Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7004 |
| ensemblid | ENSG00000197905.10 |
| hgncid | 11717 |
| symbol | TEAD4 |
| name | TEA domain transcription factor 4 |
| refseq_nuc | NM_003213.4 |
| refseq_prot | NP_003204.2 |
| ensembl_nuc | ENST00000359864.8 |
| ensembl_prot | ENSP00000352926.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 2959397 |
| end | 3040676 |
| strand | + |
| ver | v1.2 |
| region | chr12:2959397-3040676 |
| region5000 | chr12:2954397-3045676 |
| regionname0 | TEAD4_chr12_2959397_3040676 |
| regionname5000 | TEAD4_chr12_2954397_3045676 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1302 | 264 | 89 | 61 | 70 | 11 | 31 | TEAD4_chr12_2954397_3045676 | TEAD4 | TTGGA others(1297): Show |
chr12 | 2954397 | 3045676 | ||
| a0001c0002 | 0/0 | 1302 | 6 | 0 | 5 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | TTGGA others(1297): Show |
chr12 | 2954397 | 3045676 | ||
| a0001c0003 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | TTGGA others(1297): Show |
chr12 | 2954397 | 3045676 | ||
| a0001c0004 | 0/0 | 1302 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | TTGGA others(1297): Show |
chr12 | 2954397 | 3045676 | ||
| a0001c0005 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | TTGGA others(1297): Show |
chr12 | 2954397 | 3045676 | ||
| a0001c0006 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | TTGGA others(1297): Show |
chr12 | 2954397 | 3045676 | ||
| a0001c0007 | 0/0 | 1302 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | TTGGA others(1297): Show |
chr12 | 2954397 | 3045676 | ||
| a0001c0008 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | TTGGA others(1297): Show |
chr12 | 2954397 | 3045676 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1710 | 257 | 87 | 59 | 68 | 11 | 30 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0001t0002 | 0/0 | 1710 | 3 | 0 | 2 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0001t0003 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0001t0004 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0001t0005 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0001t0006 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0002t0001 | 0/0 | 1710 | 6 | 0 | 5 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0003t0001 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0004t0002 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0005t0001 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0006t0001 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0007t0001 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| a0001c0008t0001 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | ATTCC others(1705): Show |
chr12 | 2954397 | 3045676 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0003t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0004t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0005t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0007t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| a0001c0008t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | GBR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02015 | hp2 | a0001 | c0008 | t0001 | g0036 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CDX | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CDX | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02300 | hp1 | a0001 | c0007 | t0001 | g0103 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0141 | SAS | BEB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG04228 | hp2 | a0001 | c0006 | t0001 | g0129 | SAS | STU | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19002 | hp1 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | LWK | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ASW | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ASW | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0151 | EUR | TSI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | GIH | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0067 | AMR | CLM | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | USA | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | USA | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0268 | REF | REF | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0162 | REF | REF | TEAD4_chr12_2954397_3045676 | TEAD4 | chr12 | 2954397 | 3045676 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3020705 | G | A | 1 | a0001 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.655G>A | p.Val219Met | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/13 | 862/1710 | 655/1305 | 219/434 | chr12 | 3020705 | |||
| chr12:3020766 | C | T | 1 | a0001 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.716C>T | p.Pro239Leu | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/13 | 923/1710 | 716/1305 | 239/434 | chr12 | 3020766 | |||
| chr12:3021922 | C | T | 1 | a0001 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.802C>T | p.Arg268Cys | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/13 | 1009/1710 | 802/1305 | 268/434 | chr12 | 3021922 | |||
| chr12:3038037 | C | T | 1 | a0001 | 6 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(3): Show |
missense_variant | MODERATE | c.967C>T | p.Pro323Ser | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/13 | 1174/1710 | 967/1305 | 323/434 | chr12 | 3038037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2994778 | G | C | 1 | a0001c0003 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.12G>C | p.Thr4Thr | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/13 | 219/1710 | 12/1305 | 4/434 | chr12 | 2994778 | |||
| chr12:2994871 | C | T | 1 | a0001c0008 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.105C>T | p.Ile35Ile | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/13 | 312/1710 | 105/1305 | 35/434 | chr12 | 2994871 | |||
| chr12:3038063 | C | T | 1 | a0001c0005 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.993C>T | p.Ser331Ser | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/13 | 1200/1710 | 993/1305 | 331/434 | chr12 | 3038063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2959412 | G | T | 1 | a0001c0001t0006 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-192G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/13 | 35355 | chr12 | 2959412 | ||||||
| chr12:2959428 | C | G | 1 | a0001c0001t0005 | 1 | HG03834.hp2 | 5_prime_UTR_variant | MODIFIER | c.-176C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/13 | 35339 | chr12 | 2959428 | ||||||
| chr12:2959437 | A | G | 2 | a0001c0001t0002 a0001c0004t0002 |
4 | HG00735.hp1 HG01123.hp2 HG01975.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-167A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/13 | 35330 | chr12 | 2959437 | ||||||
| chr12:2960020 | C | T | 1 | a0001c0001t0004 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/13 | 34747 | chr12 | 2960020 | ||||||
| chr12:3040613 | A | G | 1 | a0001c0001t0003 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*135A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 13/13 | 135 | chr12 | 3040613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2959595 | C | T | 6 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG01192.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-123+114C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/12 | chr12 | 2959595 | |||||||
| chr12:2959729 | C | T | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG03225.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-122-219C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/12 | chr12 | 2959729 | |||||||
| chr12:2959789 | GA | G | 16 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(13): Show |
16 | HG01346.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-122-155delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 2959789 | ||||||
| chr12:2959902 | C | G | 15 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0237 others(12): Show |
15 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122-46C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/12 | chr12 | 2959902 | |||||||
| chr12:2959924 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(4): Show |
7 | HG01106.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-122-24G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/12 | chr12 | 2959924 | |||||||
| chr12:2959937 | C | A | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-122-11C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 1/12 | chr12 | 2959937 | |||||||
| chr12:2960145 | C | T | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01952.hp2 HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-30+105C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960145 | |||||||
| chr12:2960170 | C | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-30+130C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960170 | |||||||
| chr12:2960193 | G | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-30+153G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960193 | |||||||
| chr12:2960254 | C | T | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG02559.hp2 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+214C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960254 | |||||||
| chr12:2960273 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(178): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-30+233G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960273 | |||||||
| chr12:2960281 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-30+241A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960281 | |||||||
| chr12:2960363 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+323C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960363 | |||||||
| chr12:2960817 | C | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG00735.hp2 HG01167.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+777C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960817 | |||||||
| chr12:2960820 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30+780C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960820 | |||||||
| chr12:2960828 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-30+788C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960828 | |||||||
| chr12:2960989 | C | G | 24 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0185 others(21): Show |
24 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.-30+949C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2960989 | |||||||
| chr12:2961076 | T | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
46 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.-30+1036T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961076 | |||||||
| chr12:2961087 | G | A | 16 | a0001c0001t0001g0178 a0001c0001t0001g0234 a0001c0001t0001g0235 others(13): Show |
16 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+1047G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961087 | |||||||
| chr12:2961179 | C | G | 16 | a0001c0001t0001g0178 a0001c0001t0001g0234 a0001c0001t0001g0235 others(13): Show |
16 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+1139C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961179 | |||||||
| chr12:2961182 | T | C | 16 | a0001c0001t0001g0178 a0001c0001t0001g0234 a0001c0001t0001g0235 others(13): Show |
16 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+1142T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961182 | |||||||
| chr12:2961259 | C | T | 31 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.-30+1219C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961259 | |||||||
| chr12:2961263 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-30+1223A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961263 | |||||||
| chr12:2961308 | C | A | 1 | a0001c0003t0001g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-30+1268C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961308 | |||||||
| chr12:2961414 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-30+1374G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961414 | |||||||
| chr12:2961566 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG00735.hp2 HG01167.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1526G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961566 | |||||||
| chr12:2961609 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-30+1569C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961609 | |||||||
| chr12:2961708 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0192 a0001c0001t0001g0193 others(50): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.-30+1668G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2961708 | |||||||
| chr12:2962113 | T | TTTTTA | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG03225.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-30+2092_-30+2096d others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962113 | ||||||
| chr12:2962166 | C | T | 8 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+2126C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962166 | |||||||
| chr12:2962301 | A | AATATAAA others(13): Show |
41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(38): Show |
41 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-30+2273_-30+2292d others(22): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962301 | ||||||
| chr12:2962305 | TAA | T | 14 | a0001c0001t0001g0234 a0001c0001t0001g0237 a0001c0001t0001g0238 others(11): Show |
14 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+2267_-30+2268d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962305 | ||||||
| chr12:2962315 | AATAT | A | 14 | a0001c0001t0001g0234 a0001c0001t0001g0237 a0001c0001t0001g0238 others(11): Show |
14 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+2283_-30+2286d others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962315 | ||||||
| chr12:2962321 | T | TATATATA others(53): Show |
1 | a0001c0001t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-30+2286_-30+2287i others(62): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962321 | ||||||
| chr12:2962327 | A | AATATATA others(7): Show |
116 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(113): Show |
117 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-30+2292_-30+2293i others(16): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962327 | ||||||
| chr12:2962327 | A | AATATATA others(15): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG00408.hp1 NA18979.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-30+2292_-30+2293i others(24): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962327 | ||||||
| chr12:2962327 | A | AATATATA others(17): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG00639.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-30+2292_-30+2293i others(26): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962327 | ||||||
| chr12:2962327 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-30+2287A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962327 | |||||||
| chr12:2962331 | T | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(3): Show |
6 | HG01106.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+2291T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962331 | |||||||
| chr12:2962331 | TAA | T | 22 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0181 others(19): Show |
22 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30+2293_-30+2294d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962331 | ||||||
| chr12:2962333 | A | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-30+2293A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962333 | |||||||
| chr12:2962339 | TA | T | 10 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(7): Show |
10 | HG01346.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+2300delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962339 | |||||||
| chr12:2962341 | TA | T | 4 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(1): Show |
4 | HG02257.hp2 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+2302delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962341 | |||||||
| chr12:2962342 | A | AT | 34 | a0001c0001t0001g0002 a0001c0001t0001g0193 a0001c0001t0001g0194 others(31): Show |
35 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.-30+2303dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962342 | ||||||
| chr12:2962342 | A | T | 11 | a0001c0001t0001g0206 a0001c0001t0001g0255 a0001c0001t0001g0256 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30+2302A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962342 | |||||||
| chr12:2962343 | TA | T | 8 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+2304delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962343 | |||||||
| chr12:2962344 | A | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0177 a0001c0001t0001g0180 others(67): Show |
71 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-30+2304A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962344 | |||||||
| chr12:2962346 | A | ATATATT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0058 others(105): Show |
109 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-30+2307_-30+2308i others(8): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962346 | ||||||
| chr12:2962346 | A | ATATTTT | 7 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(4): Show |
7 | HG00140.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+2307_-30+2308i others(8): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2962346 | ||||||
| chr12:2962346 | A | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-30+2306A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962346 | |||||||
| chr12:2962348 | T | A | 1 | a0001c0001t0001g0013 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-30+2308T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962348 | |||||||
| chr12:2962365 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(7): Show |
10 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30+2325C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962365 | |||||||
| chr12:2962390 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0192 a0001c0001t0001g0193 others(50): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.-30+2350C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962390 | |||||||
| chr12:2962398 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG00423.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-30+2358C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962398 | |||||||
| chr12:2962428 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG01891.hp1 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+2388C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962428 | |||||||
| chr12:2962463 | G | A | 7 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+2423G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962463 | |||||||
| chr12:2962491 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-30+2451G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962491 | |||||||
| chr12:2962500 | T | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(4): Show |
7 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+2460T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962500 | |||||||
| chr12:2962544 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0148 others(50): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.-30+2504A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962544 | |||||||
| chr12:2962800 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-30+2760C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962800 | |||||||
| chr12:2962917 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-30+2877G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962917 | |||||||
| chr12:2962929 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02523.hp1 NA18960.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-30+2889C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962929 | |||||||
| chr12:2962931 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+2891C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2962931 | |||||||
| chr12:2963036 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-30+2996C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2963036 | |||||||
| chr12:2963038 | A | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30+2998A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2963038 | |||||||
| chr12:2963154 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-30+3114C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2963154 | |||||||
| chr12:2963446 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-30+3406C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2963446 | |||||||
| chr12:2963623 | C | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG00280.hp1 HG01167.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+3583C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2963623 | |||||||
| chr12:2963707 | A | C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0191 a0001c0001t0001g0224 others(1): Show |
4 | HG01358.hp1 HG01891.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+3667A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2963707 | |||||||
| chr12:2963983 | A | G | 183 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
183 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.-30+3943A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2963983 | |||||||
| chr12:2964217 | T | C | 19 | a0001c0001t0001g0073 a0001c0001t0001g0163 a0001c0001t0001g0164 others(16): Show |
19 | HG00597.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-30+4177T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964217 | |||||||
| chr12:2964285 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(1): Show |
4 | HG01496.hp2 HG02280.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+4245G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964285 | |||||||
| chr12:2964355 | T | C | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01952.hp2 HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-30+4315T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964355 | |||||||
| chr12:2964438 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-30+4398A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964438 | |||||||
| chr12:2964459 | CT | C | 7 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0074 others(4): Show |
7 | HG01070.hp1 HG01168.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+4434delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2964459 | ||||||
| chr12:2964515 | T | C | 115 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(112): Show |
115 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-30+4475T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964515 | |||||||
| chr12:2964533 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-30+4493C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964533 | |||||||
| chr12:2964621 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-30+4581C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964621 | |||||||
| chr12:2964624 | A | AT | 6 | a0001c0001t0001g0053 a0001c0001t0001g0072 a0001c0001t0001g0139 others(3): Show |
6 | HG01123.hp1 HG01346.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+4603dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2964624 | ||||||
| chr12:2964624 | AT | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
157 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.-30+4603delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2964624 | ||||||
| chr12:2964674 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-30+4634G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964674 | |||||||
| chr12:2964718 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-30+4678C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964718 | |||||||
| chr12:2964751 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-30+4711C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964751 | |||||||
| chr12:2964821 | G | A | 125 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(122): Show |
125 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-30+4781G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964821 | |||||||
| chr12:2964853 | C | G | 148 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(145): Show |
148 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-30+4813C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2964853 | |||||||
| chr12:2965021 | A | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30+4981A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965021 | |||||||
| chr12:2965375 | A | G | 158 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(155): Show |
158 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.-30+5335A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965375 | |||||||
| chr12:2965407 | A | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
180 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+5367A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965407 | |||||||
| chr12:2965418 | C | G | 126 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(123): Show |
126 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.-30+5378C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965418 | |||||||
| chr12:2965486 | TA | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
6 | HG00597.hp2 HG00738.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+5457delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2965486 | ||||||
| chr12:2965492 | A | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0235 a0001c0001t0001g0267 |
3 | HG01109.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-30+5452A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965492 | |||||||
| chr12:2965516 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-30+5476T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965516 | |||||||
| chr12:2965533 | G | A | 180 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
180 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+5493G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965533 | |||||||
| chr12:2965560 | AT | A | 20 | a0001c0001t0001g0073 a0001c0001t0001g0163 a0001c0001t0001g0164 others(17): Show |
20 | HG00597.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-30+5529delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2965560 | ||||||
| chr12:2965575 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-30+5535G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965575 | |||||||
| chr12:2965590 | C | T | 10 | a0001c0001t0001g0070 a0001c0001t0001g0138 a0001c0001t0001g0205 others(7): Show |
10 | HG00558.hp2 HG00609.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+5550C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965590 | |||||||
| chr12:2965709 | A | AT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(17): Show |
20 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-30+5676dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2965709 | ||||||
| chr12:2965727 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+5687G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965727 | |||||||
| chr12:2965765 | T | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(24): Show |
27 | HG01167.hp2 HG01496.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30+5725T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965765 | |||||||
| chr12:2965774 | T | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-30+5734T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965774 | |||||||
| chr12:2965835 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-30+5795C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965835 | |||||||
| chr12:2965879 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG00423.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-30+5839G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965879 | |||||||
