Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7111 |
| ensemblid | ENSG00000136842.14 |
| hgncid | 11871 |
| symbol | TMOD1 |
| name | tropomodulin 1 |
| refseq_nuc | NM_003275.4 |
| refseq_prot | NP_003266.1 |
| ensembl_nuc | ENST00000259365.9 |
| ensembl_prot | ENSP00000259365.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 97501666 |
| end | 97601743 |
| strand | + |
| ver | v1.2 |
| region | chr9:97501666-97601743 |
| region5000 | chr9:97496666-97606743 |
| regionname0 | TMOD1_chr9_97501666_97601743 |
| regionname5000 | TMOD1_chr9_97496666_97606743 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1077 | 325 | 81 | 66 | 128 | 14 | 34 | TMOD1_chr9_97496666_97606743 | TMOD1 | ATGTC others(1072): Show |
chr9 | 97496666 | 97606743 | ||
| a0001c0002 | 0/0 | 1077 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD1_chr9_97496666_97606743 | TMOD1 | ATGTC others(1072): Show |
chr9 | 97496666 | 97606743 | ||
| a0001c0003 | 0/0 | 1077 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | ATGTC others(1072): Show |
chr9 | 97496666 | 97606743 | ||
| a0001c0004 | 0/0 | 1077 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | ATGTC others(1072): Show |
chr9 | 97496666 | 97606743 | ||
| a0001c0005 | 0/0 | 1077 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | ATGTC others(1072): Show |
chr9 | 97496666 | 97606743 | ||
| a0001c0006 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | ATGTC others(1072): Show |
chr9 | 97496666 | 97606743 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3311 | 227 | 29 | 46 | 110 | 12 | 28 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0002 | 0/0 | 3311 | 23 | 13 | 0 | 10 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0003 | 0/0 | 3311 | 17 | 0 | 11 | 5 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0004 | 0/0 | 3311 | 11 | 10 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0005 | 0/0 | 3311 | 11 | 10 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0006 | 0/0 | 3311 | 7 | 5 | 2 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0007 | 0/0 | 3311 | 7 | 3 | 2 | 1 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0008 | 0/0 | 3311 | 5 | 5 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0009 | 0/0 | 3311 | 3 | 0 | 0 | 0 | 1 | 2 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0010 | 0/0 | 3311 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0011 | 0/0 | 3311 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0013 | 0/0 | 3311 | 2 | 0 | 1 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0014 | 0/0 | 3311 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0015 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0016 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0017 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0018 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0001t0019 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0002t0001 | 0/0 | 3311 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0003t0012 | 0/0 | 3311 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0004t0001 | 0/0 | 3311 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0005t0001 | 0/0 | 3311 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| a0001c0006t0006 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | GAGCT others(3306): Show |
chr9 | 97496666 | 97606743 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0007g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0009g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0009g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0010g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0010g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0011g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0011g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0013g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0013g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0014g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0015g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0016g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0017g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0018g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0001t0019g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0003t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0003t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| a0001c0006t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | GBR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0099 | EUR | GBR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0144 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01070 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0011 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0305 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0308 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0179 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0125 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01517 | hp2 | a0001 | c0001 | t0009 | g0018 | EUR | IBS | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0143 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01884 | hp2 | a0001 | c0001 | t0017 | g0251 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0258 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0085 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02129 | hp2 | a0001 | c0001 | t0007 | g0146 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02145 | hp1 | a0001 | c0001 | t0016 | g0334 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CDX | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CDX | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CDX | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0275 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02451 | hp2 | a0001 | c0006 | t0006 | g0252 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02630 | hp2 | a0001 | c0003 | t0012 | g0104 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0331 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0303 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0330 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02886 | hp1 | a0001 | c0003 | t0012 | g0170 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0180 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0276 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0254 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0327 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0333 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0306 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0058 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0299 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03669 | hp1 | a0001 | c0001 | t0009 | g0177 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0262 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03704 | hp1 | a0001 | c0001 | t0013 | g0123 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0241 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03831 | hp2 | a0001 | c0001 | t0014 | g0117 | SAS | BEB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG04228 | hp2 | a0001 | c0001 | t0014 | g0155 | SAS | STU | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0316 | AFR | YRI | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | YRI | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0003 | AFR | YRI | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18965 | hp2 | a0001 | c0001 | t0019 | g0190 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0300 | AFR | LWK | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | LWK | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19054 | hp1 | a0001 | c0005 | t0001 | g0137 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19082 | hp2 | a0001 | c0001 | t0018 | g0083 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19084 | hp1 | a0001 | c0005 | t0001 | g0168 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | ASW | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | ASW | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0271 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0257 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | MSL | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0277 | AFR | USA | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | USA | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | USA | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | LWK | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0086 | REF | REF | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0225 | REF | REF | TMOD1_chr9_97496666_97606743 | TMOD1 | chr9 | 97496666 | 97606743 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97546193 | G | A | 1 | a0001c0002 | 2 | HG03492.hp1 HG03688.hp2 |
synonymous_variant | LOW | c.129G>A | p.Leu43Leu | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/10 | 315/3311 | 129/1080 | 43/359 | chr9 | 97546193 | |||
| chr9:97564075 | C | T | 1 | a0001c0006 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.525C>T | p.Asp175Asp | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/10 | 711/3311 | 525/1080 | 175/359 | chr9 | 97564075 | |||
| chr9:97565943 | C | T | 1 | a0001c0005 | 2 | NA19054.hp1 NA19084.hp1 |
synonymous_variant | LOW | c.714C>T | p.Asp238Asp | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/10 | 900/3311 | 714/1080 | 238/359 | chr9 | 97565943 | |||
| chr9:97591329 | G | A | 1 | a0001c0005 | 2 | NA19054.hp1 NA19084.hp1 |
synonymous_variant | LOW | c.909G>A | p.Val303Val | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/10 | 1095/3311 | 909/1080 | 303/359 | chr9 | 97591329 | |||
| chr9:97591365 | C | T | 1 | a0001c0004 | 2 | HG03486.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.945C>T | p.Phe315Phe | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/10 | 1131/3311 | 945/1080 | 315/359 | chr9 | 97591365 | |||
| chr9:97591410 | C | T | 1 | a0001c0003 | 2 | HG02630.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.990C>T | p.Asn330Asn | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/10 | 1176/3311 | 990/1080 | 330/359 | chr9 | 97591410 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97501679 | C | G | 1 | a0001c0001t0019 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-173C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/10 | 22510 | chr9 | 97501679 | ||||||
| chr9:97501708 | G | A | 1 | a0001c0001t0011 | 2 | HG01070.hp2 HG01071.hp2 |
5_prime_UTR_variant | MODIFIER | c.-144G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/10 | 22481 | chr9 | 97501708 | ||||||
| chr9:97524149 | C | A | 2 | a0001c0001t0007 a0001c0001t0015 |
8 | HG00140.hp2 HG00738.hp1 HG01175.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/10 | 40 | chr9 | 97524149 | ||||||
| chr9:97600086 | T | C | 1 | a0001c0001t0016 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 388 | chr9 | 97600086 | ||||||
| chr9:97600300 | T | C | 1 | a0001c0001t0009 | 3 | HG01517.hp2 HG03669.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*602T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 602 | chr9 | 97600300 | ||||||
| chr9:97600317 | T | C | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(6): Show |
74 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*619T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 619 | chr9 | 97600317 | ||||||
| chr9:97600375 | C | G | 2 | a0001c0001t0006 a0001c0006t0006 |
8 | HG01109.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*677C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 677 | chr9 | 97600375 | ||||||
| chr9:97600441 | T | G | 1 | a0001c0001t0010 | 3 | HG03225.hp1 NA18906.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*743T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 743 | chr9 | 97600441 | ||||||
| chr9:97600692 | G | A | 1 | a0001c0001t0018 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*994G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 994 | chr9 | 97600692 | ||||||
| chr9:97600792 | A | G | 1 | a0001c0001t0017 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1094A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1094 | chr9 | 97600792 | ||||||
| chr9:97600793 | T | G | 1 | a0001c0001t0013 | 2 | HG01361.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1095T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1095 | chr9 | 97600793 | ||||||
| chr9:97600886 | T | C | 1 | a0001c0001t0008 | 5 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1188T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1188 | chr9 | 97600886 | ||||||
| chr9:97601035 | C | T | 1 | a0001c0001t0005 | 11 | HG01891.hp2 HG01952.hp2 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1337C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1337 | chr9 | 97601035 | ||||||
| chr9:97601171 | T | C | 1 | a0001c0001t0014 | 2 | HG03831.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1473T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1473 | chr9 | 97601171 | ||||||
| chr9:97601294 | C | T | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
73 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1596C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1596 | chr9 | 97601294 | ||||||
| chr9:97601396 | T | G | 1 | a0001c0003t0012 | 2 | HG02630.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1698T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1698 | chr9 | 97601396 | ||||||
| chr9:97601630 | A | T | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
73 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1932A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1932 | chr9 | 97601630 | ||||||
| chr9:97601652 | A | G | 2 | a0001c0001t0004 a0001c0001t0015 |
12 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1954A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 1954 | chr9 | 97601652 | ||||||
| chr9:97601739 | T | C | 1 | a0001c0001t0003 | 17 | HG01099.hp2 HG01123.hp1 HG01167.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2041T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 10/10 | 2041 | chr9 | 97601739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97501824 | G | T | 4 | a0001c0001t0001g0332 a0001c0001t0004g0333 a0001c0001t0005g0331 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+21G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97501824 | |||||||
| chr9:97502119 | G | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-49+316G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502119 | |||||||
| chr9:97502171 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(13): Show |
16 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-49+368C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502171 | |||||||
| chr9:97502231 | C | T | 2 | a0001c0001t0002g0329 a0001c0001t0005g0330 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49+428C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502231 | |||||||
| chr9:97502409 | G | A | 80 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(77): Show |
80 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-49+606G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502409 | |||||||
| chr9:97502579 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-49+776C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502579 | |||||||
| chr9:97502653 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-49+850C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502653 | |||||||
| chr9:97502771 | T | C | 1 | a0001c0001t0007g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-49+968T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502771 | |||||||
| chr9:97502797 | G | A | 7 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+994G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502797 | |||||||
| chr9:97502946 | C | A | 12 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0113 others(9): Show |
12 | HG01099.hp2 HG01192.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.-49+1143C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97502946 | |||||||
| chr9:97503262 | C | T | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49+1459C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97503262 | |||||||
| chr9:97503449 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0009g0018 |
2 | HG00280.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-49+1646G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97503449 | |||||||
| chr9:97503613 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-49+1810A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97503613 | |||||||
| chr9:97503700 | T | A | 1 | a0001c0001t0014g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-49+1897T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97503700 | |||||||
| chr9:97503967 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-49+2164G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97503967 | |||||||
| chr9:97504127 | G | C | 51 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(48): Show |
51 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-49+2324G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97504127 | |||||||
| chr9:97504277 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-49+2474G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97504277 | |||||||
| chr9:97504372 | A | G | 1 | a0001c0001t0008g0327 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-49+2569A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97504372 | |||||||
| chr9:97504461 | T | C | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49+2658T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97504461 | |||||||
| chr9:97504810 | C | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(13): Show |
16 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-49+3007C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97504810 | |||||||
| chr9:97504998 | G | A | 1 | a0001c0001t0004g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49+3195G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97504998 | |||||||
| chr9:97505291 | G | A | 7 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+3488G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97505291 | |||||||
| chr9:97505419 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-49+3616C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97505419 | |||||||
| chr9:97505484 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(21): Show |
24 | HG00408.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-49+3681A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97505484 | |||||||
| chr9:97505517 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-49+3714A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97505517 | |||||||
| chr9:97505657 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-49+3854A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97505657 | |||||||
| chr9:97505663 | TA | T | 8 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(5): Show |
8 | HG00408.hp2 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49+3862delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97505663 | ||||||
| chr9:97505744 | C | T | 156 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0113 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-49+3941C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97505744 | |||||||
| chr9:97505928 | C | T | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49+4125C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97505928 | |||||||
| chr9:97506088 | TC | T | 156 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0113 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-49+4286delC | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97506088 | |||||||
| chr9:97506328 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-49+4525C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97506328 | |||||||
| chr9:97506627 | A | G | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49+4824A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97506627 | |||||||
| chr9:97506644 | C | T | 3 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 |
3 | NA18959.hp1 NA19007.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-49+4841C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97506644 | |||||||
| chr9:97506914 | G | C | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49+5111G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97506914 | |||||||
| chr9:97507009 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(39): Show |
42 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.-49+5206C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507009 | |||||||
| chr9:97507183 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-49+5380A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507183 | |||||||
| chr9:97507232 | A | T | 2 | a0001c0001t0001g0167 a0001c0005t0001g0168 |
2 | NA19011.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-49+5429A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507232 | |||||||
| chr9:97507370 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0004g0316 |
2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-49+5567C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507370 | |||||||
| chr9:97507371 | G | A | 2 | a0001c0001t0004g0171 a0001c0003t0012g0170 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-49+5568G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507371 | |||||||
| chr9:97507387 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-49+5584G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507387 | |||||||
| chr9:97507532 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-49+5729A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507532 | |||||||
| chr9:97507773 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-49+5970G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507773 | |||||||
| chr9:97507879 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-49+6076A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507879 | |||||||
| chr9:97507916 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
179 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.-49+6113A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97507916 | |||||||
| chr9:97508006 | G | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(23): Show |
26 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-49+6203G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508006 | |||||||
| chr9:97508056 | TTCACACA others(11): Show |
T | 1 | a0001c0001t0010g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-49+6254_-49+6271d others(20): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508056 | |||||||
| chr9:97508057 | T | TCA | 22 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0037 others(19): Show |
22 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.-49+6301_-49+6302d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | T | TCACA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0157 a0001c0001t0001g0212 others(3): Show |
6 | HG00639.hp2 HG01358.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+6299_-49+6302d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | TCA | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0040 others(113): Show |
116 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-49+6301_-49+6302d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | TCACA | T | 31 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0038 others(28): Show |
31 | HG00323.hp2 HG00408.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-49+6299_-49+6302d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | TCACACA | T | 14 | a0001c0001t0001g0035 a0001c0001t0001g0059 a0001c0001t0001g0131 others(11): Show |
14 | HG00609.hp1 HG01109.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-49+6297_-49+6302d others(8): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | TCACACAC others(1): Show |
T | 11 | a0001c0001t0001g0153 a0001c0001t0001g0242 a0001c0001t0001g0324 others(8): Show |
11 | HG01884.hp2 HG02451.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.-49+6295_-49+6302d others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | TCACACAC others(5): Show |
T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0185 a0001c0001t0001g0282 |
3 | NA18947.hp2 NA18981.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-49+6291_-49+6302d others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | TCACACAC others(7): Show |
T | 2 | a0001c0001t0001g0176 a0001c0001t0008g0254 |
2 | HG02922.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-49+6289_-49+6302d others(16): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | TCACACAC others(11): Show |
T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0312 a0001c0001t0006g0013 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+6285_-49+6302d others(20): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508057 | TCACACAC others(15): Show |
T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(14): Show |
17 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-49+6281_-49+6302d others(24): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97508057 | ||||||
| chr9:97508059 | A | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0191 others(1): Show |
4 | NA18965.hp1 NA18965.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+6256A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508059 | |||||||
| chr9:97508061 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-49+6258A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508061 | |||||||
| chr9:97508063 | A | T | 1 | a0001c0001t0001g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-49+6260A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508063 | |||||||
| chr9:97508064 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49+6261C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508064 | |||||||
| chr9:97508088 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-49+6285C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508088 | |||||||
| chr9:97508251 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-49+6448C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508251 | |||||||
| chr9:97508386 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-49+6583C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508386 | |||||||
| chr9:97508410 | G | A | 1 | a0001c0001t0005g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-49+6607G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508410 | |||||||
| chr9:97508442 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0087 others(3): Show |
6 | HG02809.hp1 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+6639G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508442 | |||||||
| chr9:97508479 | C | T | 11 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0255 others(8): Show |
11 | HG00408.hp2 HG01081.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49+6676C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508479 | |||||||
| chr9:97508481 | T | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
157 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-49+6678T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508481 | |||||||
| chr9:97508564 | A | G | 54 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0094 others(51): Show |
54 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-49+6761A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508564 | |||||||
| chr9:97508604 | G | A | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
127 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-49+6801G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508604 | |||||||
| chr9:97508683 | G | T | 7 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+6880G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508683 | |||||||
| chr9:97508948 | G | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0004g0316 others(1): Show |
4 | HG01109.hp1 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+7145G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97508948 | |||||||
| chr9:97509026 | A | T | 2 | a0001c0001t0001g0304 a0001c0001t0005g0100 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-49+7223A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509026 | |||||||
| chr9:97509111 | C | T | 8 | a0001c0001t0001g0255 a0001c0001t0001g0321 a0001c0001t0001g0323 others(5): Show |
8 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+7308C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509111 | |||||||
| chr9:97509115 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(176): Show |
179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.-49+7312G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509115 | |||||||
| chr9:97509258 | G | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0066 |
3 | HG02698.hp2 HG03669.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-49+7455G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509258 | |||||||
| chr9:97509408 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-49+7605T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509408 | |||||||
| chr9:97509464 | G | A | 49 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0094 others(46): Show |
49 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-49+7661G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509464 | |||||||
| chr9:97509471 | G | T | 7 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+7668G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509471 | |||||||
| chr9:97509500 | G | GT | 7 | a0001c0001t0001g0005 a0001c0001t0001g0321 a0001c0001t0001g0323 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+7708dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97509500 | ||||||
| chr9:97509512 | G | GT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0165 others(5): Show |
8 | HG01891.hp1 HG02071.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+7715dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97509512 | ||||||
| chr9:97509512 | G | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0255 a0001c0001t0001g0326 |
3 | NA18994.hp2 NA19086.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-49+7709G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509512 | |||||||
| chr9:97509513 | T | G | 1 | a0001c0001t0001g0234 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-49+7710T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509513 | |||||||
| chr9:97509518 | TG | T | 104 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0048 others(101): Show |
104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-49+7716delG | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509518 | |||||||
| chr9:97509519 | G | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
98 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-49+7716G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509519 | |||||||
| chr9:97509521 | T | G | 1 | a0001c0001t0001g0245 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-49+7718T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509521 | |||||||
| chr9:97509522 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0004g0316 |
3 | HG02647.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-49+7719T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509522 | |||||||
| chr9:97509570 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-49+7767G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509570 | |||||||
| chr9:97509611 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0004g0316 others(1): Show |
4 | HG01109.hp1 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+7808C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509611 | |||||||
| chr9:97509707 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(7): Show |
10 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49+7904G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509707 | |||||||
| chr9:97509842 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-49+8039C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97509842 | |||||||
| chr9:97510016 | T | A | 1 | a0001c0001t0005g0100 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-49+8213T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97510016 | |||||||
| chr9:97510057 | G | A | 8 | a0001c0001t0001g0255 a0001c0001t0001g0321 a0001c0001t0001g0323 others(5): Show |
8 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+8254G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97510057 | |||||||
| chr9:97510237 | C | CT | 124 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0045 others(121): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49+8445dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97510237 | ||||||
| chr9:97510581 | C | A | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-49+8778C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97510581 | |||||||
| chr9:97510694 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-49+8891C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97510694 | |||||||
| chr9:97510720 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(179): Show |
182 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-49+8917G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97510720 | |||||||
| chr9:97510845 | G | T | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-49+9042G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97510845 | |||||||
| chr9:97510897 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-49+9094A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97510897 | |||||||
| chr9:97511023 | C | G | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-49+9220C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511023 | |||||||
| chr9:97511065 | C | T | 45 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0094 others(42): Show |
45 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-49+9262C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511065 | |||||||
| chr9:97511070 | G | GCACACAC others(9): Show |
3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0302 |
3 | HG00673.hp1 HG02056.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.-49+9282_-49+9297d others(18): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97511070 | ||||||
