Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51001 |
| ensemblid | ENSG00000156469.9 |
| hgncid | 24258 |
| symbol | MTERF3 |
| name | mitochondrial transcription termination factor 3 |
| refseq_nuc | NM_015942.5 |
| refseq_prot | NP_057026.3 |
| ensembl_nuc | ENST00000287025.4 |
| ensembl_prot | ENSP00000287025.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 96239402 |
| end | 96261610 |
| strand | - |
| ver | v1.2 |
| region | chr8:96239402-96261610 |
| region5000 | chr8:96234402-96266610 |
| regionname0 | MTERF3_chr8_96239402_96261610 |
| regionname5000 | MTERF3_chr8_96234402_96266610 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 417 | 271 | 60 | 54 | 116 | 5 | 34 | 86 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| a0002 | 0/0 | 417 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| a0003 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| a0004 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| a0005 | 0/0 | 417 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| a0006 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| a0007 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| a0008 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| a0009 | 0/0 | 417 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | MALSA others(412): Show |
chr8 | 96234402 | 96266610 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1251 | 271 | 60 | 54 | 116 | 5 | 34 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 | ||
| a0002c0002 | 0/0 | 1251 | 14 | 13 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 | ||
| a0003c0004 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 | ||
| a0004c0003 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 | ||
| a0005c0009 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 | ||
| a0006c0007 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 | ||
| a0007c0008 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 | ||
| a0008c0005 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 | ||
| a0009c0006 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 1 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | ATGGC others(1246): Show |
chr8 | 96234402 | 96266610 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1463 | 234 | 39 | 53 | 102 | 5 | 33 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0001c0001t0002 | 0/0 | 1463 | 36 | 20 | 1 | 14 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0001c0001t0003 | 0/0 | 1463 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0002c0002t0003 | 0/0 | 1463 | 14 | 13 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0003c0004t0003 | 0/0 | 1463 | 2 | 2 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0004c0003t0001 | 0/0 | 1463 | 2 | 2 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0005c0009t0001 | 0/0 | 1463 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0006c0007t0001 | 0/0 | 1463 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0007c0008t0003 | 0/0 | 1463 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0008c0005t0002 | 0/0 | 1463 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| a0009c0006t0001 | 0/0 | 1463 | 1 | 0 | 0 | 0 | 1 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | GTGTA others(1458): Show |
chr8 | 96234402 | 96266610 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 4 | 5 | 2 | 3 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0002 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0004 | 1/0 | 5 | 0 | 0 | 4 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 0 | 2 | 2 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0007 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0003 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0002c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0003c0004t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0003c0004t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0004c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0004c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0005c0009t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0006c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0007c0008t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0008c0005t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| a0009c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01109 | hp1 | a0002 | c0002 | t0003 | g0014 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG01993 | hp2 | a0005 | c0009 | t0001 | g0166 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0221 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02145 | hp2 | a0003 | c0004 | t0003 | g0215 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02257 | hp1 | a0004 | c0003 | t0001 | g0056 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02280 | hp1 | a0006 | c0007 | t0001 | g0161 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0026 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02895 | hp2 | a0002 | c0002 | t0003 | g0224 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0222 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02897 | hp2 | a0002 | c0002 | t0003 | g0223 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0217 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0218 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03041 | hp1 | a0004 | c0003 | t0001 | g0049 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03041 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03453 | hp1 | a0003 | c0004 | t0003 | g0216 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03540 | hp1 | a0007 | c0008 | t0003 | g0226 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03579 | hp2 | a0008 | c0005 | t0002 | g0039 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0219 | AFR | YRI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | YRI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | LWK | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19043 | hp1 | a0002 | c0002 | t0003 | g0220 | AFR | LWK | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | LWK | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA20805 | hp1 | a0009 | c0006 | t0001 | g0176 | EUR | TSI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | GIH | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02559 | hp1 | a0002 | c0002 | t0003 | g0014 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0225 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | USA | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0167 | REF | REF | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | MTERF3_chr8_96234402_96266610 | MTERF3 | chr8 | 96234402 | 96266610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:96250952 | T | G | 2 | a0002 a0007 |
15 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
missense_variant | MODERATE | c.631A>C | p.Lys211Gln | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/8 | 751/1463 | 631/1254 | 211/417 | chr8 | 96250952 | |||
| chr8:96257010 | G | C | 1 | a0004 | 2 | HG02257.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.439C>G | p.Arg147Gly | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/8 | 559/1463 | 439/1254 | 147/417 | chr8 | 96257010 | |||
| chr8:96257085 | T | C | 1 | a0006 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.364A>G | p.Met122Val | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/8 | 484/1463 | 364/1254 | 122/417 | chr8 | 96257085 | |||
| chr8:96257096 | G | T | 1 | a0009 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.353C>A | p.Pro118Gln | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/8 | 473/1463 | 353/1254 | 118/417 | chr8 | 96257096 | |||
| chr8:96258539 | T | C | 1 | a0003 | 2 | HG02145.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.152A>G | p.Asn51Ser | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/8 | 272/1463 | 152/1254 | 51/417 | chr8 | 96258539 | |||
| chr8:96258597 | T | C | 1 | a0007 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.94A>G | p.Arg32Gly | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/8 | 214/1463 | 94/1254 | 32/417 | chr8 | 96258597 | |||
| chr8:96258605 | C | T | 1 | a0008 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.86G>A | p.Arg29His | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/8 | 206/1463 | 86/1254 | 29/417 | chr8 | 96258605 | |||
| chr8:96258630 | T | C | 1 | a0005 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.61A>G | p.Ile21Val | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/8 | 181/1463 | 61/1254 | 21/417 | chr8 | 96258630 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:96261574 | G | A | 4 | a0001c0001t0003 a0002c0002t0003 a0003c0004t0003 others(1): Show |
18 | HG01109.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-84C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/8 | 2884 | chr8 | 96261574 | ||||||
| chr8:96261601 | C | G | 2 | a0001c0001t0002 a0008c0005t0002 |
37 | HG00423.hp1 HG01081.hp1 HG01884.hp1 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-111G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/8 | 2911 | chr8 | 96261601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:96239725 | G | A | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1060-40C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96239725 | |||||||
| chr8:96239848 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1060-163A>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96239848 | |||||||
| chr8:96239979 | G | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-294C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96239979 | |||||||
| chr8:96239999 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0160 |
2 | HG00408.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1060-314C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96239999 | |||||||
| chr8:96240220 | C | G | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1060-535G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96240220 | |||||||
| chr8:96240485 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-800C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96240485 | |||||||
| chr8:96240689 | G | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-1004C>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96240689 | |||||||
| chr8:96240822 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1060-1137A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96240822 | |||||||
| chr8:96240980 | C | T | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1060-1295G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96240980 | |||||||
| chr8:96241128 | C | T | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1060-1443G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241128 | |||||||
| chr8:96241138 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1060-1453C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241138 | |||||||
| chr8:96241142 | TGGCTCAC others(11): Show |
T | 1 | a0001c0001t0001g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1060-1475_1060-145 others(22): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241142 | |||||||
| chr8:96241145 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1060-1460G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241145 | |||||||
| chr8:96241227 | T | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 |
3 | HG01109.hp2 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1060-1542A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241227 | |||||||
| chr8:96241342 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-1657C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241342 | |||||||
