Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7140 |
| ensemblid | ENSG00000130595.20 |
| hgncid | 11950 |
| symbol | TNNT3 |
| name | troponin T3, fast skeletal type |
| refseq_nuc | NM_006757.4 |
| refseq_prot | NP_006748.1 |
| ensembl_nuc | ENST00000278317.11 |
| ensembl_prot | ENSP00000278317.6 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 1919703 |
| end | 1938702 |
| strand | + |
| ver | v1.2 |
| region | chr11:1919703-1938702 |
| region5000 | chr11:1914703-1943702 |
| regionname0 | TNNT3_chr11_1919703_1938702 |
| regionname5000 | TNNT3_chr11_1914703_1943702 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 258 | 120 | 36 | 24 | 32 | 8 | 19 | 8 | TNNT3_chr11_1914703_1943702 | TNNT3 | MSDEE others(253): Show |
chr11 | 1914703 | 1943702 |
| a0002 | 0/0 | 257 | 5 | 2 | 0 | 0 | 0 | 3 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | MSDEE others(252): Show |
chr11 | 1914703 | 1943702 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 774 | 97 | 33 | 18 | 20 | 8 | 17 | TNNT3_chr11_1914703_1943702 | TNNT3 | ATGTC others(769): Show |
chr11 | 1914703 | 1943702 | ||
| a0001c0002 | 0/0 | 774 | 21 | 1 | 6 | 12 | 0 | 2 | TNNT3_chr11_1914703_1943702 | TNNT3 | ATGTC others(769): Show |
chr11 | 1914703 | 1943702 | ||
| a0001c0004 | 0/0 | 774 | 2 | 2 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | ATGTC others(769): Show |
chr11 | 1914703 | 1943702 | ||
| a0002c0003 | 0/0 | 771 | 5 | 2 | 0 | 0 | 0 | 3 | TNNT3_chr11_1914703_1943702 | TNNT3 | ATGTC others(766): Show |
chr11 | 1914703 | 1943702 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1065 | 96 | 33 | 17 | 20 | 8 | 17 | TNNT3_chr11_1914703_1943702 | TNNT3 | AGTGC others(1060): Show |
chr11 | 1914703 | 1943702 |
| a0001c0001t0002 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | AGTGC others(1060): Show |
chr11 | 1914703 | 1943702 |
| a0001c0002t0001 | 0/0 | 1065 | 21 | 1 | 6 | 12 | 0 | 2 | TNNT3_chr11_1914703_1943702 | TNNT3 | AGTGC others(1060): Show |
chr11 | 1914703 | 1943702 |
| a0001c0004t0001 | 0/0 | 1065 | 2 | 2 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | AGTGC others(1060): Show |
chr11 | 1914703 | 1943702 |
| a0002c0003t0001 | 0/0 | 1062 | 5 | 2 | 0 | 0 | 0 | 3 | TNNT3_chr11_1914703_1943702 | TNNT3 | AGTGC others(1057): Show |
chr11 | 1914703 | 1943702 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 1 | 1 | 1 | 3 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0002 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0003 | 1/0 | 5 | 3 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0007 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0002c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | CHS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PEL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | ACB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0088 | AFR | ACB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PEL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02602 | hp1 | a0002 | c0003 | t0001 | g0038 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0087 | AFR | MSL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0027 | AFR | MSL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03688 | hp1 | a0002 | c0003 | t0001 | g0020 | SAS | STU | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | STU | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0039 | SAS | GIH | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | USA | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | LWK | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | TNNT3_chr11_1914703_1943702 | TNNT3 | chr11 | 1914703 | 1943702 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1934874 | T | C | 2 | a0001c0004 a0002c0003 |
7 | HG02258.hp2 HG02602.hp1 HG03098.hp1 others(4): Show |
synonymous_variant | LOW | c.636T>C | p.Ile212Ile | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/16 | 714/1065 | 636/777 | 212/258 | chr11 | 1934874 | |||
| chr11:1938477 | C | T | 1 | a0001c0002 | 21 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(18): Show |
synonymous_variant | LOW | c.762C>T | p.Gly254Gly | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 16/16 | 840/1065 | 762/777 | 254/258 | chr11 | 1938477 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1938528 | C | T | 1 | a0001c0001t0002 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 16/16 | 36 | chr11 | 1938528 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1919803 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02056.hp2 HG03942.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+41C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1919803 | |||||||
| chr11:1919854 | G | C | 1 | a0001c0002t0001g0016 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-19+92G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1919854 | |||||||
| chr11:1919901 | G | T | 3 | a0001c0001t0001g0086 a0001c0004t0001g0087 a0001c0004t0001g0088 |
3 | HG02258.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-19+139G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1919901 | |||||||
| chr11:1920005 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-19+243A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920005 | |||||||
| chr11:1920165 | C | T | 2 | a0001c0001t0001g0008 a0001c0002t0001g0084 |
4 | HG01361.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+403C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920165 | |||||||
| chr11:1920235 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-19+473C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920235 | |||||||
| chr11:1920251 | T | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(16): Show |
23 | HG00597.hp1 HG00597.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-19+489T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920251 | |||||||
| chr11:1920313 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-19+551G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920313 | |||||||
| chr11:1920315 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-19+553G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920315 | |||||||
| chr11:1920379 | T | C | 3 | a0001c0001t0001g0086 a0001c0004t0001g0087 a0001c0004t0001g0088 |
3 | HG02258.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-19+617T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920379 | |||||||
| chr11:1920498 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-19+736G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920498 | |||||||
| chr11:1920518 | C | G | 2 | a0001c0002t0001g0079 a0001c0002t0001g0080 |
2 | HG00621.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-19+756C>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920518 | |||||||
| chr11:1920628 | A | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
26 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19+866A>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920628 | |||||||
| chr11:1920628 | A | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(39): Show |
54 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-19+866A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920628 | |||||||
| chr11:1920637 | C | T | 5 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
