Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 375484 |
| ensemblid | ENSG00000170085.18 |
| hgncid | 24779 |
| symbol | SIMC1 |
| name | SUMO interacting motifs containing 1 |
| refseq_nuc | NM_001308195.2 |
| refseq_prot | NP_001295124.1 |
| ensembl_nuc | ENST00000429602.7 |
| ensembl_prot | ENSP00000410552.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 176238424 |
| end | 176345989 |
| strand | + |
| ver | v1.2 |
| region | chr5:176238424-176345989 |
| region5000 | chr5:176233424-176350989 |
| regionname0 | SIMC1_chr5_176238424_176345989 |
| regionname5000 | SIMC1_chr5_176233424_176350989 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 891 | 276 | 68 | 48 | 122 | 8 | 28 | 97 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0002 | 0/0 | 891 | 58 | 10 | 10 | 31 | 2 | 5 | 29 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0003 | 0/0 | 891 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0004 | 0/0 | 891 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0005 | 0/0 | 891 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0006 | 0/0 | 891 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDYI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0007 | 0/0 | 891 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0008 | 0/0 | 891 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0009 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0010 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0011 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| a0012 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | MEDFI others(886): Show |
chr5 | 176233424 | 176350989 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2673 | 275 | 68 | 48 | 121 | 8 | 28 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0001c0010 | 0/0 | 2673 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0002c0002 | 0/0 | 2673 | 49 | 5 | 8 | 29 | 2 | 5 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0002c0003 | 0/0 | 2673 | 8 | 5 | 2 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0002c0014 | 0/0 | 2673 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0003c0004 | 0/0 | 2673 | 6 | 5 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0003c0016 | 0/0 | 2673 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0004c0005 | 0/0 | 2673 | 4 | 3 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0005c0006 | 0/0 | 2673 | 4 | 0 | 0 | 4 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0006c0007 | 0/0 | 2673 | 3 | 0 | 0 | 3 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0007c0008 | 0/0 | 2673 | 2 | 0 | 0 | 1 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0008c0009 | 0/0 | 2673 | 2 | 0 | 0 | 2 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0009c0013 | 0/0 | 2673 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0010c0015 | 0/0 | 2673 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0011c0011 | 0/0 | 2673 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 | ||
| a0012c0012 | 0/0 | 2673 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | ATGGA others(2668): Show |
chr5 | 176233424 | 176350989 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3305 | 272 | 66 | 48 | 121 | 8 | 28 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0001c0001t0003 | 0/1 | 3306 | 1 | 0 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3301): Show |
chr5 | 176233424 | 176350989 |
| a0001c0001t0004 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0001c0001t0005 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0001c0010t0001 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0002c0002t0002 | 0/0 | 3305 | 49 | 5 | 8 | 29 | 2 | 5 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0002c0003t0001 | 0/0 | 3305 | 4 | 1 | 2 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0002c0003t0002 | 0/0 | 3305 | 4 | 4 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0002c0014t0002 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0003c0004t0001 | 0/0 | 3305 | 6 | 5 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0003c0016t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0004c0005t0001 | 0/0 | 3305 | 4 | 3 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0005c0006t0002 | 0/0 | 3305 | 4 | 0 | 0 | 4 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0006c0007t0001 | 0/0 | 3305 | 3 | 0 | 0 | 3 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0007c0008t0001 | 0/0 | 3305 | 2 | 0 | 0 | 1 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0008c0009t0001 | 0/0 | 3305 | 2 | 0 | 0 | 2 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0009c0013t0001 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0010c0015t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0011c0011t0001 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| a0012c0012t0001 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | GCCCC others(3300): Show |
chr5 | 176233424 | 176350989 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0003g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0001c0010t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0002t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0003t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0003t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0003t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0003t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0003t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0003t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0003t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0002c0014t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0003c0004t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0003c0004t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0003c0004t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0003c0004t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0003c0004t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0003c0004t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0003c0016t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0004c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0004c0005t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0004c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0004c0005t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0005c0006t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0005c0006t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0005c0006t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0005c0006t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0006c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0006c0007t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0006c0007t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0007c0008t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0007c0008t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0008c0009t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0008c0009t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0009c0013t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0010c0015t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0011c0011t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| a0012c0012t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0326 | EUR | GBR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | GBR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0312 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00609 | hp1 | a0009 | c0013 | t0001 | g0016 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0314 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0320 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01243 | hp2 | a0004 | c0005 | t0001 | g0164 | AMR | PUR | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0337 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0336 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0352 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0358 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01496 | hp2 | a0003 | c0004 | t0001 | g0355 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0340 | EUR | IBS | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0350 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0349 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0317 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02135 | hp2 | a0002 | c0003 | t0001 | g0351 | EAS | KHV | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0344 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02280 | hp1 | a0003 | c0004 | t0001 | g0353 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0339 | AMR | PEL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0300 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0325 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02886 | hp1 | a0002 | c0003 | t0002 | g0329 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02896 | hp1 | a0004 | c0005 | t0001 | g0163 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0212 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02897 | hp1 | a0004 | c0005 | t0001 | g0162 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02922 | hp2 | a0002 | c0003 | t0002 | g0282 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0299 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03041 | hp2 | a0003 | c0004 | t0001 | g0354 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03130 | hp1 | a0003 | c0016 | t0001 | g0348 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03516 | hp2 | a0002 | c0003 | t0002 | g0283 | AFR | ESN | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03540 | hp1 | a0002 | c0003 | t0002 | g0281 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0301 | AFR | MSL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0342 | SAS | BEB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03927 | hp1 | a0007 | c0008 | t0001 | g0242 | SAS | BEB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0308 | SAS | BEB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0338 | SAS | BEB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0306 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0324 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0001 | AFR | YRI | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18906 | hp2 | a0003 | c0004 | t0001 | g0356 | AFR | YRI | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0346 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0321 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18951 | hp2 | a0006 | c0007 | t0001 | g0195 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18961 | hp2 | a0008 | c0009 | t0001 | g0135 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0319 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18967 | hp2 | a0002 | c0014 | t0002 | g0331 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18972 | hp2 | a0008 | c0009 | t0001 | g0039 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18978 | hp2 | a0005 | c0006 | t0002 | g0335 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0345 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0347 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18992 | hp1 | a0005 | c0006 | t0002 | g0332 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18992 | hp2 | a0001 | c0010 | t0001 | g0036 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18998 | hp2 | a0007 | c0008 | t0001 | g0178 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0327 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19006 | hp2 | a0011 | c0011 | t0001 | g0021 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19030 | hp1 | a0004 | c0005 | t0001 | g0161 | AFR | LWK | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19043 | hp2 | a0003 | c0004 | t0001 | g0357 | AFR | LWK | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0341 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0343 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19077 | hp1 | a0012 | c0012 | t0001 | g0060 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19079 | hp1 | a0005 | c0006 | t0002 | g0333 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19080 | hp2 | a0006 | c0007 | t0001 | g0194 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19089 | hp2 | a0006 | c0007 | t0001 | g0198 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ASW | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ASW | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | GIH | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | GIH | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0302 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG06807 | hp1 | a0010 | c0015 | t0001 | g0183 | AFR | USA | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA18955 | hp2 | a0005 | c0006 | t0002 | g0330 | EAS | JPT | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0048 | REF | REF | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | SIMC1_chr5_176233424_176350989 | SIMC1 | chr5 | 176233424 | 176350989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176238519 | T | A | 1 | a0006 | 3 | NA18951.hp2 NA19080.hp2 NA19089.hp2 |
missense_variant | MODERATE | c.11T>A | p.Phe4Tyr | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/10 | 96/3305 | 11/2676 | 4/891 | chr5 | 176238519 | |||
| chr5:176238588 | C | T | 1 | a0003 | 7 | HG01496.hp2 HG02280.hp1 HG03041.hp2 others(4): Show |
missense_variant | MODERATE | c.80C>T | p.Pro27Leu | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/10 | 165/3305 | 80/2676 | 27/891 | chr5 | 176238588 | |||
| chr5:176289993 | A | G | 1 | a0010 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.469A>G | p.Thr157Ala | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/10 | 554/3305 | 469/2676 | 157/891 | chr5 | 176289993 | |||
| chr5:176290213 | C | T | 2 | a0002 a0005 |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
missense_variant | MODERATE | c.689C>T | p.Pro230Leu | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/10 | 774/3305 | 689/2676 | 230/891 | chr5 | 176290213 | |||
| chr5:176290393 | C | A | 1 | a0011 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.869C>A | p.Pro290Gln | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/10 | 954/3305 | 869/2676 | 290/891 | chr5 | 176290393 | |||
| chr5:176290540 | C | T | 1 | a0005 | 4 | NA18955.hp2 NA18978.hp2 NA18992.hp1 others(1): Show |
missense_variant | MODERATE | c.1016C>T | p.Pro339Leu | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/10 | 1101/3305 | 1016/2676 | 339/891 | chr5 | 176290540 | |||
| chr5:176290568 | C | A | 1 | a0011 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.1044C>A | p.Asp348Glu | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/10 | 1129/3305 | 1044/2676 | 348/891 | chr5 | 176290568 | |||
| chr5:176290677 | A | G | 1 | a0009 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.1153A>G | p.Met385Val | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/10 | 1238/3305 | 1153/2676 | 385/891 | chr5 | 176290677 | |||
| chr5:176295240 | A | G | 1 | a0004 | 4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.1642A>G | p.Met548Val | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 3/10 | 1727/3305 | 1642/2676 | 548/891 | chr5 | 176295240 | |||
| chr5:176313710 | G | A | 1 | a0007 | 2 | HG03927.hp1 NA18998.hp2 |
missense_variant | MODERATE | c.1754G>A | p.Arg585Gln | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/10 | 1839/3305 | 1754/2676 | 585/891 | chr5 | 176313710 | |||
| chr5:176313779 | G | A | 1 | a0008 | 2 | NA18961.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.1823G>A | p.Arg608Gln | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/10 | 1908/3305 | 1823/2676 | 608/891 | chr5 | 176313779 | |||
| chr5:176345437 | G | A | 1 | a0012 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.2668G>A | p.Gly890Ser | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 10/10 | 2753/3305 | 2668/2676 | 890/891 | chr5 | 176345437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176289845 | G | A | 1 | a0001c0010 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.321G>A | p.Ala107Ala | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/10 | 406/3305 | 321/2676 | 107/891 | chr5 | 176289845 | |||
| chr5:176290394 | A | G | 1 | a0011c0011 | 1 | NA19006.hp2 | synonymous_variant | LOW | c.870A>G | p.Pro290Pro | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/10 | 955/3305 | 870/2676 | 290/891 | chr5 | 176290394 | |||
| chr5:176322345 | G | A | 1 | a0002c0014 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.1962G>A | p.Thr654Thr | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/10 | 2047/3305 | 1962/2676 | 654/891 | chr5 | 176322345 | |||
| chr5:176324710 | C | T | 1 | a0003c0016 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.2124C>T | p.Ala708Ala | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/10 | 2209/3305 | 2124/2676 | 708/891 | chr5 | 176324710 | |||
| chr5:176345205 | C | T | 3 | a0002c0002 a0002c0014 a0005c0006 |
54 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
synonymous_variant | LOW | c.2436C>T | p.Ile812Ile | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 10/10 | 2521/3305 | 2436/2676 | 812/891 | chr5 | 176345205 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176238495 | C | G | 1 | a0001c0001t0005 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/10 | 14 | chr5 | 176238495 | ||||||
| chr5:176345847 | T | G | 1 | a0001c0001t0004 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 10/10 | 402 | chr5 | 176345847 | ||||||
| chr5:176345903 | A | G | 4 | a0002c0002t0002 a0002c0003t0002 a0002c0014t0002 others(1): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*458A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 10/10 | 458 | chr5 | 176345903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176238694 | C | T | 1 | a0001c0001t0001g0360 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.129+57C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176238694 | |||||||
| chr5:176239026 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.129+389C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239026 | |||||||
| chr5:176239036 | A | G | 1 | a0002c0002t0002g0358 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.129+399A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239036 | |||||||
| chr5:176239120 | A | G | 3 | a0003c0004t0001g0355 a0003c0004t0001g0356 a0003c0004t0001g0357 |
3 | HG01496.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.129+483A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239120 | |||||||
| chr5:176239190 | T | G | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+553T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239190 | |||||||
| chr5:176239341 | A | G | 356 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(353): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.129+704A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239341 | |||||||
| chr5:176239388 | A | G | 80 | a0001c0001t0001g0277 a0001c0001t0001g0285 a0001c0001t0001g0286 others(77): Show |
80 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.129+751A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239388 | |||||||
| chr5:176239634 | G | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.129+997G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239634 | |||||||
| chr5:176239849 | C | T | 10 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+1212C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239849 | |||||||
| chr5:176239875 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+1238T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239875 | |||||||
| chr5:176239899 | G | A | 147 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
147 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.129+1262G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239899 | |||||||
| chr5:176239921 | G | A | 182 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.129+1284G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176239921 | |||||||
| chr5:176240198 | C | G | 190 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
190 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.129+1561C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240198 | |||||||
| chr5:176240270 | C | G | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.129+1633C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240270 | |||||||
| chr5:176240359 | G | C | 182 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.129+1722G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240359 | |||||||
| chr5:176240391 | A | G | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+1754A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240391 | |||||||
| chr5:176240622 | A | G | 185 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(182): Show |
185 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.129+1985A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240622 | |||||||
| chr5:176240710 | T | C | 185 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(182): Show |
185 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.129+2073T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240710 | |||||||
| chr5:176240723 | T | C | 185 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(182): Show |
185 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.129+2086T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240723 | |||||||
| chr5:176240873 | A | T | 184 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
184 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.129+2236A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240873 | |||||||
| chr5:176240938 | G | T | 188 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
188 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.129+2301G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176240938 | |||||||
| chr5:176240991 | T | TCTTG | 17 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+2357_129+2358i others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176240991 | ||||||
| chr5:176240992 | C | CT | 16 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(13): Show |
16 | HG00733.hp2 HG01361.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.129+2371dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176240992 | ||||||
| chr5:176240992 | C | CTTGCT | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00558.hp2 HG00609.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+2357_129+2358i others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176240992 | ||||||
| chr5:176240992 | C | CTTGCTT | 123 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(120): Show |
123 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.129+2357_129+2358i others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176240992 | ||||||
| chr5:176240992 | CT | C | 12 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(9): Show |
12 | HG01081.hp1 HG02486.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.129+2371delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176240992 | ||||||
| chr5:176240993 | T | TTGC | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+2357_129+2358i others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176240993 | ||||||
| chr5:176241013 | G | A | 184 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
184 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.129+2376G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241013 | |||||||
| chr5:176241283 | C | T | 1 | a0008c0009t0001g0135 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.129+2646C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241283 | |||||||
| chr5:176241284 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.129+2647G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241284 | |||||||
| chr5:176241308 | CA | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+2673delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176241308 | ||||||
| chr5:176241429 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.129+2792T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241429 | |||||||
| chr5:176241430 | G | A | 1 | a0007c0008t0001g0178 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.129+2793G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241430 | |||||||
| chr5:176241442 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG02027.hp2 NA18943.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+2805A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241442 | |||||||
| chr5:176241453 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.129+2816A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241453 | |||||||
| chr5:176241571 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+2934C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241571 | |||||||
| chr5:176241579 | G | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+2942G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241579 | |||||||
| chr5:176241585 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.129+2948G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241585 | |||||||
| chr5:176241587 | G | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+2950G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241587 | |||||||
| chr5:176241632 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+2995A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241632 | |||||||
| chr5:176241874 | A | G | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG00438.hp2 HG02135.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.129+3237A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241874 | |||||||
| chr5:176241961 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+3324C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241961 | |||||||
| chr5:176241977 | A | AGT | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+3340_129+3341i others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176241977 | |||||||
| chr5:176242015 | T | A | 1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.129+3378T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242015 | |||||||
| chr5:176242130 | C | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+3493C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242130 | |||||||
| chr5:176242133 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+3496G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242133 | |||||||
| chr5:176242215 | C | T | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.129+3578C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242215 | |||||||
| chr5:176242216 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+3579G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242216 | |||||||
| chr5:176242223 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.129+3586C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242223 | |||||||
| chr5:176242247 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.129+3610T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242247 | |||||||
| chr5:176242483 | CAT | C | 27 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(24): Show |
27 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+3849_129+3850d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176242483 | ||||||
| chr5:176242514 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+3877A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242514 | |||||||
| chr5:176242543 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+3906C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242543 | |||||||
| chr5:176242546 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+3909A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242546 | |||||||
| chr5:176242639 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+4002T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242639 | |||||||
| chr5:176242717 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+4080T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242717 | |||||||
| chr5:176242842 | G | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+4205G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242842 | |||||||
| chr5:176242866 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+4229T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242866 | |||||||
| chr5:176242889 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0003c0004t0001g0001 others(2): Show |
5 | HG01081.hp2 HG02280.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+4252A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242889 | |||||||
| chr5:176242942 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+4305G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176242942 | |||||||
| chr5:176242997 | ATTATTTT | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+4370_129+4376d others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176242997 | ||||||
| chr5:176243107 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+4470A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243107 | |||||||
| chr5:176243167 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.129+4530T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243167 | |||||||
| chr5:176243320 | G | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0130 a0001c0001t0001g0179 others(3): Show |
6 | HG02280.hp1 HG03041.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+4683G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243320 | |||||||
| chr5:176243367 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+4730A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243367 | |||||||
| chr5:176243418 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.129+4781G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243418 | |||||||
| chr5:176243626 | A | G | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+4989A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243626 | |||||||
| chr5:176243668 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+5031A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243668 | |||||||
| chr5:176243696 | A | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.129+5059A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243696 | |||||||
| chr5:176243741 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.129+5104G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243741 | |||||||
| chr5:176243759 | T | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+5122T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243759 | |||||||
| chr5:176243762 | A | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+5125A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243762 | |||||||
| chr5:176243861 | G | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.129+5224G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243861 | |||||||
| chr5:176243873 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG02451.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.129+5236A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176243873 | |||||||
| chr5:176244287 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.129+5650G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244287 | |||||||
| chr5:176244535 | A | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02027.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.129+5898A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244535 | |||||||
| chr5:176244540 | G | GCATA | 4 | a0001c0001t0001g0277 a0003c0004t0001g0001 a0003c0004t0001g0353 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+5903_129+5904i others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244540 | |||||||
| chr5:176244541 | T | G | 4 | a0001c0001t0001g0277 a0003c0004t0001g0001 a0003c0004t0001g0353 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+5904T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244541 | |||||||
| chr5:176244596 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+5959G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244596 | |||||||
| chr5:176244597 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+5960C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244597 | |||||||
| chr5:176244651 | C | T | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.129+6014C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244651 | |||||||
| chr5:176244652 | A | G | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.129+6015A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244652 | |||||||
| chr5:176244717 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.129+6080T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244717 | |||||||
| chr5:176244719 | C | CT | 66 | a0001c0001t0001g0022 a0001c0001t0001g0120 a0001c0001t0001g0121 others(63): Show |
66 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.129+6101dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176244719 | ||||||
| chr5:176244719 | C | CTT | 6 | a0002c0002t0002g0342 a0002c0002t0002g0343 a0002c0002t0002g0344 others(3): Show |
6 | HG02148.hp1 HG03831.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+6100_129+6101d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176244719 | ||||||
| chr5:176244719 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.129+6082C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244719 | |||||||
| chr5:176244719 | CT | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0031 others(4): Show |
7 | HG00323.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+6101delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176244719 | ||||||
| chr5:176244782 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02293.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.129+6145C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244782 | |||||||
| chr5:176244804 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.129+6167C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176244804 | |||||||
| chr5:176245096 | A | C | 1 | a0001c0001t0001g0297 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.129+6459A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245096 | |||||||
| chr5:176245132 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.129+6495G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245132 | |||||||
| chr5:176245175 | G | A | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.129+6538G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245175 | |||||||
| chr5:176245212 | C | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+6575C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245212 | |||||||
| chr5:176245367 | A | G | 13 | a0001c0001t0001g0285 a0001c0001t0001g0287 a0001c0001t0001g0288 others(10): Show |
13 | HG00323.hp2 HG01074.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.129+6730A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245367 | |||||||
| chr5:176245373 | T | C | 182 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.129+6736T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245373 | |||||||
| chr5:176245634 | A | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+6997A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245634 | |||||||
| chr5:176245712 | G | A | 1 | a0002c0002t0002g0302 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.129+7075G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245712 | |||||||
| chr5:176245736 | A | G | 2 | a0001c0001t0001g0249 a0003c0004t0001g0353 |
2 | HG00609.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.129+7099A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176245736 | |||||||
| chr5:176246012 | G | GT | 25 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0022 others(22): Show |
25 | HG01109.hp1 HG01192.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+7391dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246012 | ||||||
| chr5:176246103 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+7466G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246103 | |||||||
| chr5:176246219 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.129+7582C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246219 | |||||||
| chr5:176246232 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0274 |
2 | HG02300.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.129+7595A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246232 | |||||||
| chr5:176246292 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.129+7655G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246292 | |||||||
| chr5:176246317 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.129+7680T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246317 | |||||||
| chr5:176246322 | T | A | 2 | a0002c0002t0002g0303 a0002c0002t0002g0304 |
2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.129+7685T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246322 | |||||||
| chr5:176246404 | AG | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0169 a0001c0001t0001g0173 others(1): Show |
4 | HG03453.hp1 HG03516.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+7771delG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246404 | ||||||
| chr5:176246407 | G | GGT | 66 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0031 others(63): Show |
66 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.129+7811_129+7812d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246407 | G | GGTGT | 19 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(16): Show |
19 | HG00438.hp2 HG01496.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.129+7809_129+7812d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246407 | G | GGTGTGTG others(3): Show |
1 | a0002c0002t0002g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.129+7803_129+7812d others(12): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246407 | G | GT | 7 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0134 others(4): Show |
7 | HG00642.hp1 HG02809.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+7770_129+7771i others(3): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246407 | |||||||
| chr5:176246407 | GGT | G | 25 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0117 others(22): Show |
25 | HG00558.hp1 HG00597.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+7811_129+7812d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246407 | GGTGT | G | 39 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(36): Show |
39 | HG00280.hp2 HG00609.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.129+7809_129+7812d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246407 | GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.129+7803_129+7812d others(12): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246407 | GGTGTGTG others(5): Show |
G | 2 | a0001c0001t0001g0240 a0002c0002t0002g0338 |
2 | HG03942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.129+7801_129+7812d others(14): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246407 | GGTGTGTG others(7): Show |
G | 1 | a0001c0001t0001g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.129+7799_129+7812d others(16): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246407 | GGTGTGTG others(17): Show |
G | 1 | a0002c0002t0002g0339 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.129+7789_129+7812d others(26): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176246407 | ||||||
| chr5:176246411 | T | G | 1 | a0010c0015t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.129+7774T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246411 | |||||||
| chr5:176246449 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.129+7812T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246449 | |||||||
| chr5:176246450 | T | G | 1 | a0001c0001t0001g0033 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.129+7813T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246450 | |||||||
| chr5:176246586 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+7949C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246586 | |||||||
| chr5:176246686 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.129+8049A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246686 | |||||||
| chr5:176246698 | C | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+8061C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246698 | |||||||
| chr5:176246708 | T | C | 6 | a0001c0001t0001g0187 a0001c0001t0001g0274 a0002c0003t0001g0349 others(3): Show |
6 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+8071T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246708 | |||||||
| chr5:176246724 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.129+8087A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246724 | |||||||
| chr5:176246748 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.129+8111A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246748 | |||||||
| chr5:176246772 | C | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG02132.hp2 NA18997.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.129+8135C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246772 | |||||||
| chr5:176246783 | G | C | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+8146G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246783 | |||||||
| chr5:176246800 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+8163A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246800 | |||||||
| chr5:176246830 | A | G | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+8193A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246830 | |||||||
| chr5:176246924 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+8287C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246924 | |||||||
| chr5:176246983 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.129+8346C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176246983 | |||||||
| chr5:176247061 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+8424A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247061 | |||||||
| chr5:176247171 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+8534G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247171 | |||||||
| chr5:176247221 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+8584T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247221 | |||||||
| chr5:176247287 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(2): Show |
5 | HG02965.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+8650A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247287 | |||||||
| chr5:176247354 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+8717A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247354 | |||||||
| chr5:176247367 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(1): Show |
4 | HG00438.hp2 NA18940.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+8730A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247367 | |||||||
| chr5:176247392 | C | T | 1 | a0002c0002t0002g0326 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.129+8755C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247392 | |||||||
| chr5:176247417 | T | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+8780T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247417 | |||||||
| chr5:176247434 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0274 |
2 | HG02300.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.129+8797C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247434 | |||||||
| chr5:176247452 | GTTGT | G | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+8822_129+8825d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176247452 | ||||||
| chr5:176247487 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.129+8850C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247487 | |||||||
| chr5:176247606 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+8969G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247606 | |||||||
| chr5:176247696 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9059G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247696 | |||||||
| chr5:176247737 | T | G | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.129+9100T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247737 | |||||||
| chr5:176247741 | G | GT | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.129+9107dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176247741 | ||||||
| chr5:176247805 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9168G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176247805 | |||||||
| chr5:176248029 | C | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0274 |
3 | HG01516.hp1 HG02257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.129+9392C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248029 | |||||||