| chr9:97511071 | C | CACACACA others(5): Show |
2 | a0001c0001t0011g0010 a0001c0001t0011g0011 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-49+9279_-49+9280i others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97511071 | ||||||
| chr9:97511085 | G | C | 2 | a0001c0001t0011g0010 a0001c0001t0011g0011 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-49+9282G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511085 | |||||||
| chr9:97511085 | G | GAC | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0232 others(1): Show |
4 | HG02698.hp2 HG03834.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+9308_-49+9309d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97511085 | ||||||
| chr9:97511085 | GAC | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(13): Show |
16 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-49+9308_-49+9309d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97511085 | ||||||
| chr9:97511085 | GACAC | G | 7 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+9306_-49+9309d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97511085 | ||||||
| chr9:97511087 | C | CACACACA others(7): Show |
171 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(168): Show |
171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-49+9297_-49+9298i others(16): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97511087 | ||||||
| chr9:97511087 | C | G | 2 | a0001c0001t0011g0010 a0001c0001t0011g0011 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-49+9284C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511087 | |||||||
| chr9:97511089 | C | CACACACA others(5): Show |
7 | a0001c0001t0001g0118 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
7 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+9297_-49+9298i others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97511089 | ||||||
| chr9:97511108 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-49+9305A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511108 | |||||||
| chr9:97511375 | C | T | 3 | a0001c0001t0002g0253 a0001c0001t0017g0251 a0001c0006t0006g0252 |
3 | HG01884.hp2 HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-49+9572C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511375 | |||||||
| chr9:97511562 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG01261.hp2 HG01496.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+9759C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511562 | |||||||
| chr9:97511596 | T | C | 1 | a0001c0001t0005g0100 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-49+9793T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511596 | |||||||
| chr9:97511631 | C | T | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49+9828C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511631 | |||||||
| chr9:97511852 | T | TG | 152 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-49+10052dupG | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97511852 | ||||||
| chr9:97511891 | C | A | 53 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0094 others(50): Show |
53 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-49+10088C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511891 | |||||||
| chr9:97511892 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.-49+10089A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511892 | |||||||
| chr9:97511946 | G | A | 1 | a0001c0001t0013g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-49+10143G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97511946 | |||||||
| chr9:97512173 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(217): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-49+10370A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512173 | |||||||
| chr9:97512197 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-49+10394G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512197 | |||||||
| chr9:97512277 | A | G | 7 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+10474A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512277 | |||||||
| chr9:97512283 | T | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-49+10480T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512283 | |||||||
| chr9:97512462 | A | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0298 a0001c0001t0005g0230 others(2): Show |
5 | HG02630.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+10659A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512462 | |||||||
| chr9:97512489 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-49+10686T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512489 | |||||||
| chr9:97512652 | C | CA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0068 a0001c0001t0001g0255 others(7): Show |
10 | HG01517.hp2 HG02976.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.-49+10861dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97512652 | ||||||
| chr9:97512664 | A | C | 1 | a0001c0001t0001g0114 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-49+10861A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512664 | |||||||
| chr9:97512665 | C | A | 3 | a0001c0001t0001g0162 a0001c0001t0003g0161 a0001c0001t0010g0003 |
3 | HG03239.hp2 NA18906.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.-49+10862C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512665 | |||||||
| chr9:97512872 | A | G | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-49+11069A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512872 | |||||||
| chr9:97512928 | T | G | 49 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0094 others(46): Show |
49 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-49+11125T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97512928 | |||||||
| chr9:97513142 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-48-10999C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97513142 | |||||||
| chr9:97513165 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-48-10976T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97513165 | |||||||
| chr9:97513217 | CTGAAGGA others(3): Show |
C | 4 | a0001c0001t0001g0312 a0001c0001t0002g0101 a0001c0001t0002g0102 others(1): Show |
4 | HG02976.hp2 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-10915_-48-1090 others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97513217 | ||||||
| chr9:97513387 | A | T | 1 | a0001c0001t0010g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48-10754A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97513387 | |||||||
| chr9:97513603 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(11): Show |
14 | HG02280.hp2 HG02630.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48-10538G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97513603 | |||||||
| chr9:97513670 | G | GTGCCCTC others(5): Show |
1 | a0001c0001t0001g0059 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-48-10469_-48-1046 others(16): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97513670 | ||||||
| chr9:97514028 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
183 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.-48-10113A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514028 | |||||||
| chr9:97514066 | A | AT | 9 | a0001c0001t0001g0312 a0001c0001t0002g0101 a0001c0001t0002g0102 others(6): Show |
9 | HG01884.hp2 HG02451.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-10062dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97514066 | ||||||
| chr9:97514239 | T | TG | 6 | a0001c0001t0001g0166 a0001c0001t0001g0309 a0001c0001t0007g0099 others(3): Show |
6 | HG00140.hp2 HG00738.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-9902_-48-9901i others(3): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514239 | |||||||
| chr9:97514239 | T | TGG | 3 | a0001c0001t0007g0069 a0001c0001t0007g0308 a0001c0001t0015g0143 |
3 | HG01175.hp1 HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-48-9902_-48-9901i others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514239 | |||||||
| chr9:97514240 | T | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0166 a0001c0001t0001g0309 others(7): Show |
10 | HG00140.hp2 HG00738.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48-9901T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514240 | |||||||
| chr9:97514240 | T | TG | 42 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0068 others(39): Show |
42 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.-48-9891dupG | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97514240 | ||||||
| chr9:97514243 | G | GGGT | 162 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-48-9896_-48-9895i others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97514243 | ||||||
| chr9:97514243 | G | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG02738.hp1 NA18979.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-48-9898G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514243 | |||||||
| chr9:97514245 | G | C | 1 | a0001c0001t0001g0059 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-48-9896G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514245 | |||||||
| chr9:97514275 | C | CT | 8 | a0001c0001t0001g0297 a0001c0001t0001g0304 a0001c0001t0002g0253 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48-9852dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97514275 | ||||||
| chr9:97514275 | CT | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0045 others(73): Show |
76 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-48-9852delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97514275 | ||||||
| chr9:97514288 | T | C | 7 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-9853T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514288 | |||||||
| chr9:97514302 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(212): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-48-9839A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514302 | |||||||
| chr9:97514303 | T | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(212): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-48-9838T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514303 | |||||||
| chr9:97514396 | G | A | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48-9745G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514396 | |||||||
| chr9:97514398 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-48-9743G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514398 | |||||||
| chr9:97514494 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(161): Show |
164 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.-48-9647C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514494 | |||||||
| chr9:97514680 | T | C | 5 | a0001c0001t0002g0253 a0001c0001t0008g0254 a0001c0001t0010g0306 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-9461T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514680 | |||||||
| chr9:97514771 | A | C | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48-9370A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514771 | |||||||
| chr9:97514797 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-48-9344C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514797 | |||||||
| chr9:97514813 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-48-9328C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514813 | |||||||
| chr9:97514939 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-48-9202T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514939 | |||||||
| chr9:97514999 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-48-9142T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97514999 | |||||||
| chr9:97515201 | G | GA | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(22): Show |
25 | HG01109.hp1 HG01361.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.-48-8927dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97515201 | ||||||
| chr9:97515201 | G | GAA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.-48-8928_-48-8927d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97515201 | ||||||
| chr9:97515201 | GA | G | 48 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0071 others(45): Show |
48 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48-8927delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97515201 | ||||||
| chr9:97515256 | C | T | 43 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0050 others(40): Show |
43 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.-48-8885C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515256 | |||||||
| chr9:97515345 | T | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG00408.hp1 HG00423.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-8796T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515345 | |||||||
| chr9:97515410 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-48-8731G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515410 | |||||||
| chr9:97515477 | G | T | 1 | a0001c0001t0001g0114 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-48-8664G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515477 | |||||||
| chr9:97515572 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-48-8569G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515572 | |||||||
| chr9:97515594 | T | C | 5 | a0001c0001t0002g0253 a0001c0001t0008g0254 a0001c0001t0010g0306 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-8547T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515594 | |||||||
| chr9:97515667 | G | A | 2 | a0001c0001t0005g0256 a0001c0001t0008g0257 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-48-8474G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515667 | |||||||
| chr9:97515671 | C | T | 2 | a0001c0001t0005g0256 a0001c0001t0008g0257 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-48-8470C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515671 | |||||||
| chr9:97515730 | A | G | 1 | a0001c0001t0005g0330 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-48-8411A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515730 | |||||||
| chr9:97515748 | A | G | 12 | a0001c0001t0001g0312 a0001c0001t0001g0321 a0001c0001t0001g0323 others(9): Show |
12 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-8393A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515748 | |||||||
| chr9:97515754 | G | C | 5 | a0001c0001t0002g0253 a0001c0001t0008g0254 a0001c0001t0010g0306 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-8387G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515754 | |||||||
| chr9:97515797 | C | T | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48-8344C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515797 | |||||||
| chr9:97515872 | A | C | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-48-8269A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515872 | |||||||
| chr9:97515886 | A | G | 5 | a0001c0001t0002g0253 a0001c0001t0008g0254 a0001c0001t0010g0306 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-8255A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515886 | |||||||
| chr9:97515924 | G | C | 1 | a0001c0001t0001g0059 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-48-8217G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515924 | |||||||
| chr9:97515925 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-48-8216C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515925 | |||||||
| chr9:97515925 | C | T | 1 | a0001c0001t0005g0100 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-48-8216C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515925 | |||||||
| chr9:97515967 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-48-8174A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515967 | |||||||
| chr9:97515971 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-48-8170T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97515971 | |||||||
| chr9:97516049 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-48-8092G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516049 | |||||||
| chr9:97516237 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-48-7904T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516237 | |||||||
| chr9:97516273 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-48-7868G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516273 | |||||||
| chr9:97516324 | C | T | 1 | a0001c0001t0005g0258 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-48-7817C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516324 | |||||||
| chr9:97516447 | C | G | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-48-7694C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516447 | |||||||
| chr9:97516475 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.-48-7666G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516475 | |||||||
| chr9:97516493 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-48-7648G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516493 | |||||||
| chr9:97516671 | G | A | 7 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-7470G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516671 | |||||||
| chr9:97516727 | A | G | 52 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0071 others(49): Show |
52 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-48-7414A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516727 | |||||||
| chr9:97516745 | A | G | 7 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-7396A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516745 | |||||||
| chr9:97516769 | C | T | 1 | a0001c0001t0004g0295 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48-7372C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516769 | |||||||
| chr9:97516770 | G | A | 4 | a0001c0001t0002g0253 a0001c0001t0008g0254 a0001c0001t0017g0251 others(1): Show |
4 | HG01884.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-7371G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516770 | |||||||
| chr9:97516958 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(9): Show |
12 | HG02280.hp2 HG02630.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-7183C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516958 | |||||||
| chr9:97516977 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(9): Show |
12 | HG02280.hp2 HG02630.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-7164C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97516977 | |||||||
| chr9:97517016 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01256.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-48-7125G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517016 | |||||||
| chr9:97517022 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0311 |
3 | HG00597.hp2 HG01993.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-48-7119A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517022 | |||||||
| chr9:97517059 | A | T | 2 | a0001c0001t0010g0003 a0001c0003t0012g0104 |
2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-48-7082A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517059 | |||||||
| chr9:97517065 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-48-7076G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517065 | |||||||
| chr9:97517084 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-48-7057C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517084 | |||||||
| chr9:97517122 | G | A | 4 | a0001c0001t0002g0329 a0001c0001t0005g0100 a0001c0001t0005g0256 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-7019G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517122 | |||||||
| chr9:97517127 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(9): Show |
12 | HG02280.hp2 HG02630.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-7014G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517127 | |||||||
| chr9:97517334 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-48-6807G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517334 | |||||||
| chr9:97517335 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-48-6806G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517335 | |||||||
| chr9:97517336 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
273 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.-48-6805G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517336 | |||||||
| chr9:97517427 | C | T | 42 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0071 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48-6714C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517427 | |||||||
| chr9:97517507 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-48-6634G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517507 | |||||||
| chr9:97517728 | C | T | 4 | a0001c0001t0001g0312 a0001c0001t0002g0101 a0001c0001t0002g0102 others(1): Show |
4 | HG02976.hp2 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-6413C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517728 | |||||||
| chr9:97517729 | G | A | 111 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(108): Show |
111 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-48-6412G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517729 | |||||||
| chr9:97517849 | G | A | 4 | a0001c0001t0001g0312 a0001c0001t0002g0101 a0001c0001t0002g0102 others(1): Show |
4 | HG02976.hp2 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-6292G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97517849 | |||||||
| chr9:97518040 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-48-6101C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97518040 | |||||||
| chr9:97518240 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-48-5901G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97518240 | |||||||
| chr9:97518282 | GA | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(51): Show |
54 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-48-5852delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 97518282 | ||||||
| chr9:97518300 | A | T | 1 | a0001c0001t0004g0012 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-48-5841A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97518300 | |||||||
| chr9:97518418 | C | T | 1 | a0001c0004t0001g0058 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-48-5723C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97518418 | |||||||
| chr9:97518507 | T | C | 21 | a0001c0001t0001g0304 a0001c0001t0001g0312 a0001c0001t0001g0321 others(18): Show |
21 | HG00408.hp2 HG01884.hp2 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.-48-5634T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97518507 | |||||||
| chr9:97518537 | C | T | 7 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-5604C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97518537 | |||||||
| chr9:97518778 | C | T | 1 | a0001c0004t0001g0058 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-48-5363C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97518778 | |||||||
| chr9:97519090 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48-5051T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519090 | |||||||
| chr9:97519167 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-48-4974A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519167 | |||||||
| chr9:97519199 | C | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG00408.hp1 HG00423.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-4942C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519199 | |||||||
| chr9:97519234 | C | T | 2 | a0001c0001t0001g0326 a0001c0001t0002g0278 |
2 | HG02523.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-48-4907C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519234 | |||||||
| chr9:97519344 | T | G | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-48-4797T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519344 | |||||||
| chr9:97519530 | C | T | 29 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0030 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-48-4611C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519530 | |||||||
| chr9:97519558 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0156 |
2 | HG01258.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-48-4583C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519558 | |||||||
| chr9:97519590 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0001g0120 a0001c0001t0001g0217 others(8): Show |
11 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48-4551C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519590 | |||||||
| chr9:97519857 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0205 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-48-4284A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519857 | |||||||
| chr9:97519957 | C | T | 1 | a0001c0001t0010g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48-4184C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97519957 | |||||||
| chr9:97520031 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-48-4110A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520031 | |||||||
| chr9:97520201 | A | G | 3 | a0001c0001t0006g0305 a0001c0001t0008g0257 a0001c0001t0008g0277 |
3 | HG01109.hp1 HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-48-3940A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520201 | |||||||
| chr9:97520282 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-48-3859A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520282 | |||||||
| chr9:97520384 | A | G | 30 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0059 others(27): Show |
30 | HG00408.hp2 HG00609.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.-48-3757A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520384 | |||||||
| chr9:97520423 | ACT | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0108 a0001c0001t0001g0126 others(4): Show |
7 | HG01070.hp1 HG01433.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-3717_-48-3716d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520423 | |||||||
| chr9:97520446 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-48-3695C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520446 | |||||||
| chr9:97520513 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-48-3628G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520513 | |||||||
| chr9:97520653 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-48-3488G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520653 | |||||||
| chr9:97520706 | G | A | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-48-3435G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520706 | |||||||
| chr9:97520763 | T | C | 3 | a0001c0001t0006g0305 a0001c0001t0008g0257 a0001c0001t0008g0277 |
3 | HG01109.hp1 HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-48-3378T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520763 | |||||||
| chr9:97520884 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48-3257C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520884 | |||||||
| chr9:97520892 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-48-3249C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97520892 | |||||||
| chr9:97521031 | A | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(7): Show |
10 | HG01256.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48-3110A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97521031 | |||||||
| chr9:97521426 | T | G | 1 | a0001c0001t0005g0188 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-48-2715T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97521426 | |||||||
| chr9:97521865 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(7): Show |
10 | HG01256.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48-2276G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97521865 | |||||||
| chr9:97521939 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-48-2202T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97521939 | |||||||
| chr9:97522054 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48-2087G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522054 | |||||||
| chr9:97522092 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-48-2049A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522092 | |||||||
| chr9:97522128 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-48-2013T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522128 | |||||||
| chr9:97522147 | C | T | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48-1994C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522147 | |||||||
| chr9:97522170 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0002g0239 |
2 | HG01081.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-48-1971C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522170 | |||||||
| chr9:97522201 | T | C | 1 | a0001c0001t0008g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-48-1940T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522201 | |||||||
| chr9:97522342 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0227 a0001c0001t0003g0072 |
3 | NA18947.hp1 NA19063.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-48-1799C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522342 | |||||||
| chr9:97522345 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-48-1796T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522345 | |||||||
| chr9:97522346 | A | G | 1 | a0001c0002t0001g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-48-1795A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522346 | |||||||
| chr9:97522354 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-48-1787C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522354 | |||||||
| chr9:97522423 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-48-1718C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522423 | |||||||
| chr9:97522580 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0004g0012 a0001c0001t0008g0014 |
3 | HG01256.hp1 HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-48-1561G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522580 | |||||||
| chr9:97522761 | C | T | 26 | a0001c0001t0001g0059 a0001c0001t0001g0108 a0001c0001t0001g0126 others(23): Show |
26 | HG00408.hp2 HG01070.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.-48-1380C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522761 | |||||||
| chr9:97522970 | C | T | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-48-1171C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97522970 | |||||||
| chr9:97523015 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.-48-1126G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97523015 | |||||||
| chr9:97523371 | C | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-48-770C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97523371 | |||||||
| chr9:97523440 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0004g0012 a0001c0001t0008g0014 |
3 | HG01256.hp1 HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-48-701G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97523440 | |||||||
| chr9:97523470 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-48-671G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97523470 | |||||||
| chr9:97523666 | A | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0233 a0001c0001t0001g0250 |
3 | HG00741.hp1 HG01934.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-48-475A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97523666 | |||||||
| chr9:97523771 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0008g0257 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-48-370C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 1/9 | chr9 | 97523771 | |||||||
| chr9:97524497 | G | GGGGTGT | 9 | a0001c0001t0001g0059 a0001c0001t0001g0108 a0001c0001t0001g0126 others(6): Show |
9 | HG01070.hp1 HG01433.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.120+190_120+191ins others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGGGTGTG others(1): Show |
14 | a0001c0001t0001g0132 a0001c0001t0001g0224 a0001c0001t0001g0261 others(11): Show |
14 | HG00408.hp2 HG01167.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+190_120+191ins others(8): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGGGTGTG others(3): Show |
4 | a0001c0001t0001g0324 a0001c0001t0001g0326 a0001c0001t0003g0031 others(1): Show |
4 | HG01934.hp1 NA18966.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+190_120+191ins others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGT | 5 | a0001c0001t0001g0026 a0001c0001t0001g0130 a0001c0001t0001g0328 others(2): Show |
5 | HG00408.hp1 HG02165.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+212_120+213dup others(2): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGT | 52 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0030 others(49): Show |
52 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.120+210_120+213dup others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGT | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(85): Show |
88 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.120+208_120+213dup others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGTG others(1): Show |
33 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0066 others(30): Show |
33 | HG00639.hp1 HG00673.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.120+206_120+213dup others(8): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGTG others(3): Show |
13 | a0001c0001t0001g0017 a0001c0001t0001g0141 a0001c0001t0001g0270 others(10): Show |
13 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+204_120+213dup others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGTG others(5): Show |
8 | a0001c0001t0001g0181 a0001c0001t0001g0229 a0001c0001t0002g0101 others(5): Show |
8 | HG01081.hp2 HG02886.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+202_120+213dup others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGTG others(7): Show |
7 | a0001c0001t0001g0142 a0001c0001t0001g0208 a0001c0001t0001g0228 others(4): Show |
7 | HG01071.hp1 HG01256.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+200_120+213dup others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGTG others(9): Show |