5 | HG01993.hp1 HG02056.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+875C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920637 | |||||||
| chr11:1920716 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
60 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-19+954T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920716 | |||||||
| chr11:1920766 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0032 others(3): Show |
9 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+1004G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920766 | |||||||
| chr11:1920774 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-19+1012C>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920774 | |||||||
| chr11:1920883 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19+1121T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920883 | |||||||
| chr11:1920905 | T | C | 3 | a0001c0001t0001g0086 a0001c0004t0001g0087 a0001c0004t0001g0088 |
3 | HG02258.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-19+1143T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920905 | |||||||
| chr11:1920922 | G | A | 1 | a0002c0003t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19+1160G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920922 | |||||||
| chr11:1920940 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-19+1178T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920940 | |||||||
| chr11:1920941 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-19+1179G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920941 | |||||||
| chr11:1920978 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-19+1216C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1920978 | |||||||
| chr11:1921112 | G | A | 3 | a0001c0001t0001g0086 a0001c0004t0001g0087 a0001c0004t0001g0088 |
3 | HG02258.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-19+1350G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921112 | |||||||
| chr11:1921284 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+1522C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921284 | |||||||
| chr11:1921312 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0043 others(3): Show |
13 | HG00099.hp1 HG00642.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-1545C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921312 | |||||||
| chr11:1921345 | C | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(44): Show |
66 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.-18-1512C>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921345 | |||||||
| chr11:1921411 | A | C | 1 | a0001c0002t0001g0073 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-18-1446A>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921411 | |||||||
| chr11:1921454 | A | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0043 others(3): Show |
13 | HG00099.hp1 HG00642.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-1403A>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921454 | |||||||
| chr11:1921456 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0031 others(8): Show |
18 | HG00099.hp1 HG00642.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18-1401C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921456 | |||||||
| chr11:1921743 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0043 others(13): Show |
23 | HG00099.hp1 HG00642.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18-1114C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921743 | |||||||
| chr11:1921890 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-18-967G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921890 | |||||||
| chr11:1921911 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18-946C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921911 | |||||||
| chr11:1921977 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18-880A>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921977 | |||||||
| chr11:1921984 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(58): Show |
82 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-18-873C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1921984 | |||||||
| chr11:1922028 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-829C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922028 | |||||||
| chr11:1922052 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18-805G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922052 | |||||||
| chr11:1922104 | C | CG | 3 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0002c0003t0001g0038 |
7 | HG00642.hp2 HG01346.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-746dupG | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr11 | 1922104 | ||||||
| chr11:1922107 | G | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-18-750G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922107 | |||||||
| chr11:1922319 | G | T | 1 | a0001c0002t0001g0071 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-18-538G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922319 | |||||||
| chr11:1922363 | G | C | 1 | a0001c0002t0001g0084 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-18-494G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922363 | |||||||
| chr11:1922375 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(68): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-18-482G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922375 | |||||||
| chr11:1922478 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-18-379C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922478 | |||||||
| chr11:1922639 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0021 |
3 | HG01070.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-18-218C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922639 | |||||||
| chr11:1922651 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-18-206C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922651 | |||||||
| chr11:1922730 | C | A | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-127C>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | chr11 | 1922730 | |||||||
| chr11:1922820 | C | CCT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0043 others(2): Show |
9 | HG00642.hp2 HG01346.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-18_-18-17dupCT | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr11 | 1922820 | ||||||
| chr11:1922972 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(69): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.18-76A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 2/15 | chr11 | 1922972 | |||||||
| chr11:1923151 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.31+90C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 3/15 | chr11 | 1923151 | |||||||
| chr11:1923406 | A | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(74): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.32-149A>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 3/15 | chr11 | 1923406 | |||||||
| chr11:1923430 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32-125C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 3/15 | chr11 | 1923430 | |||||||