| chr12:2965925 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30+5885G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2965925 | |||||||
| chr12:2966007 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(69): Show |
73 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-30+5967T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966007 | |||||||
| chr12:2966122 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-30+6082A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966122 | |||||||
| chr12:2966226 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0159 others(1): Show |
4 | HG01106.hp1 HG02647.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+6186T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966226 | |||||||
| chr12:2966314 | C | T | 6 | a0001c0001t0001g0133 a0001c0001t0001g0181 a0001c0001t0001g0183 others(3): Show |
6 | HG01167.hp2 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+6274C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966314 | |||||||
| chr12:2966318 | G | C | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30+6278G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966318 | |||||||
| chr12:2966417 | C | CT | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
57 | HG00099.hp1 HG00597.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-30+6390dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2966417 | ||||||
| chr12:2966467 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-30+6427G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966467 | |||||||
| chr12:2966548 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-30+6508T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966548 | |||||||
| chr12:2966567 | T | C | 9 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(6): Show |
9 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30+6527T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966567 | |||||||
| chr12:2966572 | A | G | 9 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(6): Show |
9 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30+6532A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966572 | |||||||
| chr12:2966633 | G | A | 1 | a0001c0001t0006g0045 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-30+6593G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966633 | |||||||
| chr12:2966707 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(22): Show |
25 | HG00738.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-30+6667G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966707 | |||||||
| chr12:2966747 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-30+6707C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966747 | |||||||
| chr12:2966792 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0166 |
2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-30+6752C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966792 | |||||||
| chr12:2966799 | T | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-30+6759T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966799 | |||||||
| chr12:2966852 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01952.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-30+6812A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2966852 | |||||||
| chr12:2967016 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0132 others(2): Show |
5 | HG01934.hp1 HG01943.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+6976G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967016 | |||||||
| chr12:2967220 | GGT | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-30+7182_-30+7183d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2967220 | ||||||
| chr12:2967235 | C | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.-30+7195C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967235 | |||||||
| chr12:2967251 | A | G | 15 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.-30+7211A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967251 | |||||||
| chr12:2967308 | C | T | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(34): Show |
37 | HG01106.hp1 HG01167.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-30+7268C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967308 | |||||||
| chr12:2967364 | AC | A | 15 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.-30+7325delC | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967364 | |||||||
| chr12:2967499 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(140): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-30+7459G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967499 | |||||||
| chr12:2967609 | A | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(140): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-30+7569A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967609 | |||||||
| chr12:2967634 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-30+7594G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967634 | |||||||
| chr12:2967840 | G | T | 32 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
32 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.-30+7800G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2967840 | |||||||
| chr12:2968016 | T | C | 16 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+7976T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968016 | |||||||
| chr12:2968033 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(140): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-30+7993G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968033 | |||||||
| chr12:2968053 | A | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-30+8013A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968053 | |||||||
| chr12:2968083 | C | CT | 5 | a0001c0001t0001g0039 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | HG00280.hp1 HG01257.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+8063dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968083 | ||||||
| chr12:2968083 | C | CTT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(133): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-30+8062_-30+8063d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968083 | ||||||
| chr12:2968083 | C | CTTT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0128 others(2): Show |
5 | HG01243.hp2 HG03831.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+8061_-30+8063d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968083 | ||||||
| chr12:2968083 | CTTTTTTT | C | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(35): Show |
38 | HG00597.hp2 HG01106.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.-30+8057_-30+8063d others(9): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968083 | ||||||
| chr12:2968119 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-30+8079T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968119 | |||||||
| chr12:2968320 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0086 others(11): Show |
14 | HG01257.hp1 HG01258.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+8280A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968320 | |||||||
| chr12:2968348 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(140): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-30+8308A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968348 | |||||||
| chr12:2968357 | A | T | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(34): Show |
37 | HG01106.hp1 HG01167.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-30+8317A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968357 | |||||||
| chr12:2968378 | G | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(34): Show |
37 | HG01106.hp1 HG01167.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-30+8338G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968378 | |||||||
| chr12:2968385 | C | CT | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(116): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-30+8372dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968385 | ||||||
| chr12:2968385 | C | CTT | 60 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(57): Show |
60 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-30+8371_-30+8372d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968385 | ||||||
| chr12:2968385 | C | CTTT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0034 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+8370_-30+8372d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968385 | ||||||
| chr12:2968385 | C | CTTTT | 14 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(11): Show |
14 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30+8369_-30+8372d others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968385 | ||||||
| chr12:2968385 | C | CTTTTT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0159 others(8): Show |
11 | HG01106.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30+8368_-30+8372d others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968385 | ||||||
| chr12:2968385 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0001g0186 |
3 | HG02145.hp1 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-30+8363_-30+8372d others(12): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968385 | ||||||
| chr12:2968385 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0250 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-30+8362_-30+8372d others(13): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968385 | ||||||
| chr12:2968385 | CTTTTT | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0168 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+8368_-30+8372d others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968385 | ||||||
| chr12:2968419 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-30+8379C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968419 | |||||||
| chr12:2968512 | C | T | 28 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.-30+8472C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968512 | |||||||
| chr12:2968569 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+8529C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968569 | |||||||
| chr12:2968792 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-30+8752G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2968792 | |||||||
| chr12:2968997 | GC | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(130): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-30+8960delC | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2968997 | ||||||
| chr12:2969096 | T | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0193 a0001c0001t0001g0206 |
3 | HG02132.hp2 HG02165.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-30+9056T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969096 | |||||||
| chr12:2969335 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0170 others(14): Show |
17 | HG01346.hp2 HG01358.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-30+9295G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969335 | |||||||
| chr12:2969395 | A | G | 16 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+9355A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969395 | |||||||
| chr12:2969549 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-30+9509G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969549 | |||||||
| chr12:2969588 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-30+9548C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969588 | |||||||
| chr12:2969596 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-30+9556G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969596 | |||||||
| chr12:2969683 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0086 others(11): Show |
14 | HG01257.hp1 HG01258.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+9643G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969683 | |||||||
| chr12:2969841 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-30+9801C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969841 | |||||||
| chr12:2969859 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+9819A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969859 | |||||||
| chr12:2969906 | C | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(226): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-30+9866C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2969906 | |||||||
| chr12:2969924 | T | TA | 2 | a0001c0001t0001g0002 a0001c0001t0001g0199 |
3 | HG03492.hp2 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-30+9885dupA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2969924 | ||||||
| chr12:2970019 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-30+9979G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970019 | |||||||
| chr12:2970146 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-30+10106C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970146 | |||||||
| chr12:2970152 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+10112C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970152 | |||||||
| chr12:2970228 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-30+10188C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970228 | |||||||
| chr12:2970260 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-30+10220G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970260 | |||||||
| chr12:2970308 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-30+10268A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970308 | |||||||
| chr12:2970346 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-30+10306C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970346 | |||||||
| chr12:2970679 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0001g0123 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+10639C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970679 | |||||||
| chr12:2970844 | G | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0168 a0001c0001t0001g0188 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+10804G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970844 | |||||||
| chr12:2970847 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-30+10807G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970847 | |||||||
| chr12:2970940 | G | A | 18 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(15): Show |
18 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30+10900G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2970940 | |||||||
| chr12:2971003 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0269 |
2 | HG01192.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-30+10963C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2971003 | |||||||
| chr12:2971106 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG01192.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+11066T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2971106 | |||||||
| chr12:2971408 | A | G | 55 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
55 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+11368A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2971408 | |||||||
| chr12:2971418 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0143 |
3 | HG00140.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-30+11378G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2971418 | |||||||
| chr12:2971728 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0135 |
2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-30+11688G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2971728 | |||||||
| chr12:2971814 | C | CT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
13 | HG00738.hp1 HG01952.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-30+11790dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2971814 | ||||||
| chr12:2971814 | CT | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(16): Show |
19 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30+11790delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2971814 | ||||||
| chr12:2971814 | CTT | C | 55 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
55 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+11789_-30+1179 others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2971814 | ||||||
| chr12:2971899 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-30+11859G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2971899 | |||||||
| chr12:2971915 | TGA | T | 55 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
55 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+11876_-30+1187 others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2971915 | |||||||
| chr12:2972329 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-30+12289G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2972329 | |||||||
| chr12:2972439 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0212 |
2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-30+12399G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2972439 | |||||||
| chr12:2972454 | C | T | 55 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
55 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+12414C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2972454 | |||||||
| chr12:2972491 | C | CT | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(125): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-30+12476dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2972491 | ||||||
| chr12:2972491 | C | CTT | 24 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0029 others(21): Show |
24 | HG00738.hp1 HG01123.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-30+12475_-30+1247 others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2972491 | ||||||
| chr12:2972491 | CT | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0019 others(17): Show |
20 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-30+12476delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2972491 | ||||||
| chr12:2972491 | CTT | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0016 others(18): Show |
21 | HG01167.hp2 HG01192.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30+12475_-30+1247 others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2972491 | ||||||
| chr12:2972491 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+12467_-30+1247 others(14): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2972491 | ||||||
| chr12:2972580 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-30+12540A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2972580 | |||||||
| chr12:2972606 | TCTC | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0170 others(15): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30+12569_-30+1257 others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2972606 | ||||||
| chr12:2972845 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-30+12805T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2972845 | |||||||
| chr12:2972875 | G | C | 55 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
55 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+12835G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2972875 | |||||||
| chr12:2972963 | C | G | 18 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(15): Show |
18 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30+12923C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2972963 | |||||||
| chr12:2972963 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0223 a0001c0001t0001g0238 |
3 | HG01884.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-30+12923C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2972963 | |||||||
| chr12:2973094 | G | GT | 23 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): Show |
23 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-30+13056dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2973094 | ||||||
| chr12:2973236 | T | G | 1 | a0001c0001t0001g0004 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-30+13196T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2973236 | |||||||
| chr12:2973317 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+13277C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2973317 | |||||||
| chr12:2973318 | G | A | 32 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(29): Show |
32 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.-30+13278G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2973318 | |||||||
| chr12:2973628 | T | C | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+13588T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2973628 | |||||||
| chr12:2973671 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-30+13631G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2973671 | |||||||
| chr12:2973741 | G | A | 1 | a0001c0001t0005g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-30+13701G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2973741 | |||||||
| chr12:2973957 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0175 a0001c0001t0001g0232 others(1): Show |
4 | HG01952.hp2 HG02055.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+13917G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2973957 | |||||||
| chr12:2974207 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+14167T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974207 | |||||||
| chr12:2974222 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-30+14182C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974222 | |||||||
| chr12:2974264 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0156 |
2 | HG01934.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-30+14224A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974264 | |||||||
| chr12:2974288 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-30+14248C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974288 | |||||||
| chr12:2974368 | G | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0050 others(11): Show |
14 | HG01106.hp1 HG02055.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30+14328G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974368 | |||||||
| chr12:2974414 | G | A | 18 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(15): Show |
18 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30+14374G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974414 | |||||||
| chr12:2974467 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0004g0176 |
2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-30+14427C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974467 | |||||||
| chr12:2974473 | C | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0050 others(13): Show |
16 | HG00597.hp2 HG01106.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+14433C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974473 | |||||||
| chr12:2974504 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-30+14464A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974504 | |||||||
| chr12:2974543 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.-30+14503A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974543 | |||||||
| chr12:2974786 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-30+14746T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974786 | |||||||
| chr12:2974923 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-30+14883C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974923 | |||||||
| chr12:2974931 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+14891A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2974931 | |||||||
| chr12:2975081 | T | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(15): Show |
18 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30+15041T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975081 | |||||||
| chr12:2975143 | C | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-30+15103C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975143 | |||||||
| chr12:2975147 | A | T | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+15107A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975147 | |||||||
| chr12:2975167 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30+15127C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975167 | |||||||
| chr12:2975171 | AAAAC | A | 16 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+15143_-30+1514 others(8): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975171 | ||||||
| chr12:2975172 | AAAC | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0212 a0001c0001t0001g0251 others(1): Show |
4 | HG00140.hp2 HG02523.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+15135_-30+1513 others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975172 | ||||||
| chr12:2975173 | AAC | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(184): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.-30+15135_-30+1513 others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975173 | ||||||
| chr12:2975174 | AC | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0112 a0001c0001t0001g0144 |
3 | HG00597.hp1 HG02257.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-30+15135delC | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975174 | |||||||
| chr12:2975179 | C | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-30+15139C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975179 | |||||||
| chr12:2975183 | C | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-30+15143C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975183 | |||||||
| chr12:2975187 | A | C | 1 | a0001c0001t0001g0223 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-30+15147A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975187 | |||||||
| chr12:2975301 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-30+15261T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975301 | |||||||
| chr12:2975352 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-30+15312G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975352 | |||||||
| chr12:2975356 | CATT | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0025 others(17): Show |
20 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-30+15360_-30+1536 others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975356 | ||||||
| chr12:2975356 | CATTATT | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0042 others(20): Show |
23 | HG00597.hp2 HG01192.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.-30+15357_-30+1536 others(10): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975356 | ||||||
| chr12:2975356 | CATTATTA others(2): Show |
C | 8 | a0001c0001t0001g0132 a0001c0001t0001g0148 a0001c0001t0001g0165 others(5): Show |
8 | HG00735.hp1 HG00741.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+15354_-30+1536 others(13): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975356 | ||||||
| chr12:2975356 | CATTATTA others(5): Show |
C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(30): Show |
33 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-30+15351_-30+1536 others(16): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975356 | ||||||
| chr12:2975356 | CATTATTA others(8): Show |
C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-30+15348_-30+1536 others(19): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975356 | ||||||
| chr12:2975356 | CATTATTA others(11): Show |
C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0204 |
2 | HG00099.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-30+15345_-30+1536 others(22): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975356 | ||||||
| chr12:2975384 | ATTATTAT others(9): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-30+15346_-30+1536 others(20): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975384 | ||||||
| chr12:2975385 | TTATTATT others(11): Show |
T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): Show |