1 | a0001c0001t0002g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.120+198_120+213dup others(16): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGTG others(11): Show |
1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+196_120+213dup others(18): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGTG others(13): Show |
1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.120+194_120+213dup others(20): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524497 | G | GGTGTGTG others(17): Show |
1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120+190_120+213dup others(24): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524497 | ||||||
| chr9:97524522 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
240 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.120+214A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524522 | |||||||
| chr9:97524538 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
240 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.120+230C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524538 | |||||||
| chr9:97524687 | G | A | 4 | a0001c0001t0002g0329 a0001c0001t0005g0256 a0001c0003t0012g0104 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+379G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524687 | |||||||
| chr9:97524734 | T | G | 14 | a0001c0001t0001g0089 a0001c0001t0001g0181 a0001c0001t0001g0228 others(11): Show |
14 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+426T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524734 | |||||||
| chr9:97524737 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.120+429G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524737 | |||||||
| chr9:97524791 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
240 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.120+483T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524791 | |||||||
| chr9:97524794 | G | A | 3 | a0001c0001t0001g0304 a0001c0001t0008g0257 a0001c0001t0008g0277 |
3 | HG02109.hp2 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.120+486G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524794 | |||||||
| chr9:97524795 | C | T | 9 | a0001c0001t0001g0089 a0001c0001t0001g0181 a0001c0001t0001g0228 others(6): Show |
9 | HG01081.hp2 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.120+487C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524795 | |||||||
| chr9:97524815 | CT | C | 4 | a0001c0001t0002g0329 a0001c0001t0005g0256 a0001c0003t0012g0104 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+514delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97524815 | ||||||
| chr9:97524827 | A | G | 1 | a0001c0001t0008g0014 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.120+519A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524827 | |||||||
| chr9:97524859 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+551C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524859 | |||||||
| chr9:97524872 | CA | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.120+565delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524872 | |||||||
| chr9:97524917 | G | A | 3 | a0001c0001t0002g0329 a0001c0001t0005g0256 a0001c0003t0012g0170 |
3 | HG01891.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.120+609G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97524917 | |||||||
| chr9:97525087 | G | GAC | 14 | a0001c0001t0001g0089 a0001c0001t0001g0181 a0001c0001t0001g0228 others(11): Show |
14 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+781_120+782dup others(2): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97525087 | ||||||
| chr9:97525095 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.120+787C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97525095 | |||||||
| chr9:97525313 | T | C | 14 | a0001c0001t0001g0089 a0001c0001t0001g0181 a0001c0001t0001g0228 others(11): Show |
14 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+1005T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97525313 | |||||||
| chr9:97525956 | A | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.120+1648A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97525956 | |||||||
| chr9:97525967 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.120+1659G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97525967 | |||||||
| chr9:97526144 | A | AC | 12 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0041 others(9): Show |
12 | HG00621.hp2 HG00673.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+1840dupC | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97526144 | ||||||
| chr9:97526346 | A | C | 2 | a0001c0001t0001g0304 a0001c0001t0008g0257 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.120+2038A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97526346 | |||||||
| chr9:97526417 | C | T | 1 | a0001c0001t0008g0014 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.120+2109C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97526417 | |||||||
| chr9:97526627 | A | G | 4 | a0001c0001t0001g0181 a0001c0001t0001g0228 a0001c0001t0001g0229 others(1): Show |
4 | HG01081.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2319A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97526627 | |||||||
| chr9:97526676 | G | A | 1 | a0001c0001t0006g0303 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120+2368G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97526676 | |||||||
| chr9:97526733 | C | A | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.120+2425C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97526733 | |||||||
| chr9:97526776 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
187 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.120+2468G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97526776 | |||||||
| chr9:97526899 | T | C | 2 | a0001c0001t0005g0256 a0001c0003t0012g0104 |
2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.120+2591T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97526899 | |||||||
| chr9:97527104 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.120+2796C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97527104 | |||||||
| chr9:97527327 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.120+3019C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97527327 | |||||||
| chr9:97527330 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.120+3022C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97527330 | |||||||
| chr9:97527465 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.120+3157A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97527465 | |||||||
| chr9:97527481 | T | C | 50 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0057 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.120+3173T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97527481 | |||||||
| chr9:97527644 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.120+3336G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97527644 | |||||||
| chr9:97527670 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.120+3362C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97527670 | |||||||
| chr9:97527927 | G | A | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+3619G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97527927 | |||||||
| chr9:97528006 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.120+3698G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528006 | |||||||
| chr9:97528036 | G | T | 26 | a0001c0001t0001g0108 a0001c0001t0001g0126 a0001c0001t0001g0127 others(23): Show |
26 | HG00408.hp2 HG01070.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.120+3728G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528036 | |||||||
| chr9:97528124 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0312 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.120+3816C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528124 | |||||||
| chr9:97528231 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.120+3923G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528231 | |||||||
| chr9:97528232 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.120+3924C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528232 | |||||||
| chr9:97528236 | C | T | 5 | a0001c0001t0001g0208 a0001c0001t0001g0255 a0001c0001t0002g0329 others(2): Show |
5 | HG01256.hp1 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+3928C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528236 | |||||||
| chr9:97528260 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.120+3952G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528260 | |||||||
| chr9:97528267 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+3959C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528267 | |||||||
| chr9:97528455 | G | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
241 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.120+4147G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528455 | |||||||
| chr9:97528507 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.120+4199A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528507 | |||||||
| chr9:97528746 | C | T | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+4438C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528746 | |||||||
| chr9:97528830 | G | T | 1 | a0001c0001t0001g0141 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.120+4522G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528830 | |||||||
| chr9:97528935 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.120+4627T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528935 | |||||||
| chr9:97528955 | C | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.120+4647C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97528955 | |||||||
| chr9:97529121 | T | C | 1 | a0001c0001t0008g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.120+4813T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529121 | |||||||
| chr9:97529174 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.120+4866G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529174 | |||||||
| chr9:97529189 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0002g0025 |
2 | HG00408.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.120+4881T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529189 | |||||||
| chr9:97529202 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.120+4894T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529202 | |||||||
| chr9:97529242 | T | C | 6 | a0001c0001t0001g0108 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG01070.hp1 HG01433.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+4934T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529242 | |||||||
| chr9:97529345 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.120+5037C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529345 | |||||||
| chr9:97529434 | G | A | 1 | a0001c0001t0007g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.120+5126G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529434 | |||||||
| chr9:97529534 | TA | T | 17 | a0001c0001t0001g0074 a0001c0001t0001g0222 a0001c0001t0001g0234 others(14): Show |
17 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.120+5241delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97529534 | ||||||
| chr9:97529656 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.120+5348C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529656 | |||||||
| chr9:97529704 | A | G | 1 | a0001c0001t0008g0327 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.120+5396A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529704 | |||||||
| chr9:97529859 | G | A | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.120+5551G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97529859 | |||||||
| chr9:97530100 | C | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.120+5792C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530100 | |||||||
| chr9:97530313 | G | A | 2 | a0001c0001t0010g0003 a0001c0001t0010g0300 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.120+6005G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530313 | |||||||
| chr9:97530327 | G | A | 1 | a0001c0001t0004g0012 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.120+6019G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530327 | |||||||
| chr9:97530489 | G | GT | 12 | a0001c0001t0001g0022 a0001c0001t0001g0140 a0001c0001t0001g0173 others(9): Show |
12 | HG01175.hp2 HG01891.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+6197dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97530489 | ||||||
| chr9:97530633 | G | A | 2 | a0001c0001t0010g0003 a0001c0001t0010g0300 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.120+6325G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530633 | |||||||
| chr9:97530637 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.120+6329G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530637 | |||||||
| chr9:97530647 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0013g0123 a0001c0001t0013g0125 |
3 | HG01361.hp2 HG01515.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.120+6339C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530647 | |||||||
| chr9:97530769 | G | A | 9 | a0001c0001t0001g0074 a0001c0001t0001g0315 a0001c0001t0001g0332 others(6): Show |
9 | HG01081.hp1 HG01255.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.120+6461G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530769 | |||||||
| chr9:97530779 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.120+6471G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530779 | |||||||
| chr9:97530787 | C | CT | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.120+6498dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97530787 | ||||||
| chr9:97530787 | C | CTT | 71 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0030 others(68): Show |
71 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.120+6497_120+6498d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97530787 | ||||||
| chr9:97530849 | G | A | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120+6541G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530849 | |||||||
| chr9:97530874 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.120+6566G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97530874 | |||||||
| chr9:97531033 | A | AC | 77 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(74): Show |
77 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.120+6728dupC | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97531033 | ||||||
| chr9:97531033 | A | ACC | 92 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0029 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.120+6727_120+6728d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97531033 | ||||||
| chr9:97531033 | A | ACCC | 61 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0040 others(58): Show |
61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.120+6726_120+6728d others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97531033 | ||||||
| chr9:97531034 | C | A | 13 | a0001c0001t0001g0074 a0001c0001t0001g0315 a0001c0001t0001g0332 others(10): Show |
13 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.120+6726C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531034 | |||||||
| chr9:97531036 | CA | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0074 a0001c0001t0001g0315 others(14): Show |
17 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.120+6729delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531036 | |||||||
| chr9:97531037 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.120+6729A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531037 | |||||||
| chr9:97531037 | A | G | 2 | a0001c0001t0002g0046 a0001c0001t0005g0047 |
2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.120+6729A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531037 | |||||||
| chr9:97531044 | C | G | 2 | a0001c0001t0006g0276 a0001c0001t0010g0306 |
2 | HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.120+6736C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531044 | |||||||
| chr9:97531475 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.120+7167G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531475 | |||||||
| chr9:97531500 | A | G | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.120+7192A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531500 | |||||||
| chr9:97531579 | C | G | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120+7271C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531579 | |||||||
| chr9:97531722 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.120+7414C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531722 | |||||||
| chr9:97531743 | C | CG | 8 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0189 others(5): Show |
8 | HG00423.hp1 HG01255.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+7437dupG | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97531743 | ||||||
| chr9:97531861 | G | T | 25 | a0001c0001t0001g0108 a0001c0001t0001g0126 a0001c0001t0001g0127 others(22): Show |
25 | HG00408.hp2 HG01070.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.120+7553G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97531861 | |||||||
| chr9:97532188 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.120+7880T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532188 | |||||||
| chr9:97532327 | C | T | 1 | a0001c0001t0008g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.120+8019C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532327 | |||||||
| chr9:97532347 | C | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.120+8039C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532347 | |||||||
| chr9:97532419 | C | G | 2 | a0001c0001t0002g0329 a0001c0003t0012g0170 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.120+8111C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532419 | |||||||
| chr9:97532443 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.120+8135A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532443 | |||||||
| chr9:97532547 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.120+8239A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532547 | |||||||
| chr9:97532618 | TA | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0079 others(4): Show |
7 | HG00738.hp2 HG01515.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+8322delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97532618 | ||||||
| chr9:97532834 | T | G | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+8526T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532834 | |||||||
| chr9:97532863 | G | T | 46 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0108 others(43): Show |
46 | HG00408.hp2 HG01070.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.120+8555G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532863 | |||||||
| chr9:97532900 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+8592C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97532900 | |||||||
| chr9:97533029 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0255 a0001c0001t0008g0014 |
3 | HG01256.hp1 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.120+8721G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533029 | |||||||
| chr9:97533310 | G | T | 25 | a0001c0001t0001g0108 a0001c0001t0001g0126 a0001c0001t0001g0127 others(22): Show |
25 | HG00408.hp2 HG01070.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.120+9002G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533310 | |||||||
| chr9:97533366 | G | T | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120+9058G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533366 | |||||||
| chr9:97533405 | C | T | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.120+9097C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533405 | |||||||
| chr9:97533639 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
284 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.120+9331A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533639 | |||||||
| chr9:97533709 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+9401A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533709 | |||||||
| chr9:97533729 | C | A | 1 | a0001c0001t0006g0276 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.120+9421C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533729 | |||||||
| chr9:97533764 | C | T | 9 | a0001c0001t0001g0074 a0001c0001t0001g0095 a0001c0001t0001g0315 others(6): Show |
9 | HG01081.hp1 HG01255.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.120+9456C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533764 | |||||||
| chr9:97533806 | G | T | 4 | a0001c0001t0002g0253 a0001c0001t0005g0100 a0001c0001t0017g0251 others(1): Show |
4 | HG01884.hp2 HG02451.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+9498G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533806 | |||||||
| chr9:97533937 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.120+9629C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533937 | |||||||
| chr9:97533972 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0312 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.120+9664G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533972 | |||||||
| chr9:97533981 | T | C | 3 | a0001c0001t0001g0272 a0001c0001t0002g0273 a0001c0001t0002g0301 |
3 | HG02622.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.120+9673T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97533981 | |||||||
| chr9:97534057 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.120+9749A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534057 | |||||||
| chr9:97534094 | A | G | 1 | a0001c0001t0008g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.120+9786A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534094 | |||||||
| chr9:97534198 | C | G | 5 | a0001c0001t0001g0208 a0001c0001t0004g0206 a0001c0001t0004g0333 others(2): Show |
5 | HG01256.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+9890C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534198 | |||||||
| chr9:97534373 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0006g0013 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.120+10065C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534373 | |||||||
| chr9:97534434 | A | C | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.120+10126A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534434 | |||||||
| chr9:97534694 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.120+10386T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534694 | |||||||
| chr9:97534728 | C | T | 13 | a0001c0001t0001g0074 a0001c0001t0001g0095 a0001c0001t0001g0315 others(10): Show |
13 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.120+10420C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534728 | |||||||
| chr9:97534773 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+10465A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534773 | |||||||
| chr9:97534864 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.120+10556T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97534864 | |||||||
| chr9:97535310 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.121-10875A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97535310 | |||||||
| chr9:97535413 | C | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0057 others(38): Show |
41 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.121-10772C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97535413 | |||||||
| chr9:97535436 | C | T | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.121-10749C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97535436 | |||||||
| chr9:97535457 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.121-10728C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97535457 | |||||||
| chr9:97535571 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-10614G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97535571 | |||||||
| chr9:97535656 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.121-10529G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97535656 | |||||||
| chr9:97535679 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-10506A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97535679 | |||||||
| chr9:97535967 | G | C | 4 | a0001c0001t0002g0253 a0001c0001t0005g0100 a0001c0001t0017g0251 others(1): Show |
4 | HG01884.hp2 HG02451.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-10218G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97535967 | |||||||
| chr9:97536299 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.121-9886G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536299 | |||||||
| chr9:97536326 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.121-9859C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536326 | |||||||
| chr9:97536425 | T | A | 9 | a0001c0001t0001g0074 a0001c0001t0001g0095 a0001c0001t0001g0315 others(6): Show |
9 | HG01081.hp1 HG01255.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.121-9760T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536425 | |||||||
| chr9:97536441 | A | G | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-9744A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536441 | |||||||
| chr9:97536473 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-9712C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536473 | |||||||
| chr9:97536491 | C | T | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.121-9694C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536491 | |||||||
| chr9:97536627 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.121-9558G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536627 | |||||||
| chr9:97536694 | G | A | 1 | a0001c0006t0006g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121-9491G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536694 | |||||||
| chr9:97536705 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.121-9480A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536705 | |||||||
| chr9:97536707 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.121-9478T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536707 | |||||||
| chr9:97536726 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0002g0246 a0001c0001t0006g0013 |
3 | HG02451.hp1 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.121-9459G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536726 | |||||||
| chr9:97536830 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0014g0155 |
2 | HG02647.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.121-9355G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536830 | |||||||
| chr9:97536949 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.121-9236G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97536949 | |||||||
| chr9:97537087 | C | T | 53 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.121-9098C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537087 | |||||||
| chr9:97537211 | G | T | 39 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0057 others(36): Show |
39 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.121-8974G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537211 | |||||||
| chr9:97537217 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(278): Show |
281 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.121-8968G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537217 | |||||||
| chr9:97537273 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.121-8912C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537273 | |||||||
| chr9:97537316 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.121-8869G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537316 | |||||||
| chr9:97537330 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.121-8855G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537330 | |||||||
| chr9:97537418 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.121-8767G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537418 | |||||||
| chr9:97537493 | T | C | 17 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0001t0001g0076 others(14): Show |
17 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.121-8692T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537493 | |||||||
| chr9:97537733 | A | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0004g0316 |
3 | HG03225.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.121-8452A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537733 | |||||||
| chr9:97537791 | T | C | 12 | a0001c0001t0001g0074 a0001c0001t0001g0095 a0001c0001t0001g0255 others(9): Show |
12 | HG01081.hp1 HG01109.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-8394T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97537791 | |||||||
| chr9:97538138 | A | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(284): Show |
287 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.121-8047A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538138 | |||||||
| chr9:97538168 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.121-8017A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538168 | |||||||
| chr9:97538182 | A | G | 18 | a0001c0001t0001g0261 a0001c0001t0001g0293 a0001c0001t0001g0321 others(15): Show |
18 | HG00408.hp2 HG01167.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.121-8003A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538182 | |||||||
| chr9:97538209 | C | T | 18 | a0001c0001t0001g0261 a0001c0001t0001g0293 a0001c0001t0001g0321 others(15): Show |
18 | HG00408.hp2 HG01167.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.121-7976C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538209 | |||||||
| chr9:97538221 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-7964C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538221 | |||||||
| chr9:97538414 | T | G | 6 | a0001c0001t0001g0141 a0001c0001t0001g0245 a0001c0001t0001g0270 others(3): Show |
6 | NA18954.hp1 NA18984.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-7771T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538414 | |||||||
| chr9:97538469 | CA | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(242): Show |
245 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.121-7705delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97538469 | ||||||
| chr9:97538526 | T | A | 2 | a0001c0001t0002g0046 a0001c0001t0005g0047 |
2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.121-7659T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538526 | |||||||
| chr9:97538714 | A | T | 2 | a0001c0001t0011g0010 a0001c0001t0011g0011 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.121-7471A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538714 | |||||||
| chr9:97538717 | C | T | 1 | a0001c0001t0010g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.121-7468C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538717 | |||||||
| chr9:97538778 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.121-7407C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538778 | |||||||
| chr9:97538779 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.121-7406G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538779 | |||||||
| chr9:97538782 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(284): Show |
287 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.121-7403A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538782 | |||||||
| chr9:97538840 | C | CA | 18 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0094 others(15): Show |
18 | HG01081.hp2 HG01109.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.121-7330dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97538840 | ||||||
| chr9:97538927 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-7258C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538927 | |||||||
| chr9:97538969 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(47): Show |
50 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.121-7216C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97538969 | |||||||
| chr9:97539005 | AAAAAC | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0208 a0001c0001t0001g0240 others(2): Show |
5 | HG01256.hp1 HG02896.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-7156_121-7152d others(7): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97539005 | ||||||
| chr9:97539005 | AAAAACAA others(3): Show |
A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0002g0253 others(8): Show |
11 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-7161_121-7152d others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97539005 | ||||||
| chr9:97539029 | A | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0087 a0001c0001t0002g0088 |
3 | HG02809.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.121-7156A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539029 | |||||||
| chr9:97539038 | C | A | 1 | a0001c0003t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121-7147C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539038 | |||||||
| chr9:97539166 | A | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(47): Show |
50 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.121-7019A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539166 | |||||||
| chr9:97539207 | A | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
10 | NA18965.hp1 NA18966.hp1 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.121-6978A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539207 | |||||||
| chr9:97539236 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.121-6949A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539236 | |||||||
| chr9:97539400 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.121-6785A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539400 | |||||||
| chr9:97539479 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0120 a0001c0001t0001g0217 |
3 | HG00733.hp1 HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.121-6706C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539479 | |||||||