| chr8:96241407 | G | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG01167.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-1722C>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241407 | |||||||
| chr8:96241408 | C | CA | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG01167.hp2 HG01175.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1060-1724dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241408 | |||||||
| chr8:96241460 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0182 a0001c0001t0001g0186 others(1): Show |
7 | NA18954.hp2 NA18999.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060-1775C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241460 | |||||||
| chr8:96241560 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(89): Show |
126 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1060-1875G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96241560 | |||||||
| chr8:96242060 | C | G | 1 | a0007c0008t0003g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1059+1859G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96242060 | |||||||
| chr8:96242144 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(111): Show |
160 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1059+1775T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96242144 | |||||||
| chr8:96242494 | CTGCCCCA others(59): Show |
C | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1059+1359_1059+142 others(70): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96242494 | |||||||
| chr8:96242565 | T | C | 5 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG01891.hp1 HG03195.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+1354A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96242565 | |||||||
| chr8:96242788 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG01167.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059+1131G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96242788 | |||||||
| chr8:96242928 | T | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG01167.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+991A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96242928 | |||||||
| chr8:96243647 | A | G | 1 | a0002c0002t0003g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1059+272T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96243647 | |||||||
| chr8:96243712 | A | T | 4 | a0002c0002t0003g0014 a0002c0002t0003g0026 a0002c0002t0003g0217 others(1): Show |
7 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059+207T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96243712 | |||||||
| chr8:96243824 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1059+95T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96243824 | |||||||
| chr8:96243910 | T | C | 10 | a0002c0002t0003g0014 a0002c0002t0003g0026 a0002c0002t0003g0217 others(7): Show |
13 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059+9A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 7/7 | chr8 | 96243910 | |||||||
| chr8:96244113 | T | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(89): Show |
126 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.898-33A>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96244113 | |||||||
| chr8:96244257 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.898-177A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96244257 | |||||||
| chr8:96244557 | T | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG01167.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-477A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96244557 | |||||||
| chr8:96244577 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0069 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.898-497A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96244577 | |||||||
| chr8:96244652 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.898-572G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96244652 | |||||||
| chr8:96245138 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.897+722G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96245138 | |||||||
| chr8:96245179 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.897+681G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96245179 | |||||||
| chr8:96245382 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
279 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.897+478G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96245382 | |||||||
| chr8:96245442 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG01167.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+418C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96245442 | |||||||
| chr8:96245548 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.897+312C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96245548 | |||||||
| chr8:96245743 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.897+117T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96245743 | |||||||
| chr8:96245754 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(46): Show |
77 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.897+106A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96245754 | |||||||
| chr8:96245803 | C | T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG02886.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+57G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 6/7 | chr8 | 96245803 | |||||||
| chr8:96246017 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.826-86C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 5/7 | chr8 | 96246017 | |||||||
| chr8:96246491 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(88): Show |
125 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.678-37G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96246491 | |||||||
| chr8:96246636 | T | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG01167.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.678-182A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96246636 | |||||||
| chr8:96246836 | AT | A | 47 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(44): Show |
63 | HG00423.hp1 HG00642.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.678-383delA | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96246836 | |||||||
| chr8:96246869 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.678-415T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96246869 | |||||||
| chr8:96246940 | G | GT | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.678-487dupA | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96246940 | |||||||
| chr8:96247058 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.678-604G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96247058 | |||||||
| chr8:96247136 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.678-682G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96247136 | |||||||
| chr8:96247285 | T | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.678-831A>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96247285 | |||||||
| chr8:96247525 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.678-1071T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96247525 | |||||||
| chr8:96247548 | T | C | 4 | a0002c0002t0003g0014 a0002c0002t0003g0026 a0002c0002t0003g0217 others(1): Show |
7 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.678-1094A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96247548 | |||||||
| chr8:96247612 | C | T | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.678-1158G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96247612 | |||||||
| chr8:96247725 | C | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(125): Show |
175 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.678-1271G>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96247725 | |||||||
| chr8:96247869 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0175 a0001c0001t0002g0044 |
4 | HG02895.hp1 HG02897.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.678-1415T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96247869 | |||||||
| chr8:96248020 | A | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.678-1566T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248020 | |||||||
| chr8:96248066 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.678-1612T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248066 | |||||||
| chr8:96248103 | A | G | 3 | a0001c0001t0001g0135 a0001c0001t0002g0015 a0001c0001t0002g0016 |
5 | NA18994.hp1 NA19054.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-1649T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248103 | |||||||
| chr8:96248139 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.678-1685T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248139 | |||||||
| chr8:96248183 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.678-1729G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248183 | |||||||
| chr8:96248208 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.678-1754G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248208 | |||||||
| chr8:96248585 | GAC | G | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.678-2133_678-2132d others(4): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248585 | |||||||
| chr8:96248802 | TTTAAAAA others(35): Show |
T | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.677+2062_677+2103d others(44): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248802 | |||||||
| chr8:96248810 | A | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0016 |
4 | NA18994.hp1 NA19054.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+2096T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96248810 | |||||||
| chr8:96249081 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0133 |
2 | NA18948.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.677+1825A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249081 | |||||||
| chr8:96249269 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0170 |
2 | HG01168.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.677+1637C>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249269 | |||||||
| chr8:96249294 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0175 a0001c0001t0002g0044 |
4 | HG02895.hp1 HG02897.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+1612G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249294 | |||||||
| chr8:96249314 | C | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0139 a0001c0001t0001g0143 others(2): Show |
5 | HG02155.hp1 NA18960.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.677+1592G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249314 | |||||||
| chr8:96249478 | TATCACTC others(5): Show |
T | 1 | a0001c0001t0001g0122 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.677+1416_677+1427d others(14): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249478 | |||||||
| chr8:96249485 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.677+1421G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249485 | |||||||
| chr8:96249654 | T | C | 13 | a0001c0001t0001g0172 a0002c0002t0003g0014 a0002c0002t0003g0026 others(10): Show |
16 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.677+1252A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249654 | |||||||
| chr8:96249728 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.677+1178A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249728 | |||||||