23 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-30+15348_-30+1536 others(22): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2975385 | ||||||
| chr12:2975410 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-30+15370T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975410 | |||||||
| chr12:2975509 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(131): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-30+15469C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975509 | |||||||
| chr12:2975537 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-30+15497C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975537 | |||||||
| chr12:2975888 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0200 |
2 | HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-30+15848G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2975888 | |||||||
| chr12:2976008 | A | AT | 34 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0029 others(31): Show |
34 | HG00597.hp2 HG00738.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-30+15983dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2976008 | ||||||
| chr12:2976008 | ATTT | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-30+15981_-30+1598 others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2976008 | ||||||
| chr12:2976128 | C | T | 33 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0029 others(30): Show |
33 | HG00597.hp2 HG00738.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.-30+16088C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976128 | |||||||
| chr12:2976130 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-30+16090C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976130 | |||||||
| chr12:2976183 | T | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-30+16143T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976183 | |||||||
| chr12:2976208 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-30+16168C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976208 | |||||||
| chr12:2976217 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-30+16177C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976217 | |||||||
| chr12:2976221 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-30+16181G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976221 | |||||||
| chr12:2976273 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-30+16233A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976273 | |||||||
| chr12:2976293 | T | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.-30+16253T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976293 | |||||||
| chr12:2976313 | T | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-30+16273T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976313 | |||||||
| chr12:2976357 | C | CCA | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-30+16318_-30+1631 others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2976357 | ||||||
| chr12:2976360 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-30+16320T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976360 | |||||||
| chr12:2976362 | C | G | 1 | a0001c0005t0001g0015 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-30+16322C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976362 | |||||||
| chr12:2976508 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-30+16468G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976508 | |||||||
| chr12:2976511 | C | T | 33 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.-30+16471C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976511 | |||||||
| chr12:2976527 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-30+16487A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976527 | |||||||
| chr12:2976625 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30+16585G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976625 | |||||||
| chr12:2976637 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-30+16597G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976637 | |||||||
| chr12:2976657 | C | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.-30+16617C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976657 | |||||||
| chr12:2976694 | CCTGAGAG others(27): Show |
C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-30+16690_-30+1672 others(38): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2976694 | ||||||
| chr12:2976781 | T | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-30+16741T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976781 | |||||||
| chr12:2976789 | C | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0050 others(13): Show |
16 | HG01106.hp1 HG02055.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-30+16749C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976789 | |||||||
| chr12:2976817 | T | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
57 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-30+16777T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976817 | |||||||
| chr12:2976922 | G | A | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-30+16882G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2976922 | |||||||
| chr12:2977042 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-30+17002C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977042 | |||||||
| chr12:2977056 | A | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-30+17016A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977056 | |||||||
| chr12:2977085 | G | GCTCCTGT | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-30+17048_-30+1704 others(11): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2977085 | ||||||
| chr12:2977169 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0040 others(12): Show |
15 | HG00597.hp2 HG00738.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-30+17129G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977169 | |||||||
| chr12:2977218 | G | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(22): Show |
25 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-30+17178G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977218 | |||||||
| chr12:2977286 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30+17246G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977286 | |||||||
| chr12:2977309 | T | TCCCCTTC others(18): Show |
1 | a0001c0007t0001g0103 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-30+17278_-30+1730 others(29): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2977309 | ||||||
| chr12:2977447 | C | T | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): Show |
74 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-29-17291C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977447 | |||||||
| chr12:2977784 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-29-16954A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977784 | |||||||
| chr12:2977837 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-29-16901T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977837 | |||||||
| chr12:2977878 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-29-16860C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977878 | |||||||
| chr12:2977913 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0040 others(12): Show |
15 | HG00597.hp2 HG00738.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-29-16825G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2977913 | |||||||
| chr12:2978216 | G | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): Show |
24 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29-16522G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978216 | |||||||
| chr12:2978376 | GT | G | 34 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.-29-16350delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2978376 | ||||||
| chr12:2978376 | GTT | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-29-16351_-29-1635 others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2978376 | ||||||
| chr12:2978384 | T | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): Show |
24 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29-16354T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978384 | |||||||
| chr12:2978398 | T | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0041 others(4): Show |
7 | HG00738.hp1 HG01952.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-16340T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978398 | |||||||
| chr12:2978407 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(64): Show |
68 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-29-16331G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978407 | |||||||
| chr12:2978456 | A | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0050 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29-16282A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978456 | |||||||
| chr12:2978487 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-16251G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978487 | |||||||
| chr12:2978543 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-29-16195A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978543 | |||||||
| chr12:2978552 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-29-16186C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978552 | |||||||
| chr12:2978655 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-29-16083C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978655 | |||||||
| chr12:2978667 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-29-16071G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978667 | |||||||
| chr12:2978695 | C | T | 15 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0040 others(12): Show |
15 | HG00597.hp2 HG00738.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-29-16043C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978695 | |||||||
| chr12:2978995 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-29-15743A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978995 | |||||||
| chr12:2978997 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-29-15741C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2978997 | |||||||
| chr12:2979040 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(165): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-29-15698C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979040 | |||||||
| chr12:2979077 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-29-15661G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979077 | |||||||
| chr12:2979195 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-29-15543C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979195 | |||||||
| chr12:2979413 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0071 a0001c0008t0001g0036 |
3 | HG02015.hp2 HG02165.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-29-15325A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979413 | |||||||
| chr12:2979489 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0115 |
2 | HG00438.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-29-15249C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979489 | |||||||
| chr12:2979558 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-29-15180A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979558 | |||||||
| chr12:2979591 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(191): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-29-15147G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979591 | |||||||
| chr12:2979643 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-29-15095A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979643 | |||||||
| chr12:2979849 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-14889C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979849 | |||||||
| chr12:2979874 | T | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.-29-14864T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2979874 | |||||||
| chr12:2980004 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-29-14734C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980004 | |||||||
| chr12:2980134 | G | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-29-14604G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980134 | |||||||
| chr12:2980169 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG01099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-29-14569C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980169 | |||||||
| chr12:2980188 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(208): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-29-14550T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980188 | |||||||
| chr12:2980238 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-29-14500G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980238 | |||||||
| chr12:2980356 | C | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0196 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-29-14382C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980356 | |||||||
| chr12:2980394 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(191): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-29-14344G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980394 | |||||||
| chr12:2980438 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(191): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-29-14300T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980438 | |||||||
| chr12:2980470 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0050 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29-14268C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980470 | |||||||
| chr12:2980499 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-29-14239G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980499 | |||||||
| chr12:2980777 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-29-13961A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980777 | |||||||
| chr12:2980799 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-29-13939G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980799 | |||||||
| chr12:2980930 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(190): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-29-13808C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2980930 | |||||||
| chr12:2981069 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-29-13669C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981069 | |||||||
| chr12:2981142 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-29-13596C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981142 | |||||||
| chr12:2981214 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01952.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-29-13524G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981214 | |||||||
| chr12:2981275 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0064 others(4): Show |
7 | HG00738.hp1 HG01952.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-13463C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981275 | |||||||
| chr12:2981351 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-29-13387C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981351 | |||||||
| chr12:2981431 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-29-13307G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981431 | |||||||
| chr12:2981579 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-29-13159A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981579 | |||||||
| chr12:2981694 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-29-13044G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981694 | |||||||
| chr12:2981746 | C | G | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(37): Show |
40 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29-12992C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981746 | |||||||
| chr12:2981819 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-29-12919G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981819 | |||||||
| chr12:2981932 | G | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-29-12806G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2981932 | |||||||
| chr12:2982136 | A | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(198): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-29-12602A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2982136 | |||||||
| chr12:2982166 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-29-12572C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2982166 | |||||||
| chr12:2982207 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-29-12531C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2982207 | |||||||
| chr12:2982323 | C | A | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-29-12415C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2982323 | |||||||
| chr12:2982586 | G | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-29-12152G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2982586 | |||||||
| chr12:2982912 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-29-11826A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2982912 | |||||||
| chr12:2982928 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0170 a0001c0001t0001g0178 others(14): Show |
17 | HG01346.hp2 HG01358.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-11810C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2982928 | |||||||
| chr12:2982938 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0227 |
3 | HG01891.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-29-11800C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2982938 | |||||||
| chr12:2983295 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(19): Show |
22 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29-11443G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2983295 | |||||||
| chr12:2983770 | C | T | 4 | a0001c0001t0001g0181 a0001c0001t0001g0250 a0001c0001t0001g0270 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-10968C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2983770 | |||||||
| chr12:2983817 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-29-10921C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2983817 | |||||||
| chr12:2983942 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-29-10796A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2983942 | |||||||
| chr12:2983994 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-29-10744G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2983994 | |||||||
| chr12:2984158 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-29-10580C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2984158 | |||||||
| chr12:2984190 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-29-10548C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2984190 | |||||||
| chr12:2984226 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-29-10512A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2984226 | |||||||
| chr12:2984394 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-29-10344C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2984394 | |||||||
| chr12:2984442 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(172): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-29-10296A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2984442 | |||||||
| chr12:2984698 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-29-10040T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2984698 | |||||||
| chr12:2984868 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-29-9870G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2984868 | |||||||
| chr12:2984994 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-29-9744C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2984994 | |||||||
| chr12:2985046 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-29-9692C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985046 | |||||||
| chr12:2985155 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG01192.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-9583C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985155 | |||||||
| chr12:2985211 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-29-9527T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985211 | |||||||
| chr12:2985254 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0004g0176 |
3 | HG02723.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-29-9484A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985254 | |||||||
| chr12:2985258 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0004g0176 |
3 | HG02723.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-29-9480A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985258 | |||||||
| chr12:2985284 | C | CTGAGGCA others(6): Show |
2 | a0001c0001t0001g0175 a0001c0001t0001g0181 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-29-9451_-29-9439d others(15): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2985284 | ||||||
| chr12:2985299 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0205 |
2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-29-9439G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985299 | |||||||
| chr12:2985311 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29-9427G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985311 | |||||||
| chr12:2985339 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0237 |
3 | HG01256.hp1 HG01258.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-29-9399T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985339 | |||||||
| chr12:2985347 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-29-9391T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985347 | |||||||
| chr12:2985349 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0196 others(2): Show |
5 | HG00558.hp1 HG01106.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-9389T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985349 | |||||||
| chr12:2985431 | C | T | 40 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(37): Show |
40 | HG00621.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29-9307C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985431 | |||||||
| chr12:2985464 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29-9274T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985464 | |||||||
| chr12:2985501 | C | CT | 36 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(33): Show |
36 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-29-9215dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2985501 | ||||||
| chr12:2985501 | CT | C | 7 | a0001c0001t0001g0040 a0001c0001t0001g0147 a0001c0001t0001g0153 others(4): Show |
7 | HG02155.hp1 HG02602.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-9215delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2985501 | ||||||
| chr12:2985501 | CTT | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(170): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-29-9216_-29-9215d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2985501 | ||||||
| chr12:2985501 | CTTT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0054 others(11): Show |
15 | HG00733.hp2 HG01168.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29-9217_-29-9215d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2985501 | ||||||
| chr12:2985528 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29-9210C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985528 | |||||||
| chr12:2985536 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-29-9202C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985536 | |||||||
| chr12:2985548 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0112 |
2 | HG00597.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-29-9190C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985548 | |||||||
| chr12:2985567 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-29-9171A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985567 | |||||||
| chr12:2985568 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-29-9170C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985568 | |||||||
| chr12:2985569 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-29-9169G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985569 | |||||||
| chr12:2985587 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-29-9151C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985587 | |||||||
| chr12:2985587 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29-9151C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985587 | |||||||
| chr12:2985591 | C | T | 5 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0232 others(2): Show |
5 | HG01952.hp2 HG02055.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-9147C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985591 | |||||||
| chr12:2985653 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29-9085G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985653 | |||||||
| chr12:2985655 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29-9083A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985655 | |||||||
| chr12:2985721 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-29-9017G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985721 | |||||||
| chr12:2985725 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-29-9013C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985725 | |||||||
| chr12:2985726 | G | A | 2 | a0001c0002t0001g0120 a0001c0002t0001g0127 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-29-9012G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985726 | |||||||
| chr12:2985845 | GGAGGCC | G | 5 | a0001c0001t0001g0183 a0001c0001t0001g0231 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp2 HG02258.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-8887_-29-8882d others(8): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2985845 | ||||||
| chr12:2985851 | C | T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0040 others(24): Show |
27 | HG01257.hp1 HG01258.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.-29-8887C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985851 | |||||||
| chr12:2985860 | T | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(66): Show |
69 | HG00597.hp2 HG00621.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.-29-8878T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985860 | |||||||
| chr12:2985905 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-29-8833G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2985905 | |||||||
| chr12:2986042 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-29-8696C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986042 | |||||||
| chr12:2986049 | G | A | 58 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-29-8689G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986049 | |||||||
| chr12:2986102 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-29-8636A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986102 | |||||||
| chr12:2986196 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-29-8542C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986196 | |||||||
| chr12:2986363 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-29-8375T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986363 | |||||||
| chr12:2986365 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-29-8373C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986365 | |||||||
| chr12:2986365 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0078 others(12): Show |
15 | HG01346.hp2 HG01358.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29-8373C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986365 | |||||||
| chr12:2986436 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0081 a0001c0001t0001g0203 |
