.834+398G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467982 | |||||||
| chr19:8468021 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.834+437T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468021 | |||||||
| chr19:8468029 | G | GA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0266 others(4): Show |
9 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.834+454dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr19 | 8468029 | ||||||
| chr19:8468214 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(83): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.835-560A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468214 | |||||||
| chr19:8468320 | C | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG00323.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.835-454C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468320 | |||||||
| chr19:8468482 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.835-292C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468482 | |||||||
| chr19:8468484 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.835-290C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468484 | |||||||
| chr19:8468620 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.835-154T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468620 | |||||||
| chr19:8468621 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.835-153G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468621 | |||||||
| chr19:8468625 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(105): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.835-149C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468625 | |||||||
| chr19:8468881 | C | A | 7 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.895+47C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8468881 | |||||||
| chr19:8468932 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.895+98G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8468932 | |||||||
| chr19:8469041 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.895+207A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469041 | |||||||
| chr19:8469098 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.895+264G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469098 | |||||||
| chr19:8469221 | G | A | 1 | a0001c0002t0001g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.895+387G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469221 | |||||||
| chr19:8469567 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.895+733G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469567 | |||||||
| chr19:8469632 | A | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(83): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.895+798A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469632 | |||||||
| chr19:8469677 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(83): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.895+843G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469677 | |||||||
| chr19:8469742 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.895+908G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469742 | |||||||
| chr19:8469794 | G | A | 45 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(42): Show |
49 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.895+960G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469794 | |||||||
| chr19:8469813 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.895+979C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469813 | |||||||
| chr19:8469970 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.895+1136A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469970 | |||||||
| chr19:8470168 | A | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.896-1158A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470168 | |||||||
| chr19:8470204 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.896-1122C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470204 | |||||||
| chr19:8470230 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.896-1096A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470230 | |||||||
| chr19:8470461 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.896-865G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470461 | |||||||
| chr19:8470495 | T | G | 19 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(16): Show |
19 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.896-831T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470495 | |||||||
| chr19:8470497 | T | TG | 6 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(3): Show |
8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.896-829_896-828ins others(1): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470497 | |||||||
| chr19:8470498 | T | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.896-828T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470498 | |||||||
| chr19:8470514 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.896-812G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470514 | |||||||
| chr19:8470731 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.896-595G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470731 | |||||||
| chr19:8470959 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG01070.hp1 HG01978.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.896-367C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470959 | |||||||
| chr19:8471100 | T | G | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.896-226T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8471100 | |||||||
| chr19:8471154 | C | T | 1 | a0001c0002t0001g0316 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.896-172C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8471154 | |||||||
| chr19:8471259 | CTT | C | 3 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0013t0001g0026 |
4 | HG02257.hp1 HG02976.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.896-64_896-63delTT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 8471259 | ||||||
| chr19:8471306 | T | G | 5 | a0001c0001t0001g0008 a0001c0002t0001g0303 a0001c0002t0001g0304 others(2): Show |
6 | HG01099.hp2 HG01261.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.896-20T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8471306 | |||||||
| chr19:8471489 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.997+62A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471489 | |||||||
| chr19:8471536 | C | A | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.997+109C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471536 | |||||||
| chr19:8471616 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.997+189T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471616 | |||||||
| chr19:8471648 | G | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.997+221G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471648 | |||||||
| chr19:8471704 | G | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0177 a0001c0001t0001g0180 others(4): Show |
8 | HG00423.hp1 HG01943.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.997+277G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471704 | |||||||
| chr19:8471870 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.997+443T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471870 | |||||||
| chr19:8472028 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.997+601G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472028 | |||||||
| chr19:8472039 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.997+612C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472039 | |||||||
| chr19:8472087 | C | G | 1 | a0001c0004t0001g0261 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.997+660C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472087 | |||||||
| chr19:8472090 | G | A | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.997+663G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472090 | |||||||
| chr19:8472172 | G | GA | 13 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0001g0081 others(10): Show |