| chr9:97539617 | A | T | 1 | a0001c0001t0001g0064 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.121-6568A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539617 | |||||||
| chr9:97539688 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.121-6497C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539688 | |||||||
| chr9:97539689 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.121-6496G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539689 | |||||||
| chr9:97539742 | G | A | 2 | a0001c0001t0002g0046 a0001c0001t0005g0047 |
2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.121-6443G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539742 | |||||||
| chr9:97539782 | T | A | 5 | a0001c0001t0001g0136 a0001c0001t0006g0090 a0001c0001t0006g0179 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-6403T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539782 | |||||||
| chr9:97539971 | C | CA | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
178 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.121-6195dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97539971 | ||||||
| chr9:97539971 | C | CAA | 10 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0176 others(7): Show |
10 | HG01255.hp1 HG01256.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-6196_121-6195d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97539971 | ||||||
| chr9:97539986 | A | G | 5 | a0001c0001t0001g0136 a0001c0001t0006g0090 a0001c0001t0006g0179 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-6199A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97539986 | |||||||
| chr9:97540235 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.121-5950T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540235 | |||||||
| chr9:97540333 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.121-5852C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540333 | |||||||
| chr9:97540347 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.121-5838G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540347 | |||||||
| chr9:97540380 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.121-5805C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540380 | |||||||
| chr9:97540404 | G | T | 1 | a0001c0001t0004g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.121-5781G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540404 | |||||||
| chr9:97540482 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0006g0090 a0001c0001t0006g0179 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-5703C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540482 | |||||||
| chr9:97540569 | T | C | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-5616T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540569 | |||||||
| chr9:97540586 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-5599C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540586 | |||||||
| chr9:97540661 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0006g0090 a0001c0001t0006g0179 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-5524C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97540661 | |||||||
| chr9:97541337 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-4848G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97541337 | |||||||
| chr9:97541477 | C | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0240 |
2 | HG01256.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.121-4708C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97541477 | |||||||
| chr9:97541529 | T | A | 24 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0126 others(21): Show |
24 | HG00408.hp2 HG00544.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.121-4656T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97541529 | |||||||
| chr9:97541574 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
75 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.121-4611G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97541574 | |||||||
| chr9:97541591 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.121-4594C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97541591 | |||||||
| chr9:97541597 | C | A | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-4588C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97541597 | |||||||
| chr9:97541606 | C | G | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-4579C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97541606 | |||||||
| chr9:97542177 | T | G | 5 | a0001c0001t0001g0136 a0001c0001t0006g0090 a0001c0001t0006g0179 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-4008T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542177 | |||||||
| chr9:97542249 | A | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(172): Show |
175 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.121-3936A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542249 | |||||||
| chr9:97542531 | C | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(152): Show |
155 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.121-3654C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542531 | |||||||
| chr9:97542579 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(162): Show |
165 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.121-3606A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542579 | |||||||
| chr9:97542785 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(18): Show |
21 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.121-3400A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542785 | |||||||
| chr9:97542798 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0006g0090 a0001c0001t0006g0179 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-3387C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542798 | |||||||
| chr9:97542800 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(160): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.121-3385A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542800 | |||||||
| chr9:97542849 | C | CAAA | 16 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0075 others(13): Show |
16 | HG00323.hp1 HG00621.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.121-3320_121-3318d others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97542849 | ||||||
| chr9:97542849 | CA | C | 171 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(168): Show |
171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.121-3318delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97542849 | ||||||
| chr9:97542910 | TG | T | 24 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0126 others(21): Show |
24 | HG00408.hp2 HG00544.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.121-3273delG | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97542910 | ||||||
| chr9:97542930 | A | G | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0304 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.121-3255A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542930 | |||||||
| chr9:97542996 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.121-3189G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97542996 | |||||||
| chr9:97543075 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(150): Show |
153 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.121-3110G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97543075 | |||||||
| chr9:97543154 | A | G | 19 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0002g0253 others(16): Show |
19 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.121-3031A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97543154 | |||||||
| chr9:97543391 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.121-2794A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97543391 | |||||||
| chr9:97543416 | A | G | 50 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(47): Show |
50 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.121-2769A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97543416 | |||||||
| chr9:97543922 | G | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0075 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.121-2263G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97543922 | |||||||
| chr9:97543985 | G | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(150): Show |
153 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.121-2200G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97543985 | |||||||
| chr9:97544303 | C | T | 1 | a0001c0001t0005g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.121-1882C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97544303 | |||||||
| chr9:97544400 | G | T | 4 | a0001c0001t0001g0095 a0001c0001t0005g0258 a0001c0001t0005g0307 others(1): Show |
4 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-1785G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97544400 | |||||||
| chr9:97544460 | C | T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(48): Show |
51 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-1725C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97544460 | |||||||
| chr9:97544467 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
286 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.121-1718T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97544467 | |||||||
| chr9:97544522 | A | G | 52 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(49): Show |
52 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.121-1663A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97544522 | |||||||
| chr9:97544535 | CA | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0136 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.121-1639delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97544535 | ||||||
| chr9:97544735 | G | T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(48): Show |
51 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-1450G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97544735 | |||||||
| chr9:97544799 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0057 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.121-1386G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97544799 | |||||||
| chr9:97545010 | C | CA | 11 | a0001c0001t0001g0135 a0001c0001t0001g0221 a0001c0001t0001g0222 others(8): Show |
11 | HG00738.hp1 HG01261.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.121-1158dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97545010 | ||||||
| chr9:97545010 | C | CAAA | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
34 | HG00323.hp1 HG00544.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.121-1160_121-1158d others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97545010 | ||||||
| chr9:97545010 | CA | C | 25 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0126 others(22): Show |
25 | HG00408.hp2 HG01070.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-1158delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 97545010 | ||||||
| chr9:97545120 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
286 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.121-1065T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545120 | |||||||
| chr9:97545157 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.121-1028C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545157 | |||||||
| chr9:97545194 | G | A | 2 | a0001c0001t0011g0010 a0001c0001t0011g0011 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.121-991G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545194 | |||||||
| chr9:97545211 | G | A | 159 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(156): Show |
159 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.121-974G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545211 | |||||||
| chr9:97545246 | T | A | 51 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(48): Show |
51 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-939T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545246 | |||||||
| chr9:97545300 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.121-885C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545300 | |||||||
| chr9:97545507 | C | T | 160 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(157): Show |
160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.121-678C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545507 | |||||||
| chr9:97545552 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.121-633C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545552 | |||||||
| chr9:97545560 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0136 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.121-625G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545560 | |||||||
| chr9:97545620 | C | T | 12 | a0001c0001t0001g0181 a0001c0001t0001g0229 a0001c0001t0002g0301 others(9): Show |
12 | HG01081.hp2 HG01891.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.121-565C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545620 | |||||||
| chr9:97545734 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
286 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.121-451T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545734 | |||||||
| chr9:97545852 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.121-333G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545852 | |||||||
| chr9:97545877 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.121-308G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545877 | |||||||
| chr9:97545949 | A | G | 51 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(48): Show |
51 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-236A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 2/9 | chr9 | 97545949 | |||||||
| chr9:97546673 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.277+332G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97546673 | |||||||
| chr9:97546776 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.277+435A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97546776 | |||||||
| chr9:97546839 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.277+498A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97546839 | |||||||
| chr9:97546923 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0040 others(47): Show |
50 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.277+582C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97546923 | |||||||
| chr9:97546929 | C | CA | 19 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0052 others(16): Show |
19 | HG00621.hp1 HG01175.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.277+611dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97546929 | ||||||
| chr9:97546929 | C | CAA | 7 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0222 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+610_277+611dup others(2): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97546929 | ||||||
| chr9:97546929 | C | CAAA | 38 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0057 others(35): Show |
38 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.277+609_277+611dup others(3): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97546929 | ||||||
| chr9:97546929 | C | CAAAA | 10 | a0001c0001t0001g0141 a0001c0001t0001g0165 a0001c0001t0001g0166 others(7): Show |
10 | HG00280.hp1 HG01175.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.277+608_277+611dup others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97546929 | ||||||
| chr9:97546929 | CA | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0324 a0001c0001t0002g0253 others(4): Show |
7 | HG01167.hp2 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.277+611delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97546929 | ||||||
| chr9:97547106 | C | T | 34 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0126 others(31): Show |
34 | HG00408.hp2 HG00544.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.277+765C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97547106 | |||||||
| chr9:97547214 | C | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0002g0273 |
3 | HG02615.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.277+873C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97547214 | |||||||
| chr9:97547638 | G | T | 1 | a0001c0001t0001g0282 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.277+1297G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97547638 | |||||||
| chr9:97548039 | G | C | 2 | a0001c0001t0010g0003 a0001c0001t0010g0300 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.277+1698G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548039 | |||||||
| chr9:97548061 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0002g0273 |
3 | HG02615.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.277+1720G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548061 | |||||||
| chr9:97548200 | T | A | 1 | a0001c0001t0002g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.277+1859T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548200 | |||||||
| chr9:97548219 | C | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0019 others(140): Show |
143 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.277+1878C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548219 | |||||||
| chr9:97548251 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.277+1910C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548251 | |||||||
| chr9:97548252 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
288 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.277+1911A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548252 | |||||||
| chr9:97548384 | C | T | 54 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(51): Show |
54 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.277+2043C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548384 | |||||||
| chr9:97548429 | C | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0019 others(79): Show |
82 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.277+2088C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548429 | |||||||
| chr9:97548568 | C | T | 33 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0126 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.277+2227C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548568 | |||||||
| chr9:97548743 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.277+2402G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548743 | |||||||
| chr9:97548831 | G | A | 16 | a0001c0001t0001g0092 a0001c0001t0001g0127 a0001c0001t0001g0134 others(13): Show |
16 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+2490G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97548831 | |||||||
| chr9:97549067 | A | T | 3 | a0001c0001t0001g0127 a0001c0001t0002g0073 a0001c0001t0009g0241 |
3 | HG02165.hp2 HG03704.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.277+2726A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549067 | |||||||
| chr9:97549092 | G | T | 1 | a0001c0001t0009g0241 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.277+2751G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549092 | |||||||
| chr9:97549164 | T | A | 92 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0026 others(89): Show |
92 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.277+2823T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549164 | |||||||
| chr9:97549197 | T | C | 4 | a0001c0001t0002g0015 a0001c0001t0005g0256 a0001c0001t0005g0331 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+2856T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549197 | |||||||
| chr9:97549398 | CAG | C | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.277+3060_277+3061d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97549398 | ||||||
| chr9:97549551 | T | C | 5 | a0001c0001t0002g0015 a0001c0001t0002g0101 a0001c0001t0002g0102 others(2): Show |
5 | HG02145.hp2 HG02976.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+3210T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549551 | |||||||
| chr9:97549595 | A | C | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.277+3254A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549595 | |||||||
| chr9:97549683 | G | T | 2 | a0001c0001t0001g0142 a0001c0001t0013g0123 |
2 | HG01071.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.277+3342G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549683 | |||||||
| chr9:97549741 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.277+3400T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549741 | |||||||
| chr9:97549744 | G | T | 3 | a0001c0001t0002g0329 a0001c0003t0012g0104 a0001c0003t0012g0170 |
3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.277+3403G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549744 | |||||||
| chr9:97549832 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.278-3449C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549832 | |||||||
| chr9:97549862 | T | C | 1 | a0001c0001t0008g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.278-3419T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97549862 | |||||||
| chr9:97550002 | T | C | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(217): Show |
220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.278-3279T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97550002 | |||||||
| chr9:97550028 | C | G | 1 | a0001c0001t0001g0020 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.278-3253C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97550028 | |||||||
| chr9:97550031 | T | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0010g0003 others(2): Show |
5 | HG02280.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-3250T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97550031 | |||||||
| chr9:97550436 | G | T | 9 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(6): Show |
9 | HG01884.hp1 HG02622.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.278-2845G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97550436 | |||||||
| chr9:97550703 | A | G | 11 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-2578A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97550703 | |||||||
| chr9:97550992 | T | TTATATAT others(5): Show |
2 | a0001c0001t0005g0271 a0001c0001t0005g0275 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.278-2277_278-2266d others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97550992 | ||||||
| chr9:97550992 | T | TTATATAT others(13): Show |
1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.278-2285_278-2266d others(22): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97550992 | ||||||
| chr9:97551010 | ATATATTT others(10): Show |
A | 2 | a0001c0001t0002g0301 a0001c0001t0003g0161 |
2 | HG03239.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.278-2269_278-2253d others(19): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551010 | ||||||
| chr9:97551012 | A | AT | 8 | a0001c0001t0001g0071 a0001c0001t0001g0162 a0001c0001t0001g0242 others(5): Show |
8 | HG00621.hp1 HG02055.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-2268dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551012 | ||||||
| chr9:97551012 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.278-2269A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551012 | |||||||
| chr9:97551012 | ATATTTTT others(6): Show |
A | 1 | a0001c0001t0008g0014 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.278-2267_278-2255d others(15): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551012 | ||||||
| chr9:97551012 | ATATTTTT others(8): Show |
A | 1 | a0001c0001t0001g0267 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.278-2267_278-2253d others(17): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551012 | ||||||
| chr9:97551012 | ATATTTTT others(10): Show |
A | 1 | a0001c0001t0013g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.278-2267_278-2251d others(19): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551012 | ||||||
| chr9:97551012 | ATATTTTT others(11): Show |
A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(2): Show |
5 | HG01884.hp2 NA18966.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-2267_278-2250d others(20): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551012 | ||||||
| chr9:97551013 | TA | T | 3 | a0001c0001t0001g0174 a0001c0001t0003g0111 a0001c0001t0009g0241 |
3 | HG00639.hp1 HG01099.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.278-2267delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551013 | |||||||
| chr9:97551014 | A | T | 36 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0026 others(33): Show |
36 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.278-2267A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551014 | |||||||
| chr9:97551014 | AT | A | 8 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG00438.hp1 HG00639.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-2239delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT | A | 25 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
25 | HG00673.hp2 HG00741.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.278-2245_278-2239d others(9): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(2): Show |
A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(20): Show |
23 | HG01081.hp1 HG01891.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.278-2247_278-2239d others(11): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(3): Show |
A | 4 | a0001c0001t0001g0255 a0001c0001t0010g0003 a0001c0001t0010g0300 others(1): Show |
4 | HG03225.hp1 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2248_278-2239d others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(4): Show |
A | 14 | a0001c0001t0002g0246 a0001c0001t0003g0203 a0001c0001t0004g0002 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.278-2249_278-2239d others(13): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0003g0106 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.278-2250_278-2239d others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(6): Show |
A | 18 | a0001c0001t0001g0323 a0001c0001t0002g0025 a0001c0001t0002g0065 others(15): Show |
18 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.278-2251_278-2239d others(15): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0293 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.278-2252_278-2239d others(16): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(8): Show |
A | 68 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(65): Show |
68 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.278-2253_278-2239d others(17): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(9): Show |
A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0084 a0001c0001t0001g0087 others(7): Show |
10 | HG00544.hp1 HG01106.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.278-2254_278-2239d others(18): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(11): Show |
A | 62 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0038 others(59): Show |
62 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.278-2256_278-2239d others(20): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551014 | ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0001g0325 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.278-2258_278-2239d others(22): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97551014 | ||||||
| chr9:97551015 | T | TA | 8 | a0001c0001t0001g0060 a0001c0001t0001g0113 a0001c0001t0001g0114 others(5): Show |
8 | HG01358.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-2266_278-2265i others(3): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551015 | |||||||
| chr9:97551015 | T | TATATATA others(10): Show |
1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.278-2266_278-2265i others(19): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551015 | |||||||
| chr9:97551016 | T | A | 6 | a0001c0001t0001g0296 a0001c0001t0002g0101 a0001c0001t0002g0102 others(3): Show |
6 | HG02109.hp1 HG02258.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-2265T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551016 | |||||||
| chr9:97551017 | T | A | 5 | a0001c0001t0002g0103 a0001c0001t0002g0186 a0001c0001t0006g0276 others(2): Show |
5 | HG02896.hp1 HG03098.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-2264T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551017 | |||||||
| chr9:97551018 | T | A | 5 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0239 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-2263T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551018 | |||||||
| chr9:97551019 | T | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0294 others(5): Show |
8 | HG01433.hp1 HG01975.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.278-2262T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551019 | |||||||
| chr9:97551020 | T | A | 5 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0239 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-2261T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551020 | |||||||
| chr9:97551021 | T | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0126 others(6): Show |
9 | HG01433.hp1 HG01975.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.278-2260T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551021 | |||||||
| chr9:97551022 | T | A | 3 | a0001c0001t0002g0239 a0001c0001t0005g0271 a0001c0001t0005g0275 |
3 | HG02109.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.278-2259T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551022 | |||||||
| chr9:97551023 | T | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0034 others(28): Show |
31 | HG00673.hp2 HG00741.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.278-2258T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551023 | |||||||
| chr9:97551024 | T | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0195 a0001c0001t0002g0239 others(2): Show |
5 | HG00323.hp2 HG00741.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-2257T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551024 | |||||||
| chr9:97551025 | T | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
54 | HG00673.hp2 HG00741.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.278-2256T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551025 | |||||||
| chr9:97551026 | T | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0195 a0001c0001t0001g0255 others(6): Show |
9 | HG00323.hp2 HG00741.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.278-2255T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551026 | |||||||
| chr9:97551027 | T | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
68 | HG00673.hp2 HG00741.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.278-2254T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551027 | |||||||
| chr9:97551028 | T | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0195 a0001c0001t0002g0239 others(5): Show |
8 | HG00323.hp2 HG00741.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.278-2253T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551028 | |||||||
| chr9:97551029 | T | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(40): Show |
43 | HG00673.hp2 HG00741.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.278-2252T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551029 | |||||||
| chr9:97551030 | T | A | 3 | a0001c0001t0002g0239 a0001c0001t0005g0271 a0001c0001t0005g0275 |
3 | HG02109.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.278-2251T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551030 | |||||||
| chr9:97551031 | T | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0033 others(66): Show |
69 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.278-2250T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551031 | |||||||
| chr9:97551032 | T | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0084 a0001c0001t0001g0087 others(7): Show |
10 | HG00544.hp1 HG01106.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.278-2249T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551032 | |||||||
| chr9:97551033 | T | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0041 others(18): Show |
21 | HG00673.hp2 HG00733.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.278-2248T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551033 | |||||||
| chr9:97551034 | T | A | 40 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0048 others(37): Show |
40 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.278-2247T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551034 | |||||||
| chr9:97551035 | T | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0138 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.278-2246T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551035 | |||||||
| chr9:97551036 | T | A | 2 | a0001c0001t0001g0313 a0001c0001t0002g0088 |
2 | HG03516.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.278-2245T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551036 | |||||||
| chr9:97551170 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.278-2111C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551170 | |||||||
| chr9:97551181 | G | A | 5 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(2): Show |
5 | HG02896.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-2100G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551181 | |||||||
| chr9:97551279 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(46): Show |
49 | HG00323.hp2 HG00673.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-2002C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551279 | |||||||
| chr9:97551366 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
209 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.278-1915G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551366 | |||||||
| chr9:97551385 | G | A | 20 | a0001c0001t0001g0293 a0001c0001t0001g0323 a0001c0001t0002g0025 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.278-1896G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551385 | |||||||