3 | HG02809.hp2 NA18950.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-29-8302G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986436 | |||||||
| chr12:2986500 | C | T | 14 | a0001c0001t0001g0081 a0001c0001t0001g0130 a0001c0001t0001g0131 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-8238C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986500 | |||||||
| chr12:2986504 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-29-8234G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986504 | |||||||
| chr12:2986533 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-29-8205G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986533 | |||||||
| chr12:2986606 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-29-8132C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986606 | |||||||
| chr12:2986646 | TA | T | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(41): Show |
44 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29-8083delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2986646 | ||||||
| chr12:2986655 | AT | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0157 others(3): Show |
6 | HG01261.hp2 HG02602.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-8082delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986655 | |||||||
| chr12:2986656 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.-29-8082T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986656 | |||||||
| chr12:2986732 | T | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(45): Show |
48 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(45): Show |
intron_variant | MODIFIER | c.-29-8006T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986732 | |||||||
| chr12:2986770 | T | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0123 a0001c0001t0001g0135 |
3 | HG01099.hp2 HG01515.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-29-7968T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986770 | |||||||
| chr12:2986920 | G | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-29-7818G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986920 | |||||||
| chr12:2986968 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-29-7770A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2986968 | |||||||
| chr12:2987416 | GTTTGT | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.-29-7293_-29-7289d others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2987416 | ||||||
| chr12:2987520 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0017 |
2 | HG02622.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-29-7218C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2987520 | |||||||
| chr12:2987527 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-29-7211C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2987527 | |||||||
| chr12:2987638 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-29-7100G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2987638 | |||||||
| chr12:2987711 | C | G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0081 a0001c0001t0001g0130 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-7027C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2987711 | |||||||
| chr12:2987752 | CTG | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0018 others(48): Show |
51 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-29-6981_-29-6980d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2987752 | ||||||
| chr12:2987760 | A | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0024 others(33): Show |
36 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-29-6978A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2987760 | |||||||
| chr12:2987793 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0181 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-29-6945C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2987793 | |||||||
| chr12:2987881 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-29-6857A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2987881 | |||||||
| chr12:2987900 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-29-6838A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2987900 | |||||||
| chr12:2988024 | C | T | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(41): Show |
44 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29-6714C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2988024 | |||||||
| chr12:2988104 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-29-6634C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2988104 | |||||||
| chr12:2988496 | G | C | 54 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0018 others(51): Show |
54 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.-29-6242G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2988496 | |||||||
| chr12:2988508 | C | CA | 49 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0039 others(46): Show |
49 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-29-6212dupA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2988508 | ||||||
| chr12:2988508 | CA | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(158): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-29-6212delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2988508 | ||||||
| chr12:2989181 | C | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0081 a0001c0001t0001g0130 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-5557C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2989181 | |||||||
| chr12:2989245 | A | T | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(41): Show |
44 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29-5493A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2989245 | |||||||
| chr12:2989254 | A | G | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(41): Show |
44 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29-5484A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2989254 | |||||||
| chr12:2989259 | G | T | 1 | a0001c0002t0001g0210 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-29-5479G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2989259 | |||||||
| chr12:2989296 | A | T | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-5442A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2989296 | |||||||
| chr12:2989460 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-29-5278A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2989460 | |||||||
| chr12:2989758 | A | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0081 a0001c0001t0001g0130 others(16): Show |
19 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-4980A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2989758 | |||||||
| chr12:2989981 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-29-4757T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2989981 | |||||||
| chr12:2990024 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-29-4714T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990024 | |||||||
| chr12:2990125 | G | A | 41 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(38): Show |
41 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.-29-4613G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990125 | |||||||
| chr12:2990145 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-29-4593G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990145 | |||||||
| chr12:2990354 | G | A | 36 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0057 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.-29-4384G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990354 | |||||||
| chr12:2990408 | C | CT | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(41): Show |
44 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29-4322dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990408 | ||||||
| chr12:2990457 | T | G | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(41): Show |
44 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29-4281T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990457 | |||||||
| chr12:2990461 | C | CT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(119): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-29-4250dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(30): Show |
34 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.-29-4251_-29-4250d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTTT | 9 | a0001c0001t0001g0040 a0001c0001t0001g0066 a0001c0001t0001g0082 others(6): Show |
9 | HG01175.hp1 HG01256.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-4252_-29-4250d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTTTT | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(20): Show |
23 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-29-4253_-29-4250d others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTTTTT | 7 | a0001c0001t0001g0014 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
7 | HG01167.hp2 HG01192.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-4254_-29-4250d others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTTTTTT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-4255_-29-4250d others(8): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTTTTTTT others(1): Show |
10 | a0001c0001t0001g0180 a0001c0001t0001g0188 a0001c0001t0001g0240 others(7): Show |
10 | HG01346.hp2 HG01358.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-4257_-29-4250d others(10): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-29-4261_-29-4250d others(14): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0186 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-29-4273_-29-4250d others(26): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990461 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0078 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-29-4274_-29-4250d others(27): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2990461 | ||||||
| chr12:2990724 | C | G | 1 | a0001c0002t0001g0102 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-29-4014C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990724 | |||||||
| chr12:2990793 | C | T | 8 | a0001c0001t0001g0038 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02132.hp2 HG02165.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-3945C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990793 | |||||||
| chr12:2990794 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0018 others(48): Show |
51 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-29-3944G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990794 | |||||||
| chr12:2990822 | G | C | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-3916G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990822 | |||||||
| chr12:2990959 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0167 |
2 | HG00597.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-29-3779A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2990959 | |||||||
| chr12:2991192 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0123 a0001c0001t0001g0135 |
3 | HG01099.hp2 HG01515.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-29-3546C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2991192 | |||||||
| chr12:2991198 | C | G | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(41): Show |
44 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29-3540C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2991198 | |||||||
| chr12:2991281 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0152 |
2 | HG00140.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.-29-3457C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2991281 | |||||||
| chr12:2991395 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-29-3343C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2991395 | |||||||
| chr12:2991767 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(128): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-29-2971G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2991767 | |||||||
| chr12:2991789 | A | G | 10 | a0001c0001t0001g0180 a0001c0001t0001g0188 a0001c0001t0001g0240 others(7): Show |
10 | HG01346.hp2 HG01358.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-2949A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2991789 | |||||||
| chr12:2991922 | G | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-29-2816G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2991922 | |||||||
| chr12:2991998 | TG | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(27): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-29-2732delG | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2991998 | ||||||
| chr12:2992000 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-29-2738G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992000 | |||||||
| chr12:2992001 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-29-2737G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992001 | |||||||
| chr12:2992016 | C | CT | 11 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0130 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.-29-2702dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2992016 | ||||||
| chr12:2992016 | C | CTT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(118): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-29-2703_-29-2702d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2992016 | ||||||
| chr12:2992016 | C | CTTT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0047 others(9): Show |
12 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29-2704_-29-2702d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2992016 | ||||||
| chr12:2992016 | CT | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0122 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-2702delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2992016 | ||||||
| chr12:2992016 | CTT | C | 94 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(91): Show |
94 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.-29-2703_-29-2702d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2992016 | ||||||
| chr12:2992016 | CTTT | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(25): Show |
28 | HG00741.hp1 HG01106.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.-29-2704_-29-2702d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2992016 | ||||||
| chr12:2992018 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-29-2720T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992018 | |||||||
| chr12:2992019 | T | C | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(44): Show |
47 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29-2719T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992019 | |||||||
| chr12:2992050 | G | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0018 others(49): Show |
52 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-29-2688G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992050 | |||||||
| chr12:2992184 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-29-2554A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992184 | |||||||
| chr12:2992333 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-29-2405G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992333 | |||||||
| chr12:2992448 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-29-2290G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992448 | |||||||
| chr12:2992627 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0037 others(25): Show |
28 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-29-2111C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992627 | |||||||
| chr12:2992704 | C | T | 5 | a0001c0001t0001g0139 a0001c0002t0001g0104 a0001c0002t0001g0120 others(2): Show |
5 | HG01109.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-2034C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992704 | |||||||
| chr12:2992781 | G | GTT | 3 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0186 |
3 | HG01884.hp2 HG02145.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-29-1956_-29-1955i others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 2992781 | ||||||
| chr12:2992988 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-29-1750G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2992988 | |||||||
| chr12:2993028 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
78 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.-29-1710C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993028 | |||||||
| chr12:2993153 | A | G | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(21): Show |
24 | HG01106.hp1 HG01952.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.-29-1585A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993153 | |||||||
| chr12:2993175 | C | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
78 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.-29-1563C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993175 | |||||||
| chr12:2993231 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0111 others(1): Show |
4 | HG01257.hp2 HG01261.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-1507G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993231 | |||||||
| chr12:2993280 | T | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(99): Show |
102 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.-29-1458T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993280 | |||||||
| chr12:2993285 | G | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(99): Show |
102 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.-29-1453G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993285 | |||||||
| chr12:2993387 | A | G | 1 | a0001c0002t0001g0102 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-29-1351A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993387 | |||||||
| chr12:2993514 | A | T | 1 | a0001c0001t0001g0004 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-29-1224A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993514 | |||||||
| chr12:2993539 | T | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0018 others(48): Show |
51 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-29-1199T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993539 | |||||||
| chr12:2993772 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-29-966C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993772 | |||||||
| chr12:2993888 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG02896.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-29-850C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993888 | |||||||
| chr12:2993927 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-29-811C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993927 | |||||||
| chr12:2993957 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(268): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-29-781G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993957 | |||||||
| chr12:2993962 | C | A | 1 | a0001c0004t0002g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-29-776C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993962 | |||||||
| chr12:2993968 | T | C | 6 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0190 others(3): Show |
6 | HG02615.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-770T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2993968 | |||||||
| chr12:2994079 | T | C | 3 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0181 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-29-659T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2994079 | |||||||
| chr12:2994114 | A | G | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(45): Show |
48 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(45): Show |
intron_variant | MODIFIER | c.-29-624A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2994114 | |||||||
| chr12:2994288 | C | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0078 others(18): Show |
21 | HG01346.hp2 HG01358.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-29-450C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2994288 | |||||||
| chr12:2994437 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0051 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-29-301G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2994437 | |||||||
| chr12:2994723 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0239 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-29-15T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 2/12 | chr12 | 2994723 | |||||||
| chr12:2995079 | A | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0170 a0001c0001t0001g0180 others(15): Show |
18 | HG01346.hp2 HG01358.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+87A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2995079 | |||||||
| chr12:2995224 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(132): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.226+232T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2995224 | |||||||
| chr12:2995237 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.226+245G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2995237 | |||||||
| chr12:2995582 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(126): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.226+590C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2995582 | |||||||
| chr12:2995675 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.226+683G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2995675 | |||||||
| chr12:2995841 | G | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0018 others(31): Show |
34 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.226+849G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2995841 | |||||||
| chr12:2995853 | A | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0018 others(31): Show |
34 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.226+861A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2995853 | |||||||
| chr12:2995900 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.226+908G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2995900 | |||||||
| chr12:2996007 | C | CAA | 45 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(42): Show |
45 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.226+1030_226+1031d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 2996007 | ||||||
| chr12:2996412 | CT | C | 21 | a0001c0001t0001g0081 a0001c0001t0001g0130 a0001c0001t0001g0131 others(18): Show |
21 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.226+1433delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 2996412 | ||||||
| chr12:2996701 | C | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0238 a0001c0001t0004g0176 |
3 | HG02818.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.226+1709C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2996701 | |||||||
| chr12:2996801 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(14): Show |
17 | HG01106.hp1 HG01952.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.226+1809C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2996801 | |||||||
| chr12:2996802 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(126): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.226+1810G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2996802 | |||||||
| chr12:2996907 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.226+1915C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2996907 | |||||||
| chr12:2996931 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0170 a0001c0001t0001g0180 others(9): Show |
12 | HG01346.hp2 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.226+1939A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2996931 | |||||||
| chr12:2997414 | C | G | 31 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0037 others(28): Show |
31 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.226+2422C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2997414 | |||||||
| chr12:2997548 | TG | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(38): Show |
41 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.226+2557delG | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2997548 | |||||||
| chr12:2997625 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(181): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.226+2633T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2997625 | |||||||
| chr12:2997687 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0215 |
2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.226+2695C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2997687 | |||||||
| chr12:2997694 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0002g0161 others(1): Show |
4 | HG02080.hp1 NA18943.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2702C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2997694 | |||||||
| chr12:2997805 | C | CG | 43 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(40): Show |
43 | HG00597.hp1 HG01070.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.226+2823dupG | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 2997805 | ||||||
| chr12:2997805 | CG | C | 43 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0024 others(40): Show |
43 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.226+2823delG | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 2997805 | ||||||
| chr12:2997806 | G | C | 1 | a0001c0003t0001g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.226+2814G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2997806 | |||||||
| chr12:2997807 | G | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0115 |
2 | HG00438.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.226+2815G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2997807 | |||||||
| chr12:2997816 | T | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0167 others(1): Show |
4 | HG00597.hp2 HG01109.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2824T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2997816 | |||||||
| chr12:2998077 | G | A | 30 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0037 others(27): Show |
30 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.226+3085G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998077 | |||||||
| chr12:2998247 | A | G | 31 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0037 others(28): Show |
31 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.226+3255A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998247 | |||||||
| chr12:2998322 | T | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0118 |
3 | HG00423.hp1 HG04184.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.226+3330T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998322 | |||||||
| chr12:2998438 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.226+3446A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998438 | |||||||
| chr12:2998490 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0238 a0001c0001t0004g0176 |
3 | HG02818.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.226+3498C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998490 | |||||||
| chr12:2998529 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.226+3537G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998529 | |||||||
| chr12:2998539 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0112 |
2 | HG00597.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.226+3547G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998539 | |||||||
| chr12:2998579 | G | T | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
57 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(54): Show |
intron_variant | MODIFIER | c.226+3587G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998579 | |||||||
| chr12:2998607 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0231 |
