Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 246175 |
| ensemblid | ENSG00000138767.14 |
| hgncid | 18042 |
| symbol | CNOT6L |
| name | CCR4-NOT transcription complex subunit 6 like |
| refseq_nuc | NM_144571.3 |
| refseq_prot | NP_653172.2 |
| ensembl_nuc | ENST00000504123.7 |
| ensembl_prot | ENSP00000424896.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 77713387 |
| end | 77819368 |
| strand | - |
| ver | v1.2 |
| region | chr4:77713387-77819368 |
| region5000 | chr4:77708387-77824368 |
| regionname0 | CNOT6L_chr4_77713387_77819368 |
| regionname5000 | CNOT6L_chr4_77708387_77824368 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 555 | 327 | 90 | 56 | 135 | 8 | 36 | 105 | CNOT6L_chr4_77708387_77824368 | CNOT6L | MRLIG others(550): Show |
chr4 | 77708387 | 77824368 |
| a0002 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | MRLIG others(550): Show |
chr4 | 77708387 | 77824368 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1665 | 326 | 89 | 56 | 135 | 8 | 36 | CNOT6L_chr4_77708387_77824368 | CNOT6L | ATGAG others(1660): Show |
chr4 | 77708387 | 77824368 | ||
| a0001c0003 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | ATGAG others(1660): Show |
chr4 | 77708387 | 77824368 | ||
| a0002c0002 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | ATGAG others(1660): Show |
chr4 | 77708387 | 77824368 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8772 | 173 | 23 | 33 | 91 | 4 | 22 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0002 | 0/0 | 8773 | 41 | 16 | 0 | 22 | 0 | 3 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0003 | 0/0 | 8772 | 18 | 1 | 10 | 5 | 2 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0004 | 0/0 | 8776 | 11 | 10 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8771): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0005 | 0/0 | 8772 | 10 | 9 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0006 | 0/0 | 8773 | 9 | 5 | 1 | 0 | 0 | 3 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0007 | 1/0 | 8772 | 8 | 1 | 1 | 0 | 1 | 4 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0008 | 0/0 | 8775 | 7 | 0 | 2 | 4 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8770): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0009 | 0/0 | 8772 | 6 | 6 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0010 | 0/0 | 8772 | 4 | 1 | 1 | 0 | 1 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0011 | 0/0 | 8773 | 3 | 2 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0012 | 0/0 | 8768 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8763): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0013 | 0/0 | 8773 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0014 | 0/0 | 8773 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0015 | 0/0 | 8772 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0016 | 0/0 | 8772 | 2 | 0 | 1 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0017 | 0/0 | 8771 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8766): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0018 | 0/0 | 8772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0019 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0020 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0021 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0022 | 0/0 | 8773 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0023 | 0/0 | 8772 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0024 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0026 | 0/0 | 8773 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0027 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0028 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0029 | 0/0 | 8772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0030 | 0/0 | 8772 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0031 | 0/0 | 8772 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0032 | 0/1 | 8749 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8744): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0033 | 0/0 | 8748 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8743): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0034 | 0/0 | 8772 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0035 | 0/0 | 8772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0036 | 0/0 | 8772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0037 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8814): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0038 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0039 | 0/0 | 8772 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0040 | 0/0 | 8775 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8770): Show |
chr4 | 77708387 | 77824368 |
| a0001c0001t0041 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0001c0003t0025 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8768): Show |
chr4 | 77708387 | 77824368 |
| a0002c0002t0001 | 0/0 | 8772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | GTGTG others(8767): Show |
chr4 | 77708387 | 77824368 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0006g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0007g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0008g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0008g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0010g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0010g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0012g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0012g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0013g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0014g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0015g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0015g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0016g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0016g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0017g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0017g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0018g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0019g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0020g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0021g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0022g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0023g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0024g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0026g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0027g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0028g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0029g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0030g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0031g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0032g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0033g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0034g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0035g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0036g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0037g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0038g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0039g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0040g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0001t0041g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0001c0003t0025g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0057 | EUR | GBR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0211 | EUR | FIN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0169 | EUR | FIN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0203 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00738 | hp1 | a0001 | c0001 | t0022 | g0181 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0059 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0073 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0106 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01175 | hp2 | a0001 | c0001 | t0023 | g0004 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01192 | hp1 | a0001 | c0001 | t0034 | g0164 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0077 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0290 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01928 | hp1 | a0001 | c0001 | t0040 | g0018 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0322 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02015 | hp2 | a0001 | c0001 | t0018 | g0289 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0170 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02083 | hp2 | a0001 | c0001 | t0026 | g0102 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0056 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0020 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02280 | hp1 | a0001 | c0001 | t0021 | g0320 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0091 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0269 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0312 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02602 | hp1 | a0001 | c0001 | t0008 | g0023 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02622 | hp1 | a0001 | c0001 | t0041 | g0076 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0089 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0090 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0268 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02735 | hp2 | a0001 | c0001 | t0010 | g0168 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0054 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02738 | hp2 | a0001 | c0001 | t0016 | g0138 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0071 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0072 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0087 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0301 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0088 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0171 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02970 | hp2 | a0001 | c0001 | t0020 | g0319 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03195 | hp2 | a0001 | c0001 | t0019 | g0310 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0213 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0074 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03516 | hp1 | a0001 | c0003 | t0025 | g0172 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ESN | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03540 | hp1 | a0001 | c0001 | t0014 | g0223 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03579 | hp2 | a0001 | c0001 | t0031 | g0112 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0053 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0050 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03704 | hp1 | a0001 | c0001 | t0037 | g0182 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0058 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0307 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0313 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0157 | AFR | YRI | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0311 | AFR | YRI | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18940 | hp1 | a0001 | c0001 | t0012 | g0186 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18941 | hp1 | a0001 | c0001 | t0035 | g0258 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18964 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18971 | hp2 | a0001 | c0001 | t0012 | g0185 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18980 | hp1 | a0001 | c0001 | t0015 | g0281 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18984 | hp1 | a0001 | c0001 | t0036 | g0274 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18992 | hp1 | a0001 | c0001 | t0012 | g0184 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18992 | hp2 | a0001 | c0001 | t0017 | g0291 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | LWK | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | LWK | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | LWK | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19058 | hp1 | a0001 | c0001 | t0029 | g0251 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19065 | hp2 | a0001 | c0001 | t0015 | g0250 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19075 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19075 | hp2 | a0001 | c0001 | t0033 | g0246 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19086 | hp2 | a0001 | c0001 | t0017 | g0287 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19240 | hp1 | a0001 | c0001 | t0024 | g0012 | AFR | YRI | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | YRI | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA20129 | hp1 | a0001 | c0001 | t0039 | g0174 | AFR | ASW | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ASW | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0145 | EUR | TSI | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG02559 | hp2 | a0001 | c0001 | t0038 | g0055 | AFR | ACB | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0075 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG03471 | hp2 | a0001 | c0001 | t0030 | g0078 | AFR | MSL | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | USA | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| HG06807 | hp2 | a0001 | c0001 | t0027 | g0318 | AFR | USA | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA20300 | hp1 | a0001 | c0001 | t0028 | g0327 | AFR | USA | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | USA | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0243 | REF | REF | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0051 | REF | REF | CNOT6L_chr4_77708387_77824368 | CNOT6L | chr4 | 77708387 | 77824368 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:77774707 | C | T | 1 | a0002 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.137G>A | p.Arg46Gln | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/12 | 197/8772 | 137/1668 | 46/555 | chr4 | 77774707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:77720482 | G | A | 1 | a0001c0003 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1617C>T | p.His539His | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 1677/8772 | 1617/1668 | 539/555 | chr4 | 77720482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:77713621 | G | GTC | 2 | a0001c0001t0008 a0001c0001t0040 |
8 | HG01928.hp1 HG02004.hp2 HG02273.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6808_*6809dupGA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 6809 | chr4 | 77713621 | ||||||
| chr4:77714154 | C | T | 1 | a0001c0001t0023 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6277G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 6277 | chr4 | 77714154 | ||||||
| chr4:77714250 | G | A | 1 | a0001c0001t0024 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6181C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 6181 | chr4 | 77714250 | ||||||
| chr4:77714429 | C | T | 1 | a0001c0001t0034 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6002G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 6002 | chr4 | 77714429 | ||||||
| chr4:77714437 | TTAAAAAA others(17): Show |
T | 1 | a0001c0001t0033 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5970_*5993delTTTT others(20): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5970 | chr4 | 77714437 | ||||||
| chr4:77714438 | T | TA | 4 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(1): Show |
14 | HG00741.hp2 HG01928.hp1 HG02080.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5992dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5992 | chr4 | 77714438 | ||||||
| chr4:77714438 | T | TAA | 3 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 |
9 | HG00673.hp2 HG02004.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5991_*5992dupTT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5992 | chr4 | 77714438 | ||||||
| chr4:77714438 | TA | T | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(3): Show |
11 | HG01109.hp2 HG02083.hp2 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5992delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5992 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0014 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5981_*5992delTTTT others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5981 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0014 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5980_*5992delTTTT others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5980 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(9): Show |
T | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0021 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5977_*5992delTTTT others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5977 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0006 | 8 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5976_*5992delTTTT others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5976 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(11): Show |
T | 2 | a0001c0001t0002 a0001c0001t0006 |
2 | HG02602.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5975_*5992delTTTT others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5975 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(12): Show |
T | 1 | a0001c0001t0041 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5974_*5992delTTTT others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5974 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(14): Show |
T | 1 | a0001c0001t0001 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5972_*5992delTTTT others(17): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5972 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(15): Show |
T | 4 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(1): Show |
16 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5971_*5992delTTTT others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5971 | chr4 | 77714438 | ||||||
| chr4:77714438 | TAAAAAAA others(16): Show |
T | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
227 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*5970_*5992delTTTT others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5970 | chr4 | 77714438 | ||||||
| chr4:77714904 | G | C | 7 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0020 others(4): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5527C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5527 | chr4 | 77714904 | ||||||
| chr4:77714921 | T | C | 1 | a0001c0001t0028 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5510A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5510 | chr4 | 77714921 | ||||||
| chr4:77715033 | G | A | 33 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(30): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*5398C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5398 | chr4 | 77715033 | ||||||
| chr4:77715073 | G | A | 1 | a0001c0001t0035 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5358C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5358 | chr4 | 77715073 | ||||||
| chr4:77715215 | C | G | 1 | a0001c0001t0018 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5216G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5216 | chr4 | 77715215 | ||||||
| chr4:77715230 | T | C | 1 | a0001c0001t0036 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5201A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5201 | chr4 | 77715230 | ||||||
| chr4:77715366 | CAATT | C | 1 | a0001c0001t0012 | 3 | NA18940.hp1 NA18971.hp2 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5061_*5064delAATT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5061 | chr4 | 77715366 | ||||||
| chr4:77715421 | T | G | 1 | a0001c0001t0006 | 9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5010A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5010 | chr4 | 77715421 | ||||||
| chr4:77715467 | A | G | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*4964T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4964 | chr4 | 77715467 | ||||||
| chr4:77715497 | C | T | 1 | a0001c0001t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4934G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4934 | chr4 | 77715497 | ||||||
| chr4:77715500 | G | A | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*4931C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4931 | chr4 | 77715500 | ||||||
| chr4:77715547 | T | C | 7 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0020 others(4): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4884A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4884 | chr4 | 77715547 | ||||||
| chr4:77715594 | T | C | 1 | a0001c0001t0016 | 2 | HG01169.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4837A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4837 | chr4 | 77715594 | ||||||
| chr4:77715792 | T | TAAAGGTG others(40): Show |
1 | a0001c0001t0037 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4592_*4638dupGGAT others(43): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4638 | chr4 | 77715792 | ||||||
| chr4:77715860 | C | T | 1 | a0001c0001t0015 | 2 | NA18980.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4571G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4571 | chr4 | 77715860 | ||||||
| chr4:77716111 | A | G | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*4320T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4320 | chr4 | 77716111 | ||||||
| chr4:77716147 | AG | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*4283delC | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4283 | chr4 | 77716147 | ||||||
| chr4:77716249 | C | A | 1 | a0001c0001t0009 | 6 | HG02280.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4182G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4182 | chr4 | 77716249 | ||||||
| chr4:77716327 | A | C | 2 | a0001c0001t0005 a0001c0001t0039 |
11 | HG00735.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4104T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 4104 | chr4 | 77716327 | ||||||
| chr4:77716558 | C | T | 1 | a0001c0001t0031 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3873G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 3873 | chr4 | 77716558 | ||||||
| chr4:77716835 | A | G | 1 | a0001c0001t0019 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3596T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 3596 | chr4 | 77716835 | ||||||
| chr4:77716955 | A | G | 1 | a0001c0001t0026 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3476T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 3476 | chr4 | 77716955 | ||||||
| chr4:77716999 | T | A | 1 | a0001c0001t0010 | 4 | HG00280.hp2 HG01192.hp2 HG02055.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3432A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 3432 | chr4 | 77716999 | ||||||
| chr4:77717197 | C | T | 1 | a0001c0001t0030 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3234G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 3234 | chr4 | 77717197 | ||||||
| chr4:77717337 | T | C | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*3094A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 3094 | chr4 | 77717337 | ||||||
| chr4:77717374 | C | T | 1 | a0001c0001t0029 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3057G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 3057 | chr4 | 77717374 | ||||||
| chr4:77717576 | T | C | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*2855A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 2855 | chr4 | 77717576 | ||||||
| chr4:77717578 | T | G | 1 | a0001c0001t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2853A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 2853 | chr4 | 77717578 | ||||||
| chr4:77717662 | G | A | 1 | a0001c0001t0011 | 3 | HG01109.hp2 HG02896.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2769C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 2769 | chr4 | 77717662 | ||||||
| chr4:77718036 | A | AT | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(36): Show |
317 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*2394dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 2394 | chr4 | 77718036 | ||||||
| chr4:77718403 | G | T | 2 | a0001c0001t0011 a0001c0001t0013 |