| chr9:97551443 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(82): Show |
85 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.278-1838C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551443 | |||||||
| chr9:97551511 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.278-1770C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551511 | |||||||
| chr9:97551524 | G | A | 2 | a0001c0001t0006g0276 a0001c0001t0008g0327 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278-1757G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551524 | |||||||
| chr9:97551554 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.278-1727T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551554 | |||||||
| chr9:97551561 | T | A | 1 | a0001c0002t0001g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.278-1720T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551561 | |||||||
| chr9:97551619 | A | G | 3 | a0001c0001t0002g0239 a0001c0001t0005g0271 a0001c0001t0005g0275 |
3 | HG02109.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.278-1662A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551619 | |||||||
| chr9:97551621 | A | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(70): Show |
73 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.278-1660A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97551621 | |||||||
| chr9:97552091 | G | C | 1 | a0001c0001t0001g0260 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.278-1190G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97552091 | |||||||
| chr9:97552331 | ACTAGC | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
242 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.278-947_278-943del others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 97552331 | ||||||
| chr9:97552458 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
248 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.278-823T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97552458 | |||||||
| chr9:97552485 | T | C | 3 | a0001c0001t0002g0329 a0001c0003t0012g0104 a0001c0003t0012g0170 |
3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.278-796T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97552485 | |||||||
| chr9:97552665 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.278-616C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97552665 | |||||||
| chr9:97552720 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.278-561C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97552720 | |||||||
| chr9:97552913 | T | C | 2 | a0001c0001t0006g0276 a0001c0001t0008g0327 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278-368T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97552913 | |||||||
| chr9:97553101 | G | A | 3 | a0001c0001t0002g0239 a0001c0001t0005g0271 a0001c0001t0005g0275 |
3 | HG02109.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.278-180G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97553101 | |||||||
| chr9:97553202 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0023 |
2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.278-79G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 3/9 | chr9 | 97553202 | |||||||
| chr9:97553493 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0181 others(5): Show |
8 | HG01891.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+93C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97553493 | |||||||
| chr9:97553559 | C | G | 15 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(12): Show |
15 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.397+159C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97553559 | |||||||
| chr9:97553824 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.397+424G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97553824 | |||||||
| chr9:97553924 | T | A | 1 | a0001c0001t0003g0106 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.397+524T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97553924 | |||||||
| chr9:97553948 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
158 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.397+548C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97553948 | |||||||
| chr9:97554051 | A | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0233 a0001c0001t0001g0250 |
3 | HG00741.hp1 HG01934.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.397+651A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97554051 | |||||||
| chr9:97554311 | G | C | 67 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(64): Show |
67 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.397+911G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97554311 | |||||||
| chr9:97554422 | T | C | 1 | a0001c0001t0007g0308 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.397+1022T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97554422 | |||||||
| chr9:97554481 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG01256.hp1 HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.397+1081G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97554481 | |||||||
| chr9:97554974 | TC | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0158 others(3): Show |
6 | HG00423.hp1 HG00597.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+1577delC | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97554974 | ||||||
| chr9:97555009 | G | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0095 others(7): Show |
10 | HG01952.hp2 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.397+1609G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97555009 | |||||||
| chr9:97555036 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.397+1636T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97555036 | |||||||
| chr9:97555203 | T | C | 5 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(2): Show |
5 | HG02896.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+1803T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97555203 | |||||||
| chr9:97555208 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.397+1808C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97555208 | |||||||
| chr9:97555291 | G | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(65): Show |
68 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.397+1891G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97555291 | |||||||
| chr9:97555993 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
140 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.397+2593G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97555993 | |||||||
| chr9:97556173 | GTGAGATT others(5): Show |
G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0261 a0001c0001t0003g0109 others(2): Show |
5 | HG01099.hp2 HG01192.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2780_397+2791d others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97556173 | ||||||
| chr9:97556176 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
253 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.397+2776A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556176 | |||||||
| chr9:97556226 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.397+2826C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556226 | |||||||
| chr9:97556238 | C | T | 20 | a0001c0001t0001g0293 a0001c0001t0001g0323 a0001c0001t0002g0025 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.397+2838C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556238 | |||||||
| chr9:97556260 | T | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(70): Show |
73 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.397+2860T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556260 | |||||||
| chr9:97556269 | C | A | 73 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(70): Show |
73 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.397+2869C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556269 | |||||||
| chr9:97556340 | G | A | 2 | a0001c0001t0011g0010 a0001c0001t0011g0011 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.397+2940G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556340 | |||||||
| chr9:97556367 | A | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0095 others(7): Show |
10 | HG01952.hp2 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.397+2967A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556367 | |||||||
| chr9:97556425 | C | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | NA18949.hp1 NA18955.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+3025C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556425 | |||||||
| chr9:97556457 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
140 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.397+3057G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556457 | |||||||
| chr9:97556501 | A | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(62): Show |
65 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.397+3101A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556501 | |||||||
| chr9:97556508 | G | A | 1 | a0001c0001t0006g0276 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.397+3108G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556508 | |||||||
| chr9:97556682 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
257 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.397+3282A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556682 | |||||||
| chr9:97556749 | C | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(58): Show |
61 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.397+3349C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556749 | |||||||
| chr9:97556750 | G | A | 12 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.397+3350G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556750 | |||||||
| chr9:97556866 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.397+3466C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556866 | |||||||
| chr9:97556998 | C | T | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(50): Show |
53 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.397+3598C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97556998 | |||||||
| chr9:97557026 | C | T | 1 | a0001c0001t0005g0331 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.397+3626C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557026 | |||||||
| chr9:97557087 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0010g0003 others(2): Show |
5 | HG02280.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+3687G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557087 | |||||||
| chr9:97557273 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0002g0088 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.397+3873C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557273 | |||||||
| chr9:97557319 | T | G | 20 | a0001c0001t0001g0233 a0001c0001t0001g0323 a0001c0001t0002g0025 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.397+3919T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557319 | |||||||
| chr9:97557366 | G | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0124 others(1): Show |
4 | HG01167.hp1 HG01168.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+3966G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557366 | |||||||
| chr9:97557377 | C | A | 1 | a0001c0001t0019g0190 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.397+3977C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557377 | |||||||
| chr9:97557575 | G | A | 69 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(66): Show |
69 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.397+4175G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557575 | |||||||
| chr9:97557591 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.397+4191T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557591 | |||||||
| chr9:97557612 | C | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(85): Show |
88 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.397+4212C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557612 | |||||||
| chr9:97557699 | C | T | 3 | a0001c0001t0002g0329 a0001c0003t0012g0104 a0001c0003t0012g0170 |
3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.397+4299C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557699 | |||||||
| chr9:97557822 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.397+4422T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97557822 | |||||||
| chr9:97557870 | TA | T | 9 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0260 others(6): Show |
9 | HG01099.hp2 HG01243.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.397+4485delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97557870 | ||||||
| chr9:97558027 | C | T | 20 | a0001c0001t0001g0293 a0001c0001t0001g0323 a0001c0001t0002g0025 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.397+4627C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558027 | |||||||
| chr9:97558212 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.398-4520A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558212 | |||||||
| chr9:97558216 | T | G | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.398-4516T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558216 | |||||||
| chr9:97558431 | CTGTT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(119): Show |
122 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.398-4275_398-4272d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97558431 | ||||||
| chr9:97558431 | CTGTTTGT others(1): Show |
C | 3 | a0001c0001t0002g0239 a0001c0001t0005g0271 a0001c0001t0005g0275 |
3 | HG02109.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.398-4279_398-4272d others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97558431 | ||||||
| chr9:97558439 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.398-4293T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558439 | |||||||
| chr9:97558548 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG01256.hp1 HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.398-4184A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558548 | |||||||
| chr9:97558589 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.398-4143G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558589 | |||||||
| chr9:97558634 | G | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
176 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.398-4098G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558634 | |||||||
| chr9:97558866 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.398-3866G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558866 | |||||||
| chr9:97558944 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.398-3788A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558944 | |||||||
| chr9:97558989 | C | T | 66 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(63): Show |
66 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.398-3743C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97558989 | |||||||
| chr9:97559135 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0018g0083 |
2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.398-3597G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559135 | |||||||
| chr9:97559162 | G | A | 3 | a0001c0001t0010g0003 a0001c0001t0010g0300 a0001c0001t0010g0306 |
3 | HG03225.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.398-3570G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559162 | |||||||
| chr9:97559420 | C | A | 12 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.398-3312C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559420 | |||||||
| chr9:97559594 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0326 |
2 | NA18967.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.398-3138G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559594 | |||||||
| chr9:97559596 | C | T | 82 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(79): Show |
82 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.398-3136C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559596 | |||||||
| chr9:97559687 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.398-3045T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559687 | |||||||
| chr9:97559689 | C | T | 3 | a0001c0001t0002g0239 a0001c0001t0005g0271 a0001c0001t0005g0275 |
3 | HG02109.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.398-3043C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559689 | |||||||
| chr9:97559759 | C | T | 67 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(64): Show |
67 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.398-2973C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559759 | |||||||
| chr9:97559769 | AT | A | 8 | a0001c0001t0001g0153 a0001c0001t0002g0065 a0001c0001t0002g0088 others(5): Show |
8 | HG01167.hp2 HG01943.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-2960delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559769 | ||||||
| chr9:97559771 | TTA | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0042 others(51): Show |
54 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.398-2960_398-2959d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAA | T | 15 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0048 others(12): Show |
15 | HG00621.hp2 HG01106.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.398-2960_398-2958d others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAAA | T | 6 | a0001c0001t0001g0133 a0001c0001t0001g0185 a0001c0001t0001g0245 others(3): Show |
6 | HG01070.hp1 HG02630.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-2960_398-2957d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAAAA | T | 29 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(26): Show |
29 | HG00597.hp2 HG01123.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.398-2960_398-2956d others(7): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAAAAA | T | 8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0183 others(5): Show |
8 | HG01433.hp2 HG02132.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-2960_398-2955d others(8): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAAAAAA | T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0051 others(15): Show |
18 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.398-2960_398-2954d others(9): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAAAAAA others(1): Show |
T | 12 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0045 others(9): Show |
12 | HG00140.hp1 HG00609.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.398-2960_398-2953d others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAAAAAA others(2): Show |
T | 9 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG01167.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-2960_398-2952d others(11): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0167 |
2 | NA19011.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.398-2960_398-2951d others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559771 | TTAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.398-2960_398-2950d others(13): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559771 | |||||||
| chr9:97559772 | T | A | 19 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0313 others(16): Show |
19 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.398-2960T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559772 | |||||||
| chr9:97559772 | TAAAAA | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0192 a0001c0001t0001g0311 others(3): Show |
6 | HG01884.hp2 HG01993.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-2941_398-2937d others(7): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559772 | ||||||
| chr9:97559772 | TAAAAAAA others(1): Show |
T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0091 a0001c0001t0001g0132 others(3): Show |
6 | HG00323.hp2 HG00733.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-2944_398-2937d others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559772 | ||||||
| chr9:97559784 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.398-2946_398-2935d others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559784 | ||||||
| chr9:97559786 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
2 | HG02040.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.398-2944_398-2935d others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559786 | ||||||
| chr9:97559787 | AAAAAAAA others(2): Show |
A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0116 a0001c0001t0001g0126 others(8): Show |
11 | HG00741.hp1 HG01258.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-2943_398-2935d others(11): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559787 | ||||||
| chr9:97559788 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0194 |
2 | HG01256.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.398-2944A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559788 | |||||||
| chr9:97559790 | A | T | 16 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0089 others(13): Show |
16 | HG00438.hp2 HG01081.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.398-2942A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559790 | |||||||
| chr9:97559792 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.398-2939_398-2938i others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559792 | ||||||
| chr9:97559792 | A | ATATATAT others(10): Show |
1 | a0001c0001t0008g0014 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.398-2940_398-2939i others(19): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559792 | |||||||
| chr9:97559792 | A | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0048 others(19): Show |
22 | HG00438.hp2 HG01081.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.398-2940A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559792 | |||||||
| chr9:97559793 | AAATATAT others(12): Show |
A | 1 | a0001c0001t0001g0317 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.398-2937_398-2919d others(21): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559793 | ||||||
| chr9:97559794 | A | AAAAAAAA others(1): Show |
7 | a0001c0001t0001g0134 a0001c0001t0001g0160 a0001c0001t0001g0181 others(4): Show |
7 | HG00621.hp1 HG02451.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-2937_398-2936i others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AAAAAAAA others(5): Show |
3 | a0001c0001t0001g0026 a0001c0001t0001g0260 a0001c0001t0003g0072 |
3 | HG00408.hp1 NA18947.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.398-2937_398-2936i others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AAAAAATA others(5): Show |
2 | a0001c0001t0001g0021 a0001c0001t0001g0071 |
2 | NA18968.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.398-2937_398-2936i others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AAAAAATA others(15): Show |
1 | a0001c0001t0001g0237 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.398-2937_398-2936i others(24): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AAAATAT | 6 | a0001c0001t0001g0060 a0001c0001t0001g0218 a0001c0001t0001g0231 others(3): Show |
6 | HG02630.hp1 HG03710.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-2937_398-2936i others(8): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AAAATATA others(3): Show |
3 | a0001c0001t0001g0149 a0001c0001t0001g0162 a0001c0001t0001g0284 |
3 | HG02083.hp1 HG02083.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.398-2937_398-2936i others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0196 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.398-2937_398-2936i others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AAAATATA others(7): Show |
1 | a0001c0001t0007g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.398-2937_398-2936i others(16): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AAATATAT others(4): Show |
2 | a0001c0001t0003g0110 a0001c0001t0003g0111 |
2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.398-2937_398-2936i others(13): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0282 a0001c0001t0008g0277 |
2 | HG06807.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.398-2917_398-2908d others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.398-2923_398-2908d others(18): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | AATATATA others(15): Show |
1 | a0001c0001t0008g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.398-2929_398-2908d others(24): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559794 | A | ATATATAT | 3 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0007g0144 |
3 | HG00738.hp1 HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.398-2938_398-2937i others(9): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559794 | |||||||
| chr9:97559794 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0198 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.398-2938_398-2937i others(21): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559794 | |||||||
| chr9:97559794 | A | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(31): Show |
34 | HG00438.hp2 HG01081.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.398-2938A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559794 | |||||||
| chr9:97559794 | AATATATA others(3): Show |
A | 2 | a0001c0001t0005g0271 a0001c0001t0005g0275 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.398-2917_398-2908d others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559794 | ||||||
| chr9:97559795 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.398-2937A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559795 | |||||||
| chr9:97559795 | ATAT | A | 7 | a0001c0001t0002g0073 a0001c0001t0003g0031 a0001c0001t0003g0032 others(4): Show |
7 | HG01123.hp1 HG01934.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2936_398-2934d others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559795 | |||||||
| chr9:97559796 | T | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0267 others(20): Show |
23 | HG00597.hp1 HG00609.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.398-2936T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559796 | |||||||
| chr9:97559797 | A | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(62): Show |
65 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.398-2935A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559797 | |||||||
| chr9:97559798 | T | A | 10 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(7): Show |
10 | HG00597.hp1 HG00609.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.398-2934T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559798 | |||||||
| chr9:97559799 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.398-2933A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559799 | |||||||
| chr9:97559800 | T | A | 16 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(13): Show |
16 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.398-2932T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559800 | |||||||
| chr9:97559801 | A | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(62): Show |
65 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.398-2931A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559801 | |||||||
| chr9:97559802 | T | A | 11 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0073 others(8): Show |
11 | HG00609.hp1 HG01123.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-2930T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559802 | |||||||
| chr9:97559803 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.398-2929A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559803 | |||||||
| chr9:97559804 | T | A | 8 | a0001c0001t0002g0065 a0001c0001t0002g0202 a0001c0001t0002g0278 others(5): Show |
8 | HG01123.hp1 HG01934.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-2928T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559804 | |||||||
| chr9:97559805 | A | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(62): Show |
65 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.398-2927A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559805 | |||||||
| chr9:97559806 | T | A | 4 | a0001c0001t0003g0182 a0001c0001t0003g0201 a0001c0001t0003g0203 others(1): Show |
4 | HG01123.hp1 HG01934.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-2926T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559806 | |||||||
| chr9:97559807 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.398-2925A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559807 | |||||||
| chr9:97559808 | T | A | 2 | a0001c0001t0003g0182 a0001c0001t0003g0281 |
2 | HG01123.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.398-2924T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559808 | |||||||
| chr9:97559809 | A | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(62): Show |
65 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.398-2923A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559809 | |||||||
| chr9:97559809 | ATATATAT others(31): Show |
A | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.398-2919_398-2882d others(40): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559809 | ||||||
| chr9:97559811 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.398-2921A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559811 | |||||||
| chr9:97559811 | ATATATAT others(7): Show |
A | 13 | a0001c0001t0001g0062 a0001c0001t0001g0142 a0001c0001t0001g0157 others(10): Show |
13 | HG00408.hp2 HG00438.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-2919_398-2906d others(16): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559811 | ||||||
| chr9:97559813 | A | C | 52 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0036 others(49): Show |
52 | HG00280.hp1 HG00544.hp2 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.398-2919A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559813 | |||||||
| chr9:97559815 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.398-2917A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559815 | |||||||
| chr9:97559815 | A | G | 1 | a0001c0001t0010g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.398-2917A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559815 | |||||||
| chr9:97559815 | ATATATAT others(3): Show |
A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0042 others(29): Show |
32 | HG01175.hp2 HG01255.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.398-2915_398-2906d others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559815 | ||||||
| chr9:97559817 | A | C | 21 | a0001c0001t0001g0036 a0001c0001t0001g0057 a0001c0001t0001g0067 others(18): Show |
21 | HG00280.hp1 HG00544.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.398-2915A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559817 | |||||||
| chr9:97559819 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.398-2913A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559819 | |||||||
| chr9:97559819 | ATATATG | A | 18 | a0001c0001t0001g0036 a0001c0001t0001g0057 a0001c0001t0001g0067 others(15): Show |
18 | HG00280.hp1 HG00544.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.398-2911_398-2906d others(8): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559819 | ||||||
| chr9:97559821 | A | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0292 a0001c0001t0001g0326 |
3 | NA18950.hp1 NA18967.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.398-2911A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559821 | |||||||
| chr9:97559821 | A | G | 6 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0005g0047 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-2911A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559821 | |||||||
| chr9:97559821 | ATATGTC | A | 16 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0077 others(13): Show |
16 | HG02135.hp2 HG02630.hp2 HG03041.hp1 others(13): Show |
intron_variant | MODIFIER | c.398-2907_398-2902d others(8): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559821 | ||||||
| chr9:97559821 | ATATGTCT others(3): Show |
A | 11 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0001t0001g0141 others(8): Show |
11 | HG01168.hp2 HG01243.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-2907_398-2898d others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559821 | ||||||
| chr9:97559821 | ATATGTCT others(7): Show |
A | 5 | a0001c0001t0001g0272 a0001c0001t0002g0025 a0001c0001t0002g0070 others(2): Show |
5 | HG00609.hp1 HG01884.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-2907_398-2894d others(16): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559821 | ||||||
| chr9:97559821 | ATATGTCT others(11): Show |
A | 1 | a0001c0001t0002g0088 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.398-2907_398-2890d others(20): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559821 | ||||||
| chr9:97559821 | ATATGTCT others(15): Show |
A | 1 | a0001c0001t0003g0204 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.398-2907_398-2886d others(24): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559821 | ||||||
| chr9:97559821 | ATATGTCT others(19): Show |
A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0035 others(11): Show |
14 | HG01256.hp2 HG02109.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-2907_398-2882d others(28): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559821 | ||||||
| chr9:97559823 | A | C | 7 | a0001c0001t0001g0266 a0001c0001t0002g0246 a0001c0001t0002g0273 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2909A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559823 | |||||||
| chr9:97559823 | ATG | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0064 a0001c0001t0001g0068 others(7): Show |
10 | HG01099.hp1 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.398-2907_398-2906d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559823 | ||||||
| chr9:97559823 | ATGTC | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0081 others(20): Show |
23 | HG00544.hp1 HG00733.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.398-2907_398-2904d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559823 | ||||||