| chr8:96249847 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.677+1059T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96249847 | |||||||
| chr8:96250075 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.677+831A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250075 | |||||||
| chr8:96250329 | G | GT | 25 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0155 others(22): Show |
29 | HG00423.hp1 HG01109.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.677+576dupA | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250329 | |||||||
| chr8:96250329 | GT | G | 26 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(23): Show |
29 | HG00408.hp1 HG00609.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.677+576delA | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250329 | |||||||
| chr8:96250330 | TTTTTTTT others(13): Show |
T | 1 | a0001c0001t0001g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.677+556_677+575del others(20): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250330 | |||||||
| chr8:96250354 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.677+552G>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250354 | |||||||
| chr8:96250394 | CAGTAATA others(6): Show |
C | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.677+499_677+511del others(13): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250394 | |||||||
| chr8:96250413 | T | TA | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0110 |
3 | HG00673.hp1 HG03834.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.677+492dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250413 | |||||||
| chr8:96250450 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
6 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+456G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250450 | |||||||
| chr8:96250531 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0182 a0001c0001t0001g0186 others(2): Show |
8 | NA18948.hp1 NA18954.hp2 NA18999.hp1 others(5): Show |
intron_variant | MODIFIER | c.677+375G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250531 | |||||||
| chr8:96250534 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(51): Show |
82 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.677+372T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250534 | |||||||
| chr8:96250536 | CCCCATCT others(22): Show |
C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.677+341_677+369del others(29): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250536 | |||||||
| chr8:96250603 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.677+303C>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250603 | |||||||
| chr8:96250606 | A | G | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.677+300T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250606 | |||||||
| chr8:96250609 | C | A | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.677+297G>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250609 | |||||||
| chr8:96250609 | C | CGGCGGAG others(569): Show |
1 | a0001c0001t0001g0127 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.677+296_677+297ins others(576): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250609 | |||||||
| chr8:96250610 | T | G | 5 | a0001c0001t0001g0080 a0001c0001t0001g0127 a0001c0001t0003g0214 others(2): Show |
5 | HG01928.hp2 HG02040.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.677+296A>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250610 | |||||||
| chr8:96250610 | T | TGAGGAGG others(622): Show |
1 | a0001c0001t0001g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.677+295_677+296ins others(629): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250610 | |||||||
| chr8:96250610 | T | TGAGGAGG others(521): Show |
1 | a0001c0001t0001g0147 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.677+295_677+296ins others(528): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250610 | |||||||
| chr8:96250610 | T | TGAGGAGG others(119): Show |
1 | a0001c0001t0001g0090 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.677+295_677+296ins others(126): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250610 | |||||||
| chr8:96250610 | T | TGAGGAGG others(143): Show |
1 | a0005c0009t0001g0166 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.677+295_677+296ins others(150): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250610 | |||||||
| chr8:96250613 | G | A | 4 | a0001c0001t0001g0080 a0001c0001t0003g0214 a0003c0004t0003g0215 others(1): Show |
4 | HG02040.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+293C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAAGACG others(128): Show |
1 | a0001c0001t0001g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.677+292_677+293ins others(135): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAAGCAG others(410): Show |
1 | a0001c0001t0001g0139 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.677+292_677+293ins others(417): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAAGCAG others(410): Show |
1 | a0001c0001t0001g0143 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.677+292_677+293ins others(417): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAAGCAG others(422): Show |
2 | a0001c0001t0001g0118 a0001c0001t0001g0145 |
2 | NA18960.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.677+292_677+293ins others(429): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAAGCAG others(425): Show |
1 | a0001c0001t0001g0171 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.677+292_677+293ins others(432): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAGGAGG others(224): Show |
1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.677+292_677+293ins others(231): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAGGAGG others(53): Show |
1 | a0001c0001t0001g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.677+292_677+293ins others(60): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAGGAGG others(56): Show |
1 | a0001c0001t0001g0170 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.677+292_677+293ins others(63): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAGGAGG others(77): Show |
1 | a0001c0001t0001g0094 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.677+292_677+293ins others(84): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250613 | G | GGAGGAGG others(539): Show |
1 | a0001c0001t0001g0128 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.677+292_677+293ins others(546): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250613 | |||||||
| chr8:96250615 | C | A | 26 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0084 others(23): Show |
26 | HG01168.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.677+291G>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CA | 4 | a0001c0001t0001g0076 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | HG00673.hp1 HG03834.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+290dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGA | 3 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0135 |
7 | HG00639.hp1 HG01081.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+285_677+290dup others(6): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(68): Show |
1 | a0001c0001t0002g0044 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.677+290_677+291ins others(75): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(55): Show |
1 | a0001c0001t0001g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.677+290_677+291ins others(62): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(58): Show |
1 | a0001c0001t0001g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.677+290_677+291ins others(65): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(67): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0175 |
3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.677+290_677+291ins others(74): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(81): Show |
1 | a0001c0001t0001g0097 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.677+290_677+291ins others(88): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(2): Show |
5 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0085 others(2): Show |
9 | HG00280.hp2 HG00597.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.677+282_677+290dup others(9): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(80): Show |
1 | a0001c0001t0001g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.677+290_677+291ins others(87): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(5): Show |
1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.677+279_677+290dup others(12): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(8): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0138 |
5 | HG00609.hp1 HG02004.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.677+276_677+290dup others(15): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(11): Show |
1 | a0001c0001t0001g0008 | 4 | HG01934.hp2 HG04115.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+273_677+290dup others(18): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(17): Show |
1 | a0001c0001t0001g0141 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.677+267_677+290dup others(24): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(20): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0142 |
2 | HG01981.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.677+264_677+290dup others(27): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(26): Show |
1 | a0001c0001t0001g0144 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.677+258_677+290dup others(33): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(29): Show |
1 | a0001c0001t0001g0020 | 2 | HG01358.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.677+255_677+290dup others(36): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(35): Show |
1 | a0001c0001t0001g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.677+249_677+290dup others(42): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(41): Show |
1 | a0001c0001t0001g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.677+243_677+290dup others(48): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(455): Show |
1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.677+290_677+291ins others(462): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(128): Show |
1 | a0001c0001t0001g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.677+290_677+291ins others(135): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(140): Show |
1 | a0001c0001t0001g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.677+290_677+291ins others(147): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(268): Show |
1 | a0001c0001t0001g0081 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.677+290_677+291ins others(275): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(488): Show |
1 | a0001c0001t0001g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.677+290_677+291ins others(495): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(156): Show |
1 | a0001c0001t0001g0134 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.677+290_677+291ins others(163): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CAGAAGAA others(79): Show |
1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.677+290_677+291ins others(86): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | C | CTGAGGCA others(951): Show |
1 | a0001c0001t0001g0159 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.677+290_677+291ins others(958): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | CAGA | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0089 a0001c0001t0001g0130 others(4): Show |