| chr5:176248045 | C | A | 1 | a0004c0005t0001g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.129+9408C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248045 | |||||||
| chr5:176248063 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0274 |
3 | HG01516.hp1 HG02257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.129+9426T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248063 | |||||||
| chr5:176248064 | T | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0274 |
3 | HG01516.hp1 HG02257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.129+9427T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248064 | |||||||
| chr5:176248117 | A | G | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.129+9480A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248117 | |||||||
| chr5:176248151 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9514G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248151 | |||||||
| chr5:176248187 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.129+9550T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248187 | |||||||
| chr5:176248189 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9552T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248189 | |||||||
| chr5:176248219 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129+9582T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248219 | |||||||
| chr5:176248280 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0274 |
2 | HG02300.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.129+9643C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248280 | |||||||
| chr5:176248308 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9671G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248308 | |||||||
| chr5:176248401 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9764T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248401 | |||||||
| chr5:176248459 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9822T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248459 | |||||||
| chr5:176248477 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9840A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248477 | |||||||
| chr5:176248559 | T | C | 67 | a0001c0001t0001g0274 a0002c0002t0002g0278 a0002c0002t0002g0279 others(64): Show |
67 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.129+9922T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248559 | |||||||
| chr5:176248617 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+9980T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248617 | |||||||
| chr5:176248662 | G | C | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10025G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248662 | |||||||
| chr5:176248675 | T | C | 258 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.129+10038T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248675 | |||||||
| chr5:176248891 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0274 |
2 | HG02300.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.129+10254G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248891 | |||||||
| chr5:176248901 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10264G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248901 | |||||||
| chr5:176248915 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10278A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248915 | |||||||
| chr5:176248936 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.129+10299T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248936 | |||||||
| chr5:176248941 | G | A | 16 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.129+10304G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248941 | |||||||
| chr5:176248999 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10362G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176248999 | |||||||
| chr5:176249050 | G | C | 2 | a0002c0002t0002g0303 a0002c0002t0002g0304 |
2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.129+10413G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249050 | |||||||
| chr5:176249065 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10428G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249065 | |||||||
| chr5:176249179 | A | G | 115 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.129+10542A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249179 | |||||||
| chr5:176249301 | A | G | 4 | a0001c0001t0001g0274 a0003c0004t0001g0001 a0003c0004t0001g0353 others(1): Show |
4 | HG02280.hp1 HG02300.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+10664A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249301 | |||||||
| chr5:176249355 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10718G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249355 | |||||||
| chr5:176249368 | A | G | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
152 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.129+10731A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249368 | |||||||
| chr5:176249445 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+10808G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249445 | |||||||
| chr5:176249472 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10835A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249472 | |||||||
| chr5:176249527 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10890A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249527 | |||||||
| chr5:176249529 | G | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.129+10892G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249529 | |||||||
| chr5:176249610 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.129+10973G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249610 | |||||||
| chr5:176249612 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+10975G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249612 | |||||||
| chr5:176249713 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.129+11076A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249713 | |||||||
| chr5:176249721 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+11084G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249721 | |||||||
| chr5:176249749 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.129+11112C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249749 | |||||||
| chr5:176249793 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.129+11156G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249793 | |||||||
| chr5:176249840 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.129+11203T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249840 | |||||||
| chr5:176249843 | C | CA | 33 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0143 others(30): Show |
33 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.129+11227dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176249843 | ||||||
| chr5:176249843 | C | CAA | 58 | a0001c0001t0001g0098 a0001c0001t0001g0142 a0001c0001t0001g0153 others(55): Show |
58 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.129+11226_129+1122 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176249843 | ||||||
| chr5:176249843 | C | CAAA | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.129+11225_129+1122 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176249843 | ||||||
| chr5:176249843 | C | CAAAA | 49 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0028 others(46): Show |
49 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.129+11224_129+1122 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176249843 | ||||||
| chr5:176249843 | C | CAAAAA | 6 | a0001c0001t0001g0038 a0001c0001t0001g0105 a0001c0001t0001g0123 others(3): Show |
6 | HG00438.hp1 HG01169.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+11223_129+1122 others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176249843 | ||||||
| chr5:176249937 | T | TA | 9 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0153 others(6): Show |
9 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+11301dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176249937 | ||||||
| chr5:176249966 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.129+11329G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176249966 | |||||||
| chr5:176250332 | G | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+11695G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250332 | |||||||
| chr5:176250343 | C | T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+11706C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250343 | |||||||
| chr5:176250568 | A | G | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.129+11931A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250568 | |||||||
| chr5:176250578 | A | G | 1 | a0002c0002t0002g0302 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.129+11941A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250578 | |||||||
| chr5:176250636 | G | T | 66 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.129+11999G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250636 | |||||||
| chr5:176250641 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.129+12004G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250641 | |||||||
| chr5:176250647 | G | C | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.129+12010G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250647 | |||||||
| chr5:176250679 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.129+12042C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250679 | |||||||
| chr5:176250915 | A | G | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.129+12278A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250915 | |||||||
| chr5:176250970 | A | C | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+12333A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176250970 | |||||||
| chr5:176251058 | G | GT | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+12426dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176251058 | ||||||
| chr5:176251089 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.129+12452C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251089 | |||||||
| chr5:176251128 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.129+12491G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251128 | |||||||
| chr5:176251173 | A | G | 9 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0153 others(6): Show |
9 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+12536A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251173 | |||||||
| chr5:176251405 | T | G | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.129+12768T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251405 | |||||||
| chr5:176251413 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.129+12776A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251413 | |||||||
| chr5:176251416 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.129+12779G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251416 | |||||||
| chr5:176251428 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | NA18940.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.129+12791C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251428 | |||||||
| chr5:176251734 | C | T | 26 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(23): Show |
26 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.129+13097C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251734 | |||||||
| chr5:176251756 | A | C | 1 | a0001c0001t0001g0224 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.129+13119A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251756 | |||||||
| chr5:176251782 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.129+13145T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251782 | |||||||
| chr5:176251788 | C | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+13151C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251788 | |||||||
| chr5:176251797 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.129+13160T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251797 | |||||||
| chr5:176251835 | C | T | 1 | a0001c0010t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.129+13198C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251835 | |||||||
| chr5:176251872 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+13235A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251872 | |||||||
| chr5:176251893 | T | G | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+13256T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251893 | |||||||
| chr5:176251966 | T | C | 251 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
251 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.129+13329T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251966 | |||||||
| chr5:176251996 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.129+13359C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251996 | |||||||
| chr5:176251997 | G | A | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.129+13360G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176251997 | |||||||
| chr5:176252076 | C | T | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+13439C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252076 | |||||||
| chr5:176252121 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+13484C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252121 | |||||||
| chr5:176252169 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.129+13532C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252169 | |||||||
| chr5:176252184 | G | A | 2 | a0001c0001t0001g0040 a0012c0012t0001g0060 |
2 | NA18965.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.129+13547G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252184 | |||||||
| chr5:176252188 | G | A | 1 | a0002c0002t0002g0344 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.129+13551G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252188 | |||||||
| chr5:176252200 | C | T | 4 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+13563C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252200 | |||||||
| chr5:176252214 | A | AC | 11 | a0002c0002t0002g0300 a0002c0002t0002g0306 a0002c0002t0002g0308 others(8): Show |
11 | HG00544.hp1 HG01361.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+13579dupC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176252214 | ||||||
| chr5:176252216 | CG | C | 162 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
162 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.129+13580delG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252216 | |||||||
| chr5:176252217 | G | C | 73 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0042 others(70): Show |
73 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.129+13580G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252217 | |||||||
| chr5:176252222 | C | G | 1 | a0012c0012t0001g0060 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.129+13585C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252222 | |||||||
| chr5:176252225 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.129+13588C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252225 | |||||||
| chr5:176252225 | C | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0247 |
2 | HG02071.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.129+13588C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252225 | |||||||
| chr5:176252267 | C | T | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.129+13630C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252267 | |||||||
| chr5:176252279 | C | T | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.129+13642C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252279 | |||||||
| chr5:176252372 | C | T | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.129+13735C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252372 | |||||||
| chr5:176252427 | G | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+13790G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252427 | |||||||
| chr5:176252500 | C | CG | 42 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(39): Show |
42 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.129+13867dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176252500 | ||||||
| chr5:176252509 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+13872G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252509 | |||||||
| chr5:176252518 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.129+13881G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252518 | |||||||
| chr5:176252527 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.129+13890A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252527 | |||||||
| chr5:176252553 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0103 others(1): Show |
4 | HG01175.hp1 HG01934.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+13916A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252553 | |||||||
| chr5:176252592 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+13955A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252592 | |||||||
| chr5:176252625 | G | A | 54 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(51): Show |
54 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.129+13988G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252625 | |||||||
| chr5:176252700 | C | T | 1 | a0012c0012t0001g0060 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.129+14063C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252700 | |||||||
| chr5:176252707 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0193 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.129+14070G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252707 | |||||||
| chr5:176252764 | G | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0258 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.129+14127G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252764 | |||||||
| chr5:176252824 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.129+14187T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252824 | |||||||
| chr5:176252850 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+14213A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252850 | |||||||
| chr5:176252895 | C | T | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+14258C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252895 | |||||||
| chr5:176252903 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.129+14266T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252903 | |||||||
| chr5:176252918 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+14281A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252918 | |||||||
| chr5:176252944 | C | T | 1 | a0010c0015t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.129+14307C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252944 | |||||||
| chr5:176252953 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(1): Show |
4 | HG02965.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+14316C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176252953 | |||||||
| chr5:176253003 | G | GGC | 3 | a0001c0001t0001g0186 a0001c0001t0001g0273 a0001c0001t0001g0277 |
3 | HG02486.hp1 HG03688.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.129+14375_129+1437 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176253003 | ||||||
| chr5:176253006 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.129+14369G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253006 | |||||||
| chr5:176253008 | G | A | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.129+14371G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253008 | |||||||
| chr5:176253009 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(2): Show |
5 | HG02965.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+14372C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253009 | |||||||
| chr5:176253012 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | NA18990.hp2 NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.129+14375G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253012 | |||||||
| chr5:176253021 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0244 |
2 | NA18945.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.129+14384C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253021 | |||||||
| chr5:176253022 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.129+14385G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253022 | |||||||
| chr5:176253103 | C | T | 3 | a0003c0004t0001g0355 a0003c0004t0001g0356 a0003c0004t0001g0357 |
3 | HG01496.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.129+14466C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253103 | |||||||
| chr5:176253105 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.129+14468G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253105 | |||||||
| chr5:176253235 | C | G | 1 | a0002c0002t0002g0311 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.129+14598C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253235 | |||||||
| chr5:176253303 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.129+14666T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253303 | |||||||
| chr5:176253333 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.129+14696C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253333 | |||||||
| chr5:176253386 | G | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+14749G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253386 | |||||||
| chr5:176253579 | T | A | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.129+14942T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253579 | |||||||
| chr5:176253603 | A | G | 1 | a0002c0002t0002g0358 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.129+14966A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253603 | |||||||
| chr5:176253824 | A | T | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.129+15187A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253824 | |||||||
| chr5:176253895 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+15258A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253895 | |||||||
| chr5:176253952 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0184 |
2 | NA19006.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.129+15315T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176253952 | |||||||
| chr5:176254000 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+15363A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176254000 | |||||||
| chr5:176254098 | A | G | 1 | a0002c0002t0002g0307 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.129+15461A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176254098 | |||||||
| chr5:176254163 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.129+15526G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176254163 | |||||||
| chr5:176254347 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+15710G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176254347 | |||||||
| chr5:176254392 | T | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
21 | HG00558.hp2 HG00609.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.129+15755T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176254392 | |||||||
| chr5:176254476 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.129+15839A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176254476 | |||||||
| chr5:176254701 | T | C | 1 | a0002c0002t0002g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.129+16064T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176254701 | |||||||
| chr5:176255013 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+16376A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176255013 | |||||||
| chr5:176255352 | C | T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0035 others(13): Show |
16 | HG00597.hp2 HG01175.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.129+16715C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176255352 | |||||||
| chr5:176255442 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+16805G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176255442 | |||||||
| chr5:176255536 | C | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.129+16899C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176255536 | |||||||
| chr5:176255577 | CT | C | 84 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0055 others(81): Show |
84 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.129+16960delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176255577 | ||||||
| chr5:176255577 | CTT | C | 160 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
160 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.129+16959_129+1696 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176255577 | ||||||
| chr5:176255674 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.129+17037A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176255674 | |||||||
| chr5:176255710 | A | G | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+17073A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176255710 | |||||||
| chr5:176255721 | T | TA | 127 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0028 others(124): Show |
127 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.129+17097dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176255721 | ||||||
| chr5:176255771 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.129+17134A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176255771 | |||||||
| chr5:176256135 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0087 |
2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.129+17498A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256135 | |||||||
| chr5:176256167 | A | G | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
153 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.129+17530A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256167 | |||||||
| chr5:176256205 | C | G | 25 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
25 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+17568C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256205 | |||||||
| chr5:176256234 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.129+17597A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256234 | |||||||
| chr5:176256321 | G | A | 1 | a0002c0014t0002g0331 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.129+17684G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256321 | |||||||
| chr5:176256349 | CATACTT | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+17716_129+1772 others(10): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176256349 | ||||||
| chr5:176256423 | G | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.129+17786G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256423 | |||||||
| chr5:176256637 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.129+18000G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256637 | |||||||
| chr5:176256695 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG02132.hp2 NA18997.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.129+18058T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256695 | |||||||
| chr5:176256915 | T | A | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+18278T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176256915 | |||||||
| chr5:176257058 | G | A | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.129+18421G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257058 | |||||||
| chr5:176257084 | TTA | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.129+18449_129+1845 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176257084 | ||||||
| chr5:176257103 | G | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | NA18941.hp1 NA18963.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.129+18466G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257103 | |||||||
| chr5:176257184 | G | A | 5 | a0001c0001t0001g0096 a0002c0003t0001g0349 a0002c0003t0001g0350 others(2): Show |
5 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+18547G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257184 | |||||||
| chr5:176257216 | G | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG00099.hp2 HG00280.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+18579G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257216 | |||||||
| chr5:176257312 | T | A | 1 | a0005c0006t0002g0332 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.129+18675T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257312 | |||||||
| chr5:176257382 | CAA | C | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+18747_129+1874 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176257382 | ||||||
| chr5:176257711 | C | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+19074C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257711 | |||||||
| chr5:176257715 | A | C | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+19078A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257715 | |||||||
| chr5:176257840 | T | C | 1 | a0001c0001t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+19203T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257840 | |||||||
| chr5:176257898 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.129+19261G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257898 | |||||||
| chr5:176257921 | A | C | 66 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.129+19284A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176257921 | |||||||
| chr5:176258009 | A | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.129+19372A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258009 | |||||||
| chr5:176258018 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.129+19381A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258018 | |||||||
| chr5:176258052 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.129+19415C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258052 | |||||||
| chr5:176258378 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.129+19741G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258378 | |||||||
| chr5:176258379 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+19742T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258379 | |||||||
| chr5:176258387 | C | T | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.129+19750C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258387 | |||||||
| chr5:176258392 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01175.hp2 HG01952.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.129+19755G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258392 | |||||||
| chr5:176258461 | T | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | NA18974.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.129+19824T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258461 | |||||||
| chr5:176258519 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.129+19882A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258519 | |||||||
| chr5:176258532 | A | G | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+19895A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258532 | |||||||
| chr5:176258541 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+19904G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258541 | |||||||
| chr5:176258555 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.129+19918C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258555 | |||||||
| chr5:176258841 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.129+20204A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258841 | |||||||
| chr5:176258895 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.129+20258C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176258895 | |||||||
| chr5:176259185 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+20548G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176259185 | |||||||
| chr5:176259292 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG03139.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.129+20655C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176259292 | |||||||
| chr5:176259722 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.129+21085G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176259722 | |||||||
| chr5:176259773 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.129+21136A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176259773 | |||||||
| chr5:176259775 | AAAT | A | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+21148_129+2115 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176259775 | ||||||
| chr5:176259926 | C | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(10): Show |
13 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.129+21289C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176259926 | |||||||
| chr5:176259966 | ATATAT | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+21334_129+2133 others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176259966 | ||||||
| chr5:176260086 | C | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+21449C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176260086 | |||||||
| chr5:176260088 | A | G | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.129+21451A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176260088 | |||||||
| chr5:176260234 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.129+21597C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176260234 | |||||||
| chr5:176260578 | C | G | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+21941C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176260578 | |||||||
| chr5:176260613 | G | GA | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
152 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.129+21984dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176260613 | ||||||
| chr5:176260673 | T | C | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+22036T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176260673 | |||||||
| chr5:176260700 | C | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.129+22063C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176260700 | |||||||
| chr5:176260928 | G | A | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG00733.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.129+22291G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176260928 | |||||||
| chr5:176260988 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+22351A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176260988 | |||||||
| chr5:176261099 | C | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+22462C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261099 | |||||||
| chr5:176261099 | C | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.129+22462C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261099 | |||||||
| chr5:176261111 | A | C | 1 | a0001c0001t0001g0229 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.129+22474A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261111 | |||||||
| chr5:176261195 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.129+22558T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261195 | |||||||
| chr5:176261196 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.129+22559G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261196 | |||||||
| chr5:176261250 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.129+22613G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261250 | |||||||
| chr5:176261388 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.129+22751T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261388 | |||||||
| chr5:176261540 | A | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+22903A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261540 | |||||||
| chr5:176261556 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.129+22919G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261556 | |||||||
| chr5:176261615 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+22978G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261615 | |||||||
| chr5:176261690 | T | C | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.129+23053T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261690 | |||||||
| chr5:176261747 | C | CA | 25 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
25 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+23120dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176261747 | ||||||
| chr5:176261748 | A | C | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+23111A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261748 | |||||||
| chr5:176261920 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.129+23283C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261920 | |||||||
| chr5:176261968 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129+23331G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176261968 | |||||||
| chr5:176262203 | T | C | 16 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.129+23566T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262203 | |||||||
| chr5:176262279 | TAAA | T | 71 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0082 others(68): Show |
71 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.129+23660_129+2366 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176262279 | ||||||
| chr5:176262279 | TAAAA | T | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
173 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.129+23659_129+2366 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176262279 | ||||||
| chr5:176262403 | G | A | 4 | a0002c0003t0002g0281 a0002c0003t0002g0282 a0002c0003t0002g0283 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+23766G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262403 | |||||||
| chr5:176262448 | ACTC | A | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+23814_129+2381 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176262448 | ||||||
| chr5:176262452 | C | T | 3 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0352 |
3 | HG01361.hp1 HG01891.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.129+23815C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262452 | |||||||
| chr5:176262558 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.129+23921A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262558 | |||||||
| chr5:176262565 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0108 |
2 | HG01257.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.129+23928G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262565 | |||||||
| chr5:176262650 | T | C | 3 | a0002c0003t0002g0281 a0002c0003t0002g0282 a0002c0003t0002g0283 |
3 | HG02922.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.129+24013T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262650 | |||||||
| chr5:176262711 | A | C | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.129+24074A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262711 | |||||||
| chr5:176262749 | G | C | 1 | a0001c0010t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.129+24112G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262749 | |||||||
| chr5:176262802 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.129+24165C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262802 | |||||||
| chr5:176262810 | A | C | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+24173A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262810 | |||||||
| chr5:176262880 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.129+24243T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176262880 | |||||||
| chr5:176263076 | C | T | 1 | a0010c0015t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.129+24439C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263076 | |||||||
| chr5:176263077 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.129+24440G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263077 | |||||||
| chr5:176263134 | C | T | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.129+24497C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263134 | |||||||
| chr5:176263134 | CAAAG | C | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+24500_129+2450 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176263134 | ||||||
| chr5:176263137 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+24500A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263137 | |||||||
| chr5:176263166 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0008c0009t0001g0135 |
3 | HG00423.hp2 HG00438.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.129+24529G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263166 | |||||||
| chr5:176263246 | G | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0075 a0001c0001t0001g0087 others(1): Show |
4 | HG00597.hp2 HG00609.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+24609G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263246 | |||||||
| chr5:176263453 | G | A | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.129+24816G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263453 | |||||||
| chr5:176263616 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.129+24979G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263616 | |||||||
| chr5:176263666 | A | C | 1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.129+25029A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263666 | |||||||
| chr5:176263758 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.129+25121A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263758 | |||||||
| chr5:176263810 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+25173A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263810 | |||||||
| chr5:176263983 | C | T | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+25346C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176263983 | |||||||
| chr5:176264014 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.129+25377T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264014 | |||||||
| chr5:176264144 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0096 |
2 | NA18963.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.129+25507T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264144 | |||||||
| chr5:176264179 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-25475C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264179 | |||||||
| chr5:176264220 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-25434C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264220 | |||||||
| chr5:176264266 | A | T | 1 | a0002c0002t0002g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.130-25388A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264266 | |||||||
| chr5:176264290 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-25364A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264290 | |||||||
| chr5:176264470 | C | T | 74 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.130-25184C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264470 | |||||||
| chr5:176264547 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.130-25107G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264547 | |||||||
| chr5:176264564 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.130-25090C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264564 | |||||||
| chr5:176264641 | C | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.130-25013C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264641 | |||||||
| chr5:176264845 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.130-24809C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264845 | |||||||
| chr5:176264919 | A | G | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130-24735A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264919 | |||||||
| chr5:176264972 | C | A | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130-24682C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176264972 | |||||||
| chr5:176265149 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.130-24505C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265149 | |||||||
| chr5:176265266 | T | TCAAA | 184 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
184 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.130-24365_130-2436 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176265266 | ||||||
| chr5:176265266 | T | TCAAACAA others(1): Show |
22 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0130 others(19): Show |