| chr11:1923476 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32-79A>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 3/15 | chr11 | 1923476 | |||||||
| chr11:1923505 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32-50C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 3/15 | chr11 | 1923505 | |||||||
| chr11:1923529 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.32-26C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 3/15 | chr11 | 1923529 | |||||||
| chr11:1923707 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02080.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.49+135T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1923707 | |||||||
| chr11:1923844 | C | G | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.49+272C>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1923844 | |||||||
| chr11:1923923 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0075 a0001c0004t0001g0087 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+351A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1923923 | |||||||
| chr11:1923926 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+354G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1923926 | |||||||
| chr11:1923926 | GCCCTGCG others(41): Show |
G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0075 a0001c0004t0001g0087 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+359_49+406delGC others(46): Show |
TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr11 | 1923926 | ||||||
| chr11:1923930 | T | C | 1 | a0002c0003t0001g0027 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+358T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1923930 | |||||||
| chr11:1923944 | T | C | 5 | a0001c0001t0001g0005 a0002c0003t0001g0020 a0002c0003t0001g0037 others(2): Show |
5 | HG02602.hp1 HG03688.hp1 NA20905.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+372T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1923944 | |||||||
| chr11:1924031 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.49+459T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924031 | |||||||
| chr11:1924062 | A | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+490A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924062 | |||||||
| chr11:1924088 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0036 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.49+516A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924088 | |||||||
| chr11:1924160 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0075 a0001c0004t0001g0087 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+588C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924160 | |||||||
| chr11:1924226 | A | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(67): Show |
89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.49+654A>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924226 | |||||||
| chr11:1924342 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.50-757G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924342 | |||||||
| chr11:1924577 | G | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
5 | HG01993.hp1 HG02056.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-522G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924577 | |||||||
| chr11:1924589 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.50-510C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924589 | |||||||
| chr11:1924654 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(39): Show |
54 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.50-445G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924654 | |||||||
| chr11:1924862 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(14): Show |
24 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.50-237C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924862 | |||||||
| chr11:1924967 | C | T | 1 | a0002c0003t0001g0020 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.50-132C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924967 | |||||||
| chr11:1924989 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0085 |
2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.50-110C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1924989 | |||||||
| chr11:1925014 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-85G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 4/15 | chr11 | 1925014 | |||||||
| chr11:1925300 | T | G | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.67+184T>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1925300 | |||||||
| chr11:1925641 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+525C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1925641 | |||||||
| chr11:1926195 | C | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
56 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.68-500C>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926195 | |||||||
| chr11:1926291 | T | C | 1 | a0001c0002t0001g0054 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.68-404T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926291 | |||||||
| chr11:1926309 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.68-386C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926309 | |||||||
| chr11:1926345 | C | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
59 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.68-350C>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926345 | |||||||
| chr11:1926348 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.68-347C>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926348 | |||||||
| chr11:1926348 | C | T | 5 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
5 | HG01993.hp1 HG02056.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-347C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926348 | |||||||
| chr11:1926448 | G | A | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.68-247G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926448 | |||||||
| chr11:1926559 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0032 others(13): Show |
19 | HG00280.hp1 HG01109.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-136G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926559 | |||||||
| chr11:1926563 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(41): Show |
60 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.68-132C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926563 | |||||||
| chr11:1926570 | C | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0032 others(4): Show |
10 | HG00280.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-125C>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926570 | |||||||
| chr11:1926613 | G | A | 1 | a0001c0002t0001g0071 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.68-82G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926613 | |||||||
| chr11:1926679 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68-16G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 5/15 | chr11 | 1926679 | |||||||
| chr11:1926823 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.82+114G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1926823 | |||||||