7 | HG02080.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+288_677+290del others(3): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | CAGAAGA | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0156 a0001c0001t0002g0040 |
3 | NA18942.hp1 NA19078.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.677+285_677+290del others(6): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | CAGAAGAA others(2): Show |
C | 3 | a0002c0002t0003g0218 a0002c0002t0003g0221 a0002c0002t0003g0224 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.677+282_677+290del others(9): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | CAGAAGAA others(5): Show |
C | 10 | a0001c0001t0001g0172 a0001c0001t0002g0028 a0002c0002t0003g0014 others(7): Show |
13 | HG01081.hp1 HG01109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.677+279_677+290del others(12): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250615 | CAGAAGAA others(8): Show |
C | 1 | a0008c0005t0002g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.677+276_677+290del others(15): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250615 | |||||||
| chr8:96250616 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0005c0009t0001g0166 |
3 | HG01358.hp2 HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.677+290T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250616 | |||||||
| chr8:96250617 | G | GAAGAAAA others(33): Show |
1 | a0001c0001t0001g0204 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.677+288_677+289ins others(40): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250617 | |||||||
| chr8:96250618 | A | AAGGAAGA others(449): Show |
1 | a0006c0007t0001g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.677+287_677+288ins others(456): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250618 | |||||||
| chr8:96250619 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.677+287T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250619 | |||||||
| chr8:96250620 | G | GA | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.677+285dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250620 | |||||||
| chr8:96250620 | G | GAA | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(32): Show |
58 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.677+284_677+285dup others(2): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250620 | |||||||
| chr8:96250620 | G | GAAAAGAA others(30): Show |
1 | a0001c0001t0001g0192 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.677+285_677+286ins others(37): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250620 | |||||||
| chr8:96250620 | G | GAAAAGAA others(37): Show |
8 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0189 others(5): Show |
12 | HG01069.hp1 HG02015.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.677+285_677+286ins others(44): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250620 | |||||||
| chr8:96250620 | G | GAAAGAAG others(54): Show |
1 | a0001c0001t0001g0098 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.677+285_677+286ins others(61): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250620 | |||||||
| chr8:96250622 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01358.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.677+284T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250622 | |||||||
| chr8:96250623 | G | GAAGAAAG others(46): Show |
1 | a0001c0001t0001g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.677+282_677+283ins others(53): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250623 | |||||||
| chr8:96250624 | A | G | 1 | a0006c0007t0001g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.677+282T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250624 | |||||||
| chr8:96250625 | A | AAGAAGAA others(418): Show |
1 | a0001c0001t0001g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.677+280_677+281ins others(425): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250625 | |||||||
| chr8:96250625 | A | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 |
4 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+281T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250625 | |||||||
| chr8:96250625 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0147 |
2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.677+281T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250625 | |||||||
| chr8:96250626 | G | GAA | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 |
3 | HG01109.hp2 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.677+278_677+279dup others(2): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250626 | |||||||
| chr8:96250626 | GA | G | 3 | a0001c0001t0001g0083 a0001c0001t0002g0029 a0001c0001t0002g0033 |
3 | HG01891.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.677+279delT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250626 | |||||||
| chr8:96250627 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.677+279T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250627 | |||||||
| chr8:96250628 | A | AGGGCGGG others(3): Show |
1 | a0001c0001t0001g0119 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.677+277_677+278ins others(10): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250628 | |||||||
| chr8:96250628 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.677+278T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250628 | |||||||
| chr8:96250629 | G | GA | 5 | a0001c0001t0001g0084 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG00609.hp2 HG01106.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.677+276dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250629 | |||||||
| chr8:96250629 | G | GAAGAAGA others(26): Show |
1 | a0001c0001t0001g0188 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.677+276_677+277ins others(33): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250629 | |||||||
| chr8:96250630 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.677+276T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250630 | |||||||
| chr8:96250631 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.677+275T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250631 | |||||||
| chr8:96250632 | G | GAAGAAGA others(23): Show |
2 | a0001c0001t0001g0178 a0001c0001t0001g0193 |
2 | HG01256.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.677+273_677+274ins others(30): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250632 | |||||||
| chr8:96250633 | A | AAGGAGAA others(263): Show |
1 | a0001c0001t0001g0122 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.677+272_677+273ins others(270): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250633 | |||||||
| chr8:96250634 | A | AGAAGAAG others(566): Show |
1 | a0001c0001t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.677+271_677+272ins others(573): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250634 | |||||||
| chr8:96250636 | A | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0149 |
2 | HG02523.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.677+270T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250636 | |||||||
| chr8:96250637 | A | AGAAGAAG others(509): Show |
1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.677+268_677+269ins others(516): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250637 | |||||||
| chr8:96250637 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.677+269T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250637 | |||||||
| chr8:96250638 | G | GA | 4 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0150 others(1): Show |
4 | HG00609.hp2 HG03831.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+267dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250638 | |||||||
| chr8:96250638 | G | GAAGAAGA others(17): Show |
1 | a0001c0001t0001g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.677+267_677+268ins others(24): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250638 | |||||||
| chr8:96250639 | A | AAGGAGGA others(17): Show |
1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.677+266_677+267ins others(24): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250639 | |||||||
| chr8:96250639 | A | AAGGAGGA others(20): Show |
7 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0063 others(4): Show |
10 | HG00642.hp1 HG00738.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.677+266_677+267ins others(27): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250639 | |||||||
| chr8:96250639 | A | AAGGAGGA others(23): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0073 |
2 | HG01167.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.677+266_677+267ins others(30): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250639 | |||||||
| chr8:96250639 | A | AAGGAGGA others(26): Show |
1 | a0001c0001t0001g0066 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.677+266_677+267ins others(33): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250639 | |||||||
| chr8:96250640 | A | AGAAGAC | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.677+265_677+266ins others(6): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250640 | |||||||
| chr8:96250642 | A | AAAGAAGA others(167): Show |
1 | a0001c0001t0001g0084 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.677+263_677+264ins others(174): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250642 | |||||||
| chr8:96250642 | A | AGGAGGAG others(25): Show |
1 | a0001c0001t0001g0072 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.677+263_677+264ins others(32): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250642 | |||||||
| chr8:96250642 | A | G | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.677+264T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250642 | |||||||
| chr8:96250643 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.677+263T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250643 | |||||||
| chr8:96250645 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.677+261T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250645 | |||||||
| chr8:96250645 | A | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(14): Show |
20 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.677+261T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250645 | |||||||
| chr8:96250646 | A | AGAGGAAG others(707): Show |
1 | a0001c0001t0001g0080 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.677+259_677+260ins others(714): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250646 | |||||||
| chr8:96250646 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.677+260T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250646 | |||||||
| chr8:96250647 | G | GA | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0150 |
3 | HG00609.hp2 NA19004.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.677+258dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250647 | |||||||
| chr8:96250647 | G | GAAAGAAG others(8): Show |
28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(25): Show |
51 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.677+258_677+259ins others(15): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250647 | |||||||
| chr8:96250648 | A | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(18): Show |
24 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.677+258T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250648 | |||||||