| chr9:97559823 | ATGTCTAT others(1): Show |
A | 27 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0027 others(24): Show |
27 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.398-2907_398-2900d others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559823 | ||||||
| chr9:97559823 | ATGTCTAT others(5): Show |
A | 15 | a0001c0001t0001g0030 a0001c0001t0001g0084 a0001c0001t0001g0163 others(12): Show |
15 | HG00597.hp1 HG01106.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.398-2907_398-2896d others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559823 | ||||||
| chr9:97559823 | ATGTCTAT others(9): Show |
A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0029 others(20): Show |
23 | HG00323.hp2 HG00673.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.398-2907_398-2892d others(18): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559823 | ||||||
| chr9:97559823 | ATGTCTAT others(13): Show |
A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0087 others(4): Show |
7 | HG00438.hp2 HG01081.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2907_398-2888d others(22): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559823 | ||||||
| chr9:97559823 | ATGTCTAT others(17): Show |
A | 6 | a0001c0001t0001g0147 a0001c0001t0001g0200 a0001c0001t0001g0312 others(3): Show |
6 | HG01884.hp2 HG01952.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-2907_398-2884d others(26): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559823 | ||||||
| chr9:97559825 | G | A | 20 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0135 others(17): Show |
20 | HG00140.hp1 HG00597.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.398-2907G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559825 | |||||||
| chr9:97559825 | G | GTCTA | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0181 others(7): Show |
10 | HG02896.hp1 HG02965.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.398-2883_398-2880d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97559825 | ||||||
| chr9:97559827 | C | A | 20 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0064 others(17): Show |
20 | HG00140.hp1 HG00597.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.398-2905C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559827 | |||||||
| chr9:97559831 | C | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0028 others(56): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.398-2901C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559831 | |||||||
| chr9:97559835 | C | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0022 others(93): Show |
96 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.398-2897C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559835 | |||||||
| chr9:97559839 | C | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0022 others(95): Show |
98 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.398-2893C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559839 | |||||||
| chr9:97559843 | C | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(69): Show |
72 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.398-2889C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559843 | |||||||
| chr9:97559847 | C | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(68): Show |
71 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.398-2885C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559847 | |||||||
| chr9:97559849 | A | C | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.398-2883A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559849 | |||||||
| chr9:97559866 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.398-2866T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559866 | |||||||
| chr9:97559886 | A | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0124 |
3 | HG01167.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.398-2846A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559886 | |||||||
| chr9:97559920 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.398-2812G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97559920 | |||||||
| chr9:97560067 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.398-2665T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560067 | |||||||
| chr9:97560142 | TA | T | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(167): Show |
170 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.398-2584delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97560142 | ||||||
| chr9:97560143 | A | T | 3 | a0001c0001t0002g0239 a0001c0001t0005g0271 a0001c0001t0005g0275 |
3 | HG02109.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.398-2589A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560143 | |||||||
| chr9:97560152 | C | T | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(167): Show |
170 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.398-2580C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560152 | |||||||
| chr9:97560291 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.398-2441A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560291 | |||||||
| chr9:97560353 | G | A | 84 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(81): Show |
84 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.398-2379G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560353 | |||||||
| chr9:97560418 | A | T | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(167): Show |
170 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.398-2314A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560418 | |||||||
| chr9:97560491 | A | T | 2 | a0001c0001t0006g0276 a0001c0001t0008g0327 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.398-2241A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560491 | |||||||
| chr9:97560494 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
252 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.398-2238C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560494 | |||||||
| chr9:97560521 | C | T | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(50): Show |
53 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.398-2211C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560521 | |||||||
| chr9:97560531 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0158 others(4): Show |
7 | HG00423.hp1 HG00597.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2201C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560531 | |||||||
| chr9:97560609 | T | C | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(167): Show |
170 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.398-2123T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560609 | |||||||
| chr9:97560669 | G | GTA | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(148): Show |
151 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.398-2048_398-2047d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97560669 | ||||||
| chr9:97560669 | G | GTATA | 18 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0015 others(15): Show |
18 | HG00609.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.398-2050_398-2047d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 97560669 | ||||||
| chr9:97560678 | T | C | 1 | a0001c0001t0001g0319 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.398-2054T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560678 | |||||||
| chr9:97560874 | T | A | 1 | a0001c0004t0001g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.398-1858T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97560874 | |||||||
| chr9:97561064 | G | T | 1 | a0001c0001t0004g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.398-1668G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561064 | |||||||
| chr9:97561088 | C | A | 1 | a0001c0001t0002g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.398-1644C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561088 | |||||||
| chr9:97561138 | A | C | 2 | a0001c0001t0003g0110 a0001c0001t0003g0111 |
2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.398-1594A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561138 | |||||||
| chr9:97561173 | C | T | 12 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.398-1559C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561173 | |||||||
| chr9:97561183 | A | G | 329 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(326): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.398-1549A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561183 | |||||||
| chr9:97561370 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.398-1362A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561370 | |||||||
| chr9:97561552 | G | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0064 others(8): Show |
11 | HG00423.hp1 HG00597.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.398-1180G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561552 | |||||||
| chr9:97561586 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0181 others(5): Show |
8 | HG01891.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.398-1146G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561586 | |||||||
| chr9:97561804 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(31): Show |
34 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.398-928C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561804 | |||||||
| chr9:97561907 | A | T | 20 | a0001c0001t0001g0267 a0001c0001t0002g0025 a0001c0001t0002g0065 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.398-825A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97561907 | |||||||
| chr9:97562199 | A | T | 79 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(76): Show |
79 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.398-533A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97562199 | |||||||
| chr9:97562262 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.398-470C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97562262 | |||||||
| chr9:97562278 | T | C | 81 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(78): Show |
81 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.398-454T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97562278 | |||||||
| chr9:97562372 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
178 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.398-360G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97562372 | |||||||
| chr9:97562482 | G | A | 7 | a0001c0001t0001g0084 a0001c0001t0001g0094 a0001c0001t0001g0129 others(4): Show |
7 | HG01106.hp1 HG01496.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-250G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97562482 | |||||||
| chr9:97562529 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.398-203G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97562529 | |||||||
| chr9:97562611 | T | A | 68 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(65): Show |
68 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.398-121T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97562611 | |||||||
| chr9:97562714 | C | T | 1 | a0001c0001t0005g0307 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.398-18C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 4/9 | chr9 | 97562714 | |||||||
| chr9:97563167 | C | T | 3 | a0001c0001t0001g0162 a0001c0001t0001g0227 a0001c0001t0001g0289 |
3 | NA18945.hp2 NA18983.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.487+346C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563167 | |||||||
| chr9:97563211 | G | A | 3 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0277 |
3 | HG02280.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.487+390G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563211 | |||||||
| chr9:97563258 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0007g0145 |
2 | HG01071.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.487+437G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563258 | |||||||
| chr9:97563636 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(32): Show |
35 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.488-402A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563636 | |||||||
| chr9:97563783 | C | G | 1 | a0001c0001t0006g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.488-255C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563783 | |||||||
| chr9:97563818 | C | G | 2 | a0001c0001t0001g0017 a0001c0001t0017g0251 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.488-220C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563818 | |||||||
| chr9:97563874 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0017g0251 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.488-164C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563874 | |||||||
| chr9:97563898 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.488-140C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563898 | |||||||
| chr9:97563921 | A | G | 1 | a0001c0001t0007g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.488-117A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563921 | |||||||
| chr9:97563935 | C | G | 66 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(63): Show |
66 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.488-103C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 5/9 | chr9 | 97563935 | |||||||
| chr9:97564542 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.618+374C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97564542 | |||||||
| chr9:97564543 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.618+375G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97564543 | |||||||
| chr9:97564583 | G | T | 1 | a0001c0001t0001g0026 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.618+415G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97564583 | |||||||
| chr9:97564859 | G | T | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.618+691G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97564859 | |||||||
| chr9:97564944 | G | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(63): Show |
66 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.618+776G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97564944 | |||||||
| chr9:97564950 | C | T | 97 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(94): Show |
97 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.618+782C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97564950 | |||||||
| chr9:97565035 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0087 others(24): Show |
27 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.619-813C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565035 | |||||||
| chr9:97565080 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.619-768G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565080 | |||||||
| chr9:97565316 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(78): Show |
81 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.619-532C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565316 | |||||||
| chr9:97565322 | A | G | 72 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(69): Show |
72 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.619-526A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565322 | |||||||
| chr9:97565368 | G | A | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.619-480G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565368 | |||||||
| chr9:97565432 | G | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(63): Show |
66 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.619-416G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565432 | |||||||
| chr9:97565481 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.619-367C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565481 | |||||||
| chr9:97565497 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.619-351A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565497 | |||||||
| chr9:97565622 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0189 |
2 | NA18965.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.619-226G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565622 | |||||||
| chr9:97565816 | G | A | 1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.619-32G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 6/9 | chr9 | 97565816 | |||||||
| chr9:97565986 | G | T | 4 | a0001c0001t0001g0272 a0001c0001t0002g0088 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+31G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97565986 | |||||||
| chr9:97566033 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0268 a0001c0001t0001g0298 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+78G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566033 | |||||||
| chr9:97566059 | T | C | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.726+104T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566059 | |||||||
| chr9:97566123 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.726+168C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566123 | |||||||
| chr9:97566138 | C | T | 9 | a0001c0001t0001g0136 a0001c0001t0006g0013 a0001c0001t0006g0090 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.726+183C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566138 | |||||||
| chr9:97566280 | G | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.726+325G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566280 | |||||||
| chr9:97566294 | C | T | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.726+339C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566294 | |||||||
| chr9:97566315 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.726+360C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566315 | |||||||
| chr9:97566474 | C | T | 1 | a0001c0001t0018g0083 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.726+519C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566474 | |||||||
| chr9:97566486 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.726+531C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566486 | |||||||
| chr9:97566526 | C | A | 68 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(65): Show |
68 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.726+571C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566526 | |||||||
| chr9:97566588 | T | C | 85 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(82): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.726+633T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566588 | |||||||
| chr9:97566624 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.726+669T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566624 | |||||||
| chr9:97566639 | C | G | 5 | a0001c0001t0002g0186 a0001c0001t0002g0239 a0001c0001t0002g0301 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+684C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566639 | |||||||
| chr9:97566649 | C | T | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.726+694C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566649 | |||||||
| chr9:97566657 | C | T | 95 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.726+702C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566657 | |||||||
| chr9:97566699 | T | A | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.726+744T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566699 | |||||||
| chr9:97566714 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.726+759G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566714 | |||||||
| chr9:97566739 | G | A | 71 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.726+784G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97566739 | |||||||
| chr9:97566844 | TATTGAG | T | 95 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.726+891_726+896del others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 97566844 | ||||||
| chr9:97567100 | A | T | 72 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(69): Show |
72 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.726+1145A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567100 | |||||||
| chr9:97567335 | G | A | 2 | a0001c0003t0012g0104 a0001c0003t0012g0170 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.726+1380G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567335 | |||||||
| chr9:97567339 | A | G | 12 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(9): Show |
12 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.726+1384A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567339 | |||||||
| chr9:97567437 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.727-1457C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567437 | |||||||
| chr9:97567456 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.727-1438C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567456 | |||||||
| chr9:97567464 | C | T | 68 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(65): Show |
68 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.727-1430C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567464 | |||||||
| chr9:97567572 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.727-1322G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567572 | |||||||
| chr9:97567722 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
213 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.727-1172G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567722 | |||||||
| chr9:97567756 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.727-1138G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567756 | |||||||
| chr9:97567789 | C | T | 4 | a0001c0001t0002g0239 a0001c0001t0002g0301 a0001c0001t0005g0271 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-1105C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567789 | |||||||
| chr9:97567818 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.727-1076G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567818 | |||||||
| chr9:97567837 | T | A | 68 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(65): Show |
68 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.727-1057T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567837 | |||||||
| chr9:97567858 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.727-1036G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567858 | |||||||
| chr9:97567900 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0017g0251 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.727-994G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567900 | |||||||
| chr9:97567907 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.727-987C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567907 | |||||||
| chr9:97567922 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.727-972A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97567922 | |||||||
| chr9:97568020 | CT | C | 15 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0051 others(12): Show |
15 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.727-873delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97568020 | |||||||
| chr9:97568411 | A | G | 5 | a0001c0001t0002g0186 a0001c0001t0002g0239 a0001c0001t0002g0301 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-483A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97568411 | |||||||
| chr9:97568456 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0087 others(24): Show |
27 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.727-438C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97568456 | |||||||
| chr9:97568534 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0218 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.727-360G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97568534 | |||||||
| chr9:97568606 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.727-288C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 7/9 | chr9 | 97568606 | |||||||
| chr9:97569229 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0087 others(24): Show |
27 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.870+192C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97569229 | |||||||
| chr9:97569252 | G | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | NA18949.hp1 NA18955.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+215G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97569252 | |||||||
| chr9:97569334 | C | T | 1 | a0001c0001t0007g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.870+297C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97569334 | |||||||
| chr9:97569456 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(45): Show |
48 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.870+419C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97569456 | |||||||
| chr9:97569488 | G | A | 97 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.870+451G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97569488 | |||||||
| chr9:97569619 | C | G | 1 | a0001c0001t0003g0107 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.870+582C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97569619 | |||||||
| chr9:97569641 | A | G | 12 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(9): Show |
12 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+604A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97569641 | |||||||
| chr9:97569795 | AAAGAT | A | 12 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(9): Show |
12 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+762_870+766del others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97569795 | ||||||
| chr9:97569918 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.870+881T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97569918 | |||||||
| chr9:97570094 | A | G | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.870+1057A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570094 | |||||||
| chr9:97570158 | G | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.870+1121G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570158 | |||||||
| chr9:97570187 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0311 |
2 | HG01993.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.870+1150G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570187 | |||||||
| chr9:97570381 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.870+1344C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570381 | |||||||
| chr9:97570638 | G | T | 9 | a0001c0001t0001g0136 a0001c0001t0006g0013 a0001c0001t0006g0090 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+1601G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570638 | |||||||
| chr9:97570651 | C | T | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.870+1614C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570651 | |||||||
| chr9:97570722 | C | T | 85 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(82): Show |
85 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.870+1685C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570722 | |||||||
| chr9:97570736 | C | G | 4 | a0001c0001t0001g0272 a0001c0001t0002g0088 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+1699C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570736 | |||||||
| chr9:97570755 | T | C | 1 | a0001c0001t0007g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.870+1718T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570755 | |||||||
| chr9:97570790 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0286 a0001c0001t0001g0288 others(1): Show |
4 | HG02135.hp1 NA18983.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+1753G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570790 | |||||||
| chr9:97570823 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.870+1786T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97570823 | |||||||
| chr9:97571024 | C | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0129 |
2 | HG01515.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.870+1987C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571024 | |||||||
| chr9:97571102 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0218 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.870+2065G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571102 | |||||||
| chr9:97571356 | C | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(111): Show |
114 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.870+2319C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571356 | |||||||
| chr9:97571389 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(87): Show |
90 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.870+2352C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571389 | |||||||
| chr9:97571490 | T | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(45): Show |
48 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.870+2453T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571490 | |||||||
| chr9:97571614 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0087 others(13): Show |
16 | HG01891.hp2 HG01952.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.870+2577C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571614 | |||||||
| chr9:97571629 | C | T | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.870+2592C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571629 | |||||||
| chr9:97571648 | A | G | 15 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(12): Show |
15 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.870+2611A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571648 | |||||||
| chr9:97571856 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.870+2819C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571856 | |||||||
| chr9:97571877 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
169 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.870+2840C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97571877 | |||||||
| chr9:97572037 | G | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(45): Show |
48 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.870+3000G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97572037 | |||||||
| chr9:97572304 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
168 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.870+3267G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97572304 | |||||||
| chr9:97572465 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0087 others(4): Show |
7 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.870+3428C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97572465 | |||||||
| chr9:97572585 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
144 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.870+3548A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97572585 | |||||||
| chr9:97573007 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.870+3970G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573007 | |||||||
| chr9:97573117 | A | G | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.870+4080A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573117 | |||||||
| chr9:97573138 | G | C | 1 | a0001c0005t0001g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.870+4101G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573138 | |||||||
| chr9:97573203 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.870+4166C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573203 | |||||||
| chr9:97573247 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.870+4210C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573247 | |||||||
| chr9:97573287 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.870+4250C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573287 | |||||||
| chr9:97573371 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
166 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.870+4334A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573371 | |||||||
| chr9:97573611 | G | C | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870+4574G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573611 | |||||||
| chr9:97573744 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.870+4707C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573744 | |||||||
| chr9:97573834 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.870+4797G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97573834 | |||||||
| chr9:97574078 | C | G | 2 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
2 | NA18966.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.870+5041C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574078 | |||||||
| chr9:97574078 | C | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(41): Show |
44 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.870+5041C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574078 | |||||||
| chr9:97574167 | T | A | 1 | a0001c0001t0005g0307 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870+5130T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574167 | |||||||
| chr9:97574202 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.870+5165T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574202 | |||||||
| chr9:97574260 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.870+5223C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574260 | |||||||
| chr9:97574414 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | NA18966.hp1 NA18967.hp2 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.870+5377G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574414 | |||||||
| chr9:97574500 | C | G | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.870+5463C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574500 | |||||||
| chr9:97574545 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.870+5508G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574545 | |||||||
| chr9:97574565 | G | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
175 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.870+5528G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574565 | |||||||
| chr9:97574666 | T | A | 68 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
68 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.870+5629T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574666 | |||||||