2 | HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.226+3615G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998607 | |||||||
| chr12:2998650 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.226+3658C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998650 | |||||||
| chr12:2998727 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.226+3735T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998727 | |||||||
| chr12:2998784 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.226+3792C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2998784 | |||||||
| chr12:2999060 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.226+4068G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999060 | |||||||
| chr12:2999450 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.226+4458G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999450 | |||||||
| chr12:2999470 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.226+4478C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999470 | |||||||
| chr12:2999526 | A | T | 9 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0181 others(6): Show |
9 | HG02615.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.226+4534A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999526 | |||||||
| chr12:2999570 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.226+4578A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999570 | |||||||
| chr12:2999605 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0111 others(1): Show |
4 | HG01257.hp2 HG01261.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+4613C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999605 | |||||||
| chr12:2999628 | G | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0167 a0001c0001t0001g0235 |
3 | HG00597.hp2 HG01109.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.226+4636G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999628 | |||||||
| chr12:2999637 | T | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(32): Show |
35 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.226+4645T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999637 | |||||||
| chr12:2999701 | T | G | 2 | a0001c0001t0001g0235 a0001c0001t0003g0236 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.226+4709T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999701 | |||||||
| chr12:2999712 | ACCT | A | 9 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0181 others(6): Show |
9 | HG02615.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.226+4724_226+4726d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 2999712 | ||||||
| chr12:2999736 | C | CGGCCT | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0076 others(18): Show |
21 | HG01106.hp1 HG01167.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.226+4745_226+4749d others(7): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 2999736 | ||||||
| chr12:2999750 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.226+4758G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999750 | |||||||
| chr12:2999767 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.226+4775C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999767 | |||||||
| chr12:2999771 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.226+4779C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999771 | |||||||
| chr12:2999779 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.226+4787C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999779 | |||||||
| chr12:2999849 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.226+4857C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999849 | |||||||
| chr12:2999955 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0111 others(1): Show |
4 | HG01257.hp2 HG01261.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+4963C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 2999955 | |||||||
| chr12:3000103 | C | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0041 a0001c0001t0001g0191 others(6): Show |
9 | HG01192.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.226+5111C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000103 | |||||||
| chr12:3000191 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.226+5199C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000191 | |||||||
| chr12:3000219 | T | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(28): Show |
31 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.226+5227T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000219 | |||||||
| chr12:3000341 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(147): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.226+5349G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000341 | |||||||
| chr12:3000350 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0111 others(1): Show |
4 | HG01257.hp2 HG01261.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+5358T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000350 | |||||||
| chr12:3000426 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0111 others(2): Show |
5 | HG01257.hp2 HG01261.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+5434A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000426 | |||||||
| chr12:3000433 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(125): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.226+5441G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000433 | |||||||
| chr12:3000438 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(204): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.226+5446A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000438 | |||||||
| chr12:3000475 | G | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.226+5483G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000475 | |||||||
| chr12:3000513 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.226+5521T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000513 | |||||||
| chr12:3000515 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.226+5523A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000515 | |||||||
| chr12:3000526 | C | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.226+5534C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000526 | |||||||
| chr12:3000537 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.226+5545C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000537 | |||||||
| chr12:3000565 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(154): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.226+5573G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000565 | |||||||
| chr12:3000593 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.226+5601A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000593 | |||||||
| chr12:3000707 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(125): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.226+5715C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000707 | |||||||
| chr12:3000715 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0167 |
3 | HG00597.hp2 HG03098.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.226+5723C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000715 | |||||||
| chr12:3000881 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(125): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.226+5889C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000881 | |||||||
| chr12:3000882 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0167 others(1): Show |
4 | HG00597.hp2 HG01109.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+5890G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000882 | |||||||
| chr12:3000949 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.226+5957G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3000949 | |||||||
| chr12:3001082 | G | A | 1 | a0001c0003t0001g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.226+6090G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001082 | |||||||
| chr12:3001208 | A | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(154): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.226+6216A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001208 | |||||||
| chr12:3001248 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(125): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.226+6256C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001248 | |||||||
| chr12:3001421 | G | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(46): Show |
49 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.226+6429G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001421 | |||||||
| chr12:3001634 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.226+6642G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001634 | |||||||
| chr12:3001776 | C | CA | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(22): Show |
25 | HG01106.hp1 HG01257.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.226+6798dupA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 3001776 | ||||||
| chr12:3001862 | G | T | 1 | a0001c0001t0001g0011 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.226+6870G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001862 | |||||||
| chr12:3001880 | C | T | 8 | a0001c0001t0001g0132 a0001c0001t0001g0148 a0001c0001t0001g0163 others(5): Show |
8 | HG00735.hp1 HG00741.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.226+6888C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001880 | |||||||
| chr12:3001881 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.226+6889A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001881 | |||||||
| chr12:3001919 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.226+6927G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3001919 | |||||||
| chr12:3002087 | A | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0050 others(19): Show |
22 | HG01952.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.226+7095A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002087 | |||||||
| chr12:3002145 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.226+7153C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002145 | |||||||
| chr12:3002147 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.226+7155G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002147 | |||||||
| chr12:3002227 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(10): Show |
13 | HG01106.hp1 HG01346.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.226+7235C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002227 | |||||||
| chr12:3002465 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0058 |
3 | HG00733.hp2 HG01168.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.226+7473C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002465 | |||||||
| chr12:3002569 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(127): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.226+7577G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002569 | |||||||
| chr12:3002695 | A | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0167 others(1): Show |
4 | HG00597.hp2 HG01109.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+7703A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002695 | |||||||
| chr12:3002702 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0076 others(16): Show |
19 | HG01106.hp1 HG01346.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+7710G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002702 | |||||||
| chr12:3002988 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0111 others(2): Show |
5 | HG01257.hp2 HG01261.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+7996C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3002988 | |||||||
| chr12:3003053 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0134 a0001c0001t0001g0221 |
3 | HG02683.hp2 HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.227-7951C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003053 | |||||||
| chr12:3003212 | G | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(195): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.227-7792G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003212 | |||||||
| chr12:3003342 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.227-7662C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003342 | |||||||
| chr12:3003360 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.227-7644T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003360 | |||||||
| chr12:3003526 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(127): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.227-7478G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003526 | |||||||
| chr12:3003552 | G | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(46): Show |
49 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.227-7452G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003552 | |||||||
| chr12:3003563 | C | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(136): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.227-7441C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003563 | |||||||
| chr12:3003624 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.227-7380C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003624 | |||||||
| chr12:3003625 | G | A | 5 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0179 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-7379G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003625 | |||||||
| chr12:3003667 | C | T | 4 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0142 others(1): Show |
4 | HG01168.hp2 HG03710.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-7337C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003667 | |||||||
| chr12:3003731 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0076 others(16): Show |
19 | HG01106.hp1 HG01346.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.227-7273G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003731 | |||||||
| chr12:3003958 | A | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
50 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.227-7046A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003958 | |||||||
| chr12:3003961 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.227-7043G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003961 | |||||||
| chr12:3003973 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0111 others(2): Show |
5 | HG01257.hp2 HG01261.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-7031C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003973 | |||||||
| chr12:3003974 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.227-7030G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003974 | |||||||
| chr12:3003980 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.227-7024C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003980 | |||||||
| chr12:3003995 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(205): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.227-7009A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3003995 | |||||||
| chr12:3004083 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.227-6921G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004083 | |||||||
| chr12:3004235 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0111 others(2): Show |
5 | HG01257.hp2 HG01261.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-6769G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004235 | |||||||
| chr12:3004236 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.227-6768C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004236 | |||||||
| chr12:3004343 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.227-6661G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004343 | |||||||
| chr12:3004414 | A | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(157): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.227-6590A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004414 | |||||||
| chr12:3004684 | T | A | 45 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(42): Show |
45 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.227-6320T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004684 | |||||||
| chr12:3004709 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0115 |
2 | HG00438.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.227-6295G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004709 | |||||||
| chr12:3004780 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0169 a0001c0001t0001g0194 |
3 | NA18612.hp2 NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.227-6224G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004780 | |||||||
| chr12:3004852 | G | A | 58 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
58 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(55): Show |
intron_variant | MODIFIER | c.227-6152G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004852 | |||||||
| chr12:3004946 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.227-6058G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004946 | |||||||
| chr12:3004967 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0157 others(8): Show |
11 | HG01257.hp2 HG02602.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.227-6037A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3004967 | |||||||
| chr12:3005029 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.227-5975A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005029 | |||||||
| chr12:3005298 | C | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0179 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-5706C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005298 | |||||||
| chr12:3005300 | T | TTTTG | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(19): Show |
22 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.227-5696_227-5693d others(6): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 3005300 | ||||||
| chr12:3005300 | T | TTTTGTTT others(1): Show |
56 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(53): Show |
56 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(53): Show |
intron_variant | MODIFIER | c.227-5700_227-5693d others(10): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 3005300 | ||||||
| chr12:3005331 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-5673C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005331 | |||||||
| chr12:3005485 | T | A | 1 | a0001c0001t0001g0026 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.227-5519T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005485 | |||||||
| chr12:3005505 | AT | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-5490delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 3005505 | ||||||
| chr12:3005529 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0041 a0001c0001t0001g0191 others(6): Show |
9 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.227-5475C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005529 | |||||||
| chr12:3005533 | A | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0157 others(10): Show |
13 | HG01192.hp1 HG01257.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.227-5471A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005533 | |||||||
| chr12:3005553 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.227-5451A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005553 | |||||||
| chr12:3005572 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-5432C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005572 | |||||||
| chr12:3005597 | A | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
78 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-5407A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005597 | |||||||
| chr12:3005615 | G | T | 2 | a0001c0001t0001g0085 a0001c0004t0002g0067 |
2 | HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.227-5389G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005615 | |||||||
| chr12:3005664 | A | ATT | 20 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(17): Show |
20 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-5333_227-5332d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 3005664 | ||||||
| chr12:3005674 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.227-5330T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005674 | |||||||
| chr12:3005699 | T | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-5305T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005699 | |||||||
| chr12:3005835 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0002g0161 |
3 | NA18943.hp1 NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.227-5169A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005835 | |||||||
| chr12:3005909 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-5095G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3005909 | |||||||
| chr12:3006040 | C | A | 43 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(40): Show |
43 | HG01167.hp2 HG01168.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.227-4964C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006040 | |||||||
| chr12:3006056 | A | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-4948A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006056 | |||||||
| chr12:3006076 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-4928G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006076 | |||||||
| chr12:3006097 | A | G | 9 | a0001c0001t0001g0081 a0001c0001t0001g0130 a0001c0001t0001g0143 others(6): Show |
9 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.227-4907A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006097 | |||||||
| chr12:3006136 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0167 a0001c0001t0001g0235 |
3 | HG00597.hp2 HG01109.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.227-4868G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006136 | |||||||
| chr12:3006222 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.227-4782G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006222 | |||||||
| chr12:3006240 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(7): Show |
10 | HG02132.hp1 HG02683.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.227-4764G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006240 | |||||||
| chr12:3006359 | A | T | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.227-4645A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006359 | |||||||
| chr12:3006458 | T | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-4546T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006458 | |||||||
| chr12:3006628 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.227-4376G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006628 | |||||||
| chr12:3006641 | G | C | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(41): Show |
44 | HG01167.hp2 HG01168.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.227-4363G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006641 | |||||||
| chr12:3006678 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-4326C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006678 | |||||||
| chr12:3006707 | T | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-4297T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006707 | |||||||
| chr12:3006950 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0181 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.227-4054C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006950 | |||||||
| chr12:3006951 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.227-4053A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006951 | |||||||
| chr12:3006968 | G | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-4036G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3006968 | |||||||
| chr12:3007036 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.227-3968A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007036 | |||||||
| chr12:3007046 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-3958C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007046 | |||||||
| chr12:3007047 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.227-3957G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007047 | |||||||
| chr12:3007087 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-3917C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007087 | |||||||
| chr12:3007088 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0181 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.227-3916G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007088 | |||||||
| chr12:3007106 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-3898C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007106 | |||||||
| chr12:3007110 | G | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
78 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-3894G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007110 | |||||||
| chr12:3007286 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.227-3718G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007286 | |||||||
| chr12:3007524 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-3480C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007524 | |||||||
| chr12:3007570 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.227-3434C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007570 | |||||||
| chr12:3007636 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.227-3368G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007636 | |||||||
| chr12:3007770 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-3234A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007770 | |||||||
| chr12:3007849 | C | T | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
57 | HG01167.hp2 HG01168.hp2 HG01192.hp1 others(54): Show |
intron_variant | MODIFIER | c.227-3155C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007849 | |||||||
| chr12:3007850 | G | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0054 a0001c0001t0001g0070 others(4): Show |
7 | HG00423.hp2 HG00558.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-3154G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007850 | |||||||
| chr12:3007895 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.227-3109C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007895 | |||||||
| chr12:3007939 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.227-3065A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3007939 | |||||||
| chr12:3008032 | G | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0190 others(4): Show |
7 | HG02615.hp1 HG02717.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-2972G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008032 | |||||||
| chr12:3008140 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.227-2864G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008140 | |||||||
| chr12:3008166 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-2838G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008166 | |||||||
| chr12:3008170 | G | C | 53 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(50): Show |
53 | HG00597.hp2 HG01109.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.227-2834G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008170 | |||||||
| chr12:3008185 | G | A | 9 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0078 others(6): Show |
9 | HG00597.hp2 HG01109.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.227-2819G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008185 | |||||||
| chr12:3008191 | G | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-2813G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008191 | |||||||
| chr12:3008200 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.227-2804T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008200 | |||||||