13 | HG01109.hp2 HG01891.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.997+765dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 8472172 | ||||||
| chr19:8472172 | GA | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(92): Show |
107 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.997+765delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 8472172 | ||||||
| chr19:8472173 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0035 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.997+746A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472173 | |||||||
| chr19:8472205 | CTTTGATG others(3): Show |
C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0051 |
2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.997+779_997+788del others(10): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472205 | |||||||
| chr19:8472212 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.997+785G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472212 | |||||||
| chr19:8472212 | G | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(83): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.997+785G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472212 | |||||||
| chr19:8472229 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0051 |
2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.997+802G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472229 | |||||||
| chr19:8472481 | A | G | 20 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(17): Show |
20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.997+1054A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472481 | |||||||
| chr19:8472599 | A | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG01109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.998-1065A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472599 | |||||||
| chr19:8472782 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.998-882A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472782 | |||||||
| chr19:8473005 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.998-659G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473005 | |||||||
| chr19:8473239 | T | C | 23 | a0001c0001t0001g0017 a0001c0001t0001g0182 a0001c0001t0001g0183 others(20): Show |
24 | HG02071.hp2 HG02074.hp2 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.998-425T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473239 | |||||||
| chr19:8473243 | A | C | 1 | a0001c0002t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.998-421A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473243 | |||||||
| chr19:8473302 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.998-362C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473302 | |||||||
| chr19:8473385 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.998-279C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473385 | |||||||
| chr19:8473459 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.998-205T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473459 | |||||||
| chr19:8473459 | TA | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
13 | HG00733.hp2 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.998-191delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 8473459 | ||||||
| chr19:8473465 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.998-199A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473465 | |||||||
| chr19:8473592 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.998-72A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473592 | |||||||
| chr19:8473614 | A | G | 10 | a0001c0001t0001g0006 a0001c0001t0001g0174 a0001c0001t0001g0266 others(7): Show |
12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.998-50A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473614 | |||||||
| chr19:8473766 | T | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0165 a0001c0001t0001g0183 others(4): Show |
8 | HG03209.hp2 NA18947.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.1042+58T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8473766 | |||||||
| chr19:8473783 | G | C | 4 | a0001c0003t0001g0020 a0001c0003t0001g0251 a0001c0003t0001g0252 others(1): Show |
5 | HG00544.hp1 HG00673.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042+75G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8473783 | |||||||
| chr19:8474002 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0121 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1043-165T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8474002 | |||||||
| chr19:8474052 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0122 |
2 | HG01934.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1043-115T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8474052 | |||||||
| chr19:8474111 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1043-56C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8474111 | |||||||
| chr19:8474529 | A | C | 1 | a0001c0013t0001g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1120+285A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474529 | |||||||
| chr19:8474567 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1120+323C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474567 | |||||||
| chr19:8474593 | C | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+349C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474593 | |||||||
| chr19:8474609 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120+365A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474609 | |||||||
| chr19:8474661 | T | C | 16 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(13): Show |
16 | HG01168.hp2 HG01934.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1120+417T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474661 | |||||||
| chr19:8474714 | C | CT | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG02451.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+488dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8474714 | ||||||
| chr19:8474714 | CT | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1120+488delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8474714 | ||||||
| chr19:8474714 | CTT | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0151 others(5): Show |
9 | HG01070.hp1 HG01169.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120+487_1120+488d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8474714 | ||||||
| chr19:8474778 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1120+534G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474778 | |||||||
| chr19:8474800 | C | T | 2 | a0001c0008t0001g0027 a0001c0008t0001g0028 |
2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1120+556C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474800 | |||||||
| chr19:8474828 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1120+584C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474828 | |||||||
| chr19:8474911 | C | A | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1120+667C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474911 | |||||||
| chr19:8474935 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+691G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474935 | |||||||
| chr19:8475015 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1120+771C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475015 | |||||||
| chr19:8475275 | GC | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(90): Show |
106 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1120+1034delC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475275 | ||||||
| chr19:8475321 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1120+1077A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475321 | |||||||
| chr19:8475347 | G | A | 1 | a0001c0004t0001g0261 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1120+1103G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475347 | |||||||
| chr19:8475376 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1120+1132T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475376 | |||||||