5 | HG01109.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2028C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 2028 | chr4 | 77718403 | ||||||
| chr4:77718480 | T | C | 1 | a0001c0001t0039 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1951A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 1951 | chr4 | 77718480 | ||||||
| chr4:77718691 | C | T | 1 | a0001c0001t0024 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1740G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 1740 | chr4 | 77718691 | ||||||
| chr4:77718877 | A | G | 2 | a0001c0001t0024 a0001c0003t0025 |
2 | HG03516.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1554T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 1554 | chr4 | 77718877 | ||||||
| chr4:77719324 | G | GAGTC | 1 | a0001c0001t0004 | 11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1103_*1106dupGACT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 1106 | chr4 | 77719324 | ||||||
| chr4:77719689 | A | G | 3 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0023 |
20 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*742T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 742 | chr4 | 77719689 | ||||||
| chr4:77720019 | C | G | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0021 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*412G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 412 | chr4 | 77720019 | ||||||
| chr4:77720088 | T | G | 1 | a0001c0001t0040 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*343A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 343 | chr4 | 77720088 | ||||||
| chr4:77720235 | G | A | 1 | a0001c0001t0041 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 196 | chr4 | 77720235 | ||||||
| chr4:77720416 | C | T | 1 | a0001c0001t0018 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 15 | chr4 | 77720416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:77720758 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1456-115C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77720758 | |||||||
| chr4:77720765 | G | A | 1 | a0001c0001t0039g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1456-122C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77720765 | |||||||
| chr4:77720840 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1456-197A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77720840 | |||||||
| chr4:77721001 | T | G | 1 | a0001c0001t0030g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1456-358A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77721001 | |||||||
| chr4:77721177 | C | T | 1 | a0001c0001t0014g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1456-534G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77721177 | |||||||
| chr4:77721235 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(137): Show |
141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1456-592C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77721235 | |||||||
| chr4:77721314 | A | C | 2 | a0001c0001t0005g0175 a0001c0001t0005g0208 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1456-671T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77721314 | |||||||
| chr4:77721318 | G | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1456-675C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77721318 | |||||||
| chr4:77721411 | A | G | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1456-768T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77721411 | |||||||
| chr4:77722052 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0037g0182 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1456-1409G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722052 | |||||||
| chr4:77722331 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1456-1688G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722331 | |||||||
| chr4:77722369 | T | C | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1456-1726A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722369 | |||||||
| chr4:77722370 | G | T | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1456-1727C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722370 | |||||||
| chr4:77722440 | G | C | 1 | a0001c0001t0002g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1456-1797C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722440 | |||||||
| chr4:77722555 | A | G | 3 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1456-1912T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722555 | |||||||
| chr4:77722637 | A | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1456-1994T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722637 | |||||||
| chr4:77722661 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1456-2018A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722661 | |||||||
| chr4:77722701 | A | C | 4 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
4 | HG01109.hp2 HG02896.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456-2058T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722701 | |||||||
| chr4:77722793 | G | T | 11 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(8): Show |
11 | HG01109.hp2 HG02717.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1456-2150C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722793 | |||||||
| chr4:77722875 | T | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1456-2232A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722875 | |||||||
| chr4:77722987 | AAT | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(239): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1456-2346_1456-234 others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77722987 | |||||||
| chr4:77723026 | T | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1456-2383A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77723026 | |||||||
| chr4:77723066 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1456-2423T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77723066 | |||||||
| chr4:77723076 | A | G | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1456-2433T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77723076 | |||||||
| chr4:77723233 | CCTT | C | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1456-2593_1456-259 others(7): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77723233 | |||||||
| chr4:77723332 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1456-2689C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77723332 | |||||||
| chr4:77723497 | T | C | 1 | a0001c0001t0009g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1455+2670A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77723497 | |||||||
| chr4:77723557 | C | T | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1455+2610G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77723557 | |||||||
| chr4:77723789 | T | C | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | HG02895.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1455+2378A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77723789 | |||||||
| chr4:77724331 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1455+1836G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724331 | |||||||
| chr4:77724339 | C | CA | 13 | a0001c0001t0001g0140 a0001c0001t0001g0284 a0001c0001t0002g0042 others(10): Show |
13 | HG01081.hp1 HG02602.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1455+1827dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724339 | |||||||
| chr4:77724443 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1455+1724T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724443 | |||||||
| chr4:77724485 | A | G | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0191 others(2): Show |
5 | HG01106.hp1 HG01934.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1455+1682T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724485 | |||||||
| chr4:77724639 | C | CA | 11 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0214 others(8): Show |
11 | HG01175.hp1 HG01175.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1455+1527dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724639 | |||||||
| chr4:77724639 | CA | C | 16 | a0001c0001t0001g0080 a0001c0001t0001g0151 a0001c0001t0001g0167 others(13): Show |
16 | HG01081.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1455+1527delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724639 | |||||||
| chr4:77724835 | CTG | C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1455+1330_1455+133 others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724835 | |||||||
| chr4:77724941 | G | GT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(119): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1455+1225dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724941 | |||||||
| chr4:77724947 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1455+1220A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724947 | |||||||
| chr4:77724948 | G | A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0133 a0001c0001t0001g0135 others(2): Show |
5 | HG00323.hp2 HG00597.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1455+1219C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77724948 | |||||||
| chr4:77725235 | C | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(316): Show |
320 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.1455+932G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77725235 | |||||||
| chr4:77725265 | G | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1455+902C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77725265 | |||||||
| chr4:77725428 | A | G | 6 | a0001c0001t0009g0087 a0001c0001t0009g0088 a0001c0001t0009g0089 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1455+739T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77725428 | |||||||
| chr4:77725475 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0037g0182 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1455+692C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77725475 | |||||||
| chr4:77725655 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1455+512T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77725655 | |||||||
| chr4:77725670 | C | G | 1 | a0001c0001t0002g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1455+497G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77725670 | |||||||
| chr4:77725938 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1455+229T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77725938 | |||||||
| chr4:77725971 | GC | G | 85 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(82): Show |
85 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1455+195delG | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77725971 | |||||||
| chr4:77726038 | T | C | 1 | a0001c0001t0030g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1455+129A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 11/11 | chr4 | 77726038 | |||||||
| chr4:77726403 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1253-34G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77726403 | |||||||
| chr4:77726864 | G | C | 11 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1253-495C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77726864 | |||||||
| chr4:77727320 | T | C | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253-951A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727320 | |||||||
| chr4:77727549 | C | T | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1253-1180G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727549 | |||||||
| chr4:77727555 | T | A | 1 | a0001c0001t0004g0303 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1253-1186A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727555 | |||||||
| chr4:77727562 | CAAAA | C | 7 | a0001c0001t0002g0028 a0001c0001t0002g0038 a0001c0001t0002g0068 others(4): Show |
7 | HG00673.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1253-1197_1253-119 others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727562 | CAAAAA | C | 21 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(18): Show |
21 | HG02083.hp2 HG02129.hp2 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.1253-1198_1253-119 others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727562 | CAAAAAA | C | 40 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0036 others(37): Show |