| chr9:97574683 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.870+5646T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574683 | |||||||
| chr9:97574698 | T | C | 15 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(12): Show |
15 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.870+5661T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574698 | |||||||
| chr9:97574938 | C | T | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.870+5901C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97574938 | |||||||
| chr9:97575029 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
151 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.870+5992G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575029 | |||||||
| chr9:97575046 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.870+6009C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575046 | |||||||
| chr9:97575065 | C | T | 2 | a0001c0001t0005g0271 a0001c0001t0005g0275 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.870+6028C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575065 | |||||||
| chr9:97575070 | T | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0185 |
2 | NA18947.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.870+6033T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575070 | |||||||
| chr9:97575192 | C | G | 71 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.870+6155C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575192 | |||||||
| chr9:97575272 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(41): Show |
44 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.870+6235G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575272 | |||||||
| chr9:97575273 | C | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(41): Show |
44 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.870+6236C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575273 | |||||||
| chr9:97575295 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0124 others(1): Show |
4 | HG01167.hp1 HG01168.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+6258G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575295 | |||||||
| chr9:97575335 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.870+6298C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575335 | |||||||
| chr9:97575406 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.870+6369G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575406 | |||||||
| chr9:97575671 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
199 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.870+6634T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575671 | |||||||
| chr9:97575902 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.870+6865C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575902 | |||||||
| chr9:97575941 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
5 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+6904C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575941 | |||||||
| chr9:97575996 | C | T | 6 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(3): Show |
6 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+6959C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97575996 | |||||||
| chr9:97576150 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
67 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.870+7113G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576150 | |||||||
| chr9:97576263 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.870+7226A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576263 | |||||||
| chr9:97576443 | G | A | 1 | a0001c0001t0007g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.870+7406G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576443 | |||||||
| chr9:97576550 | C | T | 6 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(3): Show |
6 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+7513C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576550 | |||||||
| chr9:97576629 | CT | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.870+7606delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97576629 | ||||||
| chr9:97576629 | CTT | C | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.870+7605_870+7606d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97576629 | ||||||
| chr9:97576644 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.870+7607C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576644 | |||||||
| chr9:97576645 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.870+7608T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576645 | |||||||
| chr9:97576702 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.870+7665C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576702 | |||||||
| chr9:97576795 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.870+7758A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576795 | |||||||
| chr9:97576882 | G | A | 3 | a0001c0001t0010g0003 a0001c0001t0010g0300 a0001c0001t0010g0306 |
3 | HG03225.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.870+7845G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576882 | |||||||
| chr9:97576890 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
197 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.870+7853C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576890 | |||||||
| chr9:97576918 | C | T | 23 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(20): Show |
23 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.870+7881C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576918 | |||||||
| chr9:97576927 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0259 |
2 | HG01433.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.870+7890T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576927 | |||||||
| chr9:97576956 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
69 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.870+7919C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576956 | |||||||
| chr9:97576966 | T | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.870+7929T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576966 | |||||||
| chr9:97576984 | G | A | 1 | a0001c0001t0005g0330 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.870+7947G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97576984 | |||||||
| chr9:97577096 | G | A | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.870+8059G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577096 | |||||||
| chr9:97577143 | C | CCAGAGAC others(46): Show |
4 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+8109_870+8161d others(55): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97577143 | ||||||
| chr9:97577246 | C | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(7): Show |
10 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.870+8209C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577246 | |||||||
| chr9:97577264 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870+8227G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577264 | |||||||
| chr9:97577283 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.870+8246T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577283 | |||||||
| chr9:97577305 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.870+8268G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577305 | |||||||
| chr9:97577307 | G | C | 4 | a0001c0001t0001g0074 a0001c0001t0010g0003 a0001c0001t0010g0300 others(1): Show |
4 | HG01081.hp1 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+8270G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577307 | |||||||
| chr9:97577665 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870+8628G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577665 | |||||||
| chr9:97577725 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.870+8688C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577725 | |||||||
| chr9:97577831 | G | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0001g0236 |
3 | HG00323.hp1 HG01175.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.870+8794G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577831 | |||||||
| chr9:97577843 | T | C | 4 | a0001c0001t0002g0025 a0001c0001t0002g0080 a0001c0001t0002g0202 others(1): Show |
4 | NA18970.hp2 NA18975.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+8806T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577843 | |||||||
| chr9:97577948 | G | A | 4 | a0001c0001t0001g0074 a0001c0001t0010g0003 a0001c0001t0010g0300 others(1): Show |
4 | HG01081.hp1 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+8911G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577948 | |||||||
| chr9:97577957 | C | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(7): Show |
10 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.870+8920C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97577957 | |||||||
| chr9:97578060 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.870+9023A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578060 | |||||||
| chr9:97578129 | C | T | 12 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.870+9092C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578129 | |||||||
| chr9:97578203 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(63): Show |
66 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.870+9166G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578203 | |||||||
| chr9:97578295 | C | T | 4 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+9258C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578295 | |||||||
| chr9:97578299 | C | T | 1 | a0001c0001t0005g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.870+9262C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578299 | |||||||
| chr9:97578310 | C | G | 1 | a0001c0001t0001g0227 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.870+9273C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578310 | |||||||
| chr9:97578321 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0154 a0001c0001t0001g0174 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.870+9284G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578321 | |||||||
| chr9:97578756 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
185 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.870+9719T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578756 | |||||||
| chr9:97578860 | C | T | 5 | a0001c0001t0006g0013 a0001c0001t0006g0090 a0001c0001t0006g0179 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+9823C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578860 | |||||||
| chr9:97578927 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
68 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.870+9890C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578927 | |||||||
| chr9:97578952 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.870+9915C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97578952 | |||||||
| chr9:97579085 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870+10048G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97579085 | |||||||
| chr9:97579254 | C | G | 8 | a0001c0001t0006g0013 a0001c0001t0006g0090 a0001c0001t0006g0179 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+10217C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97579254 | |||||||
| chr9:97579291 | A | G | 4 | a0001c0001t0001g0074 a0001c0001t0010g0003 a0001c0001t0010g0300 others(1): Show |
4 | HG01081.hp1 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+10254A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97579291 | |||||||
| chr9:97579417 | C | T | 2 | a0001c0001t0004g0171 a0001c0001t0004g0206 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.870+10380C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97579417 | |||||||
| chr9:97579470 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.870+10433C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97579470 | |||||||
| chr9:97579578 | G | T | 67 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(64): Show |
67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.870+10541G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97579578 | |||||||
| chr9:97580153 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
146 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.870+11116C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580153 | |||||||
| chr9:97580174 | T | C | 4 | a0001c0001t0002g0239 a0001c0001t0002g0301 a0001c0001t0005g0271 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-11117T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580174 | |||||||
| chr9:97580503 | G | A | 1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.871-10788G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580503 | |||||||
| chr9:97580554 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.871-10737C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580554 | |||||||
| chr9:97580657 | G | A | 1 | a0001c0001t0010g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.871-10634G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580657 | |||||||
| chr9:97580670 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.871-10621C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580670 | |||||||
| chr9:97580727 | G | C | 77 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(74): Show |
77 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.871-10564G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580727 | |||||||
| chr9:97580857 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.871-10434A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580857 | |||||||
| chr9:97580915 | C | T | 2 | a0001c0001t0013g0123 a0001c0001t0013g0125 |
2 | HG01361.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.871-10376C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580915 | |||||||
| chr9:97580930 | C | A | 77 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(74): Show |
77 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.871-10361C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580930 | |||||||
| chr9:97580943 | CT | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
187 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.871-10337delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97580943 | ||||||
| chr9:97580961 | G | A | 28 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(25): Show |
28 | HG00438.hp2 HG00673.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.871-10330G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97580961 | |||||||
| chr9:97580971 | T | TTTTTATT others(3): Show |
282 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(279): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.871-10311_871-1030 others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97580971 | ||||||
| chr9:97581105 | T | C | 35 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0095 others(32): Show |
35 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.871-10186T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581105 | |||||||
| chr9:97581138 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.871-10153G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581138 | |||||||
| chr9:97581150 | C | G | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-10141C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581150 | |||||||
| chr9:97581179 | G | A | 29 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(26): Show |
29 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.871-10112G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581179 | |||||||
| chr9:97581241 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-10050G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581241 | |||||||
| chr9:97581263 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.871-10028C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581263 | |||||||
| chr9:97581329 | AT | A | 5 | a0001c0001t0006g0013 a0001c0001t0006g0090 a0001c0001t0006g0179 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-9956delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97581329 | ||||||
| chr9:97581410 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.871-9881T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581410 | |||||||
| chr9:97581428 | G | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
187 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.871-9863G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581428 | |||||||
| chr9:97581443 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.871-9848C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581443 | |||||||
| chr9:97581464 | G | T | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.871-9827G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581464 | |||||||
| chr9:97581522 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-9769G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581522 | |||||||
| chr9:97581680 | C | T | 29 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(26): Show |
29 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.871-9611C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581680 | |||||||
| chr9:97581684 | A | G | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-9607A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581684 | |||||||
| chr9:97581685 | G | T | 26 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(23): Show |
26 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.871-9606G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581685 | |||||||
| chr9:97581846 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.871-9445G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581846 | |||||||
| chr9:97581846 | GT | G | 29 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(26): Show |
29 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.871-9437delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97581846 | ||||||
| chr9:97581909 | T | C | 4 | a0001c0001t0001g0272 a0001c0001t0002g0088 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-9382T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581909 | |||||||
| chr9:97581937 | T | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-9354T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97581937 | |||||||
| chr9:97582139 | C | A | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0095 others(8): Show |
11 | HG00323.hp1 HG01081.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.871-9152C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582139 | |||||||
| chr9:97582140 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0052 others(4): Show |
7 | HG00544.hp1 NA18612.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-9151G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582140 | |||||||
| chr9:97582216 | A | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG01256.hp1 HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.871-9075A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582216 | |||||||
| chr9:97582256 | A | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | NA18949.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.871-9035A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582256 | |||||||
| chr9:97582319 | G | A | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-8972G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582319 | |||||||
| chr9:97582408 | T | C | 1 | a0001c0001t0001g0320 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.871-8883T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582408 | |||||||
| chr9:97582477 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.871-8814A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582477 | |||||||
| chr9:97582543 | A | G | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0095 others(8): Show |
11 | HG00323.hp1 HG01081.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.871-8748A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582543 | |||||||
| chr9:97582555 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0087 others(9): Show |
12 | HG01891.hp2 HG01952.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.871-8736T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582555 | |||||||
| chr9:97582559 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-8732G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582559 | |||||||
| chr9:97582608 | G | A | 4 | a0001c0001t0002g0239 a0001c0001t0002g0301 a0001c0001t0005g0271 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-8683G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582608 | |||||||
| chr9:97582924 | A | T | 29 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(26): Show |
29 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.871-8367A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582924 | |||||||
| chr9:97582938 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-8353G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97582938 | |||||||
| chr9:97583034 | T | G | 7 | a0001c0001t0006g0013 a0001c0001t0006g0090 a0001c0001t0006g0179 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-8257T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583034 | |||||||
| chr9:97583045 | C | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
76 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.871-8246C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583045 | |||||||
| chr9:97583049 | T | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-8242T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583049 | |||||||
| chr9:97583133 | G | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0001g0236 others(1): Show |
4 | HG00323.hp1 HG01175.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-8158G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583133 | |||||||
| chr9:97583137 | T | C | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0095 others(8): Show |
11 | HG00323.hp1 HG01081.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.871-8154T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583137 | |||||||
| chr9:97583289 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.871-8002A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583289 | |||||||
| chr9:97583395 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.871-7896C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583395 | |||||||
| chr9:97583396 | G | A | 25 | a0001c0001t0001g0067 a0001c0001t0002g0025 a0001c0001t0002g0065 others(22): Show |
25 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.871-7895G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583396 | |||||||
| chr9:97583397 | T | G | 5 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0001g0315 others(2): Show |
5 | HG01255.hp2 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-7894T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583397 | |||||||
| chr9:97583526 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.871-7765A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583526 | |||||||
| chr9:97583548 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(156): Show |
159 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.871-7743A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583548 | |||||||
| chr9:97583652 | G | A | 14 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0049 others(11): Show |
14 | HG01123.hp1 HG01167.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-7639G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583652 | |||||||
| chr9:97583653 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.871-7638C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583653 | |||||||
| chr9:97583678 | C | A | 23 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(20): Show |
23 | HG00323.hp1 HG01081.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.871-7613C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583678 | |||||||
| chr9:97583679 | T | G | 14 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0049 others(11): Show |
14 | HG01123.hp1 HG01167.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-7612T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583679 | |||||||
| chr9:97583706 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.871-7585A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583706 | |||||||
| chr9:97583730 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.871-7561G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583730 | |||||||
| chr9:97583737 | T | C | 43 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(40): Show |
43 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.871-7554T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583737 | |||||||
| chr9:97583745 | C | G | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.871-7546C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583745 | |||||||
| chr9:97583752 | T | G | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.871-7539T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583752 | |||||||
| chr9:97583787 | G | A | 5 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-7504G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583787 | |||||||
| chr9:97583838 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.871-7453G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97583838 | |||||||
| chr9:97584018 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.871-7273C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97584018 | |||||||
| chr9:97584095 | G | A | 7 | a0001c0001t0006g0013 a0001c0001t0006g0090 a0001c0001t0006g0179 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-7196G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97584095 | |||||||
| chr9:97584176 | C | T | 38 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(35): Show |
38 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-7115C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97584176 | |||||||
| chr9:97584518 | C | T | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.871-6773C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97584518 | |||||||
| chr9:97584664 | G | T | 68 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
68 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.871-6627G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97584664 | |||||||
| chr9:97584673 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.871-6618A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97584673 | |||||||
| chr9:97584778 | G | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0187 |
3 | HG00621.hp2 NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.871-6513G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97584778 | |||||||
| chr9:97584905 | A | C | 39 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(36): Show |
39 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.871-6386A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97584905 | |||||||
| chr9:97585024 | T | C | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.871-6267T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585024 | |||||||
| chr9:97585033 | T | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.871-6258T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585033 | |||||||
| chr9:97585046 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.871-6245G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585046 | |||||||
| chr9:97585065 | T | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
72 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.871-6226T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585065 | |||||||
| chr9:97585107 | C | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0259 |
2 | HG01433.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.871-6184C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585107 | |||||||
| chr9:97585134 | G | A | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-6157G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585134 | |||||||
| chr9:97585214 | T | G | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.871-6077T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585214 | |||||||
| chr9:97585215 | C | G | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.871-6076C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585215 | |||||||
| chr9:97585351 | G | A | 10 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0051 others(7): Show |
10 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.871-5940G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585351 | |||||||
| chr9:97585365 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.871-5926G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585365 | |||||||
| chr9:97585625 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(51): Show |
54 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.871-5666A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585625 | |||||||
| chr9:97585650 | C | T | 1 | a0001c0001t0010g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.871-5641C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585650 | |||||||
| chr9:97585672 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
187 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.871-5619G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585672 | |||||||
| chr9:97585715 | T | C | 34 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(31): Show |
34 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.871-5576T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585715 | |||||||
| chr9:97585737 | T | C | 40 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(37): Show |
40 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.871-5554T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585737 | |||||||
| chr9:97585922 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
199 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.871-5369A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585922 | |||||||
| chr9:97585946 | C | T | 39 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(36): Show |
39 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.871-5345C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585946 | |||||||
| chr9:97585959 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.871-5332C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97585959 | |||||||
| chr9:97586005 | C | G | 7 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0008g0014 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-5286C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586005 | |||||||
| chr9:97586015 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-5276A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586015 | |||||||
| chr9:97586018 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-5273C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586018 | |||||||
| chr9:97586055 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0205 |
2 | HG00438.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.871-5236C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586055 | |||||||
| chr9:97586160 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0002g0025 |
2 | HG02280.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.871-5131C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586160 | |||||||
| chr9:97586379 | C | T | 75 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(72): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.871-4912C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586379 | |||||||
| chr9:97586380 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.871-4911G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586380 | |||||||
| chr9:97586509 | T | G | 1 | a0001c0006t0006g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.871-4782T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586509 | |||||||
| chr9:97586524 | G | A | 6 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(3): Show |
6 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-4767G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586524 | |||||||
| chr9:97586691 | G | A | 6 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(3): Show |
6 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-4600G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586691 | |||||||
| chr9:97586729 | C | G | 1 | a0001c0001t0001g0311 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.871-4562C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586729 | |||||||
| chr9:97586746 | CG | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-4542delG | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97586746 | ||||||
| chr9:97586753 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.871-4538G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586753 | |||||||
| chr9:97586776 | C | G | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-4515C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586776 | |||||||
| chr9:97586835 | G | A | 38 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(35): Show |
38 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-4456G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586835 | |||||||
| chr9:97586960 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0185 |
2 | NA18947.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.871-4331C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586960 | |||||||
| chr9:97586961 | G | T | 38 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(35): Show |
38 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-4330G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586961 | |||||||
| chr9:97586970 | G | A | 1 | a0001c0001t0004g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.871-4321G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586970 | |||||||
| chr9:97586972 | T | C | 39 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(36): Show |
39 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.871-4319T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586972 | |||||||
| chr9:97586979 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.871-4312G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97586979 | |||||||