| chr19:8475511 | C | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+1267C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475511 | |||||||
| chr19:8475515 | C | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0174 a0001c0001t0001g0266 others(7): Show |
12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120+1271C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475515 | |||||||
| chr19:8475540 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0144 |
3 | HG00639.hp2 HG00673.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1120+1296T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475540 | |||||||
| chr19:8475555 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(3): Show |
8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+1311G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475555 | |||||||
| chr19:8475569 | A | G | 1 | a0001c0002t0001g0318 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1120+1325A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475569 | |||||||
| chr19:8475577 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+1333A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475577 | |||||||
| chr19:8475662 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1120+1418C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475662 | |||||||
| chr19:8475905 | CT | C | 18 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0079 others(15): Show |
18 | HG01928.hp2 HG02080.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1120+1685delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475905 | ||||||
| chr19:8475905 | CTT | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1120+1684_1120+168 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475905 | ||||||
| chr19:8475905 | CTTT | C | 36 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0015 others(33): Show |
41 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1120+1683_1120+168 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475905 | ||||||
| chr19:8475905 | CTTTT | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(63): Show |
77 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1120+1682_1120+168 others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475905 | ||||||
| chr19:8475909 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1120+1665T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475909 | |||||||
| chr19:8475910 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(5): Show |
10 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120+1666T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475910 | |||||||
| chr19:8475911 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1120+1667T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475911 | |||||||
| chr19:8475931 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1120+1687A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475931 | |||||||
| chr19:8475955 | T | TTGAGTTG others(6): Show |
2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1120+1716_1120+172 others(17): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475955 | ||||||
| chr19:8476063 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1120+1819C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476063 | |||||||
| chr19:8476198 | C | T | 1 | a0001c0002t0001g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1120+1954C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476198 | |||||||
| chr19:8476219 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1120+1975C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476219 | |||||||
| chr19:8476249 | C | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+2005C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476249 | |||||||
| chr19:8476379 | C | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120+2135C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476379 | |||||||
| chr19:8476434 | G | C | 1 | a0001c0002t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1120+2190G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476434 | |||||||
| chr19:8476523 | G | A | 3 | a0001c0004t0001g0259 a0001c0004t0001g0260 a0001c0004t0001g0261 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1120+2279G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476523 | |||||||
| chr19:8476566 | T | TAA | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120+2334_1120+233 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8476566 | ||||||
| chr19:8476576 | AAAAG | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(74): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1120+2334_1120+233 others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8476576 | ||||||
| chr19:8476577 | AAAG | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(102): Show |
118 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1120+2335_1120+233 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8476577 | ||||||
| chr19:8476578 | AAG | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(80): Show |
94 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1120+2340_1120+234 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8476578 | ||||||
| chr19:8476579 | AG | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0125 a0001c0001t0001g0161 others(1): Show |
4 | NA18984.hp2 NA18998.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+2336delG | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476579 | |||||||
| chr19:8476867 | C | T | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+2623C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476867 | |||||||
| chr19:8476906 | G | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1120+2662G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476906 | |||||||
| chr19:8477049 | A | G | 2 | a0001c0003t0001g0117 a0001c0003t0001g0139 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1120+2805A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477049 | |||||||
| chr19:8477121 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1120+2877A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477121 | |||||||
| chr19:8477213 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(7): Show |
12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120+2969C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477213 | |||||||
| chr19:8477295 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1120+3051G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477295 | |||||||
| chr19:8477456 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1120+3212A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477456 | |||||||
| chr19:8477537 | A | C | 4 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0320 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+3293A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477537 | |||||||
| chr19:8477562 | G | T | 2 | a0001c0008t0001g0027 a0001c0008t0001g0028 |
2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1120+3318G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477562 | |||||||
| chr19:8477660 | CAAAA | C | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0307 others(4): Show |
7 | HG01934.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120+3446_1120+344 others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | ||||||
| chr19:8477660 | CAAAAA | C | 10 | a0001c0001t0001g0299 a0001c0002t0001g0301 a0001c0002t0001g0302 others(7): Show |
10 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120+3445_1120+344 others(9): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | ||||||
| chr19:8477660 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0007 a0001c0002t0001g0306 |
3 | HG02135.hp2 HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1120+3438_1120+344 others(16): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | ||||||
| chr19:8477660 | CAAAAAAA others(6): Show |
C | 2 | a0001c0008t0001g0027 a0001c0008t0001g0028 |
2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1120+3437_1120+344 others(17): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | ||||||
| chr19:8477660 | CAAAAAAA others(7): Show |
C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0152 others(13): Show |