40 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1253-1199_1253-119 others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727562 | CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0245 a0001c0001t0001g0265 a0001c0001t0001g0271 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253-1204_1253-119 others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727562 | CAAAAAAA others(5): Show |
C | 88 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0079 others(85): Show |
88 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1253-1205_1253-119 others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727562 | CAAAAAAA others(6): Show |
C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0080 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1253-1206_1253-119 others(17): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727562 | CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0167 a0001c0001t0003g0198 others(1): Show |
4 | HG01934.hp2 NA18906.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.1253-1207_1253-119 others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727562 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0002g0031 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1253-1209_1253-119 others(20): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727562 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1253-1210_1253-119 others(21): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727562 | |||||||
| chr4:77727690 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1252+1164A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727690 | |||||||
| chr4:77727774 | T | C | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1252+1080A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727774 | |||||||
| chr4:77727775 | A | T | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1252+1079T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727775 | |||||||
| chr4:77727776 | A | T | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1252+1078T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727776 | |||||||
| chr4:77727777 | G | A | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1252+1077C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727777 | |||||||
| chr4:77727844 | T | G | 6 | a0001c0001t0009g0087 a0001c0001t0009g0088 a0001c0001t0009g0089 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1252+1010A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727844 | |||||||
| chr4:77727967 | T | G | 20 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0001g0219 others(17): Show |
20 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1252+887A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727967 | |||||||
| chr4:77727989 | GCAGTGAT others(6): Show |
G | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1252+852_1252+864d others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77727989 | |||||||
| chr4:77728036 | G | A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0133 a0001c0001t0001g0135 others(2): Show |
5 | HG00323.hp2 HG00597.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252+818C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728036 | |||||||
| chr4:77728082 | T | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(259): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1252+772A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728082 | |||||||
| chr4:77728110 | G | A | 20 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0001g0219 others(17): Show |
20 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1252+744C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728110 | |||||||
| chr4:77728210 | T | C | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1252+644A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728210 | |||||||
| chr4:77728488 | C | T | 1 | a0001c0001t0005g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1252+366G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728488 | |||||||
| chr4:77728627 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG02132.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1252+227G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728627 | |||||||
| chr4:77728651 | T | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1252+203A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728651 | |||||||
| chr4:77728688 | G | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1252+166C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728688 | |||||||
| chr4:77728693 | T | C | 3 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1252+161A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 10/11 | chr4 | 77728693 | |||||||
| chr4:77729132 | G | A | 1 | a0001c0001t0001g0314 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1025-51C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77729132 | |||||||
| chr4:77729183 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1025-102G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77729183 | |||||||
| chr4:77729397 | A | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1025-316T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77729397 | |||||||
| chr4:77729427 | C | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1025-346G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77729427 | |||||||
| chr4:77729810 | T | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0081 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1025-729A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77729810 | |||||||
| chr4:77729826 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1025-745C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77729826 | |||||||
| chr4:77730087 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1025-1006C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730087 | |||||||
| chr4:77730234 | T | C | 1 | a0001c0001t0035g0258 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1024+1153A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730234 | |||||||
| chr4:77730331 | A | C | 1 | a0001c0001t0003g0145 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1024+1056T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730331 | |||||||
| chr4:77730440 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1024+947G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730440 | |||||||
| chr4:77730509 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1024+878A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730509 | |||||||
| chr4:77730586 | G | A | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1024+801C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730586 | |||||||
| chr4:77730796 | A | G | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1024+591T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730796 | |||||||
| chr4:77730818 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1024+569C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730818 | |||||||
| chr4:77730843 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1024+544C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730843 | |||||||
| chr4:77730857 | T | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0196 |
2 | HG01106.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1024+530A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77730857 | |||||||
| chr4:77731051 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1024+336T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77731051 | |||||||
| chr4:77731206 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1024+181A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77731206 | |||||||
| chr4:77731216 | A | C | 2 | a0001c0001t0027g0318 a0001c0001t0028g0327 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1024+171T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 9/11 | chr4 | 77731216 | |||||||
| chr4:77731718 | C | T | 18 | a0001c0001t0001g0092 a0001c0001t0005g0175 a0001c0001t0005g0176 others(15): Show |
18 | HG00735.hp1 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.873-180G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77731718 | |||||||
| chr4:77732284 | T | C | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.873-746A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77732284 | |||||||
| chr4:77732372 | A | T | 1 | a0001c0001t0001g0233 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.873-834T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77732372 | |||||||
| chr4:77732414 | A | G | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | HG02895.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.873-876T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77732414 | |||||||
| chr4:77732517 | T | C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.873-979A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77732517 | |||||||
| chr4:77732613 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.873-1075C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77732613 | |||||||
| chr4:77732864 | G | A | 1 | a0001c0001t0013g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.873-1326C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77732864 | |||||||
| chr4:77733645 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.873-2107T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77733645 | |||||||
| chr4:77733647 | C | T | 1 | a0001c0001t0014g0269 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.873-2109G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77733647 | |||||||
| chr4:77733671 | G | A | 1 | a0001c0001t0022g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.873-2133C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77733671 | |||||||
| chr4:77733862 | T | C | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.873-2324A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77733862 | |||||||
| chr4:77734052 | T | C | 13 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(10): Show |
13 | HG02145.hp1 HG02258.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.873-2514A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734052 | |||||||
| chr4:77734118 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.873-2580A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734118 | |||||||
| chr4:77734141 | C | T | 1 | a0001c0001t0017g0287 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.873-2603G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734141 | |||||||
| chr4:77734481 | T | C | 1 | a0001c0001t0026g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.873-2943A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734481 | |||||||
| chr4:77734517 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.873-2979C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734517 | |||||||
| chr4:77734624 | G | A | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.873-3086C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734624 | |||||||
| chr4:77734736 | GAT | G | 19 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0005g0175 others(16): Show |
19 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.873-3200_873-3199d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734736 | |||||||
| chr4:77734825 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.873-3287A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734825 | |||||||
| chr4:77734878 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.873-3340T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734878 | |||||||
| chr4:77734959 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0131 |
3 | HG00741.hp1 HG01346.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.873-3421A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734959 | |||||||
| chr4:77734979 | T | C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.873-3441A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77734979 | |||||||
| chr4:77735104 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.873-3566T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735104 | |||||||
| chr4:77735107 | C | T | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.873-3569G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735107 | |||||||