| chr11:1926890 | G | A | 1 | a0002c0003t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.82+181G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1926890 | |||||||
| chr11:1926956 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(25): Show |
37 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.82+247T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1926956 | |||||||
| chr11:1927095 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0032 others(4): Show |
10 | HG00280.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+386C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927095 | |||||||
| chr11:1927107 | C | G | 1 | a0002c0003t0001g0020 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.82+398C>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927107 | |||||||
| chr11:1927266 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.82+557C>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927266 | |||||||
| chr11:1927268 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.82+559C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927268 | |||||||
| chr11:1927426 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0004t0001g0087 others(1): Show |
4 | HG00642.hp1 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+717A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927426 | |||||||
| chr11:1927472 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(15): Show |
25 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.82+763C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927472 | |||||||
| chr11:1927475 | G | T | 1 | a0002c0003t0001g0020 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.82+766G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927475 | |||||||
| chr11:1927731 | T | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(26): Show |
37 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.82+1022T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927731 | |||||||
| chr11:1927809 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.82+1100C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927809 | |||||||
| chr11:1927844 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.82+1135C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927844 | |||||||
| chr11:1927912 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.82+1203C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927912 | |||||||
| chr11:1927954 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(26): Show |
37 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.83-1166G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927954 | |||||||
| chr11:1927957 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(14): Show |
22 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.83-1163C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1927957 | |||||||
| chr11:1928014 | G | T | 3 | a0001c0001t0001g0075 a0001c0004t0001g0087 a0001c0004t0001g0088 |
3 | HG02258.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.83-1106G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928014 | |||||||
| chr11:1928016 | A | C | 3 | a0001c0001t0001g0075 a0001c0004t0001g0087 a0001c0004t0001g0088 |
3 | HG02258.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.83-1104A>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928016 | |||||||
| chr11:1928020 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.83-1100G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928020 | |||||||
| chr11:1928070 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-1050T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928070 | |||||||
| chr11:1928070 | T | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(5): Show |
15 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.83-1050T>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928070 | |||||||
| chr11:1928240 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
52 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.83-880G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928240 | |||||||
| chr11:1928616 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(14): Show |
22 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.83-504A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928616 | |||||||
| chr11:1928807 | G | A | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.83-313G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928807 | |||||||
| chr11:1928832 | GCC | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.83-283_83-282delCC | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr11 | 1928832 | ||||||
| chr11:1928899 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.83-221C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1928899 | |||||||
| chr11:1928997 | AAG | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0068 |
3 | HG01258.hp1 HG01346.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.83-118_83-117delAG | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr11 | 1928997 | ||||||
| chr11:1929072 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(80): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.83-48A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1929072 | |||||||
| chr11:1929073 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83-47C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 6/15 | chr11 | 1929073 | |||||||
| chr11:1929306 | G | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0086 |
6 | HG00642.hp2 HG01346.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+163G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929306 | |||||||
| chr11:1929310 | G | T | 1 | a0001c0002t0001g0029 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.106+167G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929310 | |||||||
| chr11:1929352 | C | T | 1 | a0002c0003t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.106+209C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929352 | |||||||
| chr11:1929358 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.106+215A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929358 | |||||||
| chr11:1929361 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.106+218T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929361 | |||||||
| chr11:1929417 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(16): Show |
24 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.106+274G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929417 | |||||||
| chr11:1929427 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG01993.hp1 HG02056.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+284C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929427 | |||||||
| chr11:1929450 | G | C | 1 | a0002c0003t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.106+307G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929450 | |||||||
| chr11:1929454 | C | T | 1 | a0002c0003t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.106+311C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929454 | |||||||
| chr11:1929676 | T | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.107-134T>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929676 | |||||||