18 | HG00323.hp1 HG01109.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1120+3436_1120+344 others(18): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | ||||||
| chr19:8477660 | CAAAAAAA others(8): Show |
C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(188): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1120+3435_1120+344 others(19): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | ||||||
| chr19:8477660 | CAAAAAAA others(9): Show |
C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1120+3434_1120+344 others(20): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | ||||||
| chr19:8477660 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0281 |
2 | HG02647.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1120+3433_1120+344 others(21): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | ||||||
| chr19:8477673 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1120+3434_1120+346 others(33): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477673 | ||||||
| chr19:8477733 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0165 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+3489G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477733 | |||||||
| chr19:8477790 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0165 a0001c0001t0001g0167 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+3546C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477790 | |||||||
| chr19:8477853 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1120+3609C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477853 | |||||||
| chr19:8477949 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1120+3705A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477949 | |||||||
| chr19:8478077 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1120+3833C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478077 | |||||||
| chr19:8478155 | G | T | 1 | a0001c0008t0001g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1120+3911G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478155 | |||||||
| chr19:8478609 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120+4365A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478609 | |||||||
| chr19:8478722 | A | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-4436A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478722 | |||||||
| chr19:8478776 | G | C | 1 | a0002c0012t0001g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1121-4382G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478776 | |||||||
| chr19:8478789 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1121-4369G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478789 | |||||||
| chr19:8478829 | C | T | 15 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(12): Show |
15 | HG01168.hp2 HG01934.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1121-4329C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478829 | |||||||
| chr19:8478950 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-4208T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478950 | |||||||
| chr19:8478955 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-4203C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478955 | |||||||
| chr19:8478965 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0121 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1121-4193G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478965 | |||||||
| chr19:8479016 | G | T | 7 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121-4142G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479016 | |||||||
| chr19:8479022 | A | AT | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0285 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-4130dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479022 | ||||||
| chr19:8479037 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1121-4121G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479037 | |||||||
| chr19:8479078 | C | CT | 19 | a0001c0001t0001g0039 a0001c0001t0001g0072 a0001c0001t0001g0077 others(16): Show |
19 | HG01169.hp2 HG02080.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121-4056dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | ||||||
| chr19:8479078 | C | CTT | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1121-4057_1121-405 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | ||||||
| chr19:8479078 | C | CTTT | 29 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0033 others(26): Show |
31 | HG00423.hp1 HG00423.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1121-4058_1121-405 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | ||||||
| chr19:8479078 | C | CTTTT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0181 others(4): Show |
7 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121-4059_1121-405 others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | ||||||
| chr19:8479078 | CT | C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0160 a0001c0002t0001g0292 others(3): Show |
6 | HG02135.hp1 HG03041.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-4056delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | ||||||
| chr19:8479078 | CTTTTTT | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-4061_1121-405 others(10): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | ||||||
| chr19:8479078 | CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-4065_1121-405 others(14): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | ||||||
| chr19:8479096 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1121-4062T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479096 | |||||||
| chr19:8479096 | T | TTTC | 72 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(69): Show |
82 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1121-4060_1121-405 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479096 | ||||||
| chr19:8479102 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-4056T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479102 | |||||||
| chr19:8479142 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1121-4016A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479142 | |||||||
| chr19:8479168 | C | T | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0285 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-3990C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479168 | |||||||
| chr19:8479178 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1121-3980C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479178 | |||||||
| chr19:8479205 | A | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1121-3953A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479205 | |||||||
| chr19:8479521 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1121-3637C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479521 | |||||||
| chr19:8479646 | G | A | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-3512G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479646 | |||||||
| chr19:8479671 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1121-3487T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479671 | |||||||
| chr19:8479686 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1121-3472C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479686 | |||||||
| chr19:8479719 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1121-3439T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479719 | |||||||
| chr19:8479743 | C | G | 2 | a0001c0008t0001g0027 a0001c0008t0001g0028 |
2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1121-3415C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479743 | |||||||
| chr19:8479755 | TA | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0069 others(12): Show |
18 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1121-3386delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479755 | ||||||
| chr19:8479770 | AAAT | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG01975.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1121-3387_1121-338 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479770 | |||||||