| chr4:77735168 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.873-3630A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735168 | |||||||
| chr4:77735310 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.873-3772C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735310 | |||||||
| chr4:77735399 | C | A | 1 | a0001c0001t0006g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.873-3861G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735399 | |||||||
| chr4:77735406 | G | A | 1 | a0001c0001t0006g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.873-3868C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735406 | |||||||
| chr4:77735567 | A | G | 1 | a0001c0001t0022g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.873-4029T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735567 | |||||||
| chr4:77735632 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.873-4094A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735632 | |||||||
| chr4:77735729 | G | A | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.873-4191C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735729 | |||||||
| chr4:77735872 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.873-4334A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735872 | |||||||
| chr4:77735987 | C | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0016 |
2 | NA18940.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.873-4449G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77735987 | |||||||
| chr4:77736066 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.873-4528G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736066 | |||||||
| chr4:77736228 | T | C | 1 | a0001c0001t0001g0315 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.873-4690A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736228 | |||||||
| chr4:77736481 | A | G | 3 | a0001c0001t0008g0020 a0001c0001t0008g0032 a0001c0001t0040g0018 |
3 | HG01928.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.873-4943T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736481 | |||||||
| chr4:77736496 | T | C | 1 | a0001c0001t0008g0035 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.873-4958A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736496 | |||||||
| chr4:77736540 | T | TTC | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.873-5003_873-5002i others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736540 | |||||||
| chr4:77736620 | C | T | 1 | a0001c0001t0016g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.873-5082G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736620 | |||||||
| chr4:77736630 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.873-5092G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736630 | |||||||
| chr4:77736672 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | HG03831.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.873-5134A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736672 | |||||||
| chr4:77736679 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.873-5141A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736679 | |||||||
| chr4:77736679 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.873-5141A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736679 | |||||||
| chr4:77736781 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0101 others(42): Show |
46 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.873-5243A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736781 | |||||||
| chr4:77736985 | TAACTC | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.872+5151_872+5155d others(7): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736985 | |||||||
| chr4:77736992 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(156): Show |
160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.872+5149T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77736992 | |||||||
| chr4:77737115 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.872+5026T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737115 | |||||||
| chr4:77737205 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.872+4936G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737205 | |||||||
| chr4:77737403 | G | GTTTTTTT others(10): Show |
1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.872+4737_872+4738i others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737403 | |||||||
| chr4:77737406 | C | CT | 10 | a0001c0001t0002g0034 a0001c0001t0002g0040 a0001c0001t0002g0045 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+4734dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | C | T | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.872+4735G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CT | C | 16 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0030 others(13): Show |
16 | HG00741.hp2 HG02080.hp1 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.872+4734delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CTT | C | 17 | a0001c0001t0002g0017 a0001c0001t0002g0025 a0001c0001t0002g0026 others(14): Show |
17 | HG01928.hp1 HG02004.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.872+4733_872+4734d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0187 a0001c0001t0001g0201 a0001c0001t0001g0209 others(3): Show |
6 | HG02738.hp2 HG03516.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+4725_872+4734d others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CTTTTTTT others(4): Show |
C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(148): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.872+4724_872+4734d others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CTTTTTTT others(5): Show |
C | 87 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0132 others(84): Show |
87 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.872+4723_872+4734d others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0001g0261 a0001c0001t0001g0294 a0001c0001t0001g0316 others(3): Show |
6 | HG01169.hp2 HG01943.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+4722_872+4734d others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.872+4720_872+4734d others(17): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.872+4719_872+4734d others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737406 | CTTTTTTT others(13): Show |
C | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+4715_872+4734d others(22): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737406 | |||||||
| chr4:77737887 | T | C | 5 | a0001c0001t0004g0290 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01243.hp1 HG01891.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+4254A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77737887 | |||||||
| chr4:77738017 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.872+4124A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77738017 | |||||||
| chr4:77738173 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.872+3968T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77738173 | |||||||
| chr4:77738191 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.872+3950A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77738191 | |||||||
| chr4:77738753 | C | CAA | 27 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(24): Show |
27 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.872+3386_872+3387d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77738753 | |||||||
| chr4:77738753 | C | CAAA | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(216): Show |
220 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.872+3385_872+3387d others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77738753 | |||||||
| chr4:77738753 | C | CAAAA | 14 | a0001c0001t0001g0111 a0001c0001t0001g0155 a0001c0001t0001g0173 others(11): Show |
14 | HG01109.hp1 HG01255.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.872+3384_872+3387d others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77738753 | |||||||
| chr4:77738753 | CA | C | 14 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(11): Show |
14 | HG02145.hp1 HG02258.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.872+3387delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77738753 | |||||||
| chr4:77739010 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.872+3131A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77739010 | |||||||
| chr4:77739045 | T | C | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.872+3096A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77739045 | |||||||
| chr4:77739269 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.872+2872T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77739269 | |||||||
| chr4:77739412 | A | C | 1 | a0001c0001t0001g0253 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.872+2729T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77739412 | |||||||
| chr4:77739530 | T | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(315): Show |
319 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.872+2611A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77739530 | |||||||
| chr4:77739915 | T | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0201 a0001c0001t0001g0210 |
3 | HG03927.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.872+2226A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77739915 | |||||||
| chr4:77740027 | AT | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.872+2113delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740027 | |||||||
| chr4:77740120 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.872+2021T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740120 | |||||||
| chr4:77740126 | G | A | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.872+2015C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740126 | |||||||
| chr4:77740327 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.872+1814C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740327 | |||||||
| chr4:77740431 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.872+1710T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740431 | |||||||
| chr4:77740434 | A | G | 1 | a0001c0001t0008g0021 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.872+1707T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740434 | |||||||
| chr4:77740532 | G | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(259): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.872+1609C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740532 | |||||||
| chr4:77740791 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0293 a0001c0001t0001g0326 |
3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.872+1350C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740791 | |||||||
| chr4:77740840 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.872+1301C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740840 | |||||||
| chr4:77740952 | G | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.872+1189C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77740952 | |||||||
| chr4:77741027 | A | G | 5 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1114T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77741027 | |||||||
| chr4:77741051 | G | A | 1 | a0001c0001t0030g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.872+1090C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77741051 | |||||||
| chr4:77741385 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.872+756A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77741385 | |||||||
| chr4:77741422 | T | A | 1 | a0001c0001t0006g0307 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.872+719A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77741422 | |||||||
| chr4:77741809 | T | C | 11 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.872+332A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77741809 | |||||||
| chr4:77741952 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.872+189T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77741952 | |||||||
| chr4:77742003 | T | A | 1 | a0001c0001t0002g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.872+138A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77742003 | |||||||