| chr12:3008512 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-2492C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008512 | |||||||
| chr12:3008534 | G | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0095 others(10): Show |
13 | HG00741.hp2 HG01106.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.227-2470G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008534 | |||||||
| chr12:3008615 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.227-2389C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008615 | |||||||
| chr12:3008791 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0221 |
2 | HG02683.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.227-2213A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008791 | |||||||
| chr12:3008795 | A | G | 2 | a0001c0001t0001g0097 a0001c0007t0001g0103 |
2 | HG02300.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.227-2209A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008795 | |||||||
| chr12:3008947 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-2057G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008947 | |||||||
| chr12:3008961 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-2043G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008961 | |||||||
| chr12:3008970 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.227-2034T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3008970 | |||||||
| chr12:3009069 | G | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
85 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.227-1935G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3009069 | |||||||
| chr12:3009301 | G | A | 43 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(40): Show |
43 | HG01167.hp2 HG01168.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.227-1703G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3009301 | |||||||
| chr12:3009426 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.227-1578G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3009426 | |||||||
| chr12:3009452 | AAAG | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(19): Show |
22 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.227-1544_227-1542d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 3009452 | ||||||
| chr12:3009647 | C | T | 20 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0039 others(17): Show |
20 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-1357C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3009647 | |||||||
| chr12:3009774 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.227-1230C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3009774 | |||||||
| chr12:3009920 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0204 a0001c0001t0001g0237 |
3 | HG00099.hp1 HG01358.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.227-1084C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3009920 | |||||||
| chr12:3010028 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.227-976C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010028 | |||||||
| chr12:3010058 | C | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0157 others(10): Show |
13 | HG01192.hp1 HG01257.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.227-946C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010058 | |||||||
| chr12:3010236 | C | T | 63 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(60): Show |
63 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.227-768C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010236 | |||||||
| chr12:3010340 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(19): Show |
22 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.227-664G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010340 | |||||||
| chr12:3010341 | T | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(19): Show |
22 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.227-663T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010341 | |||||||
| chr12:3010378 | G | A | 20 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0039 others(17): Show |
20 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-626G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010378 | |||||||
| chr12:3010483 | C | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0157 others(1): Show |
4 | HG01257.hp2 HG02602.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-521C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010483 | |||||||
| chr12:3010574 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0175 a0001c0001t0001g0178 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.227-430C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010574 | |||||||
| chr12:3010575 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.227-429G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010575 | |||||||
| chr12:3010583 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.227-421C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010583 | |||||||
| chr12:3010615 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.227-389C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010615 | |||||||
| chr12:3010629 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(1): Show |
4 | HG01071.hp1 HG01099.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-375G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010629 | |||||||
| chr12:3010823 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.227-181C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010823 | |||||||
| chr12:3010829 | G | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG00738.hp1 HG01433.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.227-175G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010829 | |||||||
| chr12:3010912 | C | T | 63 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(60): Show |
63 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.227-92C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010912 | |||||||
| chr12:3010924 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(23): Show |
26 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.227-80G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 3/12 | chr12 | 3010924 | |||||||
| chr12:3011175 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.291+107C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011175 | |||||||
| chr12:3011235 | C | CTT | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(19): Show |
22 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.291+169_291+170dup others(2): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 3011235 | ||||||
| chr12:3011239 | C | T | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
65 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.291+171C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011239 | |||||||
| chr12:3011284 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(227): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.291+216A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011284 | |||||||
| chr12:3011311 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.291+243A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011311 | |||||||
| chr12:3011356 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0157 others(1): Show |
4 | HG01257.hp2 HG02602.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+288G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011356 | |||||||
| chr12:3011370 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0152 |
2 | HG00140.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.291+302A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011370 | |||||||
| chr12:3011451 | C | G | 1 | a0001c0001t0001g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.291+383C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011451 | |||||||
| chr12:3011719 | G | T | 20 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0039 others(17): Show |
20 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.292-451G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011719 | |||||||
| chr12:3011726 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0070 a0001c0001t0001g0138 others(1): Show |
4 | HG00558.hp2 HG02148.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-444C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011726 | |||||||
| chr12:3011769 | G | A | 73 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(70): Show |
73 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.292-401G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011769 | |||||||
| chr12:3011790 | C | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG00597.hp2 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.292-380C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011790 | |||||||
| chr12:3011978 | T | C | 35 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(32): Show |
35 | HG01167.hp2 HG01168.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.292-192T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011978 | |||||||
| chr12:3011993 | T | C | 87 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
87 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.292-177T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3011993 | |||||||
| chr12:3012057 | C | G | 5 | a0001c0001t0001g0139 a0001c0002t0001g0104 a0001c0002t0001g0120 others(2): Show |
5 | HG01109.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-113C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 4/12 | chr12 | 3012057 | |||||||
| chr12:3012251 | G | C | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.354+19G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3012251 | |||||||
| chr12:3012286 | A | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG00597.hp2 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+54A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3012286 | |||||||
| chr12:3012499 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.354+267C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3012499 | |||||||
| chr12:3012529 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0077 others(3): Show |
6 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.354+297C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3012529 | |||||||
| chr12:3012559 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.354+327C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3012559 | |||||||
| chr12:3012680 | T | G | 87 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
87 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.354+448T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3012680 | |||||||
| chr12:3012879 | GAC | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0167 a0001c0001t0001g0235 |
3 | HG00597.hp2 HG01109.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.354+649_354+650del others(2): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 3012879 | ||||||
| chr12:3013033 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(136): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.354+801C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013033 | |||||||
| chr12:3013133 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.354+901A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013133 | |||||||
| chr12:3013140 | T | C | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
65 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.354+908T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013140 | |||||||
| chr12:3013226 | A | G | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
65 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.354+994A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013226 | |||||||
| chr12:3013232 | A | G | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
65 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.354+1000A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013232 | |||||||
| chr12:3013254 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.354+1022C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013254 | |||||||
| chr12:3013259 | A | AT | 6 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0001g0172 others(3): Show |
6 | HG00735.hp2 HG01109.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.354+1046dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 3013259 | ||||||
| chr12:3013259 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.354+1027A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013259 | |||||||
| chr12:3013259 | AT | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(7): Show |
10 | HG01496.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+1046delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 3013259 | ||||||
| chr12:3013259 | ATTTTTTT others(1): Show |
A | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
65 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.354+1039_354+1046d others(10): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 3013259 | ||||||
| chr12:3013273 | T | C | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
65 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.354+1041T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013273 | |||||||
| chr12:3013289 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(19): Show |
22 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.354+1057C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013289 | |||||||
| chr12:3013302 | C | T | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
65 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.354+1070C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013302 | |||||||
| chr12:3013354 | C | G | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(36): Show |
39 | HG01167.hp2 HG01168.hp2 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.354+1122C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013354 | |||||||
| chr12:3013389 | C | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(19): Show |
22 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.354+1157C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013389 | |||||||
| chr12:3013508 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0124 a0001c0001t0001g0126 |
3 | HG01257.hp1 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.354+1276C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013508 | |||||||
| chr12:3013552 | G | C | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.354+1320G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013552 | |||||||
| chr12:3013719 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+1487G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013719 | |||||||
| chr12:3013814 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0196 a0001c0001t0001g0223 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+1582C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013814 | |||||||
| chr12:3013875 | ATCTCTGA others(15): Show |
A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0167 |
2 | HG00597.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.354+1645_354+1666d others(24): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 3013875 | ||||||
| chr12:3013982 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+1750G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3013982 | |||||||
| chr12:3014011 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG00597.hp2 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+1779C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014011 | |||||||
| chr12:3014107 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.354+1875G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014107 | |||||||
| chr12:3014153 | C | T | 61 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(58): Show |
61 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.354+1921C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014153 | |||||||
| chr12:3014299 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0209 |
2 | NA18962.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.354+2067G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014299 | |||||||
| chr12:3014398 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0209 |
2 | NA18962.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.354+2166C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014398 | |||||||
| chr12:3014595 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG02896.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.354+2363C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014595 | |||||||
| chr12:3014630 | C | A | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(67): Show |
70 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.354+2398C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014630 | |||||||
| chr12:3014670 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG01070.hp1 HG01071.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.354+2438G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014670 | |||||||
| chr12:3014800 | C | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(121): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.354+2568C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014800 | |||||||
| chr12:3014801 | C | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.354+2569C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014801 | |||||||
| chr12:3014803 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0075 others(4): Show |
7 | HG00597.hp2 HG01109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+2571C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014803 | |||||||
| chr12:3014901 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.355-2497C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014901 | |||||||
| chr12:3014920 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.355-2478A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014920 | |||||||
| chr12:3014966 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.355-2432A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014966 | |||||||
| chr12:3014986 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0021 others(42): Show |
46 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.355-2412T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3014986 | |||||||
| chr12:3015001 | C | T | 1 | a0001c0003t0001g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.355-2397C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3015001 | |||||||
| chr12:3015114 | AG | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.355-2279delG | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 3015114 | ||||||
| chr12:3015170 | C | T | 107 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.355-2228C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3015170 | |||||||
| chr12:3015188 | C | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.355-2210C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3015188 | |||||||
| chr12:3015345 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0033 others(45): Show |
49 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.355-2053T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3015345 | |||||||
| chr12:3015415 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.355-1983C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3015415 | |||||||
| chr12:3015641 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-1757C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3015641 | |||||||
| chr12:3015680 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.355-1718A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3015680 | |||||||
| chr12:3015689 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-1709T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3015689 | |||||||
| chr12:3016015 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355-1383T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016015 | |||||||
| chr12:3016051 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.355-1347A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016051 | |||||||
| chr12:3016102 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0239 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.355-1296A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016102 | |||||||
| chr12:3016113 | TG | T | 11 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0175 others(8): Show |
11 | HG01192.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.355-1284delG | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016113 | |||||||
| chr12:3016266 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.355-1132G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016266 | |||||||
| chr12:3016330 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.355-1068G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016330 | |||||||
| chr12:3016336 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.355-1062A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016336 | |||||||
| chr12:3016474 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-924G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016474 | |||||||
| chr12:3016482 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(143): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.355-916G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016482 | |||||||
| chr12:3016539 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.355-859A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016539 | |||||||
| chr12:3016553 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.355-845C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016553 | |||||||
| chr12:3016554 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.355-844A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016554 | |||||||
| chr12:3016604 | G | GA | 12 | a0001c0001t0001g0054 a0001c0001t0001g0076 a0001c0001t0001g0078 others(9): Show |
12 | HG01192.hp1 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.355-779dupA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 3016604 | ||||||
| chr12:3016605 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.355-793A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016605 | |||||||
| chr12:3016606 | A | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0239 |
3 | HG01167.hp2 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.355-792A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016606 | |||||||
| chr12:3016617 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0239 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.355-781A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016617 | |||||||
| chr12:3016638 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0239 |
3 | HG01167.hp2 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.355-760G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016638 | |||||||
| chr12:3016874 | C | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(153): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.355-524C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016874 | |||||||
| chr12:3016918 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0239 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.355-480C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016918 | |||||||
| chr12:3016965 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0239 |
3 | HG01167.hp2 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.355-433G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3016965 | |||||||
| chr12:3017297 | A | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0234 others(2): Show |
5 | HG01106.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-101A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3017297 | |||||||
| chr12:3017324 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.355-74C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 5/12 | chr12 | 3017324 | |||||||
| chr12:3017864 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.483+338A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3017864 | |||||||
| chr12:3017883 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.483+357G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3017883 | |||||||
| chr12:3017887 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0234 others(2): Show |
5 | HG01106.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+361G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3017887 | |||||||
| chr12:3017932 | G | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0250 a0001c0001t0001g0272 |
3 | HG02559.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.483+406G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3017932 | |||||||
| chr12:3018238 | G | A | 9 | a0001c0001t0001g0170 a0001c0001t0001g0187 a0001c0001t0001g0189 others(6): Show |
9 | HG02615.hp1 HG02717.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.484-307G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3018238 | |||||||
| chr12:3018417 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.484-128T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3018417 | |||||||
| chr12:3018429 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.484-116C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3018429 | |||||||
| chr12:3018435 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.484-110C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3018435 | |||||||
| chr12:3018450 | A | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0042 others(9): Show |
12 | HG01106.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-95A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3018450 | |||||||
| chr12:3018486 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(239): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.484-59A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 6/12 | chr12 | 3018486 | |||||||
| chr12:3018702 | G | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0227 a0001c0001t0001g0239 |
3 | HG01891.hp2 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.527+114G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 7/12 | chr12 | 3018702 | |||||||
| chr12:3018905 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0239 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.528-210G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 7/12 | chr12 | 3018905 | |||||||
| chr12:3018937 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(74): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.528-178G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 7/12 | chr12 | 3018937 | |||||||
| chr12:3018949 | C | G | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.528-166C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 7/12 | chr12 | 3018949 | |||||||
| chr12:3018955 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.528-160C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 7/12 | chr12 | 3018955 | |||||||
| chr12:3018999 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.528-116G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 7/12 | chr12 | 3018999 | |||||||
| chr12:3019203 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.583+33G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019203 | |||||||
| chr12:3019250 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(43): Show |
47 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.583+80C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019250 | |||||||
| chr12:3019257 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+87G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019257 | |||||||
| chr12:3019279 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0234 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+109C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019279 | |||||||
| chr12:3019288 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.583+118C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019288 | |||||||
| chr12:3019289 | A | T | 30 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