22 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.130-24369_130-2436 others(12): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176265266 | ||||||
| chr5:176265266 | T | TCAAACAA others(5): Show |
39 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(36): Show |
39 | HG00741.hp1 HG01257.hp1 HG01258.hp2 others(36): Show |
intron_variant | MODIFIER | c.130-24373_130-2436 others(16): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176265266 | ||||||
| chr5:176265266 | T | TCAAACAA others(9): Show |
1 | a0002c0014t0002g0331 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.130-24377_130-2436 others(20): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176265266 | ||||||
| chr5:176265291 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.130-24363C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265291 | |||||||
| chr5:176265296 | T | G | 1 | a0002c0002t0002g0315 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.130-24358T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265296 | |||||||
| chr5:176265446 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.130-24208G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265446 | |||||||
| chr5:176265510 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.130-24144A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265510 | |||||||
| chr5:176265561 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.130-24093A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265561 | |||||||
| chr5:176265854 | G | C | 5 | a0001c0001t0001g0090 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
5 | HG02027.hp2 NA18943.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-23800G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265854 | |||||||
| chr5:176265860 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-23794G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265860 | |||||||
| chr5:176265907 | T | C | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.130-23747T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265907 | |||||||
| chr5:176265919 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(1): Show |
4 | HG00438.hp2 NA18940.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-23735G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265919 | |||||||
| chr5:176265940 | T | C | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-23714T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265940 | |||||||
| chr5:176265969 | T | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-23685T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265969 | |||||||
| chr5:176265984 | G | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-23670G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176265984 | |||||||
| chr5:176266032 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.130-23622C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266032 | |||||||
| chr5:176266034 | A | G | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-23620A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266034 | |||||||
| chr5:176266147 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0203 |
2 | HG02809.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.130-23507A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266147 | |||||||
| chr5:176266257 | A | G | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-23397A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266257 | |||||||
| chr5:176266426 | G | C | 2 | a0002c0014t0002g0331 a0003c0004t0001g0001 |
2 | NA18522.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.130-23228G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266426 | |||||||
| chr5:176266431 | T | C | 2 | a0002c0014t0002g0331 a0003c0004t0001g0001 |
2 | NA18522.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.130-23223T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266431 | |||||||
| chr5:176266469 | A | G | 4 | a0002c0003t0002g0281 a0002c0003t0002g0282 a0002c0003t0002g0283 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-23185A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266469 | |||||||
| chr5:176266503 | G | T | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.130-23151G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266503 | |||||||
| chr5:176266520 | T | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.130-23134T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266520 | |||||||
| chr5:176266520 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-23134T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266520 | |||||||
| chr5:176266752 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.130-22902G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266752 | |||||||
| chr5:176266847 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.130-22807G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266847 | |||||||
| chr5:176266894 | A | G | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.130-22760A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176266894 | |||||||
| chr5:176267064 | A | G | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
247 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.130-22590A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267064 | |||||||
| chr5:176267117 | G | A | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
247 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.130-22537G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267117 | |||||||
| chr5:176267212 | T | G | 3 | a0003c0004t0001g0355 a0003c0004t0001g0356 a0003c0004t0001g0357 |
3 | HG01496.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.130-22442T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267212 | |||||||
| chr5:176267236 | G | A | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
247 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.130-22418G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267236 | |||||||
| chr5:176267240 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.130-22414A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267240 | |||||||
| chr5:176267263 | C | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-22391C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267263 | |||||||
| chr5:176267290 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.130-22364C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267290 | |||||||
| chr5:176267535 | T | C | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.130-22119T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267535 | |||||||
| chr5:176267536 | G | A | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130-22118G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267536 | |||||||
| chr5:176267689 | T | C | 246 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.130-21965T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267689 | |||||||
| chr5:176267698 | A | G | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-21956A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267698 | |||||||
| chr5:176267712 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0169 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.130-21942G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267712 | |||||||
| chr5:176267733 | G | GT | 56 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0177 others(53): Show |
56 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.130-21892dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | G | GTT | 10 | a0001c0001t0001g0186 a0001c0001t0001g0202 a0001c0001t0001g0210 others(7): Show |
10 | HG01123.hp2 HG01891.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.130-21893_130-2189 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GT | G | 46 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0038 others(43): Show |
46 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.130-21892delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTT | G | 58 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0030 others(55): Show |
58 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.130-21893_130-2189 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTTT | G | 10 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0051 others(7): Show |
10 | HG02615.hp1 HG02738.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.130-21894_130-2189 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTTTT | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
18 | HG00609.hp1 HG01069.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.130-21895_130-2189 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTTTTT | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00558.hp2 HG01070.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.130-21896_130-2189 others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTTTTTTT | G | 16 | a0001c0001t0001g0277 a0002c0002t0002g0301 a0002c0002t0002g0302 others(13): Show |
16 | HG00642.hp2 HG00741.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.130-21898_130-2189 others(11): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTTTTTTT others(1): Show |
G | 49 | a0001c0001t0001g0148 a0001c0001t0001g0270 a0001c0001t0001g0271 others(46): Show |
49 | HG00099.hp1 HG00544.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.130-21899_130-2189 others(12): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTTTTTTT others(2): Show |
G | 8 | a0001c0001t0001g0057 a0001c0001t0001g0267 a0001c0001t0001g0269 others(5): Show |
8 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-21900_130-2189 others(13): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTTTTTTT others(4): Show |
G | 3 | a0002c0002t0002g0298 a0002c0002t0002g0321 a0002c0002t0002g0328 |
3 | NA18949.hp2 NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.130-21902_130-2189 others(15): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267733 | GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0268 |
2 | NA18965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.130-21905_130-2189 others(18): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176267733 | ||||||
| chr5:176267762 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.130-21892T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267762 | |||||||
| chr5:176267997 | G | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-21657G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176267997 | |||||||
| chr5:176268202 | AAT | A | 54 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(51): Show |
54 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.130-21449_130-2144 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176268202 | ||||||
| chr5:176268242 | A | G | 74 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.130-21412A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176268242 | |||||||
| chr5:176268367 | C | T | 1 | a0010c0015t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130-21287C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176268367 | |||||||
| chr5:176268373 | C | CA | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-21271dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176268373 | ||||||
| chr5:176268455 | C | A | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.130-21199C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176268455 | |||||||
| chr5:176268738 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0001t0001g0130 |
3 | HG00597.hp2 NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.130-20916C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176268738 | |||||||
| chr5:176268766 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.130-20888C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176268766 | |||||||
| chr5:176268799 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.130-20855A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176268799 | |||||||
| chr5:176268838 | A | T | 1 | a0001c0001t0001g0218 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.130-20816A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176268838 | |||||||
| chr5:176268961 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-20693G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176268961 | |||||||
| chr5:176269054 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.130-20600A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176269054 | |||||||
| chr5:176269171 | GAGAA | G | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-20478_130-2047 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176269171 | ||||||
| chr5:176269382 | ATAT | A | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-20268_130-2026 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176269382 | ||||||
| chr5:176269567 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.130-20087G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176269567 | |||||||
| chr5:176269677 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130-19977T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176269677 | |||||||
| chr5:176269682 | C | T | 2 | a0001c0001t0001g0102 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.130-19972C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176269682 | |||||||
| chr5:176269902 | C | T | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.130-19752C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176269902 | |||||||
| chr5:176269931 | T | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01192.hp1 HG01361.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.130-19723T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176269931 | |||||||
| chr5:176269964 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-19690C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176269964 | |||||||
| chr5:176269998 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.130-19656C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176269998 | |||||||
| chr5:176270004 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.130-19650G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270004 | |||||||
| chr5:176270071 | T | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-19583T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270071 | |||||||
| chr5:176270161 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.130-19493G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270161 | |||||||
| chr5:176270287 | C | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-19367C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270287 | |||||||
| chr5:176270567 | C | T | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.130-19087C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270567 | |||||||
| chr5:176270650 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.130-19004G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270650 | |||||||
| chr5:176270710 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.130-18944C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270710 | |||||||
| chr5:176270819 | C | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-18835C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270819 | |||||||
| chr5:176270974 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-18680G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176270974 | |||||||
| chr5:176271396 | C | T | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-18258C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271396 | |||||||
| chr5:176271491 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.130-18163C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271491 | |||||||
| chr5:176271606 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.130-18048G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271606 | |||||||
| chr5:176271632 | A | G | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-18022A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271632 | |||||||
| chr5:176271775 | A | G | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-17879A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271775 | |||||||
| chr5:176271781 | C | A | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-17873C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271781 | |||||||
| chr5:176271812 | C | T | 1 | a0002c0002t0002g0358 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.130-17842C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271812 | |||||||
| chr5:176271867 | A | G | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-17787A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271867 | |||||||
| chr5:176271891 | AATT | A | 16 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.130-17757_130-1775 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176271891 | ||||||
| chr5:176271914 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(2): Show |
5 | HG02965.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-17740T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271914 | |||||||
| chr5:176271916 | GTATAT | G | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(132): Show |
135 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.130-17728_130-1772 others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176271916 | ||||||
| chr5:176271920 | A | G | 4 | a0002c0002t0002g0280 a0002c0002t0002g0305 a0002c0002t0002g0323 others(1): Show |
4 | NA18967.hp2 NA18984.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-17734A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271920 | |||||||
| chr5:176271921 | TTA | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00558.hp2 HG00609.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.130-17729_130-1772 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176271921 | ||||||
| chr5:176271930 | A | T | 128 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.130-17724A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271930 | |||||||
| chr5:176271938 | C | T | 2 | a0003c0004t0001g0001 a0003c0004t0001g0354 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-17716C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271938 | |||||||
| chr5:176271945 | A | T | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130-17709A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271945 | |||||||
| chr5:176271967 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.130-17687T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271967 | |||||||
| chr5:176271975 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-17679T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176271975 | |||||||
| chr5:176272004 | GTAATA | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0213 a0001c0001t0001g0216 others(2): Show |
5 | HG00621.hp1 HG02071.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-17642_130-1763 others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176272004 | ||||||
| chr5:176272108 | C | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-17546C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272108 | |||||||
| chr5:176272163 | C | A | 1 | a0002c0002t0002g0342 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.130-17491C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272163 | |||||||
| chr5:176272172 | C | CA | 72 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0179 others(69): Show |
72 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.130-17456dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176272172 | ||||||
| chr5:176272172 | C | CAA | 27 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(24): Show |
27 | HG00544.hp1 HG01069.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.130-17457_130-1745 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176272172 | ||||||
| chr5:176272172 | C | CAAA | 7 | a0001c0001t0001g0144 a0001c0001t0001g0153 a0001c0001t0001g0156 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-17458_130-1745 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176272172 | ||||||
| chr5:176272172 | CAAAAAAA others(5): Show |
C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-17467_130-1745 others(16): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176272172 | ||||||
| chr5:176272198 | AG | A | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
136 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.130-17454delG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176272198 | ||||||
| chr5:176272199 | G | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
15 | HG00423.hp2 HG01123.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.130-17455G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272199 | |||||||
| chr5:176272213 | A | G | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-17441A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272213 | |||||||
| chr5:176272349 | G | A | 2 | a0001c0001t0001g0040 a0012c0012t0001g0060 |
2 | NA18965.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.130-17305G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272349 | |||||||
| chr5:176272384 | C | CA | 133 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(130): Show |
133 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.130-17259dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176272384 | ||||||
| chr5:176272523 | C | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130-17131C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272523 | |||||||
| chr5:176272532 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.130-17122C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272532 | |||||||
| chr5:176272611 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-17043C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272611 | |||||||
| chr5:176272646 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-17008G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272646 | |||||||
| chr5:176272738 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-16916A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272738 | |||||||
| chr5:176272828 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.130-16826C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272828 | |||||||
| chr5:176272956 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.130-16698C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272956 | |||||||
| chr5:176272957 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.130-16697C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176272957 | |||||||
| chr5:176273130 | C | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0246 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.130-16524C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273130 | |||||||
| chr5:176273212 | G | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-16442G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273212 | |||||||
| chr5:176273255 | G | T | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.130-16399G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273255 | |||||||
| chr5:176273267 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.130-16387G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273267 | |||||||
| chr5:176273272 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.130-16382G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273272 | |||||||
| chr5:176273272 | G | T | 1 | a0002c0003t0001g0350 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.130-16382G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273272 | |||||||
| chr5:176273374 | A | C | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-16280A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273374 | |||||||
| chr5:176273428 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.130-16226T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273428 | |||||||
| chr5:176273550 | A | T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-16104A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273550 | |||||||
| chr5:176273650 | CCCCCTCA others(5): Show |
C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-15999_130-1598 others(16): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176273650 | ||||||
| chr5:176273654 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.130-16000C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273654 | |||||||
| chr5:176273750 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0074 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG00733.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-15904C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273750 | |||||||
| chr5:176273816 | C | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-15838C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273816 | |||||||
| chr5:176273836 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-15818C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273836 | |||||||
| chr5:176273875 | G | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-15779G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273875 | |||||||
| chr5:176273967 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-15687G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273967 | |||||||
| chr5:176273971 | G | A | 1 | a0002c0003t0001g0352 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.130-15683G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176273971 | |||||||
| chr5:176274017 | C | A | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-15637C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274017 | |||||||
| chr5:176274028 | G | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG00733.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.130-15626G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274028 | |||||||
| chr5:176274045 | G | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.130-15609G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274045 | |||||||
| chr5:176274058 | TAGATCCC others(2936): Show |
T | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.130-15528_130-1258 others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176274058 | ||||||
| chr5:176274168 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-15486T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274168 | |||||||
| chr5:176274261 | A | G | 354 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(351): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.130-15393A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274261 | |||||||
| chr5:176274364 | C | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-15290C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274364 | |||||||
| chr5:176274570 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-15084C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274570 | |||||||
| chr5:176274583 | G | C | 4 | a0001c0001t0001g0182 a0001c0001t0001g0190 a0001c0001t0001g0227 others(1): Show |
4 | HG00558.hp1 NA18944.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-15071G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274583 | |||||||
| chr5:176274680 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130-14974G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274680 | |||||||
| chr5:176274744 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 |
3 | HG00558.hp2 NA19067.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.130-14910A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274744 | |||||||
| chr5:176274756 | C | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-14898C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274756 | |||||||
| chr5:176274761 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.130-14893G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274761 | |||||||
| chr5:176274819 | T | C | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.130-14835T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274819 | |||||||
| chr5:176274824 | G | A | 25 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
25 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-14830G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274824 | |||||||
| chr5:176274864 | C | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-14790C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274864 | |||||||
| chr5:176274872 | T | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-14782T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274872 | |||||||
| chr5:176274893 | T | C | 5 | a0001c0001t0001g0188 a0002c0003t0001g0349 a0002c0003t0001g0350 others(2): Show |
5 | HG00423.hp1 HG01361.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-14761T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274893 | |||||||
| chr5:176274952 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.130-14702C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274952 | |||||||
| chr5:176274970 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.130-14684G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274970 | |||||||
| chr5:176274972 | T | G | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.130-14682T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176274972 | |||||||
| chr5:176274993 | GTTTTTCC others(2966): Show |
G | 1 | a0002c0002t0002g0327 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.130-14378_130-1140 others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176274993 | ||||||
| chr5:176275026 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-14628G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275026 | |||||||
| chr5:176275029 | T | C | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-14625T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275029 | |||||||
| chr5:176275100 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.130-14554A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275100 | |||||||
| chr5:176275114 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.130-14540A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275114 | |||||||
| chr5:176275117 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.130-14537G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275117 | |||||||
| chr5:176275222 | T | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-14432T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275222 | |||||||
| chr5:176275250 | A | G | 7 | a0001c0001t0001g0187 a0001c0001t0001g0233 a0001c0001t0001g0234 others(4): Show |
7 | HG00609.hp2 NA18974.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-14404A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275250 | |||||||
| chr5:176275269 | T | G | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.130-14385T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275269 | |||||||
| chr5:176275384 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.130-14270G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275384 | |||||||
| chr5:176275386 | C | G | 353 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(350): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.130-14268C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275386 | |||||||
| chr5:176275449 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-14205T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275449 | |||||||
| chr5:176275551 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0266 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130-14103A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275551 | |||||||
| chr5:176275607 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130-14047G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275607 | |||||||
| chr5:176275615 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130-14039T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275615 | |||||||
| chr5:176275706 | C | CTTTTCTG others(2971): Show |
1 | a0001c0001t0001g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.130-13904_130-1092 others(2982): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176275706 | ||||||
| chr5:176275706 | CTTTTCTG others(2971): Show |
C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130-13904_130-1092 others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176275706 | ||||||
| chr5:176275710 | T | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(2): Show |
5 | HG02965.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-13944T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275710 | |||||||
| chr5:176275835 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0011c0011t0001g0021 |
3 | NA18955.hp1 NA18961.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.130-13819G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275835 | |||||||
| chr5:176275863 | A | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.130-13791A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275863 | |||||||
| chr5:176275904 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.130-13750G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275904 | |||||||
| chr5:176275912 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.130-13742A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275912 | |||||||
| chr5:176275940 | G | T | 1 | a0002c0002t0002g0306 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.130-13714G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176275940 | |||||||
| chr5:176276037 | A | G | 179 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
179 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.130-13617A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276037 | |||||||
| chr5:176276071 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-13583G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276071 | |||||||
| chr5:176276087 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.130-13567G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276087 | |||||||
| chr5:176276225 | A | G | 115 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.130-13429A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276225 | |||||||
| chr5:176276256 | G | T | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-13398G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276256 | |||||||
| chr5:176276306 | A | T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-13348A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276306 | |||||||
| chr5:176276354 | C | A | 61 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(58): Show |
61 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.130-13300C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276354 | |||||||
| chr5:176276354 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.130-13300C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276354 | |||||||
| chr5:176276449 | CT | C | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.130-13195delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176276449 | ||||||
| chr5:176276509 | C | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-13145C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276509 | |||||||
| chr5:176276540 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.130-13114G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276540 | |||||||
| chr5:176276592 | C | T | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.130-13062C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276592 | |||||||
| chr5:176276676 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130-12978C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276676 | |||||||
| chr5:176276830 | C | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.130-12824C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276830 | |||||||
| chr5:176276896 | C | T | 3 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 |
3 | HG02896.hp1 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130-12758C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276896 | |||||||
| chr5:176276897 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-12757G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276897 | |||||||
| chr5:176276910 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-12744G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276910 | |||||||
| chr5:176276936 | G | T | 2 | a0002c0002t0002g0303 a0002c0002t0002g0304 |
2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.130-12718G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176276936 | |||||||
| chr5:176277042 | G | C | 179 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
179 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.130-12612G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277042 | |||||||
| chr5:176277083 | G | A | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130-12571G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277083 | |||||||
| chr5:176277111 | C | T | 1 | a0002c0002t0002g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-12543C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277111 | |||||||
| chr5:176277112 | G | A | 3 | a0003c0004t0001g0355 a0003c0004t0001g0356 a0003c0004t0001g0357 |
3 | HG01496.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.130-12542G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277112 | |||||||
| chr5:176277186 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.130-12468C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277186 | |||||||
| chr5:176277274 | C | T | 57 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(54): Show |
57 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.130-12380C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277274 | |||||||
| chr5:176277295 | C | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0277 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.130-12359C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277295 | |||||||
| chr5:176277322 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-12332G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277322 | |||||||
| chr5:176277351 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.130-12303C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277351 | |||||||
| chr5:176277358 | T | C | 65 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.130-12296T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277358 | |||||||
| chr5:176277386 | C | A | 57 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(54): Show |
57 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.130-12268C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277386 | |||||||
| chr5:176277389 | T | G | 1 | a0001c0001t0001g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.130-12265T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277389 | |||||||
| chr5:176277394 | A | G | 60 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(57): Show |
60 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.130-12260A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277394 | |||||||
| chr5:176277489 | T | C | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
178 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.130-12165T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277489 | |||||||
| chr5:176277509 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.130-12145G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277509 | |||||||
| chr5:176277586 | A | G | 50 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(47): Show |
50 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.130-12068A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277586 | |||||||
| chr5:176277610 | T | C | 1 | a0001c0001t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130-12044T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277610 | |||||||
| chr5:176277611 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-12043G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277611 | |||||||
| chr5:176277633 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.130-12021T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277633 | |||||||
| chr5:176277675 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-11979G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277675 | |||||||
| chr5:176277724 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.130-11930G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277724 | |||||||
| chr5:176277767 | G | A | 128 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.130-11887G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277767 | |||||||
| chr5:176277836 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.130-11818G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277836 | |||||||
| chr5:176277929 | T | C | 5 | a0001c0001t0001g0075 a0002c0003t0001g0349 a0002c0003t0001g0350 others(2): Show |
5 | HG00597.hp2 HG01361.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-11725T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277929 | |||||||
| chr5:176277966 | T | C | 57 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(54): Show |
57 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.130-11688T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277966 | |||||||
| chr5:176277979 | T | A | 128 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.130-11675T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176277979 | |||||||
| chr5:176278026 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.130-11628A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278026 | |||||||
| chr5:176278059 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.130-11595T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278059 | |||||||
| chr5:176278082 | C | T | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.130-11572C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278082 | |||||||
| chr5:176278165 | G | A | 246 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.130-11489G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278165 | |||||||
| chr5:176278258 | G | C | 1 | a0002c0002t0002g0316 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.130-11396G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278258 | |||||||
| chr5:176278349 | G | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0216 |
2 | NA18995.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.130-11305G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278349 | |||||||
| chr5:176278358 | A | G | 2 | a0002c0002t0002g0338 a0002c0002t0002g0342 |
2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.130-11296A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278358 | |||||||
| chr5:176278387 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.130-11267G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278387 | |||||||
| chr5:176278398 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-11256G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278398 | |||||||
| chr5:176278449 | C | T | 1 | a0004c0005t0001g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.130-11205C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278449 | |||||||
| chr5:176278484 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG00099.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.130-11170A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278484 | |||||||
| chr5:176278552 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0152 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.130-11102T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278552 | |||||||
| chr5:176278580 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0095 |
2 | HG00280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.130-11074G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278580 | |||||||
| chr5:176278627 | A | G | 6 | a0001c0001t0001g0056 a0001c0001t0001g0089 a0001c0001t0001g0092 others(3): Show |
6 | HG00544.hp2 NA18957.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-11027A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278627 | |||||||
| chr5:176278684 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130-10970T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278684 | |||||||
| chr5:176278728 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.130-10926C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278728 | |||||||
| chr5:176278758 | T | A | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-10896T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278758 | |||||||
| chr5:176278907 | G | T | 115 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.130-10747G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278907 | |||||||
| chr5:176278973 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.130-10681T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278973 | |||||||
| chr5:176278997 | A | G | 59 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.130-10657A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176278997 | |||||||