| chr11:1929693 | G | A | 22 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0031 others(19): Show |
28 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.107-117G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929693 | |||||||
| chr11:1929695 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(80): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.107-115T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 7/15 | chr11 | 1929695 | |||||||
| chr11:1929825 | CCAAGTGA others(52): Show |
C | 5 | a0002c0003t0001g0020 a0002c0003t0001g0027 a0002c0003t0001g0037 others(2): Show |
5 | HG02602.hp1 HG03486.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.125+26_125+84delGC others(57): Show |
TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 1929825 | ||||||
| chr11:1929878 | G | C | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125+50G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1929878 | |||||||
| chr11:1929884 | T | C | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125+56T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1929884 | |||||||
| chr11:1929884 | TCAAGTGA others(52): Show |
T | 1 | a0001c0001t0001g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.125+87_125+145delT others(58): Show |
TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 1929884 | ||||||
| chr11:1929980 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0075 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.125+152G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1929980 | |||||||
| chr11:1930265 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125+437C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1930265 | |||||||
| chr11:1930296 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(13): Show |
21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.125+468G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1930296 | |||||||
| chr11:1930335 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG01993.hp1 HG02056.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+507C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1930335 | |||||||
| chr11:1930730 | G | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0068 others(16): Show |
25 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.125+902G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1930730 | |||||||
| chr11:1930742 | G | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
5 | HG01993.hp1 HG02056.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+914G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1930742 | |||||||
| chr11:1930774 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(13): Show |
21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.125+946G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1930774 | |||||||
| chr11:1930859 | C | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0026 others(1): Show |
6 | HG00597.hp1 HG00673.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+1031C>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1930859 | |||||||
| chr11:1931163 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.126-1306A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1931163 | |||||||
| chr11:1931206 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.126-1263C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1931206 | |||||||
| chr11:1931342 | G | C | 1 | a0001c0002t0001g0029 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.126-1127G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1931342 | |||||||
| chr11:1931518 | CA | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG01993.hp1 HG02056.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-950delA | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1931518 | |||||||
| chr11:1931720 | G | GT | 13 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0030 others(10): Show |
14 | HG00597.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.126-733dupT | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 1931720 | ||||||
| chr11:1931720 | GT | G | 7 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0002c0003t0001g0020 others(4): Show |
7 | HG02602.hp1 HG02886.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.126-733delT | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 1931720 | ||||||
| chr11:1931721 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.126-748T>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1931721 | |||||||
| chr11:1931736 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.126-733T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1931736 | |||||||
| chr11:1932106 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.126-363C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1932106 | |||||||
| chr11:1932117 | A | C | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.126-352A>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1932117 | |||||||
| chr11:1932394 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126-75G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1932394 | |||||||
| chr11:1932432 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.126-37G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 8/15 | chr11 | 1932432 | |||||||
| chr11:1932843 | C | CCCAT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0040 others(6): Show |
13 | HG00642.hp2 HG01346.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.171+356_171+359dup others(4): Show |
TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 1932843 | ||||||
| chr11:1932843 | C | CCCATCCA others(1): Show |
70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.171+352_171+359dup others(8): Show |
TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 1932843 | ||||||
| chr11:1932843 | C | CCCATCCA others(5): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0085 a0001c0004t0001g0087 others(1): Show |
4 | HG02027.hp2 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+348_171+359dup others(12): Show |
TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 1932843 | ||||||
| chr11:1932955 | TAC | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(48): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.171+444_171+445del others(2): Show |
TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 1932955 | ||||||
| chr11:1933179 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.172-542C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 9/15 | chr11 | 1933179 | |||||||
| chr11:1933562 | A | C | 5 | a0002c0003t0001g0020 a0002c0003t0001g0027 a0002c0003t0001g0037 others(2): Show |
5 | HG02602.hp1 HG03486.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-159A>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 9/15 | chr11 | 1933562 | |||||||
| chr11:1933911 | A | T | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289-20A>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 10/15 | chr11 | 1933911 | |||||||
| chr11:1934147 | C | A | 7 | a0001c0004t0001g0087 a0001c0004t0001g0088 a0002c0003t0001g0020 others(4): Show |
7 | HG02258.hp2 HG02602.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.366+139C>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 11/15 | chr11 | 1934147 | |||||||