30 | HG00099.hp1 HG01167.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.583+119A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019289 | |||||||
| chr12:3019431 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(32): Show |
35 | HG00609.hp1 HG01168.hp2 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.583+261C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019431 | |||||||
| chr12:3019432 | G | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0272 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.583+262G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019432 | |||||||
| chr12:3019454 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(31): Show |
34 | HG00099.hp1 HG01106.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.583+284C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019454 | |||||||
| chr12:3019541 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0234 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+371G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019541 | |||||||
| chr12:3019555 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
34 | HG00099.hp1 HG01167.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.583+385A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019555 | |||||||
| chr12:3019707 | TAG | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0191 a0001c0001t0001g0233 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.583+538_583+539del others(2): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019707 | |||||||
| chr12:3019767 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.583+597G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019767 | |||||||
| chr12:3019976 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0234 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.584-658C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3019976 | |||||||
| chr12:3020006 | C | G | 3 | a0001c0001t0001g0264 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG02280.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.584-628C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020006 | |||||||
| chr12:3020154 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.584-480G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020154 | |||||||
| chr12:3020186 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.584-448C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020186 | |||||||
| chr12:3020187 | G | C | 1 | a0001c0001t0001g0011 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.584-447G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020187 | |||||||
| chr12:3020204 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.584-430T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020204 | |||||||
| chr12:3020259 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.584-375T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020259 | |||||||
| chr12:3020278 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0027 others(15): Show |
19 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.584-356G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020278 | |||||||
| chr12:3020384 | CG | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
160 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.584-248delG | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 3020384 | ||||||
| chr12:3020486 | C | T | 3 | a0001c0001t0001g0264 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG02280.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.584-148C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020486 | |||||||
| chr12:3020574 | G | C | 5 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(2): Show |
5 | HG01358.hp1 HG02055.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.584-60G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020574 | |||||||
| chr12:3020589 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.584-45G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020589 | |||||||
| chr12:3020611 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.584-23T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 8/12 | chr12 | 3020611 | |||||||
| chr12:3020878 | C | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0051 others(12): Show |
15 | HG00099.hp1 HG01192.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.723+105C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3020878 | |||||||
| chr12:3021010 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0175 a0001c0001t0001g0178 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.723+237C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021010 | |||||||
| chr12:3021011 | C | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0123 others(1): Show |
4 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+238C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021011 | |||||||
| chr12:3021110 | C | T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
5 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+337C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021110 | |||||||
| chr12:3021260 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0087 others(6): Show |
9 | HG01099.hp2 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.723+487A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021260 | |||||||
| chr12:3021300 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0087 others(6): Show |
9 | HG01099.hp2 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.723+527C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021300 | |||||||
| chr12:3021307 | C | CT | 194 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.724-520dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 3021307 | ||||||
| chr12:3021307 | C | CTT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(36): Show |
40 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.724-521_724-520dup others(2): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 3021307 | ||||||
| chr12:3021307 | CT | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0087 others(6): Show |
9 | HG01099.hp2 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.724-520delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 3021307 | ||||||
| chr12:3021362 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.724-482G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021362 | |||||||
| chr12:3021434 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.724-410C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021434 | |||||||
| chr12:3021530 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.724-314T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021530 | |||||||
| chr12:3021587 | C | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0041 others(4): Show |
7 | HG01891.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.724-257C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021587 | |||||||
| chr12:3021602 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0265 |
3 | HG02723.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.724-242C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021602 | |||||||
| chr12:3021603 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.724-241A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021603 | |||||||
| chr12:3021772 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.724-72A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021772 | |||||||
| chr12:3021806 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.724-38C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 9/12 | chr12 | 3021806 | |||||||
| chr12:3022023 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(18): Show |
21 | HG01099.hp2 HG01167.hp2 HG01261.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.897+6C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022023 | |||||||
| chr12:3022033 | C | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(18): Show |
21 | HG01099.hp2 HG01167.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.897+16C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022033 | |||||||
| chr12:3022040 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0020 others(156): Show |
160 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.897+23T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022040 | |||||||
| chr12:3022072 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.897+55A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022072 | |||||||
| chr12:3022125 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0265 |
3 | HG02723.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.897+108G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022125 | |||||||
| chr12:3022204 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.897+187T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022204 | |||||||
| chr12:3022233 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.897+216C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022233 | |||||||
| chr12:3022244 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0128 |
2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.897+227G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022244 | |||||||
| chr12:3022304 | G | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0123 others(1): Show |
4 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+287G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022304 | |||||||
| chr12:3022319 | A | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0265 |
3 | HG02723.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.897+302A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022319 | |||||||
| chr12:3022362 | C | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(25): Show |
28 | HG00099.hp1 HG01109.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.897+345C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022362 | |||||||
| chr12:3022481 | A | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(155): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.897+464A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022481 | |||||||
| chr12:3022513 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.897+496C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022513 | |||||||
| chr12:3022645 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.897+628C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022645 | |||||||
| chr12:3022724 | G | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01099.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.897+707G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022724 | |||||||
| chr12:3022727 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0227 a0001c0001t0003g0236 |
3 | HG01891.hp2 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.897+710C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022727 | |||||||
| chr12:3022811 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(202): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.897+794G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022811 | |||||||
| chr12:3022999 | G | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(156): Show |
160 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.897+982G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3022999 | |||||||
| chr12:3023035 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.897+1018G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3023035 | |||||||
| chr12:3023141 | A | T | 1 | a0001c0008t0001g0036 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.897+1124A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3023141 | |||||||
| chr12:3023481 | C | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(198): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.897+1464C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3023481 | |||||||
| chr12:3023528 | C | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.897+1511C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3023528 | |||||||
| chr12:3023544 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.897+1527T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3023544 | |||||||
| chr12:3023642 | T | A | 4 | a0001c0001t0001g0240 a0001c0001t0001g0254 a0001c0001t0001g0258 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+1625T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3023642 | |||||||
| chr12:3023780 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.897+1763G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3023780 | |||||||
| chr12:3023783 | A | T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
5 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.897+1766A>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3023783 | |||||||
| chr12:3023790 | C | CA | 9 | a0001c0001t0001g0007 a0001c0001t0001g0180 a0001c0001t0001g0191 others(6): Show |
9 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.897+1789dupA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3023790 | ||||||
| chr12:3023790 | C | CAA | 176 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.897+1788_897+1789d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3023790 | ||||||
| chr12:3023790 | CA | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0057 others(7): Show |
11 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.897+1789delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3023790 | ||||||
| chr12:3024033 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.897+2016A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024033 | |||||||
| chr12:3024161 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.897+2144G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024161 | |||||||
| chr12:3024163 | C | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.897+2146C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024163 | |||||||
| chr12:3024203 | T | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(197): Show |
201 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.897+2186T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024203 | |||||||
| chr12:3024266 | C | T | 2 | a0001c0001t0001g0142 a0001c0006t0001g0129 |
2 | HG01168.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.897+2249C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024266 | |||||||
| chr12:3024267 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(191): Show |
195 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.897+2250G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024267 | |||||||
| chr12:3024342 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0265 |
3 | HG02723.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.897+2325A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024342 | |||||||
| chr12:3024423 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.897+2406C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024423 | |||||||
| chr12:3024537 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0123 |
3 | HG01099.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.897+2520G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024537 | |||||||
| chr12:3024615 | C | T | 8 | a0001c0001t0001g0180 a0001c0001t0001g0191 a0001c0001t0001g0227 others(5): Show |
8 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.897+2598C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024615 | |||||||
| chr12:3024666 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.897+2649A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024666 | |||||||
| chr12:3024733 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.897+2716C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024733 | |||||||
| chr12:3024863 | G | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.897+2846G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3024863 | |||||||
| chr12:3024913 | T | TGCC | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.897+2897_897+2899d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3024913 | ||||||
| chr12:3024947 | CT | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.897+2945delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3024947 | ||||||
| chr12:3024947 | CTT | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(205): Show |
209 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.897+2944_897+2945d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3024947 | ||||||
| chr12:3025094 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.897+3077A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025094 | |||||||
| chr12:3025181 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0265 |
3 | HG02723.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.897+3164C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025181 | |||||||
| chr12:3025185 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0239 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.897+3168C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025185 | |||||||
| chr12:3025233 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0265 |
3 | HG02723.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.897+3216C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025233 | |||||||
| chr12:3025248 | T | A | 70 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.897+3231T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025248 | |||||||
| chr12:3025271 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.897+3254C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025271 | |||||||
| chr12:3025273 | G | A | 70 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.897+3256G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025273 | |||||||
| chr12:3025350 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.897+3333C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025350 | |||||||
| chr12:3025470 | G | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.897+3453G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025470 | |||||||
| chr12:3025524 | C | CT | 7 | a0001c0001t0001g0180 a0001c0001t0001g0191 a0001c0001t0001g0233 others(4): Show |
7 | HG01358.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.897+3519dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3025524 | ||||||
| chr12:3025524 | CT | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0175 a0001c0001t0001g0177 others(11): Show |
14 | HG02451.hp1 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.897+3519delT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3025524 | ||||||
| chr12:3025597 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0107 a0001c0001t0001g0111 others(2): Show |
5 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.897+3580C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025597 | |||||||
| chr12:3025663 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(15): Show |
19 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.897+3646G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025663 | |||||||
| chr12:3025789 | G | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.897+3772G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025789 | |||||||
| chr12:3025792 | C | T | 26 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(23): Show |
26 | HG01109.hp1 HG01192.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.897+3775C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025792 | |||||||
| chr12:3025891 | T | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0123 |
3 | HG01099.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.897+3874T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025891 | |||||||
| chr12:3025906 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.897+3889C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025906 | |||||||
| chr12:3025918 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.897+3901C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3025918 | |||||||
| chr12:3025936 | C | CT | 221 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.897+3929dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3025936 | ||||||
| chr12:3026091 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.897+4074A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026091 | |||||||
| chr12:3026098 | G | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.897+4081G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026098 | |||||||
| chr12:3026106 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0181 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.897+4089A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026106 | |||||||
| chr12:3026137 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.897+4120T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026137 | |||||||
| chr12:3026236 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.897+4219C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026236 | |||||||
| chr12:3026241 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.897+4224T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026241 | |||||||
| chr12:3026242 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.897+4225A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026242 | |||||||
| chr12:3026269 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0265 |
3 | HG02723.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.897+4252C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026269 | |||||||
| chr12:3026496 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(15): Show |
19 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.897+4479C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026496 | |||||||
| chr12:3026513 | C | T | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(24): Show |
27 | HG01109.hp1 HG01192.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.897+4496C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026513 | |||||||
| chr12:3026557 | G | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(3): Show |
6 | HG02155.hp2 NA18950.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.897+4540G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026557 | |||||||
| chr12:3026626 | C | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.897+4609C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026626 | |||||||
| chr12:3026642 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(15): Show |
19 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.897+4625T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3026642 | |||||||
| chr12:3027008 | G | A | 26 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(23): Show |
26 | HG01109.hp1 HG01192.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.897+4991G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027008 | |||||||
| chr12:3027087 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.897+5070A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027087 | |||||||
| chr12:3027188 | T | C | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.897+5171T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027188 | |||||||
| chr12:3027437 | C | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0240 a0001c0001t0001g0254 others(2): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.897+5420C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027437 | |||||||
| chr12:3027466 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.897+5449T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027466 | |||||||
| chr12:3027617 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897+5600T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027617 | |||||||
| chr12:3027618 | A | G | 1 | a0001c0003t0001g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.897+5601A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027618 | |||||||
| chr12:3027724 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(232): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.897+5707A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027724 | |||||||
| chr12:3027738 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.897+5721G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027738 | |||||||
| chr12:3027742 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0057 others(12): Show |
16 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.897+5725C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027742 | |||||||
| chr12:3027901 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0057 others(8): Show |
12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.897+5884A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3027901 | |||||||
| chr12:3028140 | A | G | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.897+6123A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3028140 | |||||||
| chr12:3028156 | G | A | 4 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0123 others(1): Show |
4 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+6139G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3028156 | |||||||
| chr12:3028296 | G | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(232): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.897+6279G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3028296 | |||||||
| chr12:3028416 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0057 others(8): Show |
12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.897+6399C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3028416 | |||||||
| chr12:3028462 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0057 others(8): Show |
12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.897+6445C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3028462 | |||||||
| chr12:3028689 | G | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(2): Show |
5 | HG01358.hp1 HG02055.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.897+6672G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3028689 | |||||||
| chr12:3028968 | A | G | 15 | a0001c0001t0001g0017 a0001c0001t0001g0175 a0001c0001t0001g0177 others(12): Show |
15 | HG02451.hp1 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.897+6951A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3028968 | |||||||
| chr12:3029094 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.897+7077G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029094 | |||||||
| chr12:3029126 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.897+7109T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029126 | |||||||
| chr12:3029178 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.897+7161C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029178 | |||||||
| chr12:3029179 | G | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0057 others(8): Show |
12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.897+7162G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029179 | |||||||
| chr12:3029233 | A | AT | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(136): Show |
140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.897+7238dupT | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3029233 | ||||||
| chr12:3029233 | A | ATT | 19 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0107 others(16): Show |
19 | HG01099.hp2 HG01106.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.897+7237_897+7238d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3029233 | ||||||
| chr12:3029233 | A | ATTT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0057 others(9): Show |
13 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.897+7236_897+7238d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3029233 | ||||||
| chr12:3029233 | ATTTTTT | A | 67 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
67 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.897+7233_897+7238d others(8): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3029233 | ||||||
| chr12:3029364 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(162): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.897+7347G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029364 | |||||||