| chr5:176279003 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-10651T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279003 | |||||||
| chr5:176279034 | C | T | 2 | a0001c0001t0001g0245 a0010c0015t0001g0183 |
2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.130-10620C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279034 | |||||||
| chr5:176279044 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.130-10610C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279044 | |||||||
| chr5:176279080 | T | C | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130-10574T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279080 | |||||||
| chr5:176279095 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0193 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.130-10559T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279095 | |||||||
| chr5:176279203 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.130-10451A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279203 | |||||||
| chr5:176279236 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.130-10418G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279236 | |||||||
| chr5:176279236 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-10418G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279236 | |||||||
| chr5:176279258 | C | A | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.130-10396C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279258 | |||||||
| chr5:176279398 | A | G | 2 | a0002c0002t0002g0322 a0002c0002t0002g0345 |
2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.130-10256A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279398 | |||||||
| chr5:176279416 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.130-10238A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279416 | |||||||
| chr5:176279480 | C | G | 16 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.130-10174C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279480 | |||||||
| chr5:176279514 | A | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.130-10140A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279514 | |||||||
| chr5:176279546 | G | A | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130-10108G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279546 | |||||||
| chr5:176279666 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0130 |
2 | NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.130-9988A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279666 | |||||||
| chr5:176279686 | T | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
22 | HG00558.hp2 HG00609.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.130-9968T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279686 | |||||||
| chr5:176279699 | A | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0035 others(8): Show |
11 | HG00597.hp2 HG01175.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.130-9955A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279699 | |||||||
| chr5:176279700 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.130-9954C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279700 | |||||||
| chr5:176279732 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130-9922C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279732 | |||||||
| chr5:176279752 | A | C | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130-9902A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279752 | |||||||
| chr5:176279779 | G | C | 66 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.130-9875G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279779 | |||||||
| chr5:176279934 | A | G | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130-9720A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279934 | |||||||
| chr5:176279991 | C | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-9663C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176279991 | |||||||
| chr5:176280016 | T | C | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130-9638T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280016 | |||||||
| chr5:176280021 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0216 |
2 | NA18995.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.130-9633G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280021 | |||||||
| chr5:176280153 | T | G | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.130-9501T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280153 | |||||||
| chr5:176280175 | A | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-9479A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280175 | |||||||
| chr5:176280236 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.130-9418C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280236 | |||||||
| chr5:176280334 | C | G | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130-9320C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280334 | |||||||
| chr5:176280485 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.130-9169T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280485 | |||||||
| chr5:176280575 | G | A | 50 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(47): Show |
50 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.130-9079G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280575 | |||||||
| chr5:176280617 | G | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0277 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.130-9037G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280617 | |||||||
| chr5:176280620 | C | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0277 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.130-9034C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280620 | |||||||
| chr5:176280799 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.130-8855C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280799 | |||||||
| chr5:176280800 | G | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-8854G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280800 | |||||||
| chr5:176280812 | G | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-8842G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280812 | |||||||
| chr5:176280836 | C | T | 1 | a0002c0002t0002g0310 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.130-8818C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280836 | |||||||
| chr5:176280942 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-8712G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280942 | |||||||
| chr5:176280958 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-8696C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280958 | |||||||
| chr5:176280992 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.130-8662G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176280992 | |||||||
| chr5:176281077 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130-8577G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281077 | |||||||
| chr5:176281077 | G | T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-8577G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281077 | |||||||
| chr5:176281110 | C | T | 7 | a0002c0002t0002g0280 a0002c0002t0002g0305 a0002c0002t0002g0311 others(4): Show |
7 | NA18953.hp1 NA18965.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-8544C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281110 | |||||||
| chr5:176281193 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.130-8461G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281193 | |||||||
| chr5:176281200 | C | A | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-8454C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281200 | |||||||
| chr5:176281251 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.130-8403G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281251 | |||||||
| chr5:176281259 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(2): Show |
5 | HG02965.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-8395C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281259 | |||||||
| chr5:176281276 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | NA18946.hp1 NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.130-8378C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281276 | |||||||
| chr5:176281294 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130-8360G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281294 | |||||||
| chr5:176281310 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.130-8344G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281310 | |||||||
| chr5:176281326 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130-8328A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281326 | |||||||
| chr5:176281404 | G | A | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-8250G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281404 | |||||||
| chr5:176281418 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.130-8236T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281418 | |||||||
| chr5:176281427 | T | A | 1 | a0001c0001t0001g0030 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.130-8227T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281427 | |||||||
| chr5:176281430 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.130-8224T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281430 | |||||||
| chr5:176281590 | G | A | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-8064G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281590 | |||||||
| chr5:176281591 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.130-8063T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281591 | |||||||
| chr5:176281593 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.130-8061C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281593 | |||||||
| chr5:176281725 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0241 |
2 | HG00323.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.130-7929G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281725 | |||||||
| chr5:176281759 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-7895G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281759 | |||||||
| chr5:176281767 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.130-7887C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281767 | |||||||
| chr5:176281815 | G | A | 1 | a0002c0003t0001g0351 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.130-7839G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281815 | |||||||
| chr5:176281910 | C | T | 8 | a0001c0001t0001g0175 a0001c0001t0001g0196 a0001c0001t0001g0205 others(5): Show |
8 | HG02074.hp2 HG02293.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-7744C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281910 | |||||||
| chr5:176281926 | G | A | 1 | a0002c0003t0002g0329 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130-7728G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281926 | |||||||
| chr5:176281999 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-7655C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176281999 | |||||||
| chr5:176282074 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.130-7580T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282074 | |||||||
| chr5:176282135 | G | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-7519G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282135 | |||||||
| chr5:176282164 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.130-7490G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282164 | |||||||
| chr5:176282171 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.130-7483A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282171 | |||||||
| chr5:176282216 | G | A | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-7438G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282216 | |||||||
| chr5:176282245 | A | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-7409A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282245 | |||||||
| chr5:176282261 | C | T | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-7393C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282261 | |||||||
| chr5:176282288 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.130-7366C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282288 | |||||||
| chr5:176282402 | G | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
153 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.130-7252G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282402 | |||||||
| chr5:176282408 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0218 a0001c0001t0001g0254 |
3 | NA18946.hp2 NA19000.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.130-7246C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282408 | |||||||
| chr5:176282416 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-7238C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282416 | |||||||
| chr5:176282418 | C | T | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(1): Show |
4 | HG00438.hp2 NA18940.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-7236C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282418 | |||||||
| chr5:176282419 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-7235G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282419 | |||||||
| chr5:176282427 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0096 |
2 | NA18963.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.130-7227C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282427 | |||||||
| chr5:176282447 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-7207G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282447 | |||||||
| chr5:176282481 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-7173C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282481 | |||||||
| chr5:176282548 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-7106G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282548 | |||||||
| chr5:176282563 | C | T | 3 | a0001c0001t0001g0243 a0007c0008t0001g0178 a0007c0008t0001g0242 |
3 | HG03927.hp1 NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.130-7091C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282563 | |||||||
| chr5:176282687 | G | A | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-6967G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282687 | |||||||
| chr5:176282781 | G | C | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-6873G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282781 | |||||||
| chr5:176282858 | C | T | 1 | a0008c0009t0001g0135 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.130-6796C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282858 | |||||||
| chr5:176282888 | A | G | 2 | a0001c0001t0001g0040 a0012c0012t0001g0060 |
2 | NA18965.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.130-6766A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282888 | |||||||
| chr5:176282895 | G | A | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-6759G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282895 | |||||||
| chr5:176282910 | A | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | NA18946.hp1 NA18972.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-6744A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176282910 | |||||||
| chr5:176283067 | T | C | 251 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
251 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.130-6587T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283067 | |||||||
| chr5:176283100 | T | G | 5 | a0001c0001t0001g0117 a0002c0003t0002g0281 a0002c0003t0002g0282 others(2): Show |
5 | HG02886.hp1 HG02922.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-6554T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283100 | |||||||
| chr5:176283140 | A | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-6514A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283140 | |||||||
| chr5:176283231 | A | C | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.130-6423A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283231 | |||||||
| chr5:176283268 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.130-6386C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283268 | |||||||
| chr5:176283357 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.130-6297G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283357 | |||||||
| chr5:176283399 | A | C | 63 | a0001c0001t0001g0115 a0002c0002t0002g0278 a0002c0002t0002g0279 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-6255A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283399 | |||||||
| chr5:176283503 | C | G | 5 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0237 others(2): Show |
5 | NA18974.hp1 NA19003.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-6151C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283503 | |||||||
| chr5:176283544 | G | C | 66 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.130-6110G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283544 | |||||||
| chr5:176283567 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-6087A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283567 | |||||||
| chr5:176283702 | A | G | 2 | a0002c0002t0002g0300 a0002c0002t0002g0301 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.130-5952A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283702 | |||||||
| chr5:176283872 | A | C | 1 | a0002c0002t0002g0328 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.130-5782A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283872 | |||||||
| chr5:176283920 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-5734G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176283920 | |||||||
| chr5:176284043 | C | A | 1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.130-5611C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284043 | |||||||
| chr5:176284044 | A | C | 1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.130-5610A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284044 | |||||||
| chr5:176284135 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-5519A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284135 | |||||||
| chr5:176284235 | C | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-5419C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284235 | |||||||
| chr5:176284323 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-5331T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284323 | |||||||
| chr5:176284413 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-5241T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284413 | |||||||
| chr5:176284425 | TG | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-5225delG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176284425 | ||||||
| chr5:176284433 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130-5221A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284433 | |||||||
| chr5:176284494 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-5160A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284494 | |||||||
| chr5:176284618 | C | G | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-5036C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284618 | |||||||
| chr5:176284733 | T | C | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-4921T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284733 | |||||||
| chr5:176284808 | A | G | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-4846A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284808 | |||||||
| chr5:176284852 | A | C | 19 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(16): Show |
19 | HG00438.hp2 HG02135.hp1 NA18940.hp2 others(16): Show |
intron_variant | MODIFIER | c.130-4802A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284852 | |||||||
| chr5:176284969 | A | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0065 a0001c0001t0001g0067 others(3): Show |
6 | HG00621.hp2 HG02071.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-4685A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284969 | |||||||
| chr5:176284992 | A | G | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-4662A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284992 | |||||||
| chr5:176284993 | C | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-4661C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176284993 | |||||||
| chr5:176285052 | A | C | 1 | a0010c0015t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130-4602A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285052 | |||||||
| chr5:176285058 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.130-4596A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285058 | |||||||
| chr5:176285075 | C | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-4579C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285075 | |||||||
| chr5:176285117 | A | G | 2 | a0007c0008t0001g0178 a0007c0008t0001g0242 |
2 | HG03927.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.130-4537A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285117 | |||||||
| chr5:176285204 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0266 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130-4450A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285204 | |||||||
| chr5:176285226 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-4428C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285226 | |||||||
| chr5:176285287 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.130-4367C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285287 | |||||||
| chr5:176285337 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130-4317A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285337 | |||||||
| chr5:176285439 | A | C | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.130-4215A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285439 | |||||||
| chr5:176285466 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.130-4188T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285466 | |||||||
| chr5:176285482 | G | A | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-4172G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285482 | |||||||
| chr5:176285482 | G | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130-4172G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285482 | |||||||
| chr5:176285502 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.130-4152C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285502 | |||||||
| chr5:176285504 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-4150G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285504 | |||||||
| chr5:176285505 | T | A | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130-4149T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285505 | |||||||
| chr5:176285506 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-4148T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285506 | |||||||
| chr5:176285590 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.130-4064C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285590 | |||||||
| chr5:176285630 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.130-4024C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285630 | |||||||
| chr5:176285642 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.130-4012A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285642 | |||||||
| chr5:176285741 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130-3913A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285741 | |||||||
| chr5:176285743 | C | T | 3 | a0001c0001t0001g0148 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.130-3911C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285743 | |||||||
| chr5:176285755 | A | G | 25 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
25 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-3899A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285755 | |||||||
| chr5:176285836 | G | A | 2 | a0001c0001t0001g0176 a0002c0002t0002g0346 |
2 | HG01081.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.130-3818G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285836 | |||||||
| chr5:176285855 | A | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130-3799A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285855 | |||||||
| chr5:176285885 | A | G | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-3769A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285885 | |||||||
| chr5:176285902 | A | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-3752A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285902 | |||||||
| chr5:176285932 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-3722T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176285932 | |||||||
| chr5:176286023 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-3631A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286023 | |||||||
| chr5:176286029 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-3625G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286029 | |||||||
| chr5:176286050 | G | T | 1 | a0002c0002t0002g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-3604G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286050 | |||||||
| chr5:176286091 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-3563C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286091 | |||||||
| chr5:176286217 | T | C | 66 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.130-3437T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286217 | |||||||
| chr5:176286230 | C | T | 4 | a0002c0002t0002g0280 a0002c0002t0002g0305 a0002c0002t0002g0323 others(1): Show |
4 | NA18967.hp2 NA18984.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-3424C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286230 | |||||||
| chr5:176286303 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-3351A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286303 | |||||||
| chr5:176286331 | C | G | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-3323C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286331 | |||||||
| chr5:176286367 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | NA18990.hp2 NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.130-3287A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286367 | |||||||
| chr5:176286436 | G | T | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.130-3218G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286436 | |||||||
| chr5:176286466 | T | C | 251 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
251 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.130-3188T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286466 | |||||||
| chr5:176286494 | G | C | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-3160G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286494 | |||||||
| chr5:176286506 | A | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130-3148A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286506 | |||||||
| chr5:176286507 | A | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-3147A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286507 | |||||||
| chr5:176286516 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-3138T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286516 | |||||||
| chr5:176286523 | G | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-3131G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286523 | |||||||
| chr5:176286574 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.130-3080T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286574 | |||||||
| chr5:176286594 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-3060A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286594 | |||||||
| chr5:176286897 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.130-2757A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286897 | |||||||
| chr5:176286905 | A | G | 1 | a0002c0002t0002g0306 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.130-2749A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286905 | |||||||
| chr5:176286960 | A | G | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.130-2694A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286960 | |||||||
| chr5:176286966 | A | C | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-2688A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176286966 | |||||||
| chr5:176287035 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130-2619T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287035 | |||||||
| chr5:176287075 | T | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-2579T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287075 | |||||||
| chr5:176287152 | T | C | 129 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(126): Show |
129 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.130-2502T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287152 | |||||||
| chr5:176287248 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-2406C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287248 | |||||||
| chr5:176287271 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.130-2383C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287271 | |||||||
| chr5:176287395 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.130-2259T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287395 | |||||||
| chr5:176287400 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.130-2254G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287400 | |||||||
| chr5:176287489 | T | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-2165T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287489 | |||||||
| chr5:176287508 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.130-2146A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287508 | |||||||
| chr5:176287549 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130-2105C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287549 | |||||||
| chr5:176287579 | T | C | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
178 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.130-2075T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287579 | |||||||
| chr5:176287598 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-2056G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287598 | |||||||
| chr5:176287644 | TTAAAAAT others(3): Show |
T | 16 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.130-1999_130-1990d others(12): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176287644 | ||||||
| chr5:176287647 | AAAAT | A | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
162 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.130-1999_130-1996d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176287647 | ||||||
| chr5:176287696 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.130-1958A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176287696 | |||||||
| chr5:176287714 | GA | G | 9 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0148 others(6): Show |
9 | HG02280.hp1 HG03041.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.130-1930delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176287714 | ||||||
| chr5:176288100 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130-1554G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288100 | |||||||
| chr5:176288179 | C | G | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.130-1475C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288179 | |||||||
| chr5:176288199 | G | C | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130-1455G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288199 | |||||||
| chr5:176288324 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.130-1330C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288324 | |||||||
| chr5:176288410 | A | AGAAT | 8 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
8 | HG02080.hp1 HG02280.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-1231_130-1228d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288410 | ||||||
| chr5:176288419 | G | GAATA | 5 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0001g0074 others(2): Show |
5 | HG00733.hp1 HG01070.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-1232_130-1231i others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288419 | ||||||
| chr5:176288419 | GAATGAAT others(5): Show |
G | 60 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(57): Show |
60 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.130-1231_130-1220d others(14): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288419 | ||||||
| chr5:176288423 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0001g0074 others(3): Show |
6 | HG00323.hp1 HG00733.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-1231G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288423 | |||||||
| chr5:176288423 | G | GAATA | 32 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0017 others(29): Show |
32 | HG00609.hp1 HG01069.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.130-1199_130-1196d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | G | GAATAAAT others(1): Show |
23 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0028 others(20): Show |
23 | HG01069.hp1 HG02055.hp1 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.130-1203_130-1196d others(10): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | G | GAATAAAT others(5): Show |
70 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0030 others(67): Show |
70 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.130-1207_130-1196d others(14): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | G | GAATAAAT others(9): Show |
14 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0061 others(11): Show |
14 | HG00280.hp1 HG01975.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.130-1211_130-1196d others(18): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | G | GAATGAAT others(1): Show |
4 | a0001c0001t0001g0109 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG01175.hp2 HG01952.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1228_130-1227i others(10): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | G | GAATGAAT others(5): Show |
20 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0049 others(17): Show |
20 | HG00423.hp2 HG00544.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.130-1228_130-1227i others(14): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | G | GAATGAAT others(9): Show |
1 | a0001c0001t0001g0065 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.130-1228_130-1227i others(18): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | G | GAATGAAT others(5): Show |
1 | a0001c0010t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.130-1228_130-1227i others(14): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | G | GAATGAAT others(9): Show |
1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-1228_130-1227i others(18): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | GAATAAAT others(5): Show |
G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-1207_130-1196d others(14): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288423 | GAATAAAT others(9): Show |
G | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.130-1211_130-1196d others(18): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176288423 | ||||||
| chr5:176288427 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0261 others(2): Show |
5 | HG01081.hp2 HG02280.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-1227A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288427 | |||||||
| chr5:176288529 | G | C | 1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.130-1125G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288529 | |||||||
| chr5:176288530 | C | G | 1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.130-1124C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288530 | |||||||
| chr5:176288584 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130-1070G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288584 | |||||||
| chr5:176288647 | C | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
8 | HG00733.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-1007C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288647 | |||||||
| chr5:176288754 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
24 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-900C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288754 | |||||||
| chr5:176288912 | T | C | 3 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0248 |
3 | HG00597.hp1 NA18957.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.130-742T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288912 | |||||||
| chr5:176288927 | G | A | 1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.130-727G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288927 | |||||||
| chr5:176288958 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.130-696A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176288958 | |||||||
| chr5:176289190 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.130-464G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176289190 | |||||||
| chr5:176289206 | C | A | 1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.130-448C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176289206 | |||||||
| chr5:176289378 | G | A | 1 | a0002c0002t0002g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-276G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176289378 | |||||||
| chr5:176289415 | GA | G | 60 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0002t0002g0278 others(57): Show |
60 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.130-227delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 176289415 | ||||||
| chr5:176289576 | A | T | 1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.130-78A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176289576 | |||||||
| chr5:176289631 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.130-23T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176289631 | |||||||
| chr5:176289640 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.130-14C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 1/9 | chr5 | 176289640 | |||||||
| chr5:176291011 | G | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1431+56G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291011 | |||||||
| chr5:176291122 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1431+167T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291122 | |||||||
| chr5:176291159 | C | CT | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
220 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1431+226dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176291159 | ||||||
| chr5:176291159 | C | CTT | 9 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0120 others(6): Show |
9 | HG02027.hp2 HG03486.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.1431+225_1431+226d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176291159 | ||||||
| chr5:176291330 | A | AT | 13 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0190 others(10): Show |
13 | HG01358.hp2 HG02074.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1431+399dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176291330 | ||||||
| chr5:176291330 | AT | A | 54 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0052 others(51): Show |
54 | HG00423.hp2 HG00642.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1431+399delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176291330 | ||||||
| chr5:176291330 | ATT | A | 186 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1431+398_1431+399d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176291330 | ||||||
| chr5:176291330 | ATTT | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0170 a0001c0001t0001g0171 others(8): Show |
11 | HG01257.hp1 HG01361.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1431+397_1431+399d others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176291330 | ||||||
| chr5:176291438 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1431+483G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291438 | |||||||
| chr5:176291472 | G | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1431+517G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291472 | |||||||
| chr5:176291552 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1431+597G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291552 | |||||||
| chr5:176291616 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1431+661G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291616 | |||||||
| chr5:176291625 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
24 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1431+670C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291625 | |||||||
| chr5:176291628 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0096 |
2 | NA18963.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1431+673G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291628 | |||||||
| chr5:176291721 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1431+766A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291721 | |||||||
| chr5:176291725 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1431+770G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291725 | |||||||
| chr5:176291768 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1431+813G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291768 | |||||||
| chr5:176291790 | T | G | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1431+835T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291790 | |||||||
| chr5:176291795 | A | G | 249 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1431+840A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291795 | |||||||
| chr5:176291846 | G | A | 1 | a0002c0002t0002g0344 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1431+891G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291846 | |||||||
| chr5:176291865 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1431+910G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291865 | |||||||
| chr5:176291910 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1431+955G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291910 | |||||||
| chr5:176291914 | G | T | 1 | a0002c0003t0002g0329 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1431+959G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291914 | |||||||
| chr5:176291973 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1431+1018C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176291973 | |||||||
| chr5:176292089 | A | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1431+1134A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292089 | |||||||
| chr5:176292192 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1431+1237G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292192 | |||||||
| chr5:176292215 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1431+1260T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292215 | |||||||
| chr5:176292303 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1431+1348C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292303 | |||||||
| chr5:176292309 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1431+1354A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292309 | |||||||
| chr5:176292338 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(16): Show |
19 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1431+1383C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292338 | |||||||
| chr5:176292475 | T | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1431+1520T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292475 | |||||||
| chr5:176292560 | G | A | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1431+1605G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292560 | |||||||
| chr5:176292604 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1431+1649G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292604 | |||||||
| chr5:176292669 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1431+1714C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292669 | |||||||
| chr5:176292710 | T | C | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1431+1755T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292710 | |||||||
| chr5:176292732 | G | T | 12 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0284 others(9): Show |