| chr4:77742057 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.872+84T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77742057 | |||||||
| chr4:77742062 | G | A | 3 | a0001c0001t0008g0020 a0001c0001t0008g0032 a0001c0001t0040g0018 |
3 | HG01928.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.872+79C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77742062 | |||||||
| chr4:77742117 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.872+24A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 8/11 | chr4 | 77742117 | |||||||
| chr4:77742677 | T | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.718-382A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77742677 | |||||||
| chr4:77742698 | C | A | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-403G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77742698 | |||||||
| chr4:77743047 | G | C | 1 | a0001c0001t0028g0327 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.718-752C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743047 | |||||||
| chr4:77743317 | G | T | 3 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.718-1022C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743317 | |||||||
| chr4:77743419 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.718-1124A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743419 | |||||||
| chr4:77743469 | T | A | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-1174A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743469 | |||||||
| chr4:77743525 | T | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.717+1193A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743525 | |||||||
| chr4:77743529 | T | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.717+1189A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743529 | |||||||
| chr4:77743586 | C | CT | 9 | a0001c0001t0002g0046 a0001c0001t0002g0049 a0001c0001t0007g0053 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+1131dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.717+1120_717+1131d others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | CT | C | 36 | a0001c0001t0001g0224 a0001c0001t0002g0014 a0001c0001t0002g0017 others(33): Show |
36 | HG01081.hp1 HG01928.hp1 HG02004.hp2 others(33): Show |
intron_variant | MODIFIER | c.717+1131delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | CTT | C | 13 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0149 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.717+1130_717+1131d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | CTTT | C | 79 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(76): Show |
79 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.717+1129_717+1131d others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | CTTTT | C | 92 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0109 others(89): Show |
92 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.717+1128_717+1131d others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.717+1122_717+1131d others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0085 a0001c0001t0001g0098 a0001c0001t0001g0126 others(1): Show |
4 | HG00597.hp2 NA19010.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+1119_717+1131d others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | CTTTTTTT others(7): Show |
C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0084 others(50): Show |
54 | HG00544.hp1 HG00558.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.717+1118_717+1131d others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743586 | CTTTTTTT others(17): Show |
C | 1 | a0001c0001t0001g0221 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.717+1108_717+1131d others(26): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743586 | |||||||
| chr4:77743598 | T | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.717+1120A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743598 | |||||||
| chr4:77743684 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.717+1034G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743684 | |||||||
| chr4:77743697 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.717+1021C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743697 | |||||||
| chr4:77743768 | A | G | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.717+950T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743768 | |||||||
| chr4:77743848 | C | T | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.717+870G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77743848 | |||||||
| chr4:77744081 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.717+637T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744081 | |||||||
| chr4:77744146 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.717+572T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744146 | |||||||
| chr4:77744239 | A | G | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.717+479T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744239 | |||||||
| chr4:77744306 | T | C | 3 | a0001c0001t0004g0300 a0001c0001t0004g0301 a0001c0001t0004g0305 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.717+412A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744306 | |||||||
| chr4:77744353 | T | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0101 others(45): Show |
49 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.717+365A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744353 | |||||||
| chr4:77744353 | T | TA | 17 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0005g0175 others(14): Show |
17 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.717+364dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744353 | |||||||
| chr4:77744354 | A | T | 1 | a0001c0001t0001g0265 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.717+364T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744354 | |||||||
| chr4:77744355 | A | T | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.717+363T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744355 | |||||||
| chr4:77744436 | C | A | 1 | a0001c0001t0002g0036 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.717+282G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744436 | |||||||
| chr4:77744660 | T | C | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.717+58A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | 77744660 | |||||||
| chr4:77744990 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560-115A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77744990 | |||||||
| chr4:77745256 | T | C | 1 | a0001c0001t0004g0298 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.560-381A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77745256 | |||||||
| chr4:77745392 | C | T | 1 | a0001c0001t0038g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.560-517G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77745392 | |||||||
| chr4:77745438 | T | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.560-563A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77745438 | |||||||
| chr4:77745510 | C | T | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.560-635G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77745510 | |||||||
| chr4:77745892 | T | A | 1 | a0001c0001t0013g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.560-1017A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77745892 | |||||||
| chr4:77745920 | G | A | 1 | a0001c0001t0038g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.560-1045C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77745920 | |||||||
| chr4:77745930 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.560-1055G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77745930 | |||||||
| chr4:77745935 | G | T | 1 | a0001c0001t0014g0269 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560-1060C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77745935 | |||||||
| chr4:77746047 | T | A | 4 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0249 others(1): Show |
4 | HG02523.hp2 NA18963.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-1172A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77746047 | |||||||
| chr4:77746265 | G | A | 1 | a0001c0001t0016g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.560-1390C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77746265 | |||||||
| chr4:77746536 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.560-1661A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77746536 | |||||||
| chr4:77746759 | G | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.559+1557C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77746759 | |||||||
| chr4:77747051 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.559+1265T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747051 | |||||||
| chr4:77747130 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.559+1186A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747130 | |||||||
| chr4:77747269 | C | T | 18 | a0001c0001t0001g0092 a0001c0001t0005g0175 a0001c0001t0005g0176 others(15): Show |
18 | HG00735.hp1 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.559+1047G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747269 | |||||||
| chr4:77747296 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559+1020T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747296 | |||||||
| chr4:77747427 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.559+889G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747427 | |||||||
| chr4:77747449 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559+867A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747449 | |||||||
| chr4:77747586 | T | TA | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(156): Show |
160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.559+729dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747586 | |||||||
| chr4:77747595 | G | A | 1 | a0001c0001t0012g0184 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.559+721C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747595 | |||||||
| chr4:77747603 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.559+713C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747603 | |||||||
| chr4:77747646 | C | A | 26 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(23): Show |
26 | HG00673.hp2 HG01928.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.559+670G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77747646 | |||||||
| chr4:77748002 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0019 a0001c0001t0008g0035 |
3 | NA18964.hp1 NA19004.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.559+314A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77748002 | |||||||
| chr4:77748054 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0007 |
2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.559+262T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77748054 | |||||||
| chr4:77748124 | C | T | 7 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(4): Show |
7 | HG02602.hp2 HG03490.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+192G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77748124 | |||||||
| chr4:77748254 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.559+62C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77748254 | |||||||
| chr4:77748300 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.559+16T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 6/11 | chr4 | 77748300 | |||||||
| chr4:77748433 | C | G | 3 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.491-49G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77748433 | |||||||
| chr4:77748686 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.491-302T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77748686 | |||||||
| chr4:77748866 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.491-482C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77748866 | |||||||
| chr4:77748918 | A | C | 5 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0074 others(2): Show |
5 | HG01109.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-534T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77748918 | |||||||