| chr8:96250649 | A | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.677+257T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250649 | |||||||
| chr8:96250650 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0002g0029 a0001c0001t0002g0033 |
3 | HG01891.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.677+256C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250650 | |||||||
| chr8:96250650 | G | GAAAGAAG others(8): Show |
1 | a0001c0001t0001g0187 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.677+255_677+256ins others(15): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250650 | |||||||
| chr8:96250651 | A | AAGAAGGA others(1079): Show |
1 | a0001c0001t0001g0115 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.677+254_677+255ins others(1086): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250651 | |||||||
| chr8:96250651 | A | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(13): Show |
19 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.677+255T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250651 | |||||||
| chr8:96250652 | A | AGAAGAAG others(625): Show |
1 | a0001c0001t0001g0121 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.677+253_677+254ins others(632): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250652 | |||||||
| chr8:96250652 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.677+254T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250652 | |||||||
| chr8:96250654 | A | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(15): Show |
21 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.677+252T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250654 | |||||||
| chr8:96250655 | A | AG | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0150 |
3 | HG00609.hp2 NA19004.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.677+250dupC | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250655 | |||||||
| chr8:96250657 | A | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(14): Show |
20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.677+249T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250657 | |||||||
| chr8:96250658 | A | C | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.677+248T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250658 | |||||||
| chr8:96250658 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0126 a0001c0001t0001g0163 |
3 | HG02040.hp1 HG02273.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.677+248T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250658 | |||||||
| chr8:96250660 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(16): Show |
22 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.677+246T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250660 | |||||||
| chr8:96250661 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02040.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.677+245T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250661 | |||||||
| chr8:96250663 | A | AAGGAGGA others(95): Show |
1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.677+242_677+243ins others(102): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250663 | |||||||
| chr8:96250663 | A | G | 5 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0070 others(2): Show |
5 | HG02451.hp1 HG02523.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.677+243T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250663 | |||||||
| chr8:96250666 | A | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(15): Show |
21 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.677+240T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250666 | |||||||
| chr8:96250667 | A | AGAAGAAG others(164): Show |
1 | a0001c0001t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.677+238_677+239ins others(171): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250667 | |||||||
| chr8:96250667 | A | C | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.677+239T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250667 | |||||||
| chr8:96250667 | A | G | 1 | a0007c0008t0003g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.677+239T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250667 | |||||||
| chr8:96250667 | AG | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0110 |
3 | HG00673.hp1 HG03834.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.677+238delC | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250667 | |||||||
| chr8:96250669 | A | AAGGAGGA others(68): Show |
1 | a0001c0001t0002g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.677+236_677+237ins others(75): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250669 | |||||||
| chr8:96250669 | A | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0070 others(3): Show |
6 | HG02451.hp1 HG02683.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+237T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250669 | |||||||
| chr8:96250670 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.677+236T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250670 | |||||||
| chr8:96250672 | A | AAGGAGGA others(71): Show |
1 | a0001c0001t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.677+233_677+234ins others(78): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250672 | |||||||
| chr8:96250672 | A | AAGGAGGA others(128): Show |
1 | a0001c0001t0001g0150 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.677+233_677+234ins others(135): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250672 | |||||||
| chr8:96250672 | A | G | 29 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0050 others(26): Show |
34 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.677+234T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250672 | |||||||
| chr8:96250673 | A | G | 2 | a0001c0001t0001g0050 a0007c0008t0003g0226 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.677+233T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250673 | |||||||
| chr8:96250675 | A | AAGGAGGA others(113): Show |
1 | a0001c0001t0001g0109 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.677+230_677+231ins others(120): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250675 | |||||||
| chr8:96250675 | A | AAGGAGGA others(122): Show |
1 | a0001c0001t0001g0108 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.677+230_677+231ins others(129): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250675 | |||||||
| chr8:96250675 | A | G | 27 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0001g0068 others(24): Show |
36 | HG00609.hp2 HG01109.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.677+231T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250675 | |||||||
| chr8:96250676 | A | C | 2 | a0003c0004t0003g0215 a0003c0004t0003g0216 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.677+230T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250676 | |||||||
| chr8:96250676 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0189 others(3): Show |
10 | HG01069.hp1 HG02015.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.677+230T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250676 | |||||||
| chr8:96250678 | A | AAAGAAGA others(129): Show |
1 | a0001c0001t0001g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.677+227_677+228ins others(136): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | AAAGAAGA others(189): Show |
1 | a0001c0001t0001g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.677+227_677+228ins others(196): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | AAAGAAGA others(198): Show |
1 | a0001c0001t0001g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.677+227_677+228ins others(205): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | AAGGAGAA others(227): Show |
1 | a0001c0001t0001g0113 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.677+227_677+228ins others(234): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | AAGGAGG | 3 | a0001c0001t0001g0092 a0001c0001t0002g0011 a0001c0001t0002g0015 |
6 | HG02155.hp2 NA18970.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.677+227_677+228ins others(6): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | ACGAGGAA others(137): Show |
1 | a0001c0001t0001g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.677+227_677+228ins others(144): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | AGATGAAG others(4): Show |
1 | a0001c0001t0002g0030 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.677+227_677+228ins others(11): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | AGGAAGAA others(427): Show |
1 | a0001c0001t0001g0076 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.677+227_677+228ins others(434): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.677+228T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250678 | A | G | 43 | a0001c0001t0001g0050 a0001c0001t0001g0059 a0001c0001t0001g0062 others(40): Show |
52 | HG00609.hp2 HG01081.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.677+228T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250678 | |||||||
| chr8:96250679 | A | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(8): Show |
15 | HG01069.hp1 HG01255.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.677+227T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250679 | |||||||
| chr8:96250681 | A | AAAAGAAG others(160): Show |
1 | a0001c0001t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(167): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAAGAAGA others(199): Show |
1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(206): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAAAG others(175): Show |
1 | a0001c0001t0001g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(182): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAAAG others(178): Show |
1 | a0001c0001t0001g0107 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(185): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAA others(127): Show |
1 | a0001c0001t0001g0162 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(134): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAA others(626): Show |
1 | a0001c0001t0001g0120 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(633): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAA others(326): Show |
1 | a0001c0001t0001g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(333): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAA others(365): Show |
1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(372): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAA others(32): Show |
1 | a0001c0001t0002g0043 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(39): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAA others(20): Show |
1 | a0001c0001t0001g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(27): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAA others(23): Show |
1 | a0001c0001t0002g0035 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(30): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAA others(8): Show |
1 | a0001c0001t0001g0160 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(15): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAC others(167): Show |
1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(174): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAC others(161): Show |
1 | a0001c0001t0001g0021 | 2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.677+224_677+225ins others(168): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGAAGAC others(161): Show |