12 | HG01257.hp1 HG01258.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.1431+1777G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292732 | |||||||
| chr5:176292741 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1431+1786A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292741 | |||||||
| chr5:176292777 | G | A | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1431+1822G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292777 | |||||||
| chr5:176292820 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1431+1865C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292820 | |||||||
| chr5:176292847 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1431+1892G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292847 | |||||||
| chr5:176292902 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1431+1947A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176292902 | |||||||
| chr5:176293151 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1432-1879T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176293151 | |||||||
| chr5:176293343 | G | T | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1432-1687G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176293343 | |||||||
| chr5:176293518 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0190 |
2 | HG00558.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1432-1512T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176293518 | |||||||
| chr5:176293747 | C | CA | 27 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0140 others(24): Show |
27 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1432-1267dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176293747 | ||||||
| chr5:176293747 | CA | C | 71 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0062 others(68): Show |
71 | HG00544.hp1 HG00642.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.1432-1267delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176293747 | ||||||
| chr5:176293816 | G | A | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1432-1214G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176293816 | |||||||
| chr5:176293878 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1432-1152A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176293878 | |||||||
| chr5:176293947 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1432-1083G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176293947 | |||||||
| chr5:176294223 | G | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1432-807G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294223 | |||||||
| chr5:176294227 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1432-803T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294227 | |||||||
| chr5:176294291 | C | CTGTT | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1432-737_1432-734d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176294291 | ||||||
| chr5:176294426 | G | A | 115 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1432-604G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294426 | |||||||
| chr5:176294435 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1432-595C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294435 | |||||||
| chr5:176294539 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1432-491A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294539 | |||||||
| chr5:176294640 | G | C | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1432-390G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294640 | |||||||
| chr5:176294666 | T | C | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1432-364T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294666 | |||||||
| chr5:176294678 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1432-352C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294678 | |||||||
| chr5:176294697 | T | C | 1 | a0002c0002t0002g0298 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1432-333T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294697 | |||||||
| chr5:176294734 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1432-296A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294734 | |||||||
| chr5:176294785 | AC | A | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0265 |
3 | HG02258.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1432-242delC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176294785 | ||||||
| chr5:176294804 | T | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1432-226T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294804 | |||||||
| chr5:176294829 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0297 |
2 | HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1432-201G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294829 | |||||||
| chr5:176294831 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1432-199G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294831 | |||||||
| chr5:176294893 | A | T | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1432-137A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294893 | |||||||
| chr5:176294959 | C | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1432-71C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294959 | |||||||
| chr5:176294963 | T | TC | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1432-66dupC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176294963 | ||||||
| chr5:176294964 | C | CA | 11 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0243 others(8): Show |
11 | HG00609.hp1 HG02109.hp1 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.1432-44dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176294964 | ||||||
| chr5:176294964 | CA | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
150 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1432-44delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176294964 | ||||||
| chr5:176294964 | CAA | C | 11 | a0001c0001t0001g0068 a0001c0001t0001g0116 a0001c0001t0001g0149 others(8): Show |
11 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432-45_1432-44del others(2): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 176294964 | ||||||
| chr5:176294982 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0100 |
2 | HG02257.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1432-48A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 2/9 | chr5 | 176294982 | |||||||
| chr5:176295381 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0169 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1664+119G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 3/9 | chr5 | 176295381 | |||||||
| chr5:176295510 | T | C | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1664+248T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 3/9 | chr5 | 176295510 | |||||||
| chr5:176295611 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1664+349C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 3/9 | chr5 | 176295611 | |||||||
| chr5:176295975 | G | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1665-276G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 3/9 | chr5 | 176295975 | |||||||
| chr5:176296153 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1665-98G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 3/9 | chr5 | 176296153 | |||||||
| chr5:176296753 | A | AG | 5 | a0001c0001t0001g0181 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG00099.hp2 HG00280.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734+433_1734+434i others(3): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176296753 | |||||||
| chr5:176296956 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1734+636C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176296956 | |||||||
| chr5:176296976 | T | C | 260 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
260 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1734+656T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176296976 | |||||||
| chr5:176297059 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1734+739A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297059 | |||||||
| chr5:176297078 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1734+758A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297078 | |||||||
| chr5:176297351 | AT | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+1034delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176297351 | ||||||
| chr5:176297427 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1734+1107A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297427 | |||||||
| chr5:176297469 | TC | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0137 |
3 | HG02630.hp2 HG02738.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1734+1150delC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297469 | |||||||
| chr5:176297502 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1734+1182C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297502 | |||||||
| chr5:176297502 | C | CA | 100 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0012 others(97): Show |
100 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1734+1207dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176297502 | ||||||
| chr5:176297502 | CA | C | 51 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0140 others(48): Show |
51 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1734+1207delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176297502 | ||||||
| chr5:176297547 | A | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1734+1227A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297547 | |||||||
| chr5:176297548 | A | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1734+1228A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297548 | |||||||
| chr5:176297549 | T | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1734+1229T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297549 | |||||||
| chr5:176297550 | A | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1734+1230A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297550 | |||||||
| chr5:176297551 | A | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1734+1231A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297551 | |||||||
| chr5:176297643 | C | T | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1734+1323C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297643 | |||||||
| chr5:176297647 | C | G | 183 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(180): Show |
183 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1734+1327C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297647 | |||||||
| chr5:176297672 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(2): Show |
5 | HG02965.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734+1352T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297672 | |||||||
| chr5:176297761 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1734+1441G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297761 | |||||||
| chr5:176297896 | T | C | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1734+1576T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176297896 | |||||||
| chr5:176298376 | A | G | 66 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1734+2056A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298376 | |||||||
| chr5:176298388 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1734+2068G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298388 | |||||||
| chr5:176298424 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1734+2104G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298424 | |||||||
| chr5:176298465 | C | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1734+2145C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298465 | |||||||
| chr5:176298495 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1734+2175G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298495 | |||||||
| chr5:176298498 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1734+2178G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298498 | |||||||
| chr5:176298559 | A | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1734+2239A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298559 | |||||||
| chr5:176298616 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1734+2296C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298616 | |||||||
| chr5:176298700 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1734+2380G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298700 | |||||||
| chr5:176298759 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+2439T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298759 | |||||||
| chr5:176298929 | G | A | 1 | a0002c0003t0002g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1734+2609G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298929 | |||||||
| chr5:176298994 | T | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG00733.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1734+2674T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176298994 | |||||||
| chr5:176299007 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1734+2687C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176299007 | |||||||
| chr5:176299131 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1734+2811C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176299131 | |||||||
| chr5:176299132 | G | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0220 others(1): Show |
4 | HG02071.hp1 HG02155.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+2812G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176299132 | |||||||
| chr5:176299392 | TA | T | 58 | a0001c0001t0001g0205 a0002c0002t0002g0278 a0002c0002t0002g0279 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1734+3086delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176299392 | ||||||
| chr5:176299566 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+3246A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176299566 | |||||||
| chr5:176299764 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0066 |
2 | NA18942.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1734+3444A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176299764 | |||||||
| chr5:176299780 | CCATAGA | C | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+3465_1734+347 others(10): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176299780 | ||||||
| chr5:176299923 | A | G | 4 | a0002c0003t0002g0281 a0002c0003t0002g0282 a0002c0003t0002g0283 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734+3603A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176299923 | |||||||
| chr5:176300111 | A | C | 1 | a0001c0001t0001g0294 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1734+3791A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300111 | |||||||
| chr5:176300184 | C | T | 1 | a0002c0002t0002g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1734+3864C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300184 | |||||||
| chr5:176300364 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1734+4044G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300364 | |||||||
| chr5:176300417 | C | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1734+4097C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300417 | |||||||
| chr5:176300485 | A | AT | 246 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1734+4171dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176300485 | ||||||
| chr5:176300504 | C | A | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1734+4184C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300504 | |||||||
| chr5:176300520 | CT | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+4201delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300520 | |||||||
| chr5:176300522 | A | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+4202A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300522 | |||||||
| chr5:176300523 | A | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+4203A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300523 | |||||||
| chr5:176300544 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1734+4224A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300544 | |||||||
| chr5:176300563 | T | C | 54 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(51): Show |
54 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1734+4243T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300563 | |||||||
| chr5:176300587 | A | G | 54 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(51): Show |
54 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1734+4267A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300587 | |||||||
| chr5:176300766 | G | A | 1 | a0001c0010t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1734+4446G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300766 | |||||||
| chr5:176300809 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+4489A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300809 | |||||||
| chr5:176300811 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1734+4491A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300811 | |||||||
| chr5:176300819 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1734+4499C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300819 | |||||||
| chr5:176300882 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1734+4562A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300882 | |||||||
| chr5:176300891 | C | T | 1 | a0009c0013t0001g0016 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1734+4571C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300891 | |||||||
| chr5:176300892 | A | G | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1734+4572A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176300892 | |||||||
| chr5:176301212 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1734+4892G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301212 | |||||||
| chr5:176301338 | C | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+5018C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301338 | |||||||
| chr5:176301339 | T | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+5019T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301339 | |||||||
| chr5:176301410 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1734+5090C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301410 | |||||||
| chr5:176301411 | A | G | 125 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(122): Show |
125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1734+5091A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301411 | |||||||
| chr5:176301411 | A | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0001t0001g0130 |
3 | HG00597.hp2 NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1734+5091A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301411 | |||||||
| chr5:176301553 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1734+5233G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301553 | |||||||
| chr5:176301701 | C | G | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.1734+5381C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301701 | |||||||
| chr5:176301742 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1734+5422G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301742 | |||||||
| chr5:176301778 | C | CA | 65 | a0001c0001t0001g0122 a0001c0001t0001g0243 a0002c0002t0002g0278 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1734+5473dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176301778 | ||||||
| chr5:176301972 | T | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG00733.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1734+5652T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176301972 | |||||||
| chr5:176302050 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1734+5730C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176302050 | |||||||
| chr5:176302177 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1734+5857G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176302177 | |||||||
| chr5:176302675 | A | C | 3 | a0003c0004t0001g0355 a0003c0004t0001g0356 a0003c0004t0001g0357 |
3 | HG01496.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1734+6355A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176302675 | |||||||
| chr5:176303267 | T | C | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+6947T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303267 | |||||||
| chr5:176303268 | T | TA | 9 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0277 others(6): Show |
9 | HG00544.hp1 HG00733.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1734+6967dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176303268 | ||||||
| chr5:176303268 | TA | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0076 a0001c0001t0001g0094 others(77): Show |
80 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1734+6967delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176303268 | ||||||
| chr5:176303268 | TAA | T | 174 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1734+6966_1734+696 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176303268 | ||||||
| chr5:176303325 | A | AT | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(173): Show |
176 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1734+7024dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176303325 | ||||||
| chr5:176303325 | A | ATT | 34 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0046 others(31): Show |
34 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1734+7023_1734+702 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176303325 | ||||||
| chr5:176303325 | AT | A | 8 | a0001c0001t0001g0153 a0001c0001t0001g0187 a0001c0001t0001g0220 others(5): Show |
8 | HG02055.hp1 HG02155.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1734+7024delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176303325 | ||||||
| chr5:176303333 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1734+7013T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303333 | |||||||
| chr5:176303388 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+7068C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303388 | |||||||
| chr5:176303392 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1734+7072A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303392 | |||||||
| chr5:176303409 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1734+7089C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303409 | |||||||
| chr5:176303470 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1734+7150C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303470 | |||||||
| chr5:176303476 | C | G | 13 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(10): Show |
13 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1734+7156C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303476 | |||||||
| chr5:176303482 | C | T | 1 | a0002c0002t0002g0315 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1734+7162C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303482 | |||||||
| chr5:176303483 | G | A | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1734+7163G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303483 | |||||||
| chr5:176303537 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1734+7217C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303537 | |||||||
| chr5:176303567 | G | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1734+7247G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303567 | |||||||
| chr5:176303572 | G | A | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+7252G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303572 | |||||||
| chr5:176303646 | A | G | 1 | a0002c0002t0002g0310 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1734+7326A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303646 | |||||||
| chr5:176303804 | G | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1734+7484G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303804 | |||||||
| chr5:176303833 | T | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
22 | HG00558.hp2 HG00609.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1734+7513T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176303833 | |||||||
| chr5:176303896 | ATTAAC | A | 14 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(11): Show |
14 | HG00544.hp2 HG02027.hp2 NA18943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1734+7581_1734+758 others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176303896 | ||||||
| chr5:176304056 | A | G | 1 | a0002c0002t0002g0308 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1734+7736A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304056 | |||||||
| chr5:176304187 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1734+7867A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304187 | |||||||
| chr5:176304189 | AT | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1734+7870delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304189 | |||||||
| chr5:176304212 | A | AGCTCCCT others(5): Show |
1 | a0001c0001t0001g0232 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1734+7893_1734+790 others(16): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176304212 | ||||||
| chr5:176304213 | G | GCTCCCT | 170 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
170 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1734+7915_1734+792 others(10): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176304213 | ||||||
| chr5:176304213 | G | GCTCCCTC others(5): Show |
11 | a0001c0001t0001g0131 a0002c0002t0002g0299 a0002c0002t0002g0300 others(8): Show |
11 | HG02027.hp2 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1734+7909_1734+792 others(16): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176304213 | ||||||
| chr5:176304213 | G | GCTCCCTC others(11): Show |
50 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(47): Show |
50 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1734+7903_1734+792 others(22): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176304213 | ||||||
| chr5:176304213 | G | GCTCCCTC others(17): Show |
6 | a0002c0002t0002g0306 a0002c0002t0002g0344 a0002c0003t0001g0349 others(3): Show |
6 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734+7897_1734+792 others(28): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176304213 | ||||||
| chr5:176304235 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1734+7915C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304235 | |||||||
| chr5:176304251 | G | A | 31 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0033 others(28): Show |
31 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1734+7931G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304251 | |||||||
| chr5:176304261 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1734+7941T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304261 | |||||||
| chr5:176304325 | G | C | 128 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1734+8005G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304325 | |||||||
| chr5:176304350 | A | G | 66 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1734+8030A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304350 | |||||||
| chr5:176304353 | A | G | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1734+8033A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304353 | |||||||
| chr5:176304402 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+8082C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304402 | |||||||
| chr5:176304421 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1734+8101G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304421 | |||||||
| chr5:176304457 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1734+8137G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304457 | |||||||
| chr5:176304468 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1734+8148T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304468 | |||||||
| chr5:176304476 | C | T | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1734+8156C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304476 | |||||||
| chr5:176304500 | C | G | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1734+8180C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304500 | |||||||
| chr5:176304556 | G | A | 1 | a0002c0002t0002g0358 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1734+8236G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304556 | |||||||
| chr5:176304566 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1734+8246G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304566 | |||||||
| chr5:176304581 | G | A | 4 | a0005c0006t0002g0330 a0005c0006t0002g0332 a0005c0006t0002g0333 others(1): Show |
4 | NA18955.hp2 NA18978.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+8261G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304581 | |||||||
| chr5:176304607 | A | AC | 14 | a0001c0001t0001g0023 a0001c0001t0001g0067 a0001c0001t0001g0132 others(11): Show |
14 | HG00621.hp2 HG01257.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1734+8291dupC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176304607 | ||||||
| chr5:176304611 | C | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0248 |
2 | NA18957.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1734+8291C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304611 | |||||||
| chr5:176304611 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(7): Show |
10 | HG00558.hp2 HG00609.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1734+8291C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304611 | |||||||
| chr5:176304651 | G | A | 1 | a0002c0002t0002g0342 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1734+8331G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304651 | |||||||
| chr5:176304711 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+8391C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304711 | |||||||
| chr5:176304751 | T | C | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1734+8431T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304751 | |||||||
| chr5:176304795 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1734+8475G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304795 | |||||||
| chr5:176304843 | A | T | 2 | a0002c0002t0002g0336 a0002c0002t0002g0337 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1734+8523A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304843 | |||||||
| chr5:176304883 | G | A | 1 | a0002c0002t0002g0346 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1734+8563G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304883 | |||||||
| chr5:176304892 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0070 |
3 | NA18941.hp2 NA18959.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1734+8572G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304892 | |||||||
| chr5:176304896 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1734+8576C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304896 | |||||||
| chr5:176304911 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1734+8591G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304911 | |||||||
| chr5:176304920 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1734+8600G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304920 | |||||||
| chr5:176304949 | G | A | 128 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1734+8629G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304949 | |||||||
| chr5:176304960 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1734+8640G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304960 | |||||||
| chr5:176304987 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0148 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1734+8667C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304987 | |||||||
| chr5:176304999 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1734+8679C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176304999 | |||||||
| chr5:176305027 | C | T | 5 | a0001c0001t0001g0148 a0002c0003t0001g0349 a0002c0003t0001g0350 others(2): Show |
5 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-8664C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305027 | |||||||
| chr5:176305028 | G | C | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1735-8663G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305028 | |||||||
| chr5:176305060 | C | T | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1735-8631C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305060 | |||||||
| chr5:176305094 | T | TG | 10 | a0001c0001t0001g0023 a0001c0001t0001g0140 a0001c0001t0001g0141 others(7): Show |
10 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1735-8591dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305094 | ||||||
| chr5:176305104 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1735-8587G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305104 | |||||||
| chr5:176305115 | C | T | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1735-8576C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305115 | |||||||
| chr5:176305136 | A | AG | 39 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0174 others(36): Show |
39 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1735-8544dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | A | AGCG | 26 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1735-8554_1735-855 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | A | AGCGGGG | 25 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(22): Show |
25 | HG00438.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1735-8554_1735-855 others(10): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | A | AGCGGGGG | 56 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0033 others(53): Show |
56 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1735-8554_1735-855 others(11): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | A | AGCGGGGG others(1): Show |
24 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0041 others(21): Show |
24 | HG00280.hp1 HG01256.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1735-8554_1735-855 others(12): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | A | AGCGGGGG others(3): Show |
2 | a0001c0001t0001g0087 a0001c0001t0001g0092 |
2 | HG03704.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1735-8554_1735-855 others(14): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | A | AGCGGGGG others(4): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0109 a0001c0001t0001g0169 |
3 | HG03453.hp1 NA18957.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1735-8554_1735-855 others(15): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | A | AGCGGGGG others(5): Show |
3 | a0001c0001t0001g0094 a0001c0001t0001g0111 a0001c0001t0001g0137 |
3 | HG02738.hp1 HG03492.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1735-8554_1735-855 others(16): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | A | AGCGGGGG others(6): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0268 |
2 | NA19082.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1735-8554_1735-855 others(17): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305136 | AG | A | 46 | a0001c0001t0001g0176 a0002c0002t0002g0278 a0002c0002t0002g0279 others(43): Show |
46 | HG00099.hp1 HG00741.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1735-8544delG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305136 | ||||||
| chr5:176305138 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1735-8553G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305138 | |||||||
| chr5:176305139 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1735-8552G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305139 | |||||||
| chr5:176305139 | G | C | 1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1735-8552G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305139 | |||||||
| chr5:176305141 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1735-8550G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305141 | |||||||
| chr5:176305147 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1735-8544G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305147 | |||||||
| chr5:176305166 | AGCCGT | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-8519_1735-851 others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305166 | ||||||
| chr5:176305169 | C | T | 1 | a0003c0004t0001g0357 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1735-8522C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305169 | |||||||
| chr5:176305178 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1735-8513C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305178 | |||||||
| chr5:176305189 | T | TG | 245 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
245 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1735-8496dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305189 | ||||||
| chr5:176305217 | C | T | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8474C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305217 | |||||||
| chr5:176305218 | G | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1735-8473G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305218 | |||||||
| chr5:176305226 | T | C | 128 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1735-8465T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305226 | |||||||
| chr5:176305254 | C | T | 1 | a0001c0010t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1735-8437C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305254 | |||||||
| chr5:176305290 | C | CCAGCCAC others(476): Show |
1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1735-8387_1735-838 others(487): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(473): Show |
5 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0271 others(2): Show |
5 | HG00741.hp2 HG01975.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1735-8387_1735-838 others(484): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(531): Show |
1 | a0001c0001t0001g0359 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(542): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(485): Show |
1 | a0001c0001t0001g0216 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(496): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(484): Show |
1 | a0001c0001t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(495): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(484): Show |
1 | a0001c0001t0001g0213 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(495): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(484): Show |
1 | a0001c0001t0001g0220 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(495): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(531): Show |
1 | a0001c0001t0001g0177 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(542): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(531): Show |
1 | a0001c0001t0001g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(542): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(531): Show |
1 | a0001c0001t0001g0197 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(542): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(528): Show |
1 | a0001c0001t0001g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(539): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(479): Show |
3 | a0001c0001t0001g0201 a0006c0007t0001g0195 a0006c0007t0001g0198 |
3 | HG00621.hp1 NA18951.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(490): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(477): Show |
1 | a0001c0001t0001g0232 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(488): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(531): Show |
1 | a0001c0001t0001g0237 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(542): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(529): Show |
1 | a0001c0001t0001g0186 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(540): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(529): Show |
2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | NA19003.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(540): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(528): Show |
11 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0203 others(8): Show |
11 | HG01256.hp1 HG01261.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(539): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(527): Show |
2 | a0001c0001t0001g0261 a0001c0001t0001g0263 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(538): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(527): Show |
1 | a0007c0008t0001g0178 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(538): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(527): Show |
38 | a0001c0001t0001g0004 a0001c0001t0001g0175 a0001c0001t0001g0176 others(35): Show |
38 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(538): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(527): Show |
1 | a0001c0001t0001g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(538): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(526): Show |
5 | a0001c0001t0001g0259 a0001c0001t0001g0262 a0001c0001t0001g0264 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(537): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(526): Show |
20 | a0001c0001t0001g0139 a0001c0001t0001g0180 a0001c0001t0001g0204 others(17): Show |
20 | HG01891.hp2 HG02109.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(537): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(1279): Show |
1 | a0001c0001t0001g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(1290): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(526): Show |
1 | a0001c0001t0001g0222 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(537): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(752): Show |
2 | a0001c0001t0001g0227 a0001c0001t0001g0235 |
2 | NA19007.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(763): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(751): Show |
2 | a0001c0001t0001g0182 a0001c0001t0001g0190 |
2 | HG00558.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(762): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(528): Show |
1 | a0001c0001t0001g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(539): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(527): Show |
1 | a0001c0001t0001g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(538): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305290 | C | CCAGCCAC others(527): Show |
1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(538): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305290 | ||||||
| chr5:176305304 | C | T | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1735-8387C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305304 | |||||||
| chr5:176305304 | CGGGAGGG others(208): Show |
C | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-8369_1735-815 others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305304 | ||||||
| chr5:176305314 | G | A | 6 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00741.hp2 HG01975.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1735-8377G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305314 | |||||||
| chr5:176305314 | G | GTGGGGGG others(477): Show |
1 | a0001c0001t0001g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(488): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(475): Show |
1 | a0001c0001t0001g0093 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(486): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(474): Show |
1 | a0001c0001t0001g0066 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(485): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(479): Show |
1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(490): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(478): Show |
1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(489): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(475): Show |
1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(486): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(474): Show |
1 | a0001c0001t0001g0114 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(485): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(478): Show |
4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG01884.hp1 HG02897.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(489): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(478): Show |