| chr19:8479771 | A | AT | 8 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0043 others(5): Show |
8 | HG01169.hp2 HG01928.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121-3387_1121-338 others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479771 | |||||||
| chr19:8479771 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1121-3387A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479771 | |||||||
| chr19:8479771 | AAT | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0076 a0001c0001t0001g0083 others(9): Show |
12 | HG01981.hp1 HG02723.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121-3386_1121-338 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479771 | |||||||
| chr19:8479771 | AATT | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(173): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1121-3386_1121-338 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479771 | |||||||
| chr19:8479772 | A | AAT | 17 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(14): Show |
17 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.1121-3386_1121-338 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479772 | |||||||
| chr19:8479772 | A | AT | 9 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0002t0001g0283 others(6): Show |
9 | HG00741.hp2 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1121-3366dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479772 | ||||||
| chr19:8479772 | A | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(47): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1121-3386A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479772 | |||||||
| chr19:8479772 | ATT | A | 8 | a0001c0001t0001g0079 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG00438.hp2 HG01943.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121-3367_1121-336 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479772 | ||||||
| chr19:8479811 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
133 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1121-3347A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479811 | |||||||
| chr19:8479935 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1121-3223C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479935 | |||||||
| chr19:8480132 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1121-3026C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480132 | |||||||
| chr19:8480232 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1121-2926C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480232 | |||||||
| chr19:8480343 | C | CA | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1121-2798dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8480343 | ||||||
| chr19:8480343 | C | CAA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0082 others(4): Show |
8 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121-2799_1121-279 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8480343 | ||||||
| chr19:8480344 | A | C | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-2814A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480344 | |||||||
| chr19:8480518 | T | G | 2 | a0001c0001t0001g0234 a0001c0003t0001g0252 |
2 | HG00673.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1121-2640T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480518 | |||||||
| chr19:8480527 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0143 |
2 | HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1121-2631C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480527 | |||||||
| chr19:8480576 | T | C | 1 | a0004c0010t0001g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1121-2582T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480576 | |||||||
| chr19:8480627 | C | T | 19 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(16): Show |
19 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1121-2531C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480627 | |||||||
| chr19:8480875 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1121-2283C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480875 | |||||||
| chr19:8480965 | A | G | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-2193A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480965 | |||||||
| chr19:8481114 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1121-2044C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481114 | |||||||
| chr19:8481133 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1121-2025T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481133 | |||||||
| chr19:8481230 | G | A | 1 | a0001c0003t0001g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1121-1928G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481230 | |||||||
| chr19:8481241 | T | C | 19 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(16): Show |
19 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1121-1917T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481241 | |||||||
| chr19:8481254 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(67): Show |
81 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1121-1904C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481254 | |||||||
| chr19:8481380 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1121-1778G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481380 | |||||||
| chr19:8481390 | C | T | 7 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121-1768C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481390 | |||||||
| chr19:8481397 | C | T | 5 | a0001c0003t0001g0154 a0001c0003t0001g0155 a0001c0003t0001g0156 others(2): Show |
5 | HG01081.hp1 HG01243.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121-1761C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481397 | |||||||
| chr19:8481400 | C | T | 1 | a0001c0002t0001g0284 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1121-1758C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481400 | |||||||
| chr19:8481410 | A | G | 3 | a0001c0001t0001g0007 a0001c0008t0001g0027 a0001c0008t0001g0028 |
4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121-1748A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481410 | |||||||
| chr19:8481423 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1121-1735G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481423 | |||||||
| chr19:8481500 | GC | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(98): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1121-1656delC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481500 | ||||||
| chr19:8481516 | C | G | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-1642C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481516 | |||||||
| chr19:8481587 | G | A | 3 | a0001c0001t0001g0007 a0001c0008t0001g0027 a0001c0008t0001g0028 |
4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121-1571G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481587 | |||||||
| chr19:8481943 | TTTG | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-1200_1121-119 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481943 | ||||||
| chr19:8481967 | C | CT | 6 | a0001c0001t0001g0286 a0001c0002t0001g0024 a0001c0002t0001g0288 others(3): Show |
7 | HG02109.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121-1170dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481967 | ||||||
| chr19:8481967 | CT | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(65): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1121-1170delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481967 | ||||||
| chr19:8481967 | CTT | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(132): Show |
149 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1121-1171_1121-117 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481967 | ||||||
| chr19:8481967 | CTTT | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(82): Show |
97 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1121-1172_1121-117 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481967 | ||||||