| chr4:77749012 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.491-628A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749012 | |||||||
| chr4:77749050 | C | T | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.491-666G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749050 | |||||||
| chr4:77749053 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.491-669C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749053 | |||||||
| chr4:77749135 | A | C | 4 | a0001c0001t0004g0300 a0001c0001t0004g0301 a0001c0001t0004g0305 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-751T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749135 | |||||||
| chr4:77749144 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0304 |
2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.491-760A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749144 | |||||||
| chr4:77749151 | A | G | 3 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0205 |
3 | NA18947.hp2 NA18974.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.491-767T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749151 | |||||||
| chr4:77749205 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.491-821T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749205 | |||||||
| chr4:77749305 | G | A | 1 | a0001c0001t0040g0018 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.491-921C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749305 | |||||||
| chr4:77749415 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.491-1031A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749415 | |||||||
| chr4:77749431 | G | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.491-1047C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749431 | |||||||
| chr4:77749466 | T | C | 1 | a0001c0001t0003g0005 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.491-1082A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749466 | |||||||
| chr4:77749661 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.491-1277C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749661 | |||||||
| chr4:77749763 | C | T | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.491-1379G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749763 | |||||||
| chr4:77749906 | A | G | 1 | a0001c0001t0026g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.491-1522T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77749906 | |||||||
| chr4:77750360 | T | C | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.491-1976A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77750360 | |||||||
| chr4:77750362 | G | GT | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.491-1979dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77750362 | |||||||
| chr4:77750595 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(148): Show |
152 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.491-2211G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77750595 | |||||||
| chr4:77750756 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG00438.hp1 HG02074.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.491-2372T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77750756 | |||||||
| chr4:77750828 | C | A | 1 | a0001c0001t0014g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.491-2444G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77750828 | |||||||
| chr4:77750866 | G | A | 18 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0006 others(15): Show |
18 | HG00738.hp1 HG01069.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.491-2482C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77750866 | |||||||
| chr4:77751014 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.491-2630G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77751014 | |||||||
| chr4:77751383 | A | G | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.491-2999T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77751383 | |||||||
| chr4:77751405 | T | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.491-3021A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77751405 | |||||||
| chr4:77751534 | C | T | 1 | a0001c0001t0008g0035 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.491-3150G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77751534 | |||||||
| chr4:77751535 | A | G | 1 | a0001c0001t0020g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491-3151T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77751535 | |||||||
| chr4:77751587 | G | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.491-3203C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77751587 | |||||||
| chr4:77752043 | G | T | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.491-3659C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77752043 | |||||||
| chr4:77752295 | GAAGA | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0006 others(15): Show |
18 | HG00738.hp1 HG01069.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.491-3915_491-3912d others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77752295 | |||||||
| chr4:77752325 | G | C | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-3941C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77752325 | |||||||
| chr4:77752821 | T | C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.490+4041A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77752821 | |||||||
| chr4:77753123 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.490+3739C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753123 | |||||||
| chr4:77753124 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.490+3738T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753124 | |||||||
| chr4:77753191 | G | GA | 92 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0081 others(89): Show |
92 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.490+3670dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753191 | |||||||
| chr4:77753191 | GA | G | 16 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(13): Show |
16 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.490+3670delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753191 | |||||||
| chr4:77753194 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.490+3667_490+3668i others(23): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753194 | |||||||
| chr4:77753264 | G | A | 16 | a0001c0001t0001g0218 a0001c0001t0001g0228 a0001c0001t0001g0231 others(13): Show |
16 | HG01993.hp2 HG02083.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.490+3598C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753264 | |||||||
| chr4:77753283 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.490+3579A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753283 | |||||||
| chr4:77753359 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0081 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.490+3503G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753359 | |||||||
| chr4:77753408 | A | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.490+3454T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753408 | |||||||
| chr4:77753449 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
2 | NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.490+3413A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753449 | |||||||
| chr4:77753503 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.490+3359A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753503 | |||||||
| chr4:77753563 | C | T | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.490+3299G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753563 | |||||||
| chr4:77753642 | G | GC | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+3219dupG | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753642 | |||||||
| chr4:77753901 | TA | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(159): Show |
163 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.490+2960delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753901 | |||||||
| chr4:77753901 | TAA | T | 83 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(80): Show |
83 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.490+2959_490+2960d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753901 | |||||||
| chr4:77753921 | T | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.490+2941A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77753921 | |||||||
| chr4:77754344 | A | T | 1 | a0001c0001t0007g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.490+2518T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754344 | |||||||
| chr4:77754417 | A | T | 1 | a0001c0001t0005g0208 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490+2445T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754417 | |||||||
| chr4:77754485 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.490+2377A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754485 | |||||||
| chr4:77754712 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.490+2150G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754712 | |||||||
| chr4:77754846 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.490+2016T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754846 | |||||||
| chr4:77754860 | C | T | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+2002G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754860 | |||||||
| chr4:77754888 | T | TA | 20 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0038 others(17): Show |
20 | HG00673.hp2 HG00741.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.490+1973dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAA | 7 | a0001c0001t0001g0219 a0001c0001t0002g0024 a0001c0001t0002g0033 others(4): Show |
7 | HG02145.hp1 HG02602.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.490+1972_490+1973d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAA | 6 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0194 others(3): Show |
6 | HG01993.hp1 HG03540.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+1970_490+1973d others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0113 others(6): Show |
10 | HG01175.hp1 HG01261.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.490+1969_490+1973d others(7): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA | 28 | a0001c0001t0001g0011 a0001c0001t0001g0217 a0001c0001t0001g0226 others(25): Show |
28 | HG00558.hp2 HG01081.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.490+1967_490+1973d others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(1): Show |
47 | a0001c0001t0001g0173 a0001c0001t0001g0188 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.490+1966_490+1973d others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(2): Show |
28 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0119 others(25): Show |
28 | HG00558.hp1 HG01169.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.490+1965_490+1973d others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(3): Show |
23 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0122 others(20): Show |
23 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.490+1964_490+1973d others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(4): Show |
25 | a0001c0001t0001g0083 a0001c0001t0001g0097 a0001c0001t0001g0101 others(22): Show |
25 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.490+1963_490+1973d others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(5): Show |
18 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0096 others(15): Show |
18 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.490+1962_490+1973d others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(6): Show |
16 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0100 others(13): Show |
16 | HG00738.hp1 HG01069.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.490+1961_490+1973d others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(7): Show |
3 | a0001c0001t0001g0115 a0001c0001t0003g0144 a0001c0001t0003g0145 |
3 | HG01358.hp1 HG02165.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.490+1960_490+1973d others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0180 |