4 | a0001c0001t0001g0153 a0001c0001t0001g0158 a0004c0005t0001g0161 others(1): Show |
4 | HG02055.hp1 HG02897.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(489): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(478): Show |
1 | a0001c0001t0001g0012 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(489): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(477): Show |
4 | a0001c0001t0001g0140 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG01109.hp2 HG01167.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(488): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(477): Show |
15 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(12): Show |
15 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(488): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(477): Show |
14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(11): Show |
14 | HG00558.hp2 HG00609.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(488): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(476): Show |
2 | a0003c0004t0001g0356 a0003c0004t0001g0357 |
2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(487): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(476): Show |
1 | a0003c0004t0001g0355 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(487): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(476): Show |
1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(487): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(477): Show |
1 | a0001c0001t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(488): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(477): Show |
1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(488): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(474): Show |
1 | a0001c0001t0001g0109 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(485): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(475): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0086 |
2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(486): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(474): Show |
1 | a0001c0001t0001g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(485): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(474): Show |
1 | a0001c0001t0001g0127 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(485): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(473): Show |
1 | a0001c0001t0001g0070 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(484): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(476): Show |
1 | a0001c0001t0001g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(487): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(474): Show |
1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(485): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(474): Show |
5 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0080 others(2): Show |
5 | HG00597.hp2 HG00621.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(485): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(473): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0360 |
3 | NA18946.hp1 NA18980.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(484): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(474): Show |
2 | a0001c0001t0001g0046 a0001c0001t0001g0132 |
2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(485): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(473): Show |
84 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(81): Show |
84 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1735-8370_1735-836 others(484): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(472): Show |
1 | a0001c0001t0001g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(483): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305314 | G | GTGGGGGG others(785): Show |
1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(796): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305314 | ||||||
| chr5:176305315 | T | TG | 58 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1735-8370dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305315 | ||||||
| chr5:176305315 | T | TGGGGGGG others(531): Show |
1 | a0001c0001t0001g0234 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(542): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305315 | ||||||
| chr5:176305315 | T | TGGGGGGG others(529): Show |
1 | a0001c0001t0001g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(540): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305315 | ||||||
| chr5:176305315 | T | TGGGGGGG others(476): Show |
1 | a0001c0001t0001g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1735-8370_1735-836 others(487): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305315 | ||||||
| chr5:176305315 | TGGGGGGT others(34): Show |
T | 21 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(18): Show |
21 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1735-8369_1735-832 others(45): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305315 | ||||||
| chr5:176305329 | CG | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8361delG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305329 | |||||||
| chr5:176305331 | A | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8360A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305331 | |||||||
| chr5:176305336 | C | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8355C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305336 | |||||||
| chr5:176305346 | T | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8345T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305346 | |||||||
| chr5:176305347 | G | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8344G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305347 | |||||||
| chr5:176305350 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(5): Show |
8 | HG01081.hp2 HG01361.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1735-8341A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305350 | |||||||
| chr5:176305353 | C | CG | 74 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0175 others(71): Show |
74 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1735-8328dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305353 | ||||||
| chr5:176305353 | C | CGG | 44 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0082 others(41): Show |
44 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1735-8329_1735-832 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305353 | ||||||
| chr5:176305353 | C | CGGG | 44 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(41): Show |
44 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1735-8330_1735-832 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305353 | ||||||
| chr5:176305353 | C | CGGGG | 89 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(86): Show |
89 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1735-8331_1735-832 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305353 | ||||||
| chr5:176305353 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0148 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1735-8338C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305353 | |||||||
| chr5:176305356 | G | GAGGGAGG others(129): Show |
2 | a0002c0002t0002g0308 a0002c0002t0002g0315 |
2 | HG03927.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1735-8335_1735-833 others(140): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305356 | |||||||
| chr5:176305356 | G | GAGGGAGG others(128): Show |
1 | a0002c0002t0002g0319 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1735-8335_1735-833 others(139): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305356 | |||||||
| chr5:176305356 | G | GAGGGAGG others(128): Show |
55 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(52): Show |
55 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1735-8335_1735-833 others(139): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305356 | |||||||
| chr5:176305356 | G | GAGGGAGG others(177): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0026 |
2 | HG01081.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1735-8335_1735-833 others(188): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305356 | |||||||
| chr5:176305356 | G | GAGGGAGG others(226): Show |
1 | a0001c0001t0001g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1735-8335_1735-833 others(237): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305356 | |||||||
| chr5:176305356 | G | GAGGGAGG others(275): Show |
1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1735-8335_1735-833 others(286): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305356 | |||||||
| chr5:176305367 | G | GC | 352 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(349): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.1735-8319dupC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305367 | ||||||
| chr5:176305376 | T | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8315T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305376 | |||||||
| chr5:176305386 | T | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(80): Show |
83 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.1735-8305T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305386 | |||||||
| chr5:176305387 | G | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(80): Show |
83 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.1735-8304G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305387 | |||||||
| chr5:176305390 | G | A | 1 | a0002c0002t0002g0321 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1735-8301G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305390 | |||||||
| chr5:176305404 | T | TG | 63 | a0001c0001t0001g0061 a0001c0001t0001g0197 a0001c0001t0001g0232 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1735-8280dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305404 | ||||||
| chr5:176305415 | G | GC | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(267): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1735-8271dupC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305415 | ||||||
| chr5:176305418 | C | CT | 21 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(18): Show |
21 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1735-8273_1735-827 others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305418 | |||||||
| chr5:176305420 | C | CCT | 59 | a0001c0001t0001g0277 a0002c0002t0002g0278 a0002c0002t0002g0279 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1735-8271_1735-827 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305420 | |||||||
| chr5:176305421 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0193 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1735-8270G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305421 | |||||||
| chr5:176305421 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1735-8270G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305421 | |||||||
| chr5:176305430 | G | A | 20 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(17): Show |
20 | HG01175.hp2 HG01952.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1735-8261G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305430 | |||||||
| chr5:176305430 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1735-8261G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305430 | |||||||
| chr5:176305433 | G | C | 21 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(18): Show |
21 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1735-8258G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305433 | |||||||
| chr5:176305437 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0246 |
2 | HG03209.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1735-8254C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305437 | |||||||
| chr5:176305441 | T | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0215 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8250T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305441 | |||||||
| chr5:176305443 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1735-8248G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305443 | |||||||
| chr5:176305456 | G | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1735-8235G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305456 | |||||||
| chr5:176305458 | C | T | 59 | a0001c0001t0001g0277 a0002c0002t0002g0278 a0002c0002t0002g0279 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1735-8233C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305458 | |||||||
| chr5:176305469 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1735-8222C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305469 | |||||||
| chr5:176305498 | A | T | 83 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(80): Show |
83 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.1735-8193A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305498 | |||||||
| chr5:176305502 | C | CGGCAGCT others(166): Show |
1 | a0001c0001t0001g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1735-8186_1735-818 others(177): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305502 | ||||||
| chr5:176305505 | C | CAGCTGCC others(72): Show |
1 | a0001c0001t0001g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1735-8186_1735-818 others(83): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305505 | |||||||
| chr5:176305505 | C | CAGCTGCC others(72): Show |
1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1735-8186_1735-818 others(83): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305505 | |||||||
| chr5:176305511 | A | G | 81 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0115 others(78): Show |
81 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1735-8180A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305511 | |||||||
| chr5:176305512 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1735-8179C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305512 | |||||||
| chr5:176305513 | C | G | 1 | a0001c0001t0001g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1735-8178C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305513 | |||||||
| chr5:176305516 | G | A | 59 | a0001c0001t0001g0277 a0002c0002t0002g0278 a0002c0002t0002g0279 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1735-8175G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305516 | |||||||
| chr5:176305519 | T | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(80): Show |
83 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.1735-8172T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305519 | |||||||
| chr5:176305527 | A | AGATGGGG others(38): Show |
1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1735-8163_1735-816 others(49): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305527 | ||||||
| chr5:176305530 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1735-8161T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305530 | |||||||
| chr5:176305530 | T | TG | 10 | a0001c0001t0001g0132 a0001c0001t0001g0177 a0001c0001t0001g0226 others(7): Show |
10 | HG00597.hp1 HG01934.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1735-8154dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305530 | ||||||
| chr5:176305530 | T | TGGGGGGT others(35): Show |
1 | a0001c0001t0001g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1735-8155_1735-815 others(46): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305530 | ||||||
| chr5:176305545 | CCCGCCTG others(120): Show |
C | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1735-8144_1735-801 others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305545 | ||||||
| chr5:176305547 | C | T | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1735-8144C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305547 | |||||||
| chr5:176305551 | T | C | 80 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0115 others(77): Show |
80 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.1735-8140T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305551 | |||||||
| chr5:176305560 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG02451.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1735-8131G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305560 | |||||||
| chr5:176305560 | G | GCCCCGTC others(71): Show |
1 | a0001c0001t0001g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1735-8124_1735-812 others(82): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305560 | ||||||
| chr5:176305561 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0215 |
2 | HG01081.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1735-8130C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305561 | |||||||
| chr5:176305562 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0215 |
2 | HG01081.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1735-8129C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305562 | |||||||
| chr5:176305565 | G | A | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-8126G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305565 | |||||||
| chr5:176305579 | T | TGGG | 46 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(43): Show |
46 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.1735-8107_1735-810 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305579 | ||||||
| chr5:176305590 | G | GC | 5 | a0001c0001t0001g0277 a0002c0003t0001g0349 a0002c0003t0001g0350 others(2): Show |
5 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-8098dupC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305590 | ||||||
| chr5:176305590 | G | GCCCCCCG others(45): Show |
12 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(9): Show |
12 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1735-8098_1735-809 others(56): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305590 | ||||||
| chr5:176305590 | G | GCCCCCCG others(46): Show |
1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1735-8098_1735-809 others(57): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305590 | ||||||
| chr5:176305590 | G | GCCCCCCG others(96): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0244 |
2 | NA18945.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1735-8098_1735-809 others(107): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305590 | ||||||
| chr5:176305590 | G | GCCCCCCG others(95): Show |
1 | a0001c0001t0001g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1735-8098_1735-809 others(106): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305590 | ||||||
| chr5:176305594 | T | C | 81 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0115 others(78): Show |
81 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1735-8097T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305594 | |||||||
| chr5:176305596 | C | CT | 56 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(53): Show |
56 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1735-8095_1735-809 others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305596 | |||||||
| chr5:176305596 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0143 |
2 | HG01884.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1735-8095C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305596 | |||||||
| chr5:176305606 | A | G | 81 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0115 others(78): Show |
81 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1735-8085A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305606 | |||||||
| chr5:176305609 | C | G | 81 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0115 others(78): Show |
81 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1735-8082C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305609 | |||||||
| chr5:176305617 | T | A | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1735-8074T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305617 | |||||||
| chr5:176305617 | T | C | 78 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(75): Show |
78 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1735-8074T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305617 | |||||||
| chr5:176305626 | A | G | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1735-8065A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305626 | |||||||
| chr5:176305629 | G | T | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1735-8062G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305629 | |||||||
| chr5:176305630 | GCGCCTCT others(17): Show |
G | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1735-8060_1735-803 others(28): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305630 | |||||||
| chr5:176305631 | C | G | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1735-8060C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305631 | |||||||
| chr5:176305632 | G | A | 2 | a0001c0001t0001g0148 a0002c0002t0002g0321 |
2 | NA18906.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-8059G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305632 | |||||||
| chr5:176305633 | C | T | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1735-8058C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305633 | |||||||
| chr5:176305634 | C | T | 3 | a0001c0001t0001g0078 a0002c0002t0002g0321 a0003c0016t0001g0348 |
3 | HG03130.hp1 NA18949.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1735-8057C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305634 | |||||||
| chr5:176305634 | CTCTGCCC others(24): Show |
C | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1735-8056_1735-802 others(35): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305634 | |||||||
| chr5:176305645 | T | C | 79 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0115 others(76): Show |
79 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.1735-8046T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305645 | |||||||
| chr5:176305658 | A | G | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1735-8033A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305658 | |||||||
| chr5:176305659 | A | G | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1735-8032A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305659 | |||||||
| chr5:176305662 | G | C | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1735-8029G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305662 | |||||||
| chr5:176305672 | T | C | 1 | a0003c0004t0001g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1735-8019T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305672 | |||||||
| chr5:176305674 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0215 |
2 | HG01081.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1735-8017T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305674 | |||||||
| chr5:176305674 | T | C | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1735-8017T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305674 | |||||||
| chr5:176305678 | C | CGGCAGCT others(167): Show |
1 | a0001c0001t0001g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1735-8010_1735-800 others(178): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305678 | ||||||
| chr5:176305678 | C | CGGCAGCT others(166): Show |
1 | a0001c0001t0001g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1735-8010_1735-800 others(177): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305678 | ||||||
| chr5:176305680 | GC | G | 62 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8009delC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305680 | ||||||
| chr5:176305681 | C | CAGCTGCC others(72): Show |
1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1735-8010_1735-800 others(83): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305681 | |||||||
| chr5:176305681 | C | CAGCTGCC others(72): Show |
1 | a0001c0001t0001g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1735-8010_1735-800 others(83): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305681 | |||||||
| chr5:176305681 | C | CAGCTGCC others(72): Show |
4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-8010_1735-800 others(83): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305681 | |||||||
| chr5:176305681 | C | CAGCTGCC others(72): Show |
1 | a0002c0002t0002g0319 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1735-8010_1735-800 others(83): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305681 | |||||||
| chr5:176305681 | C | CAGCTGCC others(72): Show |
4 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02630.hp2 HG02738.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-8010_1735-800 others(83): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305681 | |||||||
| chr5:176305686 | C | T | 62 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-8005C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305686 | |||||||
| chr5:176305687 | G | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0115 others(10): Show |
13 | HG01081.hp2 HG01361.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1735-8004G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305687 | |||||||
| chr5:176305688 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0169 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1735-8003C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305688 | |||||||
| chr5:176305689 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0169 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1735-8002C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305689 | |||||||
| chr5:176305691 | C | G | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1735-8000C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305691 | |||||||
| chr5:176305691 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0008c0009t0001g0135 |
3 | HG00423.hp2 HG00438.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1735-8000C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305691 | |||||||
| chr5:176305692 | G | A | 3 | a0002c0002t0002g0319 a0002c0002t0002g0321 a0003c0016t0001g0348 |
3 | HG03130.hp1 NA18949.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1735-7999G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305692 | |||||||
| chr5:176305695 | C | T | 64 | a0001c0001t0001g0026 a0001c0001t0001g0117 a0001c0001t0001g0118 others(61): Show |
64 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1735-7996C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305695 | |||||||
| chr5:176305697 | G | A | 62 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-7994G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305697 | |||||||
| chr5:176305699 | A | AAGTGAGG others(29): Show |
9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7992_1735-799 others(40): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305699 | |||||||
| chr5:176305699 | A | AAGTGAGG others(118): Show |
53 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(50): Show |
53 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1735-7992_1735-799 others(129): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305699 | |||||||
| chr5:176305703 | A | AGATGGGG others(38): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0137 |
2 | HG02738.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1735-7987_1735-798 others(49): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305703 | ||||||
| chr5:176305703 | A | AGATGGGG others(39): Show |
1 | a0001c0001t0001g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1735-7987_1735-798 others(50): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305703 | ||||||
| chr5:176305703 | A | AGATGGGG others(40): Show |
1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1735-7987_1735-798 others(51): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305703 | ||||||
| chr5:176305703 | A | G | 53 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(50): Show |
53 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1735-7988A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305703 | |||||||
| chr5:176305704 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7987G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305704 | |||||||
| chr5:176305706 | T | A | 53 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(50): Show |
53 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1735-7985T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305706 | |||||||
| chr5:176305706 | T | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02630.hp2 HG02738.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-7985T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305706 | |||||||
| chr5:176305706 | T | TGGGGGGT others(35): Show |
2 | a0001c0001t0001g0258 a0001c0001t0001g0277 |
2 | HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1735-7979_1735-797 others(46): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305706 | ||||||
| chr5:176305706 | T | TGGGGGGT others(38): Show |
4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-7979_1735-797 others(49): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305706 | ||||||
| chr5:176305706 | T | TGGGGGGT others(39): Show |
1 | a0002c0002t0002g0319 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1735-7979_1735-797 others(50): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305706 | ||||||
| chr5:176305708 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7983G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305708 | |||||||
| chr5:176305708 | GGGGGGTC others(42): Show |
G | 7 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0082 others(4): Show |
7 | HG03688.hp1 NA18971.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-7967_1735-791 others(53): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305708 | ||||||
| chr5:176305710 | GGGGTC | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7980_1735-797 others(9): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305710 | |||||||
| chr5:176305712 | GGTCAGCC others(91): Show |
G | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7934_1735-783 others(102): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305712 | ||||||
| chr5:176305718 | C | CG | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1735-7973_1735-797 others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305718 | |||||||
| chr5:176305719 | C | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1735-7972C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305719 | |||||||
| chr5:176305720 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1735-7971C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305720 | |||||||
| chr5:176305721 | C | T | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7970C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305721 | |||||||
| chr5:176305724 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1735-7967G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305724 | |||||||
| chr5:176305727 | C | T | 65 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0115 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1735-7964C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305727 | |||||||
| chr5:176305729 | GC | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7960delC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305729 | ||||||
| chr5:176305736 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7955G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305736 | |||||||
| chr5:176305737 | C | T | 64 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(61): Show |
64 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1735-7954C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305737 | |||||||
| chr5:176305738 | C | G | 64 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(61): Show |
64 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1735-7953C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305738 | |||||||
| chr5:176305741 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1735-7950G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305741 | |||||||
| chr5:176305754 | G | A | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1735-7937G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305754 | |||||||
| chr5:176305755 | T | TG | 7 | a0001c0001t0001g0012 a0001c0001t0001g0063 a0001c0001t0001g0108 others(4): Show |
7 | HG01261.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1735-7935dupG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305755 | ||||||
| chr5:176305756 | G | A | 57 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(54): Show |
57 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1735-7935G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305756 | |||||||
| chr5:176305756 | GA | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7934delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305756 | |||||||
| chr5:176305757 | A | G | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
233 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1735-7934A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305757 | |||||||
| chr5:176305761 | G | A | 1 | a0002c0002t0002g0319 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1735-7930G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305761 | |||||||
| chr5:176305770 | C | CG | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7921_1735-792 others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305770 | |||||||
| chr5:176305770 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1735-7921C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305770 | |||||||
| chr5:176305771 | C | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7920C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305771 | |||||||
| chr5:176305772 | C | CCGCCCGG others(72): Show |
2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1735-7919_1735-791 others(83): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305772 | |||||||
| chr5:176305772 | C | CGCCCGGC others(71): Show |
1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1735-7919_1735-791 others(82): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305772 | |||||||
| chr5:176305773 | A | G | 96 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0115 others(93): Show |
96 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1735-7918A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305773 | |||||||
| chr5:176305785 | G | GCCCCGTC others(71): Show |
60 | a0001c0001t0001g0258 a0001c0001t0001g0277 a0002c0002t0002g0278 others(57): Show |
60 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1735-7899_1735-789 others(82): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305785 | ||||||
| chr5:176305786 | C | T | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7905C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305786 | |||||||
| chr5:176305787 | C | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7904C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305787 | |||||||
| chr5:176305790 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-7901G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305790 | |||||||
| chr5:176305791 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1735-7900T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305791 | |||||||
| chr5:176305793 | C | T | 59 | a0001c0001t0001g0258 a0002c0002t0002g0278 a0002c0002t0002g0279 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1735-7898C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305793 | |||||||
| chr5:176305797 | A | AGGTGAGG others(195): Show |
1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1735-7892_1735-789 others(206): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305797 | ||||||
| chr5:176305797 | A | G | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1735-7894A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305797 | |||||||
| chr5:176305800 | GAGGT | G | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1735-7890_1735-788 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305800 | |||||||
| chr5:176305801 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1735-7890A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305801 | |||||||
| chr5:176305803 | G | GGGCGCCT others(195): Show |
1 | a0002c0002t0002g0321 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1735-7888_1735-788 others(206): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305803 | |||||||
| chr5:176305804 | T | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1735-7887T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305804 | |||||||
| chr5:176305804 | T | G | 4 | a0001c0001t0001g0173 a0001c0001t0001g0219 a0001c0001t0001g0244 others(1): Show |
4 | HG03516.hp1 NA18945.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-7887T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305804 | |||||||
| chr5:176305810 | C | G | 246 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1735-7881C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305810 | |||||||
| chr5:176305821 | C | T | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1735-7870C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305821 | |||||||
| chr5:176305822 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp1 HG02630.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-7869G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305822 | |||||||
| chr5:176305825 | C | T | 70 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(67): Show |
70 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1735-7866C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305825 | |||||||
| chr5:176305835 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(8): Show |
11 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1735-7856C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305835 | |||||||
| chr5:176305836 | C | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(8): Show |
11 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1735-7855C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305836 | |||||||
| chr5:176305836 | C | T | 54 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(51): Show |
54 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1735-7855C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305836 | |||||||
| chr5:176305853 | TG | T | 71 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(68): Show |
71 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1735-7830delG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305853 | ||||||
| chr5:176305855 | G | A | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7836G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305855 | |||||||
| chr5:176305861 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1735-7830G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305861 | |||||||
| chr5:176305861 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1735-7830G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305861 | |||||||
| chr5:176305869 | C | T | 59 | a0001c0001t0001g0258 a0002c0002t0002g0278 a0002c0002t0002g0279 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1735-7822C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305869 | |||||||
| chr5:176305871 | CT | C | 70 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(67): Show |
70 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1735-7819delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305871 | |||||||
| chr5:176305872 | T | C | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1735-7819T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305872 | |||||||
| chr5:176305882 | G | A | 59 | a0001c0001t0001g0258 a0002c0002t0002g0278 a0002c0002t0002g0279 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1735-7809G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305882 | |||||||
| chr5:176305885 | G | C | 59 | a0001c0001t0001g0258 a0002c0002t0002g0278 a0002c0002t0002g0279 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1735-7806G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305885 | |||||||
| chr5:176305893 | C | T | 63 | a0001c0001t0001g0219 a0001c0001t0001g0244 a0001c0001t0001g0258 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1735-7798C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305893 | |||||||
| chr5:176305908 | G | A | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7783G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305908 | |||||||
| chr5:176305910 | T | C | 66 | a0001c0001t0001g0219 a0001c0001t0001g0244 a0001c0001t0001g0258 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1735-7781T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305910 | |||||||
| chr5:176305921 | C | T | 59 | a0001c0001t0001g0258 a0002c0002t0002g0278 a0002c0002t0002g0279 others(56): Show |
59 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1735-7770C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305921 | |||||||
| chr5:176305950 | T | A | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7741T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305950 | |||||||
| chr5:176305950 | T | TGCCCGGC others(42): Show |
3 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0352 |
3 | HG01361.hp1 HG01891.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1735-7724_1735-772 others(53): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305950 | ||||||
| chr5:176305963 | G | A | 4 | a0001c0001t0001g0139 a0001c0001t0001g0246 a0002c0002t0002g0321 others(1): Show |
4 | HG02809.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-7728G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305963 | |||||||
| chr5:176305968 | A | G | 64 | a0001c0001t0001g0258 a0002c0002t0002g0278 a0002c0002t0002g0279 others(61): Show |
64 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1735-7723A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305968 | |||||||
| chr5:176305971 | C | T | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7720C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305971 | |||||||
| chr5:176305988 | G | C | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1735-7703G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305988 | |||||||
| chr5:176305993 | G | GCCCCCCG others(578): Show |
1 | a0001c0001t0001g0197 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1735-7640_1735-763 others(589): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176305993 | ||||||
| chr5:176305999 | C | T | 2 | a0003c0004t0001g0001 a0003c0004t0001g0353 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1735-7692C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176305999 | |||||||
| chr5:176306003 | C | T | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7688C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306003 | |||||||
| chr5:176306014 | C | T | 1 | a0002c0002t0002g0321 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1735-7677C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306014 | |||||||
| chr5:176306015 | CCGTCCGG others(4): Show |
C | 1 | a0001c0001t0001g0093 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1735-7675_1735-766 others(15): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306015 | |||||||
| chr5:176306017 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1735-7674G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306017 | |||||||
| chr5:176306020 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1735-7671C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306020 | |||||||
| chr5:176306030 | GT | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0148 a0001c0001t0001g0150 others(4): Show |
7 | HG02486.hp1 HG03579.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-7659delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306030 | ||||||
| chr5:176306031 | T | TG | 23 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0042 others(20): Show |
23 | HG00438.hp2 HG00597.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1735-7660_1735-765 others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306031 | |||||||
| chr5:176306031 | T | TGAGGGGG others(90): Show |
1 | a0001c0001t0001g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1735-7660_1735-765 others(101): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306031 | |||||||
| chr5:176306031 | T | TGGGGGGG others(43): Show |
1 | a0002c0003t0001g0351 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1735-7660_1735-765 others(54): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306031 | |||||||
| chr5:176306031 | T | TGGGGGGG others(139): Show |
2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1735-7660_1735-765 others(150): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306031 | |||||||
| chr5:176306032 | T | G | 237 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