1 | a0001c0001t0001g0168 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(168): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGGAGAA others(836): Show |
1 | a0001c0001t0001g0119 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(843): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGGAGGA others(29): Show |
1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(36): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AAGGAGGA others(56): Show |
1 | a0001c0001t0001g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(63): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AGGAAGAA others(422): Show |
1 | a0001c0001t0001g0077 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(429): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AGGAAGAA others(332): Show |
1 | a0001c0001t0001g0098 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(339): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AGGAAGAA others(317): Show |
1 | a0001c0001t0001g0097 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(324): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AGGAAGAG others(14): Show |
1 | a0001c0001t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(21): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AGGAGGG | 3 | a0001c0001t0001g0178 a0001c0001t0001g0193 a0001c0001t0001g0205 |
3 | HG01256.hp1 HG02055.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.677+224_677+225ins others(6): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AGGAGGGA others(17): Show |
1 | a0001c0001t0001g0094 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.677+224_677+225ins others(24): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AGGAGGGA others(5): Show |
7 | a0001c0001t0001g0022 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
8 | HG02698.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.677+224_677+225ins others(12): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | AGGGAGGA others(14): Show |
1 | a0001c0001t0001g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.677+224_677+225ins others(21): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250681 | A | G | 74 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(71): Show |
92 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.677+225T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250681 | |||||||
| chr8:96250682 | A | AGAAGAAG others(47): Show |
1 | a0001c0001t0001g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.677+223_677+224ins others(54): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(34): Show |
1 | a0001c0001t0001g0195 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.677+223_677+224ins others(41): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(32): Show |
1 | a0001c0001t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.677+223_677+224ins others(39): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(26): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0095 others(7): Show |
19 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.677+223_677+224ins others(33): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(31): Show |
1 | a0001c0001t0001g0187 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.677+223_677+224ins others(38): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(24): Show |
1 | a0001c0001t0001g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.677+223_677+224ins others(31): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(23): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0001g0180 others(10): Show |
26 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.677+223_677+224ins others(30): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(24): Show |
2 | a0001c0001t0001g0194 a0001c0001t0001g0209 |
2 | HG01884.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.677+223_677+224ins others(31): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(20): Show |
1 | a0001c0001t0001g0024 | 2 | HG03130.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.677+223_677+224ins others(27): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(23): Show |
1 | a0001c0001t0001g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.677+223_677+224ins others(30): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(35): Show |
1 | a0001c0001t0001g0047 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.677+223_677+224ins others(42): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAAG others(17): Show |
1 | a0001c0001t0001g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.677+223_677+224ins others(24): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | AGAAGAGG others(23): Show |
1 | a0001c0001t0001g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.677+223_677+224ins others(30): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250682 | A | G | 5 | a0001c0001t0001g0170 a0001c0001t0001g0188 a0001c0001t0001g0199 others(2): Show |
5 | HG01168.hp2 HG01255.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677+224T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250682 | |||||||
| chr8:96250684 | G | A | 9 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0060 others(6): Show |
9 | HG00673.hp2 HG01167.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.677+222C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250684 | |||||||
| chr8:96250685 | A | AAGAAGAA others(35): Show |
1 | a0001c0001t0001g0186 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.677+220_677+221ins others(42): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250685 | |||||||
| chr8:96250685 | A | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(17): Show |
25 | HG01069.hp1 HG01099.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.677+221T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250685 | |||||||
| chr8:96250687 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0149 |
2 | HG02523.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.677+219C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250687 | |||||||
| chr8:96250688 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(37): Show |
63 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.677+218T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250688 | |||||||
| chr8:96250691 | A | AGAAGAAG others(538): Show |
1 | a0001c0001t0001g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.677+214_677+215ins others(545): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250691 | |||||||
| chr8:96250691 | A | AGAAGGAG others(60): Show |
1 | a0001c0001t0001g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.677+214_677+215ins others(67): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250691 | |||||||
| chr8:96250691 | A | AGAAGGAG others(61): Show |
1 | a0001c0001t0001g0068 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.677+214_677+215ins others(68): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250691 | |||||||
| chr8:96250691 | A | G | 22 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(19): Show |
27 | HG01069.hp1 HG01099.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.677+215T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250691 | |||||||
| chr8:96250694 | A | AG | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(43): Show |
65 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.677+211dupC | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250694 | A | AGGAG | 7 | a0001c0001t0001g0060 a0001c0001t0001g0080 a0001c0001t0001g0132 others(4): Show |
8 | HG00673.hp2 HG02040.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.677+211_677+212ins others(4): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250694 | A | AGGAGGAG | 5 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0001c0001t0001g0171 others(2): Show |
7 | HG01069.hp2 HG02155.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+211_677+212ins others(7): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250694 | A | AGGAGGAG others(3): Show |
2 | a0001c0001t0001g0139 a0001c0001t0002g0018 |
2 | NA19005.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.677+211_677+212ins others(10): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250694 | A | AGGAGGAG others(15): Show |
1 | a0001c0001t0001g0170 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.677+211_677+212ins others(22): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250694 | A | AGGAGGAG others(30): Show |
1 | a0001c0001t0001g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.677+211_677+212ins others(37): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250694 | A | AGGAGGAG others(51): Show |
1 | a0001c0001t0001g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.677+211_677+212ins others(58): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250694 | A | AGGAGGAG others(3): Show |
1 | a0001c0001t0001g0143 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.677+211_677+212ins others(10): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250694 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(38): Show |
64 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.677+212T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250694 | |||||||
| chr8:96250695 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.677+211C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250695 | |||||||
| chr8:96250695 | G | GGAGGAGG others(67): Show |
1 | a0001c0001t0002g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.677+210_677+211ins others(74): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250695 | |||||||
| chr8:96250695 | G | GGGGGAGG others(49): Show |
1 | a0001c0001t0001g0072 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.677+210_677+211ins others(56): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250695 | |||||||
| chr8:96250696 | G | GA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(26): Show |
52 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.677+209_677+210ins others(1): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GAGGAGGA others(80): Show |
1 | a0001c0001t0001g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.677+209_677+210ins others(87): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GAGGAGGA others(87): Show |
1 | a0003c0004t0003g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.677+209_677+210ins others(94): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GAGGAGGA others(83): Show |
2 | a0001c0001t0003g0214 a0003c0004t0003g0216 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.677+209_677+210ins others(90): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GAGGGGGA others(6): Show |
2 | a0001c0001t0001g0199 a0001c0001t0001g0207 |
2 | NA18939.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.677+209_677+210ins others(13): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GAGGGGGA others(31): Show |
1 | a0001c0001t0001g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.677+209_677+210ins others(38): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGAGGGGG others(8): Show |
1 | a0001c0001t0001g0188 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.677+209_677+210ins others(15): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGA | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0052 others(10): Show |
15 | HG01069.hp1 HG01256.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.677+209_677+210ins others(4): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGAGGG others(3): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