| chr12:3029382 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.897+7365C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029382 | |||||||
| chr12:3029485 | G | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0057 others(8): Show |
12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.897+7468G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029485 | |||||||
| chr12:3029504 | C | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0239 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.897+7487C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029504 | |||||||
| chr12:3029527 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0239 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.897+7510C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029527 | |||||||
| chr12:3029806 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.897+7789G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029806 | |||||||
| chr12:3029883 | A | G | 23 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
23 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.897+7866A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029883 | |||||||
| chr12:3029892 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.897+7875A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029892 | |||||||
| chr12:3029919 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.897+7902T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029919 | |||||||
| chr12:3029922 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.897+7905C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029922 | |||||||
| chr12:3029950 | C | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.897+7933C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029950 | |||||||
| chr12:3029992 | G | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(25): Show |
28 | HG01109.hp1 HG01192.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.897+7975G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3029992 | |||||||
| chr12:3030022 | G | T | 10 | a0001c0001t0001g0042 a0001c0001t0001g0187 a0001c0001t0001g0189 others(7): Show |
10 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.898-7946G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030022 | |||||||
| chr12:3030080 | C | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(25): Show |
28 | HG01109.hp1 HG01192.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.898-7888C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030080 | |||||||
| chr12:3030081 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.898-7887C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030081 | |||||||
| chr12:3030096 | T | G | 1 | a0001c0001t0001g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.898-7872T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030096 | |||||||
| chr12:3030123 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.898-7845T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030123 | |||||||
| chr12:3030186 | G | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(2): Show |
5 | HG01358.hp1 HG02055.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-7782G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030186 | |||||||
| chr12:3030235 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.898-7733C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030235 | |||||||
| chr12:3030252 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.898-7716G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030252 | |||||||
| chr12:3030447 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.898-7521C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030447 | |||||||
| chr12:3030590 | TG | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0098 a0001c0001t0001g0203 |
3 | NA18950.hp2 NA18962.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.898-7376delG | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3030590 | ||||||
| chr12:3030828 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.898-7140T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030828 | |||||||
| chr12:3030914 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.898-7054G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030914 | |||||||
| chr12:3030917 | C | T | 1 | a0001c0003t0001g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.898-7051C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030917 | |||||||
| chr12:3030949 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-7019T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3030949 | |||||||
| chr12:3031007 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.898-6961T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031007 | |||||||
| chr12:3031009 | T | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(11): Show |
14 | HG01099.hp2 HG01261.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.898-6959T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031009 | |||||||
| chr12:3031092 | G | A | 1 | a0001c0002t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.898-6876G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031092 | |||||||
| chr12:3031129 | T | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0088 a0001c0001t0001g0095 others(3): Show |
6 | HG00639.hp2 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.898-6839T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031129 | |||||||
| chr12:3031171 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.898-6797A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031171 | |||||||
| chr12:3031399 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-6569C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031399 | |||||||
| chr12:3031508 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.898-6460G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031508 | |||||||
| chr12:3031702 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-6266A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031702 | |||||||
| chr12:3031721 | C | CTG | 9 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-6246_898-6245d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3031721 | ||||||
| chr12:3031767 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-6201G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031767 | |||||||
| chr12:3031813 | C | T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): Show |
69 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.898-6155C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031813 | |||||||
| chr12:3031823 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-6145G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031823 | |||||||
| chr12:3031929 | TCTC | T | 7 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-6036_898-6034d others(5): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3031929 | ||||||
| chr12:3031957 | A | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-6011A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3031957 | |||||||
| chr12:3032041 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-5927A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032041 | |||||||
| chr12:3032049 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0226 a0001c0001t0001g0262 others(2): Show |
5 | HG02622.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-5919C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032049 | |||||||
| chr12:3032069 | G | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0123 others(1): Show |
4 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-5899G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032069 | |||||||
| chr12:3032120 | G | A | 4 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0123 others(1): Show |
4 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-5848G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032120 | |||||||
| chr12:3032202 | T | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
45 | HG01109.hp1 HG01167.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.898-5766T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032202 | |||||||
| chr12:3032273 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.898-5695A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032273 | |||||||
| chr12:3032295 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0241 a0001c0001t0001g0243 others(1): Show |
4 | HG02970.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-5673C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032295 | |||||||
| chr12:3032329 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.898-5639C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032329 | |||||||
| chr12:3032386 | C | T | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(34): Show |
37 | HG01109.hp1 HG01192.hp1 HG01358.hp1 others(34): Show |
intron_variant | MODIFIER | c.898-5582C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032386 | |||||||
| chr12:3032442 | C | A | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.898-5526C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032442 | |||||||
| chr12:3032469 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0245 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.898-5499G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032469 | |||||||
| chr12:3032527 | T | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-5441T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032527 | |||||||
| chr12:3032595 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0234 a0001c0001t0001g0247 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-5373G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032595 | |||||||
| chr12:3032731 | A | AGGGTGAG others(4): Show |
7 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-5235_898-5234i others(13): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3032731 | ||||||
| chr12:3032732 | GGTGAAAT others(4): Show |
G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.898-5234_898-5224d others(13): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3032732 | ||||||
| chr12:3032745 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.898-5223A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032745 | |||||||
| chr12:3032798 | G | A | 17 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(14): Show |
17 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.898-5170G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032798 | |||||||
| chr12:3032908 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0124 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.898-5060G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032908 | |||||||
| chr12:3032976 | C | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0171 others(2): Show |
5 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-4992C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3032976 | |||||||
| chr12:3033028 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.898-4940T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033028 | |||||||
| chr12:3033047 | C | T | 5 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(2): Show |
5 | HG01358.hp1 HG02055.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-4921C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033047 | |||||||
| chr12:3033082 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.898-4886G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033082 | |||||||
| chr12:3033103 | A | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0199 |
3 | HG03492.hp2 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.898-4865A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033103 | |||||||
| chr12:3033135 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0202 |
3 | HG00621.hp2 NA18948.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.898-4833A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033135 | |||||||
| chr12:3033151 | G | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-4817G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033151 | |||||||
| chr12:3033152 | G | T | 22 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-4816G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033152 | |||||||
| chr12:3033287 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(3): Show |
6 | HG02155.hp2 NA18950.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.898-4681C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033287 | |||||||
| chr12:3033357 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.898-4611T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033357 | |||||||
| chr12:3033375 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.898-4593C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033375 | |||||||
| chr12:3033384 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.898-4584T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033384 | |||||||
| chr12:3033390 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0105 a0001c0001t0001g0205 |
3 | HG00738.hp1 HG01433.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.898-4578C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033390 | |||||||
| chr12:3033464 | A | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(159): Show |
163 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.898-4504A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033464 | |||||||
| chr12:3033480 | A | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(159): Show |
163 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.898-4488A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033480 | |||||||
| chr12:3033503 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.898-4465C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033503 | |||||||
| chr12:3033584 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.898-4384T>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033584 | |||||||
| chr12:3033632 | G | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(2): Show |
5 | HG01358.hp1 HG02055.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-4336G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033632 | |||||||
| chr12:3033679 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-4289C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033679 | |||||||
| chr12:3033780 | C | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(38): Show |
41 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.898-4188C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033780 | |||||||
| chr12:3033833 | T | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.898-4135T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033833 | |||||||
| chr12:3033847 | GGGATATG others(380): Show |
G | 5 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(2): Show |
5 | HG01358.hp1 HG02055.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-4119_898-3733d others(2): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3033847 | ||||||
| chr12:3033938 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.898-4030C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033938 | |||||||
| chr12:3033969 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.898-3999T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3033969 | |||||||
| chr12:3034054 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0234 a0001c0001t0001g0247 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-3914C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3034054 | |||||||
| chr12:3034177 | C | T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.898-3791C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3034177 | |||||||
| chr12:3034285 | G | A | 6 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0117 others(3): Show |
6 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.898-3683G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3034285 | |||||||
| chr12:3034623 | A | G | 1 | a0001c0008t0001g0036 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.898-3345A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3034623 | |||||||
| chr12:3034687 | C | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0269 |
2 | HG01192.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.898-3281C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3034687 | |||||||
| chr12:3034804 | T | C | 6 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0117 others(3): Show |
6 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.898-3164T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3034804 | |||||||
| chr12:3034860 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.898-3108G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3034860 | |||||||
| chr12:3034931 | T | TA | 14 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0117 others(11): Show |
14 | HG00735.hp2 HG01099.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.898-3025dupA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3034931 | ||||||
| chr12:3034931 | TA | T | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.898-3025delA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3034931 | ||||||
| chr12:3035028 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.898-2940C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035028 | |||||||
| chr12:3035113 | T | TA | 142 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(139): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.898-2848dupA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3035113 | ||||||
| chr12:3035244 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.898-2724G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035244 | |||||||
| chr12:3035280 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0265 |
2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.898-2688T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035280 | |||||||
| chr12:3035352 | G | A | 6 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(3): Show |
6 | HG01358.hp1 HG02055.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.898-2616G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035352 | |||||||
| chr12:3035484 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0081 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-2484G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035484 | |||||||
| chr12:3035523 | C | T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(3): Show |
6 | HG01358.hp1 HG02055.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.898-2445C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035523 | |||||||
| chr12:3035546 | G | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.898-2422G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035546 | |||||||
| chr12:3035641 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0191 a0001c0001t0001g0234 others(2): Show |
5 | HG01106.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-2327G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035641 | |||||||
| chr12:3035658 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0197 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.898-2310A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035658 | |||||||
| chr12:3035683 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG01358.hp1 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-2285G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035683 | |||||||
| chr12:3035776 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0081 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-2192T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035776 | |||||||
| chr12:3035823 | C | CA | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.898-2130dupA | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3035823 | ||||||
| chr12:3035823 | C | CAA | 14 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0055 others(11): Show |
14 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.898-2131_898-2130d others(4): Show |
TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 3035823 | ||||||
| chr12:3035839 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.898-2129G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035839 | |||||||
| chr12:3035842 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.898-2126G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035842 | |||||||
| chr12:3035851 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.898-2117G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035851 | |||||||
| chr12:3035933 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0138 others(1): Show |
4 | HG01981.hp1 HG02148.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-2035G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035933 | |||||||
| chr12:3035978 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.898-1990T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035978 | |||||||
| chr12:3035989 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.898-1979C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3035989 | |||||||
| chr12:3036079 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0081 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-1889G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3036079 | |||||||
| chr12:3036375 | A | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.898-1593A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3036375 | |||||||
| chr12:3036409 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0081 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-1559A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3036409 | |||||||
| chr12:3036693 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.898-1275G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3036693 | |||||||
| chr12:3036737 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.898-1231G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3036737 | |||||||
| chr12:3036867 | C | T | 13 | a0001c0001t0001g0042 a0001c0001t0001g0177 a0001c0001t0001g0178 others(10): Show |
13 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.898-1101C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3036867 | |||||||
| chr12:3036882 | C | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
40 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.898-1086C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3036882 | |||||||
| chr12:3037006 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(140): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.898-962G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3037006 | |||||||
| chr12:3037067 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.898-901C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3037067 | |||||||
| chr12:3037219 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.898-749C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3037219 | |||||||
| chr12:3037245 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0191 a0001c0001t0001g0234 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-723G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3037245 | |||||||
| chr12:3037270 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.898-698G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3037270 | |||||||
| chr12:3037602 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.898-366A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3037602 | |||||||
| chr12:3037797 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.898-171C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3037797 | |||||||
| chr12:3037914 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.898-54C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 10/12 | chr12 | 3037914 | |||||||
| chr12:3038200 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1038+92G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038200 | |||||||
| chr12:3038296 | A | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1038+188A>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038296 | |||||||
| chr12:3038354 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1038+246G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038354 | |||||||
| chr12:3038465 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1038+357C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038465 | |||||||
| chr12:3038469 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0237 |
2 | NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1038+361C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038469 | |||||||
| chr12:3038726 | G | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1038+618G>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038726 | |||||||
| chr12:3038751 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1038+643G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038751 | |||||||
| chr12:3038786 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0191 a0001c0001t0001g0234 others(2): Show |
5 | HG01106.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+678T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038786 | |||||||
| chr12:3038853 | C | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(140): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1038+745C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038853 | |||||||
| chr12:3038859 | G | A | 6 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0117 others(3): Show |
6 | HG01099.hp2 HG01261.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+751G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3038859 | |||||||
| chr12:3039074 | C | T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(3): Show |
6 | HG01358.hp1 HG02055.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+966C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039074 | |||||||
| chr12:3039238 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1039-869T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039238 | |||||||
| chr12:3039310 | C | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(38): Show |
41 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1039-797C>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039310 | |||||||
| chr12:3039457 | C | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0171 |
3 | HG02258.hp2 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1039-650C>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039457 | |||||||
| chr12:3039498 | G | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(44): Show |
47 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1039-609G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039498 | |||||||
| chr12:3039560 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1039-547T>C | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039560 | |||||||
| chr12:3039698 | T | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1039-409T>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039698 | |||||||
| chr12:3039751 | G | A | 6 | a0001c0001t0001g0180 a0001c0001t0001g0233 a0001c0001t0001g0251 others(3): Show |
6 | HG01358.hp1 HG02055.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-356G>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039751 | |||||||
| chr12:3039835 | G | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(144): Show |
148 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1039-272G>T | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039835 | |||||||
| chr12:3039962 | C | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0001g0245 |
3 | HG02486.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1039-145C>A | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 11/12 | chr12 | 3039962 | |||||||
| chr12:3040317 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(151): Show |
155 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1192-48A>G | TEAD4 | ENSG00000197905.10 | transcript | ENST00000359864.8 | protein_coding | 12/12 | chr12 | 3040317 |