237 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.1735-7659T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306032 | |||||||
| chr5:176306049 | C | T | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7642C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306049 | |||||||
| chr5:176306051 | C | T | 4 | a0001c0001t0001g0148 a0002c0002t0002g0299 a0002c0002t0002g0300 others(1): Show |
4 | HG02615.hp2 HG02976.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-7640C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306051 | |||||||
| chr5:176306051 | CGCCCGGC others(120): Show |
C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0158 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1735-7625_1735-749 others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306051 | ||||||
| chr5:176306056 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1735-7635G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306056 | |||||||
| chr5:176306061 | G | A | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7630G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306061 | |||||||
| chr5:176306064 | G | C | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7627G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306064 | |||||||
| chr5:176306066 | T | C | 9 | a0001c0001t0001g0148 a0002c0002t0002g0299 a0002c0002t0002g0300 others(6): Show |
9 | HG02280.hp1 HG02615.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1735-7625T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306066 | |||||||
| chr5:176306066 | TCCGTCCG others(120): Show |
T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1735-7524_1735-739 others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306066 | ||||||
| chr5:176306068 | C | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1735-7623C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306068 | |||||||
| chr5:176306069 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1735-7622G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306069 | |||||||
| chr5:176306072 | C | T | 60 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(57): Show |
60 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1735-7619C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306072 | |||||||
| chr5:176306100 | C | T | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7591C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306100 | |||||||
| chr5:176306122 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1735-7569G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306122 | |||||||
| chr5:176306125 | C | A | 1 | a0001c0001t0001g0243 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1735-7566C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306125 | |||||||
| chr5:176306135 | GC | G | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7554delC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306135 | ||||||
| chr5:176306141 | C | T | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7550C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306141 | |||||||
| chr5:176306146 | C | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1735-7545C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306146 | |||||||
| chr5:176306148 | TCCGGGAG others(79): Show |
T | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7541_1735-745 others(90): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306148 | ||||||
| chr5:176306167 | C | G | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7524C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306167 | |||||||
| chr5:176306168 | G | A | 127 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(124): Show |
127 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1735-7523G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306168 | |||||||
| chr5:176306172 | G | GCCCCCTG others(44): Show |
3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1735-7486_1735-748 others(55): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306172 | ||||||
| chr5:176306176 | CCTGCCCG others(71): Show |
C | 1 | a0001c0001t0001g0172 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1735-7485_1735-740 others(82): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306176 | ||||||
| chr5:176306178 | T | C | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7513T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306178 | |||||||
| chr5:176306178 | T | TGCCCGGC others(44): Show |
1 | a0001c0001t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1735-7486_1735-748 others(55): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306178 | ||||||
| chr5:176306178 | T | TGCCCGGC others(45): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0120 others(2): Show |
5 | HG00544.hp1 HG01192.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1735-7486_1735-748 others(56): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306178 | ||||||
| chr5:176306178 | T | TGCCCGGC others(44): Show |
225 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
225 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1735-7486_1735-748 others(55): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306178 | ||||||
| chr5:176306178 | T | TGCCCGGC others(45): Show |
2 | a0001c0001t0001g0110 a0011c0011t0001g0021 |
2 | HG01109.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1735-7486_1735-748 others(56): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306178 | ||||||
| chr5:176306185 | C | CCAGCCGC others(27): Show |
1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1735-7486_1735-748 others(38): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306185 | ||||||
| chr5:176306190 | C | CGCCCCGT others(44): Show |
1 | a0001c0001t0001g0038 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1735-7486_1735-748 others(55): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306190 | ||||||
| chr5:176306199 | C | CGGGAGGG others(45): Show |
1 | a0002c0002t0002g0321 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1735-7486_1735-748 others(56): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306199 | ||||||
| chr5:176306199 | C | CGGGAGGG others(94): Show |
1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1735-7486_1735-748 others(105): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306199 | ||||||
| chr5:176306224 | GGCCGCCC others(120): Show |
G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0246 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1735-7429_1735-730 others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306224 | ||||||
| chr5:176306227 | C | T | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1735-7464C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306227 | |||||||
| chr5:176306232 | C | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
8 | HG00733.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1735-7459C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306232 | |||||||
| chr5:176306236 | T | G | 1 | a0002c0002t0002g0343 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1735-7455T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306236 | |||||||
| chr5:176306238 | G | A | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7453G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306238 | |||||||
| chr5:176306248 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1735-7443A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306248 | |||||||
| chr5:176306262 | GC | G | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7427delC | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306262 | ||||||
| chr5:176306268 | C | T | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7423C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306268 | |||||||
| chr5:176306274 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0214 a0001c0001t0001g0217 |
3 | HG01358.hp2 HG02280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1735-7417G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306274 | |||||||
| chr5:176306275 | TCCGGGAG others(79): Show |
T | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7414_1735-732 others(90): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306275 | ||||||
| chr5:176306278 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1735-7413G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306278 | |||||||
| chr5:176306279 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1735-7412G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306279 | |||||||
| chr5:176306289 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1735-7402G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306289 | |||||||
| chr5:176306294 | G | C | 2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7397G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306294 | |||||||
| chr5:176306299 | G | GCCCCCTG others(44): Show |
2 | a0002c0002t0002g0321 a0003c0016t0001g0348 |
2 | HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7387_1735-738 others(55): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306299 | ||||||
| chr5:176306307 | T | C | 3 | a0001c0001t0001g0172 a0002c0002t0002g0321 a0003c0016t0001g0348 |
3 | HG02258.hp1 HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7384T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306307 | |||||||
| chr5:176306323 | A | G | 3 | a0001c0001t0001g0172 a0002c0002t0002g0321 a0003c0016t0001g0348 |
3 | HG02258.hp1 HG03130.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1735-7368A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306323 | |||||||
| chr5:176306341 | A | G | 2 | a0001c0001t0001g0172 a0003c0016t0001g0348 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1735-7350A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306341 | |||||||
| chr5:176306351 | A | G | 2 | a0001c0001t0001g0172 a0003c0016t0001g0348 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1735-7340A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306351 | |||||||
| chr5:176306365 | G | A | 3 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0002c0002t0002g0301 |
3 | HG02615.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7326G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306365 | |||||||
| chr5:176306387 | CGA | C | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(98): Show |
101 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1735-7303_1735-730 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306387 | |||||||
| chr5:176306389 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1735-7302A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306389 | |||||||
| chr5:176306392 | A | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(98): Show |
101 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1735-7299A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306392 | |||||||
| chr5:176306395 | A | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(98): Show |
101 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1735-7296A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306395 | |||||||
| chr5:176306397 | C | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(98): Show |
101 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1735-7294C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306397 | |||||||
| chr5:176306400 | G | C | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(98): Show |
101 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1735-7291G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306400 | |||||||
| chr5:176306402 | C | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(98): Show |
101 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1735-7289C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306402 | |||||||
| chr5:176306403 | T | TCTCCTTC others(221): Show |
1 | a0001c0001t0001g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1735-7288_1735-728 others(232): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306403 | |||||||
| chr5:176306403 | T | TCTCCTTC others(220): Show |
100 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(97): Show |
100 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1735-7288_1735-728 others(231): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306403 | |||||||
| chr5:176306404 | G | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(98): Show |
101 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1735-7287G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306404 | |||||||
| chr5:176306406 | G | C | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(98): Show |
101 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1735-7285G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306406 | |||||||
| chr5:176306426 | T | C | 1 | a0002c0002t0002g0316 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1735-7265T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306426 | |||||||
| chr5:176306439 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1735-7252A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306439 | |||||||
| chr5:176306440 | G | A | 2 | a0002c0002t0002g0300 a0002c0002t0002g0301 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735-7251G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306440 | |||||||
| chr5:176306526 | AAAG | A | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1735-7161_1735-715 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306526 | ||||||
| chr5:176306546 | G | C | 1 | a0001c0001t0001g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1735-7145G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306546 | |||||||
| chr5:176306623 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1735-7068G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306623 | |||||||
| chr5:176306644 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1735-7047G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306644 | |||||||
| chr5:176306649 | C | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1735-7042C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306649 | |||||||
| chr5:176306777 | G | GA | 66 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1735-6913dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306777 | ||||||
| chr5:176306844 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1735-6847C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306844 | |||||||
| chr5:176306862 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1735-6829G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306862 | |||||||
| chr5:176306903 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1735-6788A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306903 | |||||||
| chr5:176306919 | A | AT | 73 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(70): Show |
73 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1735-6770dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176306919 | ||||||
| chr5:176306922 | A | T | 6 | a0001c0001t0001g0176 a0002c0002t0002g0298 a0002c0002t0002g0321 others(3): Show |
6 | HG01081.hp1 HG01891.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1735-6769A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306922 | |||||||
| chr5:176306928 | A | AT | 25 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
25 | HG00558.hp2 HG01069.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1735-6763_1735-676 others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306928 | |||||||
| chr5:176306931 | A | AT | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
138 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1735-6760_1735-675 others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306931 | |||||||
| chr5:176306931 | A | T | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(39): Show |
42 | HG00544.hp2 HG00558.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1735-6760A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176306931 | |||||||
| chr5:176307183 | T | C | 1 | a0002c0002t0002g0342 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1735-6508T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307183 | |||||||
| chr5:176307282 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1735-6409T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307282 | |||||||
| chr5:176307405 | A | G | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1735-6286A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307405 | |||||||
| chr5:176307433 | C | T | 1 | a0002c0002t0002g0319 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1735-6258C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307433 | |||||||
| chr5:176307506 | T | G | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1735-6185T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307506 | |||||||
| chr5:176307545 | C | T | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
153 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1735-6146C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307545 | |||||||
| chr5:176307586 | G | C | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1735-6105G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307586 | |||||||
| chr5:176307670 | G | T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-6021G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307670 | |||||||
| chr5:176307671 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1735-6020A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307671 | |||||||
| chr5:176307872 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1735-5819A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307872 | |||||||
| chr5:176307936 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1735-5755C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176307936 | |||||||
| chr5:176308030 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1735-5661A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176308030 | |||||||
| chr5:176308284 | TCGTTCTG others(12): Show |
T | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1735-5404_1735-538 others(23): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176308284 | ||||||
| chr5:176308472 | C | T | 1 | a0002c0002t0002g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1735-5219C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176308472 | |||||||
| chr5:176308515 | G | T | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1735-5176G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176308515 | |||||||
| chr5:176308535 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1735-5156A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176308535 | |||||||
| chr5:176308644 | C | G | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1735-5047C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176308644 | |||||||
| chr5:176308699 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1735-4992C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176308699 | |||||||
| chr5:176308733 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1735-4958A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176308733 | |||||||
| chr5:176309052 | G | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0220 others(1): Show |
4 | HG02071.hp1 HG02155.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-4639G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176309052 | |||||||
| chr5:176309127 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1735-4564C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176309127 | |||||||
| chr5:176309479 | G | T | 1 | a0002c0002t0002g0316 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1735-4212G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176309479 | |||||||
| chr5:176309748 | A | C | 1 | a0002c0002t0002g0341 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1735-3943A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176309748 | |||||||
| chr5:176309762 | C | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1735-3929C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176309762 | |||||||
| chr5:176309791 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1735-3900A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176309791 | |||||||
| chr5:176310148 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1735-3543A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176310148 | |||||||
| chr5:176310317 | A | G | 1 | a0002c0002t0002g0306 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1735-3374A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176310317 | |||||||
| chr5:176310422 | T | C | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-3269T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176310422 | |||||||
| chr5:176310492 | C | G | 1 | a0001c0001t0001g0238 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1735-3199C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176310492 | |||||||
| chr5:176310685 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1735-3006C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176310685 | |||||||
| chr5:176310841 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0158 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1735-2850G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176310841 | |||||||
| chr5:176310848 | T | C | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1735-2843T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176310848 | |||||||
| chr5:176310860 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0103 others(1): Show |
4 | HG01175.hp1 HG01934.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-2831G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176310860 | |||||||
| chr5:176311229 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1735-2462A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176311229 | |||||||
| chr5:176311403 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1735-2288A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176311403 | |||||||
| chr5:176311756 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1735-1935G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176311756 | |||||||
| chr5:176311783 | C | A | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1735-1908C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176311783 | |||||||
| chr5:176311797 | A | G | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1735-1894A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176311797 | |||||||
| chr5:176311847 | C | CAATTTTA others(17): Show |
1 | a0002c0002t0002g0298 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1735-1841_1735-181 others(28): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176311847 | ||||||
| chr5:176311876 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1735-1815G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176311876 | |||||||
| chr5:176312024 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0147 |
2 | HG01167.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1735-1667G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176312024 | |||||||
| chr5:176312266 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1735-1425C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176312266 | |||||||
| chr5:176312280 | A | C | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1735-1411A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176312280 | |||||||
| chr5:176312301 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1735-1390C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176312301 | |||||||
| chr5:176312434 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1735-1257G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176312434 | |||||||
| chr5:176312491 | G | A | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG01109.hp2 HG01884.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-1200G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176312491 | |||||||
| chr5:176312522 | CA | C | 355 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(352): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1735-1166delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176312522 | ||||||
| chr5:176312536 | CA | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1735-1131delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176312536 | ||||||
| chr5:176312536 | CAA | C | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
162 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1735-1132_1735-113 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 176312536 | ||||||
| chr5:176312560 | A | G | 1 | a0002c0002t0002g0328 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1735-1131A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176312560 | |||||||
| chr5:176313126 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1735-565C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176313126 | |||||||
| chr5:176313154 | T | C | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1735-537T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176313154 | |||||||
| chr5:176313169 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1735-522G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176313169 | |||||||
| chr5:176313437 | TTTGAACA others(17): Show |
T | 1 | a0002c0002t0002g0298 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1735-253_1735-230d others(26): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176313437 | |||||||
| chr5:176313603 | C | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1735-88C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176313603 | |||||||
| chr5:176313657 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1735-34A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | chr5 | 176313657 | |||||||
| chr5:176313884 | G | A | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1889+39G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176313884 | |||||||
| chr5:176314063 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1889+218T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176314063 | |||||||
| chr5:176314127 | C | T | 63 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1889+282C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176314127 | |||||||
| chr5:176314132 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1889+287T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176314132 | |||||||
| chr5:176314271 | ATAAT | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0064 a0001c0001t0001g0084 others(3): Show |
6 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1889+436_1889+439d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176314271 | ||||||
| chr5:176314496 | C | T | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1889+651C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176314496 | |||||||
| chr5:176314707 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1889+862G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176314707 | |||||||
| chr5:176314844 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1889+999A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176314844 | |||||||
| chr5:176314930 | A | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1889+1085A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176314930 | |||||||
| chr5:176315273 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1889+1428G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176315273 | |||||||
| chr5:176315312 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1889+1467G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176315312 | |||||||
| chr5:176315425 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1889+1580T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176315425 | |||||||
| chr5:176315575 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0147 |
2 | HG01167.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1889+1730T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176315575 | |||||||
| chr5:176315593 | T | C | 4 | a0002c0003t0002g0281 a0002c0003t0002g0282 a0002c0003t0002g0283 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1889+1748T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176315593 | |||||||
| chr5:176315706 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1889+1861C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176315706 | |||||||
| chr5:176315894 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1889+2049G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176315894 | |||||||
| chr5:176316123 | C | T | 1 | a0002c0003t0002g0329 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1889+2278C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176316123 | |||||||
| chr5:176316377 | G | T | 1 | a0001c0001t0001g0009 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1889+2532G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176316377 | |||||||
| chr5:176316513 | C | CA | 63 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0197 others(60): Show |
63 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1889+2685dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176316513 | ||||||
| chr5:176316513 | C | CAA | 9 | a0002c0002t0002g0314 a0002c0002t0002g0320 a0002c0002t0002g0323 others(6): Show |
9 | HG00642.hp2 HG00741.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1889+2684_1889+268 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176316513 | ||||||
| chr5:176316513 | CA | C | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1889+2685delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176316513 | ||||||
| chr5:176316620 | T | C | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1889+2775T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176316620 | |||||||
| chr5:176316670 | CAA | C | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1889+2826_1889+282 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176316670 | |||||||
| chr5:176316901 | C | A | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.1889+3056C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176316901 | |||||||
| chr5:176317020 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1889+3175G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176317020 | |||||||
| chr5:176317026 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1889+3181T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176317026 | |||||||
| chr5:176317550 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0292 a0001c0001t0001g0297 |
3 | HG01934.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1889+3705C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176317550 | |||||||
| chr5:176317567 | A | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | NA18946.hp1 NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1889+3722A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176317567 | |||||||
| chr5:176317637 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1889+3792C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176317637 | |||||||
| chr5:176317947 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1889+4102G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176317947 | |||||||
| chr5:176318243 | C | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(2): Show |
5 | HG02965.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890-4030C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176318243 | |||||||
| chr5:176318391 | G | T | 1 | a0002c0002t0002g0341 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1890-3882G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176318391 | |||||||
| chr5:176318397 | A | G | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-3876A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176318397 | |||||||
| chr5:176318565 | T | A | 1 | a0001c0001t0001g0268 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1890-3708T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176318565 | |||||||
| chr5:176318653 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1890-3620A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176318653 | |||||||
| chr5:176318769 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1890-3504G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176318769 | |||||||
| chr5:176318829 | G | A | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.1890-3444G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176318829 | |||||||
| chr5:176319108 | CA | C | 6 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(3): Show |
6 | HG01074.hp1 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890-3164delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176319108 | |||||||
| chr5:176319266 | A | G | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-3007A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176319266 | |||||||
| chr5:176319399 | C | T | 250 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
250 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1890-2874C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176319399 | |||||||
| chr5:176319532 | A | G | 3 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0352 |
3 | HG01361.hp1 HG01891.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1890-2741A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176319532 | |||||||
| chr5:176319605 | G | C | 250 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
250 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1890-2668G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176319605 | |||||||
| chr5:176319676 | A | T | 12 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0284 others(9): Show |
12 | HG01257.hp1 HG01258.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.1890-2597A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176319676 | |||||||
| chr5:176319712 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1890-2561A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176319712 | |||||||
| chr5:176319763 | TTC | T | 24 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(21): Show |
24 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1890-2506_1890-250 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176319763 | ||||||
| chr5:176319991 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1890-2282A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176319991 | |||||||
| chr5:176320306 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1890-1967A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176320306 | |||||||
| chr5:176320330 | A | ATTTT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(4): Show |
7 | HG02132.hp2 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1890-1942_1890-193 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176320330 | ||||||
| chr5:176320331 | T | TTTTA | 15 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(12): Show |
15 | HG00558.hp1 HG00558.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1890-1894_1890-189 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176320331 | ||||||
| chr5:176320331 | TTTTA | T | 63 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0020 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1890-1894_1890-189 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176320331 | ||||||
| chr5:176320331 | TTTTATTT others(1): Show |
T | 10 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
10 | HG01516.hp1 HG02027.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1890-1898_1890-189 others(12): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176320331 | ||||||
| chr5:176320331 | TTTTATTT others(5): Show |
T | 190 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0030 others(187): Show |
190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1890-1902_1890-189 others(16): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176320331 | ||||||
| chr5:176320331 | TTTTATTT others(9): Show |
T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-1906_1890-189 others(20): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176320331 | ||||||
| chr5:176320335 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1890-1938A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176320335 | |||||||
| chr5:176320343 | A | T | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1890-1930A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176320343 | |||||||
| chr5:176320413 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1890-1860G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176320413 | |||||||
| chr5:176320784 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0091 |
2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1890-1489C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176320784 | |||||||
| chr5:176320909 | T | C | 65 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0002g0278 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1890-1364T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176320909 | |||||||
| chr5:176321192 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1890-1081A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176321192 | |||||||
| chr5:176321305 | G | T | 250 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
250 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1890-968G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176321305 | |||||||
| chr5:176321428 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1890-845C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176321428 | |||||||
| chr5:176321559 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1890-714G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176321559 | |||||||
| chr5:176321579 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1890-694T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176321579 | |||||||
| chr5:176321812 | G | A | 65 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0002g0278 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1890-461G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176321812 | |||||||
| chr5:176321885 | C | CT | 170 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
170 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1890-367dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176321885 | ||||||
| chr5:176321885 | C | CTT | 71 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0024 others(68): Show |
71 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1890-368_1890-367d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176321885 | ||||||
| chr5:176321885 | C | CTTT | 12 | a0001c0001t0001g0257 a0002c0002t0002g0304 a0002c0002t0002g0309 others(9): Show |
12 | HG01361.hp1 HG01361.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1890-369_1890-367d others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176321885 | ||||||
| chr5:176321885 | CT | C | 6 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0001g0205 others(3): Show |
6 | HG02280.hp1 HG03041.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.1890-367delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 176321885 | ||||||
| chr5:176321935 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1890-338A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 5/9 | chr5 | 176321935 | |||||||
| chr5:176322676 | C | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
8 | HG00733.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042+251C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176322676 | |||||||
| chr5:176322756 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.2042+331T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176322756 | |||||||
| chr5:176322881 | C | A | 2 | a0005c0006t0002g0330 a0005c0006t0002g0333 |
2 | NA18955.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2042+456C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176322881 | |||||||
| chr5:176323071 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0214 |
2 | HG01358.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2042+646A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323071 | |||||||
| chr5:176323148 | T | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(10): Show |
13 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2042+723T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323148 | |||||||
| chr5:176323338 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2042+913A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323338 | |||||||
| chr5:176323482 | T | C | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.2042+1057T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323482 | |||||||
| chr5:176323582 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2043-1047A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323582 | |||||||
| chr5:176323795 | G | A | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2043-834G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323795 | |||||||
| chr5:176323987 | C | CA | 27 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0179 others(24): Show |
27 | HG00423.hp1 HG01074.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.2043-615dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 176323987 | ||||||
| chr5:176323987 | CA | C | 8 | a0001c0001t0001g0139 a0001c0001t0001g0191 a0001c0001t0001g0205 others(5): Show |
8 | HG02280.hp1 HG02809.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2043-615delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 176323987 | ||||||
| chr5:176323994 | A | T | 252 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(249): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.2043-635A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323994 | |||||||
| chr5:176323995 | A | T | 4 | a0001c0001t0001g0262 a0003c0004t0001g0001 a0003c0004t0001g0353 others(1): Show |
4 | HG02280.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2043-634A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323995 | |||||||
| chr5:176323998 | A | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2043-631A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323998 | |||||||
| chr5:176323999 | A | T | 2 | a0002c0002t0002g0304 a0002c0014t0002g0331 |
2 | NA18967.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.2043-630A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176323999 | |||||||
| chr5:176324000 | A | T | 245 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
245 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.2043-629A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176324000 | |||||||
| chr5:176324001 | A | T | 4 | a0001c0001t0001g0256 a0003c0004t0001g0001 a0003c0004t0001g0353 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2043-628A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176324001 | |||||||
| chr5:176324007 | A | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2043-622A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176324007 | |||||||
| chr5:176324015 | C | A | 1 | a0002c0003t0001g0351 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2043-614C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176324015 | |||||||
| chr5:176324071 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0074 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG00733.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043-558G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176324071 | |||||||
| chr5:176324266 | T | A | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2043-363T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176324266 | |||||||
| chr5:176324425 | C | T | 1 | a0002c0002t0002g0328 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2043-204C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 6/9 | chr5 | 176324425 | |||||||
| chr5:176325115 | C | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2171+358C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325115 | |||||||
| chr5:176325156 | C | T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2171+399C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325156 | |||||||
| chr5:176325157 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2171+400G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325157 | |||||||
| chr5:176325230 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2171+473T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325230 | |||||||
| chr5:176325295 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2171+538G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325295 | |||||||
| chr5:176325310 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2171+553C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325310 | |||||||
| chr5:176325318 | G | A | 1 | a0011c0011t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2171+561G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325318 | |||||||
| chr5:176325408 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2171+651G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325408 | |||||||