8 | HG02148.hp1 HG02273.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.677+209_677+210ins others(10): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGAGGG others(33): Show |
1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.677+209_677+210ins others(40): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGAGGG others(42): Show |
1 | a0001c0001t0001g0012 | 3 | HG02886.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.677+209_677+210ins others(49): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGAGGG others(44): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0074 |
3 | HG02004.hp2 HG02976.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.677+209_677+210ins others(51): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGAGGG others(45): Show |
4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0069 others(1): Show |
4 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+209_677+210ins others(52): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGAGGG others(45): Show |
1 | a0001c0001t0001g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.677+209_677+210ins others(52): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGAGGG others(46): Show |
1 | a0001c0001t0001g0019 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.677+209_677+210ins others(53): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGAGG others(4): Show |
1 | a0001c0001t0001g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.677+209_677+210ins others(11): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGAG others(5): Show |
1 | a0001c0001t0001g0068 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.677+198_677+209dup others(12): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGAG others(17): Show |
1 | a0002c0002t0003g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.677+209_677+210ins others(24): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGAG others(41): Show |
1 | a0002c0002t0003g0014 | 3 | HG01109.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.677+209_677+210ins others(48): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGAG others(47): Show |
3 | a0002c0002t0003g0217 a0002c0002t0003g0218 a0002c0002t0003g0223 |
3 | HG02897.hp2 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.677+209_677+210ins others(54): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGAG others(59): Show |
1 | a0002c0002t0003g0224 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.677+209_677+210ins others(66): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGAG others(66): Show |
1 | a0002c0002t0003g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.677+209_677+210ins others(73): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGGA others(42): Show |
1 | a0002c0002t0003g0026 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.677+209_677+210ins others(49): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGGA others(48): Show |
1 | a0002c0002t0003g0222 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.677+209_677+210ins others(55): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGGA others(79): Show |
1 | a0002c0002t0003g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.677+209_677+210ins others(86): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGGA others(32): Show |
1 | a0002c0002t0003g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.677+209_677+210ins others(39): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250696 | G | GGGGGGGG others(32): Show |
1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.677+209_677+210ins others(39): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250696 | |||||||
| chr8:96250697 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0104 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.677+209C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250697 | |||||||
| chr8:96250699 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.677+207C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250699 | |||||||
| chr8:96250700 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.677+206C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250700 | |||||||
| chr8:96250702 | A | AGGAGGAG others(166): Show |
1 | a0001c0001t0001g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.677+203_677+204ins others(173): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250702 | |||||||
| chr8:96250702 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
4 | HG00738.hp1 HG01109.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+204T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250702 | |||||||
| chr8:96250708 | A | AGGGGGGA others(45): Show |
1 | a0001c0001t0001g0071 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.677+197_677+198ins others(52): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250708 | |||||||
| chr8:96250711 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(50): Show |
81 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.677+195C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250711 | |||||||
| chr8:96250716 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0155 |
2 | HG03225.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.677+190T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250716 | |||||||
| chr8:96250784 | C | CA | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(58): Show |
89 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.677+121dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250784 | |||||||
| chr8:96250792 | A | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.677+114T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | 96250792 | |||||||
| chr8:96251190 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(129): Show |
179 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.488-95G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96251190 | |||||||
| chr8:96251449 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.488-354C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96251449 | |||||||
| chr8:96251505 | C | G | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.488-410G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96251505 | |||||||
| chr8:96251587 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.488-492C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96251587 | |||||||
| chr8:96251611 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.488-516G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96251611 | |||||||
| chr8:96251702 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(52): Show |
83 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.488-607A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96251702 | |||||||
| chr8:96252001 | T | C | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.488-906A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252001 | |||||||
| chr8:96252022 | C | T | 9 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
12 | HG01109.hp1 HG01167.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.488-927G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252022 | |||||||
| chr8:96252211 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.488-1116C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252211 | |||||||
| chr8:96252226 | T | C | 15 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.488-1131A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252226 | |||||||
| chr8:96252228 | C | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(47): Show |
78 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.488-1133G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252228 | |||||||
| chr8:96252303 | A | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(15): Show |
21 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.488-1208T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252303 | |||||||
| chr8:96252553 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.488-1458G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252553 | |||||||
| chr8:96252584 | A | G | 5 | a0002c0002t0003g0014 a0002c0002t0003g0026 a0002c0002t0003g0217 others(2): Show |
8 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-1489T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252584 | |||||||
| chr8:96252587 | T | G | 1 | a0001c0001t0001g0093 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.488-1492A>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252587 | |||||||
| chr8:96252603 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.488-1508G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252603 | |||||||
| chr8:96252721 | C | G | 1 | a0002c0002t0003g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.488-1626G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252721 | |||||||
| chr8:96252722 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.488-1627C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96252722 | |||||||
| chr8:96253040 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.488-1945C>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253040 | |||||||
| chr8:96253085 | G | A | 5 | a0002c0002t0003g0221 a0002c0002t0003g0222 a0002c0002t0003g0223 others(2): Show |
5 | HG02145.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-1990C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253085 | |||||||
| chr8:96253205 | T | C | 3 | a0001c0001t0003g0214 a0003c0004t0003g0215 a0003c0004t0003g0216 |
3 | HG02145.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.488-2110A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253205 | |||||||
| chr8:96253254 | A | C | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.488-2159T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253254 | |||||||
| chr8:96253267 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0204 |
3 | NA18939.hp2 NA19088.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.488-2172C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253267 | |||||||
| chr8:96253419 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.488-2324A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253419 | |||||||
| chr8:96253714 | A | G | 24 | a0001c0001t0001g0092 a0001c0001t0002g0003 a0001c0001t0002g0010 others(21): Show |
36 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.488-2619T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253714 | |||||||
| chr8:96253840 | AT | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0062 others(20): Show |
26 | HG00597.hp2 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.488-2746delA | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253840 | |||||||
| chr8:96253842 | T | TA | 12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0151 others(9): Show |
12 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.488-2748_488-2747i others(3): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253842 | |||||||
| chr8:96253843 | T | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(195): Show |
259 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.488-2748A>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253843 | |||||||
| chr8:96253843 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.488-2748A>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253843 | |||||||
| chr8:96253909 | G | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02965.hp2 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.488-2814C>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96253909 | |||||||
| chr8:96254221 | T | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+2741A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96254221 | |||||||