| chr19:8482036 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(97): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1121-1122G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482036 | |||||||
| chr19:8482041 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1121-1117C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482041 | |||||||
| chr19:8482068 | G | C | 1 | a0001c0003t0001g0138 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1121-1090G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482068 | |||||||
| chr19:8482129 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0127 a0001c0001t0001g0253 others(1): Show |
6 | NA18961.hp2 NA18963.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-1029T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482129 | |||||||
| chr19:8482138 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1121-1020A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482138 | |||||||
| chr19:8482165 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-993A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482165 | |||||||
| chr19:8482217 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1121-941A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482217 | |||||||
| chr19:8482255 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-903G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482255 | |||||||
| chr19:8482296 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1121-862C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482296 | |||||||
| chr19:8482309 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-849G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482309 | |||||||
| chr19:8482353 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1121-805C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482353 | |||||||
| chr19:8482377 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-781A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482377 | |||||||
| chr19:8482573 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1121-585A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482573 | |||||||
| chr19:8482689 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1121-469T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482689 | |||||||
| chr19:8482906 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0093 others(9): Show |
15 | HG02071.hp1 HG02135.hp1 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.1121-252G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482906 | |||||||
| chr19:8483036 | AC | A | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0285 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-118delC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8483036 | ||||||
| chr19:8483135 | T | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121-23T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8483135 | |||||||
| chr19:8483238 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1174+27G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483238 | |||||||
| chr19:8483251 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1174+40A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483251 | |||||||
| chr19:8483291 | A | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1174+80A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483291 | |||||||
| chr19:8483295 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1174+84C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483295 | |||||||
| chr19:8483565 | A | G | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1174+354A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483565 | |||||||
| chr19:8483613 | A | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1174+402A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483613 | |||||||
| chr19:8483618 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1174+407T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483618 | |||||||
| chr19:8483657 | A | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0071 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1174+446A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483657 | |||||||
| chr19:8483705 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1174+494G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483705 | |||||||
| chr19:8483845 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+634G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483845 | |||||||
| chr19:8483854 | T | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(49): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1174+643T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483854 | |||||||
| chr19:8483870 | A | G | 1 | a0001c0014t0001g0310 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1174+659A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483870 | |||||||
| chr19:8483991 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1174+780C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483991 | |||||||
| chr19:8484011 | G | A | 1 | a0001c0004t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1174+800G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484011 | |||||||
| chr19:8484173 | C | CT | 12 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0150 others(9): Show |
12 | HG02080.hp1 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1174+981dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 8484173 | ||||||
| chr19:8484173 | CT | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1174+981delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 8484173 | ||||||
| chr19:8484173 | CTT | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0193 a0001c0001t0001g0200 others(5): Show |
8 | HG01169.hp2 HG02071.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174+980_1174+981d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 8484173 | ||||||
| chr19:8484173 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+972_1174+981d others(12): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 8484173 | ||||||
| chr19:8484177 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(6): Show |
11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1174+966T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484177 | |||||||
| chr19:8484193 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1174+982G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484193 | |||||||
| chr19:8484200 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1174+989G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484200 | |||||||
| chr19:8484240 | G | A | 6 | a0001c0001t0001g0075 a0001c0001t0001g0141 a0001c0001t0001g0145 others(3): Show |
6 | HG02080.hp1 NA18971.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+1029G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484240 | |||||||
| chr19:8484326 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1174+1115G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484326 | |||||||
| chr19:8484333 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1174+1122T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484333 | |||||||
| chr19:8484377 | A | G | 1 | a0001c0002t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1174+1166A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484377 | |||||||
| chr19:8484396 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0266 a0001c0001t0001g0268 others(3): Show |
8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1185C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484396 | |||||||
| chr19:8484441 | G | A | 1 | a0001c0013t0001g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1175-1162G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484441 | |||||||
| chr19:8484533 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1175-1070T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484533 | |||||||
| chr19:8484576 | T | A | 16 | a0001c0002t0001g0303 a0001c0002t0001g0304 a0001c0002t0001g0305 others(13): Show |
16 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.1175-1027T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484576 | |||||||
| chr19:8484635 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1175-968G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484635 | |||||||