| chr5:176325501 | C | T | 3 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0352 |
3 | HG01361.hp1 HG01891.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2171+744C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325501 | |||||||
| chr5:176325543 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | NA18990.hp2 NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2171+786G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325543 | |||||||
| chr5:176325594 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2171+837G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325594 | |||||||
| chr5:176325699 | T | G | 128 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.2171+942T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325699 | |||||||
| chr5:176325734 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2171+977A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325734 | |||||||
| chr5:176325791 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2171+1034G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325791 | |||||||
| chr5:176325832 | G | A | 4 | a0002c0003t0002g0281 a0002c0003t0002g0282 a0002c0003t0002g0283 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2171+1075G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325832 | |||||||
| chr5:176325833 | A | G | 4 | a0002c0003t0002g0281 a0002c0003t0002g0282 a0002c0003t0002g0283 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2171+1076A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325833 | |||||||
| chr5:176325929 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2171+1172C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325929 | |||||||
| chr5:176325935 | A | G | 250 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
250 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.2171+1178A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325935 | |||||||
| chr5:176325974 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0066 |
2 | NA18942.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2171+1217A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176325974 | |||||||
| chr5:176326056 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2171+1299A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326056 | |||||||
| chr5:176326167 | C | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2171+1410C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326167 | |||||||
| chr5:176326179 | G | A | 4 | a0005c0006t0002g0330 a0005c0006t0002g0332 a0005c0006t0002g0333 others(1): Show |
4 | NA18955.hp2 NA18978.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2171+1422G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326179 | |||||||
| chr5:176326269 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2171+1512G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326269 | |||||||
| chr5:176326328 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(8): Show |
11 | HG00558.hp2 HG00609.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2171+1571T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326328 | |||||||
| chr5:176326383 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2171+1626T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326383 | |||||||
| chr5:176326466 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2171+1709C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326466 | |||||||
| chr5:176326560 | C | CTATT | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2171+1817_2171+182 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176326560 | ||||||
| chr5:176326744 | T | C | 54 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(51): Show |
54 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.2171+1987T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326744 | |||||||
| chr5:176326814 | C | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0008c0009t0001g0135 |
3 | HG00423.hp2 HG00438.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.2171+2057C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326814 | |||||||
| chr5:176326849 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2171+2092A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326849 | |||||||
| chr5:176326871 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2171+2114T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176326871 | |||||||
| chr5:176327161 | A | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2171+2404A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327161 | |||||||
| chr5:176327193 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2171+2436T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327193 | |||||||
| chr5:176327255 | C | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0214 a0001c0001t0001g0217 |
3 | HG01358.hp2 HG02280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2171+2498C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327255 | |||||||
| chr5:176327478 | G | A | 3 | a0002c0002t0002g0312 a0002c0002t0002g0313 a0002c0002t0002g0334 |
3 | HG00544.hp1 NA18979.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2171+2721G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327478 | |||||||
| chr5:176327526 | G | A | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2171+2769G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327526 | |||||||
| chr5:176327677 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2171+2920G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327677 | |||||||
| chr5:176327778 | A | C | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2171+3021A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327778 | |||||||
| chr5:176327789 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2171+3032G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327789 | |||||||
| chr5:176327818 | T | C | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2171+3061T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327818 | |||||||
| chr5:176327905 | A | T | 1 | a0001c0001t0001g0294 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2171+3148A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176327905 | |||||||
| chr5:176328109 | C | T | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2171+3352C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328109 | |||||||
| chr5:176328197 | C | T | 16 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2171+3440C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328197 | |||||||
| chr5:176328271 | C | A | 1 | a0001c0001t0001g0269 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2171+3514C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328271 | |||||||
| chr5:176328314 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01081.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2171+3557T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328314 | |||||||
| chr5:176328409 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.2171+3652G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328409 | |||||||
| chr5:176328411 | A | T | 12 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0284 others(9): Show |
12 | HG01257.hp1 HG01258.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.2171+3654A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328411 | |||||||
| chr5:176328430 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2171+3673G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328430 | |||||||
| chr5:176328460 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2171+3703T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328460 | |||||||
| chr5:176328631 | G | C | 1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2171+3874G>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328631 | |||||||
| chr5:176328711 | C | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2171+3954C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328711 | |||||||
| chr5:176328925 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2171+4168A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328925 | |||||||
| chr5:176328957 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2171+4200A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176328957 | |||||||
| chr5:176329160 | G | A | 1 | a0003c0004t0001g0353 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2171+4403G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176329160 | |||||||
| chr5:176329236 | C | CCGAGACT others(15): Show |
1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2171+4481_2171+450 others(26): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176329236 | ||||||
| chr5:176329246 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2171+4489C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176329246 | |||||||
| chr5:176329323 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2171+4566T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176329323 | |||||||
| chr5:176329395 | C | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.2171+4638C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176329395 | |||||||
| chr5:176329496 | T | TA | 179 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
179 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.2171+4760dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176329496 | ||||||
| chr5:176329496 | T | TAA | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0056 others(12): Show |
15 | HG01891.hp2 HG02135.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2171+4759_2171+476 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176329496 | ||||||
| chr5:176329496 | TA | T | 57 | a0001c0001t0001g0205 a0001c0001t0001g0258 a0002c0002t0002g0278 others(54): Show |
57 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.2171+4760delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176329496 | ||||||
| chr5:176329736 | A | C | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2171+4979A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176329736 | |||||||
| chr5:176329794 | T | A | 251 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
251 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.2171+5037T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176329794 | |||||||
| chr5:176329835 | A | G | 64 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0002g0278 others(61): Show |
64 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.2171+5078A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176329835 | |||||||
| chr5:176329953 | G | A | 251 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
251 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.2171+5196G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176329953 | |||||||
| chr5:176330013 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2171+5256C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330013 | |||||||
| chr5:176330046 | CTT | C | 14 | a0001c0001t0001g0182 a0001c0001t0001g0190 a0001c0001t0001g0222 others(11): Show |
14 | HG00558.hp1 HG00597.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.2171+5290_2171+529 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330046 | |||||||
| chr5:176330104 | A | G | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2171+5347A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330104 | |||||||
| chr5:176330253 | T | C | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2171+5496T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330253 | |||||||
| chr5:176330400 | CA | C | 72 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0066 others(69): Show |
72 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.2171+5659delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176330400 | ||||||
| chr5:176330496 | T | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | NA18989.hp1 NA18997.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2171+5739T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330496 | |||||||
| chr5:176330597 | A | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2171+5840A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330597 | |||||||
| chr5:176330713 | C | G | 158 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(155): Show |
158 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.2171+5956C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330713 | |||||||
| chr5:176330754 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2172-5966T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330754 | |||||||
| chr5:176330884 | T | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG01069.hp2 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2172-5836T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330884 | |||||||
| chr5:176330918 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2172-5802A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330918 | |||||||
| chr5:176330943 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2172-5777G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176330943 | |||||||
| chr5:176331000 | A | G | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2172-5720A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331000 | |||||||
| chr5:176331077 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2172-5643G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331077 | |||||||
| chr5:176331089 | A | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2172-5631A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331089 | |||||||
| chr5:176331142 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2172-5578G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331142 | |||||||
| chr5:176331161 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2172-5559G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331161 | |||||||
| chr5:176331187 | A | G | 4 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0245 others(1): Show |
4 | HG01169.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2172-5533A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331187 | |||||||
| chr5:176331302 | G | A | 21 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0035 others(18): Show |
21 | HG00597.hp2 HG01175.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.2172-5418G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331302 | |||||||
| chr5:176331306 | C | G | 1 | a0002c0002t0002g0307 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2172-5414C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331306 | |||||||
| chr5:176331349 | G | A | 1 | a0001c0001t0001g0360 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2172-5371G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331349 | |||||||
| chr5:176331355 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2172-5365G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331355 | |||||||
| chr5:176331368 | TA | T | 218 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(215): Show |
218 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.2172-5335delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176331368 | ||||||
| chr5:176331403 | CAAAGCAA others(3): Show |
C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02027.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2172-5308_2172-529 others(14): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176331403 | ||||||
| chr5:176331466 | C | A | 155 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(152): Show |
155 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.2172-5254C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331466 | |||||||
| chr5:176331819 | A | C | 1 | a0001c0001t0001g0202 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2172-4901A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331819 | |||||||
| chr5:176331857 | T | C | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG00099.hp2 HG01123.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2172-4863T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331857 | |||||||
| chr5:176331901 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2172-4819C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331901 | |||||||
| chr5:176331904 | G | A | 156 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(153): Show |
156 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.2172-4816G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331904 | |||||||
| chr5:176331973 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2172-4747A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176331973 | |||||||
| chr5:176332048 | A | G | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2172-4672A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332048 | |||||||
| chr5:176332077 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2172-4643A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332077 | |||||||
| chr5:176332127 | T | G | 250 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
250 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.2172-4593T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332127 | |||||||
| chr5:176332146 | T | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2172-4574T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332146 | |||||||
| chr5:176332277 | T | A | 16 | a0002c0002t0002g0280 a0002c0002t0002g0305 a0002c0002t0002g0311 others(13): Show |
16 | HG00544.hp1 HG00741.hp1 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.2172-4443T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332277 | |||||||
| chr5:176332347 | A | G | 156 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(153): Show |
156 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.2172-4373A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332347 | |||||||
| chr5:176332371 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(2): Show |
5 | HG02965.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2172-4349A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332371 | |||||||
| chr5:176332377 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2172-4343G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332377 | |||||||
| chr5:176332412 | T | C | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2172-4308T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332412 | |||||||
| chr5:176332451 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0138 |
2 | NA18999.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.2172-4269C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332451 | |||||||
| chr5:176332458 | C | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2172-4262C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332458 | |||||||
| chr5:176332517 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(1): Show |
4 | HG00558.hp2 HG00609.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.2172-4203C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332517 | |||||||
| chr5:176332558 | G | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02027.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2172-4162G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332558 | |||||||
| chr5:176332580 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2172-4140G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332580 | |||||||
| chr5:176332590 | T | G | 1 | a0001c0001t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2172-4130T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332590 | |||||||
| chr5:176332868 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2172-3852T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176332868 | |||||||
| chr5:176333021 | G | A | 4 | a0002c0002t0002g0298 a0002c0002t0002g0307 a0002c0002t0002g0321 others(1): Show |
4 | NA18949.hp2 NA18995.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.2172-3699G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333021 | |||||||
| chr5:176333121 | C | T | 1 | a0002c0002t0002g0278 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2172-3599C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333121 | |||||||
| chr5:176333343 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2172-3377T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333343 | |||||||
| chr5:176333417 | G | GT | 6 | a0001c0001t0001g0010 a0001c0001t0001g0199 a0001c0001t0001g0226 others(3): Show |
6 | HG00597.hp1 HG01978.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.2172-3296dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176333417 | ||||||
| chr5:176333458 | T | TG | 3 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | NA18990.hp2 NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2172-3262_2172-326 others(5): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333458 | |||||||
| chr5:176333459 | C | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | NA18990.hp2 NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2172-3261C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333459 | |||||||
| chr5:176333468 | G | A | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2172-3252G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333468 | |||||||
| chr5:176333472 | A | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | NA18990.hp2 NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2172-3248A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333472 | |||||||
| chr5:176333489 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0193 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2172-3231T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333489 | |||||||
| chr5:176333676 | C | T | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2172-3044C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333676 | |||||||
| chr5:176333887 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2172-2833A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176333887 | |||||||
| chr5:176334270 | T | C | 355 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(352): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.2172-2450T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176334270 | |||||||
| chr5:176334534 | C | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(7): Show |
10 | HG00558.hp2 HG00609.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.2172-2186C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176334534 | |||||||
| chr5:176334573 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2172-2147C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176334573 | |||||||
| chr5:176334890 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2172-1830G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176334890 | |||||||
| chr5:176334906 | A | G | 12 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0284 others(9): Show |
12 | HG01257.hp1 HG01258.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.2172-1814A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176334906 | |||||||
| chr5:176334996 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2172-1724T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176334996 | |||||||
| chr5:176334999 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2172-1721G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176334999 | |||||||
| chr5:176335023 | G | T | 114 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(111): Show |
114 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.2172-1697G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335023 | |||||||
| chr5:176335054 | G | A | 12 | a0001c0001t0001g0057 a0001c0001t0001g0136 a0001c0001t0001g0267 others(9): Show |
12 | HG00741.hp2 HG01123.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.2172-1666G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335054 | |||||||
| chr5:176335104 | A | T | 25 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
25 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2172-1616A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335104 | |||||||
| chr5:176335107 | A | T | 215 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(212): Show |
215 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.2172-1613A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335107 | |||||||
| chr5:176335110 | T | A | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2172-1610T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335110 | |||||||
| chr5:176335120 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2172-1600A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335120 | |||||||
| chr5:176335201 | T | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02027.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2172-1519T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335201 | |||||||
| chr5:176335273 | C | CT | 27 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0027 others(24): Show |
27 | HG01069.hp1 HG01169.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.2172-1425dupT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176335273 | ||||||
| chr5:176335273 | C | CTT | 142 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(139): Show |
142 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.2172-1426_2172-142 others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176335273 | ||||||
| chr5:176335273 | C | CTTT | 10 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0075 others(7): Show |
10 | HG00597.hp2 HG00642.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.2172-1427_2172-142 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176335273 | ||||||
| chr5:176335273 | CT | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(5): Show |
8 | HG00099.hp1 HG01169.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2172-1425delT | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176335273 | ||||||
| chr5:176335434 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2172-1286G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335434 | |||||||
| chr5:176335454 | T | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2172-1266T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335454 | |||||||
| chr5:176335609 | AG | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.2172-1109delG | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176335609 | ||||||
| chr5:176335633 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2172-1087C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335633 | |||||||
| chr5:176335693 | G | A | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2172-1027G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335693 | |||||||
| chr5:176335780 | C | CT | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2172-940_2172-939i others(3): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335780 | |||||||
| chr5:176335859 | A | T | 157 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(154): Show |
157 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.2172-861A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335859 | |||||||
| chr5:176335869 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2172-851C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335869 | |||||||
| chr5:176335897 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2172-823G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176335897 | |||||||
| chr5:176336027 | G | T | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.2172-693G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176336027 | |||||||
| chr5:176336068 | A | AAGGG | 251 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
251 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.2172-649_2172-646d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176336068 | ||||||
| chr5:176336095 | GGA | G | 4 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 others(1): Show |
4 | HG02280.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2172-604_2172-603d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 176336095 | ||||||
| chr5:176336188 | C | T | 1 | a0002c0002t0002g0324 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2172-532C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176336188 | |||||||
| chr5:176336224 | C | G | 54 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(51): Show |
54 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.2172-496C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176336224 | |||||||
| chr5:176336352 | T | G | 1 | a0001c0001t0001g0127 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2172-368T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176336352 | |||||||
| chr5:176336593 | G | A | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
88 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.2172-127G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176336593 | |||||||
| chr5:176336594 | C | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2172-126C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 7/9 | chr5 | 176336594 | |||||||
| chr5:176336881 | A | T | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.2328+5A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 8/9 | chr5 | 176336881 | |||||||
| chr5:176336907 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2328+31A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 8/9 | chr5 | 176336907 | |||||||
| chr5:176336957 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2328+81T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 8/9 | chr5 | 176336957 | |||||||
| chr5:176337259 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2413+113A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176337259 | |||||||
| chr5:176337365 | T | C | 158 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(155): Show |
158 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.2413+219T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176337365 | |||||||
| chr5:176337455 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2413+309G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176337455 | |||||||
| chr5:176337556 | T | G | 2 | a0003c0004t0001g0353 a0003c0004t0001g0354 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2413+410T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176337556 | |||||||
| chr5:176337602 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
27 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2413+456C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176337602 | |||||||
| chr5:176337734 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2413+588C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176337734 | |||||||
| chr5:176337791 | C | T | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2413+645C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176337791 | |||||||
| chr5:176337867 | A | G | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2413+721A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176337867 | |||||||
| chr5:176338083 | G | A | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413+937G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176338083 | |||||||
| chr5:176338353 | C | T | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2413+1207C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176338353 | |||||||
| chr5:176338508 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2413+1362A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176338508 | |||||||
| chr5:176338541 | A | G | 62 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2413+1395A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176338541 | |||||||
| chr5:176338633 | T | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2413+1487T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176338633 | |||||||
| chr5:176338703 | T | C | 250 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
250 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.2413+1557T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176338703 | |||||||
| chr5:176338795 | TA | T | 222 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(219): Show |
222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.2413+1664delA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176338795 | ||||||
| chr5:176338985 | A | G | 64 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0002g0278 others(61): Show |
64 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.2413+1839A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176338985 | |||||||
| chr5:176339135 | G | A | 4 | a0004c0005t0001g0161 a0004c0005t0001g0162 a0004c0005t0001g0163 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2413+1989G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339135 | |||||||
| chr5:176339180 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | NA18943.hp2 NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.2413+2034G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339180 | |||||||
| chr5:176339230 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2413+2084G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339230 | |||||||
| chr5:176339283 | G | GA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(6): Show |
9 | HG00558.hp2 HG00609.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.2413+2139dupA | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176339283 | ||||||
| chr5:176339289 | G | A | 1 | a0002c0002t0002g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2413+2143G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339289 | |||||||
| chr5:176339430 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0137 |
2 | HG02738.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2413+2284T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339430 | |||||||
| chr5:176339476 | G | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(10): Show |
13 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2413+2330G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339476 | |||||||
| chr5:176339500 | C | T | 1 | a0003c0004t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2413+2354C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339500 | |||||||
| chr5:176339626 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2413+2480C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339626 | |||||||
| chr5:176339741 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2413+2595T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176339741 | |||||||
| chr5:176340065 | C | G | 157 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(154): Show |
157 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.2413+2919C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340065 | |||||||
| chr5:176340199 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2413+3053G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340199 | |||||||
| chr5:176340316 | C | A | 60 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(57): Show |
60 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.2413+3170C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340316 | |||||||
| chr5:176340334 | A | G | 252 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(249): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.2413+3188A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340334 | |||||||
| chr5:176340470 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2413+3324G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340470 | |||||||
| chr5:176340539 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.2413+3393G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340539 | |||||||
| chr5:176340578 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0003c0004t0001g0353 |
3 | HG02280.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2413+3432G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340578 | |||||||
| chr5:176340621 | T | C | 17 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(14): Show |
17 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2413+3475T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340621 | |||||||
| chr5:176340674 | C | T | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413+3528C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340674 | |||||||
| chr5:176340873 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0218 |
2 | NA18946.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2413+3727G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340873 | |||||||
| chr5:176340982 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2413+3836A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176340982 | |||||||
| chr5:176341493 | G | T | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2414-3690G>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176341493 | |||||||
| chr5:176341620 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2414-3563C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176341620 | |||||||
| chr5:176341626 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2414-3557C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176341626 | |||||||
| chr5:176341748 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2414-3435T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176341748 | |||||||
| chr5:176341750 | G | GTGA | 4 | a0001c0001t0001g0087 a0001c0001t0001g0226 a0001c0001t0001g0231 others(1): Show |
4 | HG00597.hp1 HG03704.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.2414-3405_2414-340 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176341750 | ||||||
| chr5:176341750 | GTGA | G | 4 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 others(1): Show |
4 | HG02280.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414-3405_2414-340 others(7): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176341750 | ||||||
| chr5:176341750 | GTGATGA | G | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
88 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.2414-3408_2414-340 others(10): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176341750 | ||||||
| chr5:176341853 | T | C | 1 | a0002c0002t0002g0321 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2414-3330T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176341853 | |||||||
| chr5:176341934 | G | A | 58 | a0002c0002t0002g0278 a0002c0002t0002g0279 a0002c0002t0002g0280 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.2414-3249G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176341934 | |||||||
| chr5:176342393 | T | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2414-2790T>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176342393 | |||||||
| chr5:176342496 | T | C | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2414-2687T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176342496 | |||||||
| chr5:176342741 | C | T | 156 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(153): Show |
156 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.2414-2442C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176342741 | |||||||
| chr5:176342801 | GATTT | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0248 |
3 | HG00597.hp1 NA18957.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2414-2373_2414-237 others(8): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176342801 | ||||||
| chr5:176342920 | C | G | 3 | a0003c0004t0001g0001 a0003c0004t0001g0353 a0003c0004t0001g0354 |
3 | HG02280.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2414-2263C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176342920 | |||||||
| chr5:176343118 | G | A | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2414-2065G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343118 | |||||||
| chr5:176343418 | G | A | 155 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(152): Show |
155 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.2414-1765G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343418 | |||||||
| chr5:176343419 | C | T | 155 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(152): Show |
155 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.2414-1764C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343419 | |||||||
| chr5:176343587 | T | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
94 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.2414-1596T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343587 | |||||||
| chr5:176343637 | T | G | 1 | a0002c0002t0002g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2414-1546T>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343637 | |||||||
| chr5:176343675 | T | C | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2414-1508T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343675 | |||||||
| chr5:176343762 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | NA18946.hp1 NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2414-1421C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343762 | |||||||
| chr5:176343817 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(20): Show |
23 | HG00558.hp2 HG00609.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.2414-1366G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343817 | |||||||
| chr5:176343976 | T | C | 1 | a0003c0016t0001g0348 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2414-1207T>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176343976 | |||||||
| chr5:176344146 | A | C | 260 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
260 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.2414-1037A>C | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176344146 | |||||||
| chr5:176344345 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2414-838G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176344345 | |||||||
| chr5:176344436 | C | G | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2414-747C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176344436 | |||||||
| chr5:176344446 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2414-737G>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176344446 | |||||||
| chr5:176344466 | TATAC | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2414-715_2414-712d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176344466 | ||||||
| chr5:176344468 | T | TAC | 5 | a0001c0001t0001g0221 a0001c0001t0001g0226 a0001c0001t0001g0231 others(2): Show |
5 | HG00597.hp1 HG02109.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2414-678_2414-677d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176344468 | ||||||
| chr5:176344468 | TAC | T | 186 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(183): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.2414-678_2414-677d others(4): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176344468 | ||||||
| chr5:176344468 | TACAC | T | 39 | a0001c0001t0001g0028 a0001c0001t0001g0086 a0001c0001t0001g0116 others(36): Show |
39 | HG01109.hp2 HG01167.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.2414-680_2414-677d others(6): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176344468 | ||||||
| chr5:176344468 | TACACACA others(15): Show |
T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
90 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.2414-698_2414-677d others(24): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 176344468 | ||||||
| chr5:176344470 | C | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0245 |
3 | HG01169.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2414-713C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176344470 | |||||||
| chr5:176344478 | C | T | 1 | a0010c0015t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2414-705C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176344478 | |||||||
| chr5:176344687 | A | T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414-496A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176344687 | |||||||
| chr5:176344984 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2414-199C>A | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176344984 | |||||||
| chr5:176345012 | C | G | 156 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0028 others(153): Show |
156 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.2414-171C>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176345012 | |||||||
| chr5:176345019 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2414-164C>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176345019 | |||||||
| chr5:176345052 | A | T | 4 | a0002c0003t0001g0349 a0002c0003t0001g0350 a0002c0003t0001g0351 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414-131A>T | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176345052 | |||||||
| chr5:176345160 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0068 |
2 | NA18951.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2414-23A>G | SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 9/9 | chr5 | 176345160 |