| chr8:96254804 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.487+2158A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96254804 | |||||||
| chr8:96254847 | A | G | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.487+2115T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96254847 | |||||||
| chr8:96254956 | T | G | 12 | a0002c0002t0003g0014 a0002c0002t0003g0026 a0002c0002t0003g0217 others(9): Show |
15 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.487+2006A>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96254956 | |||||||
| chr8:96255150 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.487+1812A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255150 | |||||||
| chr8:96255285 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.487+1677A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255285 | |||||||
| chr8:96255294 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.487+1668A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255294 | |||||||
| chr8:96255576 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.487+1386C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255576 | |||||||
| chr8:96255583 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.487+1379C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255583 | |||||||
| chr8:96255639 | G | GA | 15 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0085 others(12): Show |
15 | HG00423.hp1 HG00438.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.487+1322dupT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255639 | |||||||
| chr8:96255639 | GA | G | 11 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0051 others(8): Show |
11 | HG02717.hp2 HG02809.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+1322delT | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255639 | |||||||
| chr8:96255741 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487+1221A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255741 | |||||||
| chr8:96255849 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(41): Show |
71 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.487+1113C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255849 | |||||||
| chr8:96255864 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.487+1098C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255864 | |||||||
| chr8:96255900 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0209 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.487+1062C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255900 | |||||||
| chr8:96255912 | G | A | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.487+1050C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96255912 | |||||||
| chr8:96256018 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.487+944C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96256018 | |||||||
| chr8:96256039 | C | T | 8 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+923G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96256039 | |||||||
| chr8:96256180 | G | A | 13 | a0001c0001t0001g0172 a0002c0002t0003g0014 a0002c0002t0003g0026 others(10): Show |
16 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+782C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96256180 | |||||||
| chr8:96256238 | G | A | 10 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(7): Show |
10 | HG01167.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.487+724C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96256238 | |||||||
| chr8:96256287 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.487+675T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96256287 | |||||||
| chr8:96256616 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.487+346C>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96256616 | |||||||
| chr8:96256796 | C | G | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.487+166G>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96256796 | |||||||
| chr8:96256818 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.487+144C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 3/7 | chr8 | 96256818 | |||||||
| chr8:96257197 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.335-83A>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257197 | |||||||
| chr8:96257217 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.335-103A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257217 | |||||||
| chr8:96257312 | T | C | 25 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(22): Show |
37 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.335-198A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257312 | |||||||
| chr8:96257326 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.335-212A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257326 | |||||||
| chr8:96257510 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(89): Show |
126 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.335-396G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257510 | |||||||
| chr8:96257572 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | NA18747.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.335-458T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257572 | |||||||
| chr8:96257735 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.335-621C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257735 | |||||||
| chr8:96257790 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.334+567A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257790 | |||||||
| chr8:96257867 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
11 | HG00642.hp1 HG00738.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.334+490G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257867 | |||||||
| chr8:96257870 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334+487G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96257870 | |||||||
| chr8:96258072 | A | T | 1 | a0002c0002t0003g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334+285T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96258072 | |||||||
| chr8:96258076 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.334+281G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 2/7 | chr8 | 96258076 | |||||||
| chr8:96258721 | C | T | 12 | a0002c0002t0003g0014 a0002c0002t0003g0026 a0002c0002t0003g0217 others(9): Show |
15 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-21G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96258721 | |||||||
| chr8:96258751 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-10-51T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96258751 | |||||||
| chr8:96258763 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(89): Show |
126 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-10-63C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96258763 | |||||||
| chr8:96258941 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 |
4 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-241G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96258941 | |||||||
| chr8:96259040 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10-340C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259040 | |||||||
| chr8:96259097 | G | T | 1 | a0001c0001t0002g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10-397C>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259097 | |||||||
| chr8:96259155 | G | A | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-455C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259155 | |||||||
| chr8:96259244 | C | T | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-544G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259244 | |||||||
| chr8:96259480 | A | C | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-780T>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259480 | |||||||
| chr8:96259601 | G | A | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-901C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259601 | |||||||
| chr8:96259734 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-10-1034A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259734 | |||||||
| chr8:96259805 | C | T | 2 | a0004c0003t0001g0049 a0004c0003t0001g0056 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-1105G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259805 | |||||||
| chr8:96259895 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-10-1195T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259895 | |||||||
| chr8:96259904 | A | T | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-10-1204T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259904 | |||||||
| chr8:96259907 | A | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG01167.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-10-1207T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259907 | |||||||
| chr8:96259910 | A | T | 10 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(7): Show |
10 | HG01167.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-1210T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259910 | |||||||
| chr8:96259913 | A | T | 39 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0045 others(36): Show |
45 | HG00438.hp1 HG00642.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-10-1213T>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259913 | |||||||
| chr8:96259916 | T | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(55): Show |
87 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-10-1216A>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259916 | |||||||
| chr8:96259958 | A | G | 12 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
12 | HG01167.hp2 HG02257.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-1258T>C | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259958 | |||||||
| chr8:96259970 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-10-1270A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96259970 | |||||||
| chr8:96260243 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11+1258G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96260243 | |||||||
| chr8:96260381 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-11+1120C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96260381 | |||||||
| chr8:96260494 | T | C | 1 | a0001c0001t0002g0043 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-11+1007A>G | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96260494 | |||||||
| chr8:96261183 | G | A | 12 | a0002c0002t0003g0014 a0002c0002t0003g0026 a0002c0002t0003g0217 others(9): Show |
15 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+318C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96261183 | |||||||
| chr8:96261249 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11+252A>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96261249 | |||||||
| chr8:96261285 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(47): Show |
78 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-11+216G>A | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96261285 | |||||||
| chr8:96261315 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(47): Show |
78 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-11+186C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96261315 | |||||||
| chr8:96261436 | G | A | 12 | a0002c0002t0003g0014 a0002c0002t0003g0026 a0002c0002t0003g0217 others(9): Show |
15 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+65C>T | MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 1/7 | chr8 | 96261436 |