| chr9:97587032 | A | C | 38 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(35): Show |
38 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-4259A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587032 | |||||||
| chr9:97587097 | T | C | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-4194T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587097 | |||||||
| chr9:97587099 | A | T | 1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.871-4192A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587099 | |||||||
| chr9:97587471 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0314 |
2 | HG00438.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.871-3820C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587471 | |||||||
| chr9:97587489 | G | C | 75 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(72): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.871-3802G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587489 | |||||||
| chr9:97587511 | G | A | 1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.871-3780G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587511 | |||||||
| chr9:97587567 | G | GT | 15 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(12): Show |
15 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.871-3714dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97587567 | ||||||
| chr9:97587567 | G | GTT | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-3715_871-3714d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97587567 | ||||||
| chr9:97587567 | G | T | 1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.871-3724G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587567 | |||||||
| chr9:97587567 | GT | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(40): Show |
43 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.871-3714delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97587567 | ||||||
| chr9:97587567 | GTTTT | G | 75 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(72): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.871-3717_871-3714d others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97587567 | ||||||
| chr9:97587680 | C | T | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-3611C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587680 | |||||||
| chr9:97587717 | A | C | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.871-3574A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97587717 | |||||||
| chr9:97588091 | T | C | 5 | a0001c0001t0001g0091 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG00733.hp2 HG01168.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-3200T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97588091 | |||||||
| chr9:97588350 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.871-2941A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97588350 | |||||||
| chr9:97588364 | A | G | 9 | a0001c0001t0001g0315 a0001c0001t0008g0014 a0001c0001t0008g0254 others(6): Show |
9 | HG01255.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-2927A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97588364 | |||||||
| chr9:97588538 | G | A | 12 | a0001c0001t0004g0002 a0001c0001t0004g0012 a0001c0001t0004g0016 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.871-2753G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97588538 | |||||||
| chr9:97588565 | G | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.871-2726G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97588565 | |||||||
| chr9:97588989 | C | T | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.871-2302C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97588989 | |||||||
| chr9:97589117 | C | CA | 7 | a0001c0001t0001g0059 a0001c0001t0001g0114 a0001c0001t0001g0261 others(4): Show |
7 | HG01981.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-2156dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97589117 | ||||||
| chr9:97589117 | CA | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0075 others(23): Show |
26 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.871-2156delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97589117 | ||||||
| chr9:97589133 | A | AG | 4 | a0001c0001t0001g0079 a0001c0001t0001g0108 a0001c0001t0001g0158 others(1): Show |
4 | HG00597.hp2 HG01978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2158_871-2157i others(3): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589133 | |||||||
| chr9:97589133 | A | G | 67 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(64): Show |
67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.871-2158A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589133 | |||||||
| chr9:97589279 | A | AT | 8 | a0001c0001t0001g0114 a0001c0001t0001g0175 a0001c0001t0001g0292 others(5): Show |
8 | HG01109.hp2 HG01175.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.871-1992dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97589279 | ||||||
| chr9:97589279 | AT | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(162): Show |
165 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.871-1992delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97589279 | ||||||
| chr9:97589316 | C | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0248 |
2 | HG02135.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.871-1975C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589316 | |||||||
| chr9:97589344 | G | A | 10 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0060 others(7): Show |
10 | HG02071.hp2 HG02165.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.871-1947G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589344 | |||||||
| chr9:97589344 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0260 |
2 | NA18968.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.871-1947G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589344 | |||||||
| chr9:97589397 | G | C | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871-1894G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589397 | |||||||
| chr9:97589420 | C | T | 7 | a0001c0001t0006g0013 a0001c0001t0006g0090 a0001c0001t0006g0179 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-1871C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589420 | |||||||
| chr9:97589428 | C | T | 8 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(5): Show |
8 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-1863C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589428 | |||||||
| chr9:97589446 | AT | A | 9 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-1831delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97589446 | ||||||
| chr9:97589500 | G | C | 8 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(5): Show |
8 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-1791G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589500 | |||||||
| chr9:97589575 | G | A | 30 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(27): Show |
30 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.871-1716G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589575 | |||||||
| chr9:97589613 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.871-1678A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589613 | |||||||
| chr9:97589793 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.871-1498A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589793 | |||||||
| chr9:97589842 | C | T | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.871-1449C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97589842 | |||||||
| chr9:97590003 | T | C | 6 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(3): Show |
6 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-1288T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590003 | |||||||
| chr9:97590155 | C | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0325 |
3 | HG00408.hp1 NA18612.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.871-1136C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590155 | |||||||
| chr9:97590459 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.871-832C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590459 | |||||||
| chr9:97590471 | C | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | NA18977.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.871-820C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590471 | |||||||
| chr9:97590492 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0156 |
2 | HG00323.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.871-799C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590492 | |||||||
| chr9:97590545 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.871-746T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590545 | |||||||
| chr9:97590558 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.871-733A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590558 | |||||||
| chr9:97590621 | G | GT | 14 | a0001c0001t0001g0074 a0001c0001t0001g0311 a0001c0001t0004g0002 others(11): Show |
14 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-659dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97590621 | ||||||
| chr9:97590622 | T | G | 79 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(76): Show |
79 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.871-669T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590622 | |||||||
| chr9:97590623 | T | G | 1 | a0001c0006t0006g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.871-668T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590623 | |||||||
| chr9:97590692 | C | T | 8 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(5): Show |
8 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-599C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590692 | |||||||
| chr9:97590889 | A | G | 51 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(48): Show |
51 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.871-402A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97590889 | |||||||
| chr9:97591168 | G | C | 7 | a0001c0001t0006g0013 a0001c0001t0006g0090 a0001c0001t0006g0179 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-123G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | chr9 | 97591168 | |||||||
| chr9:97591183 | TC | T | 8 | a0001c0001t0008g0014 a0001c0001t0008g0254 a0001c0001t0008g0257 others(5): Show |
8 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-104delC | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 97591183 | ||||||
| chr9:97591519 | G | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
70 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.1015+84G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97591519 | |||||||
| chr9:97591588 | T | C | 3 | a0001c0001t0010g0003 a0001c0001t0010g0300 a0001c0001t0010g0306 |
3 | HG03225.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1015+153T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97591588 | |||||||
| chr9:97591631 | G | C | 2 | a0001c0003t0012g0104 a0001c0003t0012g0170 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1015+196G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97591631 | |||||||
| chr9:97591741 | G | A | 2 | a0001c0001t0003g0049 a0001c0001t0003g0063 |
2 | NA18968.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1015+306G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97591741 | |||||||
| chr9:97591743 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1015+308C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97591743 | |||||||
| chr9:97591782 | C | T | 31 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(28): Show |
31 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1015+347C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97591782 | |||||||
| chr9:97591989 | AATT | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(47): Show |
50 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1015+560_1015+562d others(5): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97591989 | ||||||
| chr9:97592016 | A | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
180 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1015+581A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592016 | |||||||
| chr9:97592070 | T | TA | 180 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
180 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1015+637dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97592070 | ||||||
| chr9:97592074 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
180 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1015+639G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592074 | |||||||
| chr9:97592093 | T | G | 7 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0156 others(4): Show |
7 | HG00323.hp1 HG01081.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1015+658T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592093 | |||||||
| chr9:97592097 | C | T | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1015+662C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592097 | |||||||
| chr9:97592234 | T | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1015+799T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592234 | |||||||
| chr9:97592406 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1015+971A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592406 | |||||||
| chr9:97592429 | GA | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
179 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.1015+1006delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97592429 | ||||||
| chr9:97592650 | C | G | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1015+1215C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592650 | |||||||
| chr9:97592876 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1015+1441G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592876 | |||||||
| chr9:97592917 | T | G | 3 | a0001c0001t0010g0003 a0001c0001t0010g0300 a0001c0001t0010g0306 |
3 | HG03225.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1015+1482T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97592917 | |||||||
| chr9:97593023 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1015+1588G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593023 | |||||||
| chr9:97593056 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015+1621C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593056 | |||||||
| chr9:97593062 | C | T | 1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1015+1627C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593062 | |||||||
| chr9:97593063 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1015+1628G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593063 | |||||||
| chr9:97593200 | G | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0197 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1015+1765G>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593200 | |||||||
| chr9:97593328 | C | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0087 others(24): Show |
27 | HG01891.hp1 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.1015+1893C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593328 | |||||||
| chr9:97593337 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1015+1902A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593337 | |||||||
| chr9:97593528 | C | T | 2 | a0001c0003t0012g0104 a0001c0003t0012g0170 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1015+2093C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593528 | |||||||
| chr9:97593531 | C | T | 23 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0073 others(20): Show |
23 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1015+2096C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593531 | |||||||
| chr9:97593626 | A | T | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1015+2191A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593626 | |||||||
| chr9:97593636 | G | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(103): Show |
106 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1015+2201G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593636 | |||||||
| chr9:97593740 | G | A | 4 | a0001c0001t0001g0272 a0001c0001t0002g0088 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015+2305G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593740 | |||||||
| chr9:97593854 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0234 |
2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1015+2419A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593854 | |||||||
| chr9:97593871 | T | C | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1015+2436T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593871 | |||||||
| chr9:97593897 | A | G | 1 | a0001c0001t0005g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1015+2462A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593897 | |||||||
| chr9:97593899 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015+2464C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97593899 | |||||||
| chr9:97594036 | G | A | 62 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(59): Show |
62 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1015+2601G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594036 | |||||||
| chr9:97594189 | T | C | 24 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(21): Show |
24 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1015+2754T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594189 | |||||||
| chr9:97594377 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
115 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1015+2942A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594377 | |||||||
| chr9:97594459 | C | T | 97 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(94): Show |
97 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1015+3024C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594459 | |||||||
| chr9:97594460 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0210 |
2 | HG02071.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1015+3025G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594460 | |||||||
| chr9:97594502 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1015+3067T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594502 | |||||||
| chr9:97594531 | C | T | 1 | a0001c0005t0001g0168 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1015+3096C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594531 | |||||||
| chr9:97594557 | G | C | 69 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(66): Show |
69 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1015+3122G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594557 | |||||||
| chr9:97594688 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1015+3253C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594688 | |||||||
| chr9:97594860 | CT | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(274): Show |
277 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.1015+3427delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97594860 | ||||||
| chr9:97594873 | A | C | 29 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(26): Show |
29 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.1015+3438A>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594873 | |||||||
| chr9:97594877 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1015+3442C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594877 | |||||||
| chr9:97594973 | C | T | 1 | a0001c0001t0002g0025 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1015+3538C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594973 | |||||||
| chr9:97594974 | A | G | 99 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(96): Show |
99 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1015+3539A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97594974 | |||||||
| chr9:97595037 | C | T | 1 | a0001c0001t0004g0171 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1015+3602C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595037 | |||||||
| chr9:97595155 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1015+3720T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595155 | |||||||
| chr9:97595177 | AAAATT | A | 3 | a0001c0001t0001g0148 a0001c0001t0002g0246 a0001c0001t0002g0273 |
3 | HG02451.hp1 HG02523.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1015+3750_1015+375 others(9): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97595177 | ||||||
| chr9:97595234 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1015+3799C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595234 | |||||||
| chr9:97595376 | C | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(59): Show |
62 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1015+3941C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595376 | |||||||
| chr9:97595533 | C | CT | 65 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1016-4081dupT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97595533 | ||||||
| chr9:97595533 | C | CTT | 44 | a0001c0001t0001g0294 a0001c0001t0002g0015 a0001c0001t0002g0025 others(41): Show |
44 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.1016-4082_1016-408 others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97595533 | ||||||
| chr9:97595533 | CT | C | 10 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0075 others(7): Show |
10 | HG00323.hp1 HG01496.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1016-4081delT | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97595533 | ||||||
| chr9:97595577 | C | T | 100 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(97): Show |
100 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1016-4057C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595577 | |||||||
| chr9:97595838 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0301 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1016-3796C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595838 | |||||||
| chr9:97595848 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0326 |
2 | NA19086.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1016-3786G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595848 | |||||||
| chr9:97595935 | A | G | 1 | a0001c0001t0007g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1016-3699A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595935 | |||||||
| chr9:97595977 | G | C | 1 | a0001c0001t0001g0293 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1016-3657G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97595977 | |||||||
| chr9:97596233 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
118 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1016-3401T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596233 | |||||||
| chr9:97596235 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1016-3399T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596235 | |||||||
| chr9:97596268 | CA | C | 27 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0070 others(24): Show |
27 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1016-3365delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596268 | |||||||
| chr9:97596273 | C | T | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1016-3361C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596273 | |||||||
| chr9:97596323 | A | G | 1 | a0001c0001t0018g0083 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1016-3311A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596323 | |||||||
| chr9:97596578 | C | T | 58 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0046 others(55): Show |
58 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.1016-3056C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596578 | |||||||
| chr9:97596719 | C | A | 74 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0046 others(71): Show |
74 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.1016-2915C>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596719 | |||||||
| chr9:97596791 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
51 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1016-2843C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596791 | |||||||
| chr9:97596917 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1016-2717A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97596917 | |||||||
| chr9:97597065 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1016-2569T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597065 | |||||||
| chr9:97597210 | AAGTAAAG | A | 5 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG01099.hp1 HG01123.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-2422_1016-241 others(11): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597210 | ||||||
| chr9:97597445 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0154 a0001c0001t0001g0174 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016-2189T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597445 | |||||||
| chr9:97597445 | T | G | 73 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0046 others(70): Show |
73 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.1016-2189T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597445 | |||||||
| chr9:97597461 | A | G | 73 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0046 others(70): Show |
73 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.1016-2173A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597461 | |||||||
| chr9:97597465 | G | A | 1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1016-2169G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597465 | |||||||
| chr9:97597514 | T | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1016-2120T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597514 | |||||||
| chr9:97597525 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1016-2109T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597525 | |||||||
| chr9:97597539 | A | G | 73 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0046 others(70): Show |
73 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.1016-2095A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597539 | |||||||
| chr9:97597566 | T | C | 74 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0046 others(71): Show |
74 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.1016-2068T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597566 | |||||||
| chr9:97597696 | C | CA | 36 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(33): Show |
36 | HG00280.hp2 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1016-1920dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597696 | ||||||
| chr9:97597696 | C | CAAAAA | 16 | a0001c0001t0002g0015 a0001c0001t0002g0046 a0001c0001t0002g0088 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1016-1924_1016-192 others(9): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597696 | ||||||
| chr9:97597696 | C | CAAAAAA | 52 | a0001c0001t0001g0075 a0001c0001t0001g0156 a0001c0001t0001g0157 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1016-1925_1016-192 others(10): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597696 | ||||||
| chr9:97597696 | C | CAAAAAAA | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1016-1926_1016-192 others(11): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597696 | ||||||
| chr9:97597696 | C | CAAAAAAA others(1): Show |
71 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0020 others(68): Show |
71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1016-1927_1016-192 others(12): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597696 | ||||||
| chr9:97597696 | C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0120 others(9): Show |
12 | HG00621.hp2 HG00733.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1016-1928_1016-192 others(13): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597696 | ||||||
| chr9:97597696 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0079 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1016-1929_1016-192 others(14): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597696 | ||||||
| chr9:97597806 | C | G | 1 | a0001c0001t0005g0331 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1016-1828C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597806 | |||||||
| chr9:97597886 | C | T | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1016-1748C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597886 | |||||||
| chr9:97597959 | GATATGGA others(21): Show |
G | 1 | a0001c0001t0001g0317 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1016-1673_1016-164 others(32): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97597959 | ||||||
| chr9:97597988 | A | G | 1 | a0001c0001t0001g0317 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1016-1646A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597988 | |||||||
| chr9:97597991 | T | G | 1 | a0001c0001t0001g0317 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1016-1643T>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597991 | |||||||
| chr9:97597993 | T | A | 1 | a0001c0001t0001g0317 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1016-1641T>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597993 | |||||||
| chr9:97597994 | A | T | 1 | a0001c0001t0001g0317 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1016-1640A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97597994 | |||||||
| chr9:97598157 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1016-1477C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598157 | |||||||
| chr9:97598215 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1016-1419G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598215 | |||||||
| chr9:97598261 | G | A | 73 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0046 others(70): Show |
73 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.1016-1373G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598261 | |||||||
| chr9:97598327 | C | CA | 28 | a0001c0001t0001g0105 a0001c0001t0001g0198 a0001c0001t0001g0212 others(25): Show |
28 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1016-1285dupA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97598327 | ||||||
| chr9:97598327 | C | CAA | 11 | a0001c0001t0002g0015 a0001c0001t0004g0016 a0001c0001t0005g0100 others(8): Show |
11 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1016-1286_1016-128 others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97598327 | ||||||
| chr9:97598327 | C | CAAAAA | 23 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0073 others(20): Show |
23 | HG00597.hp1 HG00609.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1016-1289_1016-128 others(9): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97598327 | ||||||
| chr9:97598327 | CA | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1016-1285delA | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97598327 | ||||||
| chr9:97598327 | CAA | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0001g0133 others(3): Show |
6 | HG01070.hp1 HG01070.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016-1286_1016-128 others(6): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97598327 | ||||||
| chr9:97598458 | C | T | 1 | a0001c0001t0008g0327 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1016-1176C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598458 | |||||||
| chr9:97598463 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1016-1171G>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598463 | |||||||
| chr9:97598554 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1016-1080C>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598554 | |||||||
| chr9:97598564 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1016-1070G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598564 | |||||||
| chr9:97598744 | C | T | 2 | a0001c0003t0012g0104 a0001c0003t0012g0170 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1016-890C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598744 | |||||||
| chr9:97598768 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1016-866G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598768 | |||||||
| chr9:97598805 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0198 |
2 | HG00423.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1016-829C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97598805 | |||||||
| chr9:97599013 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0245 |
2 | HG00597.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1016-621T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97599013 | |||||||
| chr9:97599132 | G | A | 1 | a0001c0001t0008g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1016-502G>A | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97599132 | |||||||
| chr9:97599180 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1016-454A>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97599180 | |||||||
| chr9:97599187 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0135 |
2 | HG00733.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1016-447C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97599187 | |||||||
| chr9:97599196 | ACT | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0075 a0001c0001t0001g0095 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.1016-434_1016-433d others(4): Show |
TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 97599196 | ||||||
| chr9:97599294 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1016-340T>C | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97599294 | |||||||
| chr9:97599451 | A | G | 1 | a0001c0001t0017g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1016-183A>G | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97599451 | |||||||
| chr9:97599582 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
216 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.1016-52C>T | TMOD1 | ENSG00000136842.14 | transcript | ENST00000259365.9 | protein_coding | 9/9 | chr9 | 97599582 |