| chr19:8484684 | T | A | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1175-919T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484684 | |||||||
| chr19:8484762 | C | T | 9 | a0001c0001t0001g0076 a0001c0001t0001g0083 a0001c0001t0001g0087 others(6): Show |
9 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1175-841C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484762 | |||||||
| chr19:8484774 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1175-829G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484774 | |||||||
| chr19:8485003 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1175-600G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485003 | |||||||
| chr19:8485065 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0002t0001g0025 others(3): Show |
7 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-538G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485065 | |||||||
| chr19:8485172 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(5): Show |
10 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1175-431C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485172 | |||||||
| chr19:8485201 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1175-402T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485201 | |||||||
| chr19:8485223 | G | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1175-380G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485223 | |||||||
| chr19:8485224 | G | C | 1 | a0001c0001t0001g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1175-379G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485224 | |||||||
| chr19:8485386 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0211 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1175-217A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485386 | |||||||
| chr19:8485417 | C | T | 1 | a0001c0002t0001g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1175-186C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485417 | |||||||
| chr19:8485489 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1175-114T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485489 | |||||||
| chr19:8486468 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1977+63T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486468 | |||||||
| chr19:8486625 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1977+220C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486625 | |||||||
| chr19:8486626 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1977+221G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486626 | |||||||
| chr19:8486649 | CTGAT | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1977+247_1977+250d others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr19 | 8486649 | ||||||
| chr19:8486726 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1978-298C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486726 | |||||||
| chr19:8486755 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1978-269T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486755 | |||||||
| chr19:8486802 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1978-222C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486802 | |||||||
| chr19:8486824 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1978-200C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486824 | |||||||
| chr19:8486846 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1978-178C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486846 | |||||||
| chr19:8486968 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1978-56A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486968 | |||||||
| chr19:8487119 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2029+44T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487119 | |||||||
| chr19:8487132 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2029+57C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487132 | |||||||
| chr19:8487152 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2029+77C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487152 | |||||||
| chr19:8487283 | C | T | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.2029+208C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487283 | |||||||
| chr19:8487327 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0254 |
2 | NA18961.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2029+252C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487327 | |||||||
| chr19:8487329 | C | G | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2029+254C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487329 | |||||||
| chr19:8487389 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(85): Show |
100 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2029+314A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487389 | |||||||
| chr19:8487418 | C | T | 7 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2029+343C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487418 | |||||||
| chr19:8487569 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2029+494C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487569 | |||||||
| chr19:8487704 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2029+629C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487704 | |||||||
| chr19:8487755 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2029+680T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487755 | |||||||
| chr19:8487887 | C | G | 25 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0084 others(22): Show |
27 | HG00423.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2030-804C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487887 | |||||||
| chr19:8487916 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0148 |
2 | HG02523.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2030-775C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487916 | |||||||
| chr19:8487981 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2030-710A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487981 | |||||||
| chr19:8487995 | C | T | 5 | a0001c0001t0001g0007 a0001c0002t0001g0025 a0001c0008t0001g0027 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2030-696C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487995 | |||||||
| chr19:8488039 | G | A | 1 | a0001c0002t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2030-652G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488039 | |||||||
| chr19:8488058 | CA | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.2030-631delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 8488058 | ||||||
| chr19:8488071 | GTCT | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2030-615_2030-613d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 8488071 | ||||||
| chr19:8488245 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2030-446C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488245 | |||||||
| chr19:8488438 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2030-253C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488438 | |||||||
| chr19:8488516 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(83): Show |
98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2030-175G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488516 | |||||||
| chr19:8488557 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2030-134G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488557 | |||||||
| chr19:8488573 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0054 others(2): Show |
6 | HG00733.hp1 HG00741.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.2030-118G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488573 | |||||||
| chr19:8488586 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0266 |
3 | HG01891.hp2 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2030-105G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488586 | |||||||
| chr19:8488610 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2030-81G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488610 |