| chr11:1934174 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.367-158C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 11/15 | chr11 | 1934174 | |||||||
| chr11:1934316 | A | G | 7 | a0001c0004t0001g0087 a0001c0004t0001g0088 a0002c0003t0001g0020 others(4): Show |
7 | HG02258.hp2 HG02602.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.367-16A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 11/15 | chr11 | 1934316 | |||||||
| chr11:1934323 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.367-9T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 11/15 | chr11 | 1934323 | |||||||
| chr11:1934455 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.480+10G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 12/15 | chr11 | 1934455 | |||||||
| chr11:1934468 | C | T | 1 | a0001c0002t0001g0060 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.480+23C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 12/15 | chr11 | 1934468 | |||||||
| chr11:1934541 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.481-5T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 12/15 | chr11 | 1934541 | |||||||
| chr11:1934688 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.590+33C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 13/15 | chr11 | 1934688 | |||||||
| chr11:1934928 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.681+9C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1934928 | |||||||
| chr11:1934982 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.681+63T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1934982 | |||||||
| chr11:1935108 | G | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.681+189G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1935108 | |||||||
| chr11:1935112 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.681+193G>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1935112 | |||||||
| chr11:1935135 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.681+216G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1935135 | |||||||
| chr11:1935247 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.681+328C>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1935247 | |||||||
| chr11:1935549 | G | C | 7 | a0001c0004t0001g0087 a0001c0004t0001g0088 a0002c0003t0001g0020 others(4): Show |
7 | HG02258.hp2 HG02602.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.681+630G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1935549 | |||||||
| chr11:1935600 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 |
4 | HG01109.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+681C>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1935600 | |||||||
| chr11:1935712 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.681+793T>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1935712 | |||||||
| chr11:1935791 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(78): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.681+872A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1935791 | |||||||
| chr11:1936016 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
6 | HG00738.hp2 HG00741.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-947C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936016 | |||||||
| chr11:1936048 | T | C | 1 | a0002c0003t0001g0027 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.682-915T>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936048 | |||||||
| chr11:1936286 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.682-677C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936286 | |||||||
| chr11:1936388 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.682-575G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936388 | |||||||
| chr11:1936614 | C | T | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.682-349C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936614 | |||||||
| chr11:1936651 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(21): Show |
33 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.682-312G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936651 | |||||||
| chr11:1936785 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682-178A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936785 | |||||||
| chr11:1936786 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG01993.hp1 HG02056.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-177C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936786 | |||||||
| chr11:1936871 | C | T | 5 | a0002c0003t0001g0020 a0002c0003t0001g0027 a0002c0003t0001g0037 others(2): Show |
5 | HG02602.hp1 HG03486.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-92C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 14/15 | chr11 | 1936871 | |||||||
| chr11:1937172 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0075 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.722+169C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937172 | |||||||
| chr11:1937263 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.722+260C>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937263 | |||||||
| chr11:1937402 | G | C | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.722+399G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937402 | |||||||
| chr11:1937415 | G | A | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.722+412G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937415 | |||||||
| chr11:1937550 | C | T | 5 | a0002c0003t0001g0020 a0002c0003t0001g0027 a0002c0003t0001g0037 others(2): Show |
5 | HG02602.hp1 HG03486.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.722+547C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937550 | |||||||
| chr11:1937766 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(61): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.723-672C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937766 | |||||||
| chr11:1937780 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.723-658G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937780 | |||||||
| chr11:1937879 | C | T | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.723-559C>T | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937879 | |||||||
| chr11:1937985 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0086 others(7): Show |
14 | HG00642.hp2 HG01346.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.723-453A>G | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1937985 | |||||||
| chr11:1938012 | G | A | 2 | a0001c0004t0001g0087 a0001c0004t0001g0088 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.723-426G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1938012 | |||||||
| chr11:1938253 | G | C | 1 | a0001c0002t0001g0058 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.723-185G>C | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1938253 | |||||||
| chr11:1938298 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0034 |
2 | HG01515.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.723-140G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1938298 | |||||||
| chr11:1938376 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.723-62G>A | TNNT3 | ENSG00000130595.20 | transcript | ENST00000278317.11 | protein_coding | 15/15 | chr11 | 1938376 |