2 | HG00642.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.490+1959_490+1973d others(17): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(9): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0105 |
2 | HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.490+1958_490+1973d others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0094 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.490+1957_490+1973d others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | TA | T | 6 | a0001c0001t0002g0037 a0001c0001t0004g0302 a0001c0001t0004g0305 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+1973delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | TAA | T | 11 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+1972_490+1973d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | TAAA | T | 14 | a0001c0001t0001g0196 a0001c0001t0006g0171 a0001c0001t0006g0206 others(11): Show |
14 | HG00639.hp1 HG01106.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.490+1971_490+1973d others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77754888 | TAAAAAAA others(2): Show |
T | 8 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
8 | HG00323.hp1 HG01192.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+1965_490+1973d others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77754888 | |||||||
| chr4:77755098 | C | T | 5 | a0001c0001t0002g0014 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02129.hp2 NA18747.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+1764G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755098 | |||||||
| chr4:77755187 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.490+1675A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755187 | |||||||
| chr4:77755223 | GT | G | 13 | a0001c0001t0002g0014 a0001c0001t0002g0022 a0001c0001t0002g0025 others(10): Show |
13 | HG00673.hp2 HG01928.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.490+1638delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTT | G | 11 | a0001c0001t0002g0015 a0001c0001t0002g0039 a0001c0001t0002g0040 others(8): Show |
11 | HG00099.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.490+1637_490+1638d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTT | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0036 a0001c0001t0002g0042 others(8): Show |
11 | HG02145.hp1 HG02602.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+1636_490+1638d others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTTT | G | 8 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0048 others(5): Show |
8 | HG01081.hp1 HG02895.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.490+1635_490+1638d others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTTTTT | G | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0098 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+1633_490+1638d others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTTTTTT | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0081 a0001c0001t0001g0082 others(61): Show |
64 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.490+1632_490+1638d others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTTTTTT others(1): Show |
G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.490+1631_490+1638d others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTTTTTT others(2): Show |
G | 64 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0217 others(61): Show |
64 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.490+1630_490+1638d others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTTTTTT others(3): Show |
G | 12 | a0001c0001t0006g0171 a0001c0001t0006g0213 a0001c0001t0006g0222 others(9): Show |
12 | HG00639.hp1 HG02015.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.490+1629_490+1638d others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490+1628_490+1638d others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755223 | GTTTTTTT others(12): Show |
G | 1 | a0001c0001t0007g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.490+1620_490+1638d others(21): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755223 | |||||||
| chr4:77755238 | T | G | 1 | a0001c0001t0003g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.490+1624A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755238 | |||||||
| chr4:77755244 | T | G | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490+1618A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755244 | |||||||
| chr4:77755259 | G | C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.490+1603C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755259 | |||||||
| chr4:77755310 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.490+1552C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755310 | |||||||
| chr4:77755458 | C | A | 23 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0104 others(20): Show |
23 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.490+1404G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755458 | |||||||
| chr4:77755458 | C | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
240 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.490+1404G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755458 | |||||||
| chr4:77755625 | T | C | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+1237A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755625 | |||||||
| chr4:77755743 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.490+1119G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755743 | |||||||
| chr4:77755750 | C | T | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.490+1112G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755750 | |||||||
| chr4:77755994 | A | AT | 10 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.490+867dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77755994 | |||||||
| chr4:77756047 | G | A | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.490+815C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77756047 | |||||||
| chr4:77756288 | C | T | 1 | a0001c0001t0004g0286 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.490+574G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77756288 | |||||||
| chr4:77756681 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.490+181C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77756681 | |||||||
| chr4:77756710 | G | C | 1 | a0001c0001t0001g0229 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.490+152C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77756710 | |||||||
| chr4:77756717 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.490+145C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | 77756717 | |||||||
| chr4:77757098 | A | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
2 | NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.401-147T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77757098 | |||||||
| chr4:77757241 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.401-290G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77757241 | |||||||
| chr4:77757300 | C | T | 3 | a0001c0001t0001g0224 a0001c0001t0001g0293 a0001c0001t0001g0326 |
3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.401-349G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77757300 | |||||||
| chr4:77757361 | A | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.401-410T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77757361 | |||||||
| chr4:77757648 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.401-697C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77757648 | |||||||
| chr4:77757671 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.401-720G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77757671 | |||||||
| chr4:77757734 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.401-783G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77757734 | |||||||
| chr4:77757810 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.401-859C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77757810 | |||||||
| chr4:77758165 | G | A | 23 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0104 others(20): Show |
23 | HG00323.hp1 HG00438.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.401-1214C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77758165 | |||||||
| chr4:77758190 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.401-1239C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77758190 | |||||||
| chr4:77758222 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.401-1271A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77758222 | |||||||
| chr4:77758346 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.401-1395A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77758346 | |||||||
| chr4:77758384 | A | C | 1 | a0001c0001t0037g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.401-1433T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77758384 | |||||||
| chr4:77758522 | G | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0201 a0001c0001t0001g0210 |
3 | HG03927.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.401-1571C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77758522 | |||||||
| chr4:77758729 | A | G | 2 | a0001c0001t0004g0297 a0001c0001t0004g0298 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.401-1778T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77758729 | |||||||
| chr4:77758768 | T | C | 1 | a0001c0001t0002g0024 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.401-1817A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77758768 | |||||||
| chr4:77759016 | C | T | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-2065G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759016 | |||||||
| chr4:77759284 | G | A | 11 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.401-2333C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759284 | |||||||
| chr4:77759393 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.401-2442C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759393 | |||||||
| chr4:77759518 | T | C | 4 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0249 others(1): Show |
4 | HG02523.hp2 NA18963.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-2567A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759518 | |||||||
| chr4:77759528 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.401-2577C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759528 | |||||||
| chr4:77759575 | G | GA | 121 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(118): Show |
121 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.401-2625dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759575 | |||||||
| chr4:77759640 | A | G | 1 | a0001c0001t0028g0327 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.401-2689T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759640 | |||||||
| chr4:77759853 | G | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.401-2902C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759853 | |||||||
| chr4:77759896 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0314 |
2 | NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.401-2945C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77759896 | |||||||
| chr4:77760061 | T | C | 1 | a0001c0001t0014g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.401-3110A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760061 | |||||||
| chr4:77760121 | C | G | 19 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0005g0175 others(16): Show |
19 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.401-3170G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760121 | |||||||
| chr4:77760444 | A | G | 1 | a0001c0001t0010g0170 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.401-3493T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760444 | |||||||
| chr4:77760533 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.401-3582T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760533 | |||||||
| chr4:77760577 | A | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(81): Show |
84 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.401-3626T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760577 | |||||||
| chr4:77760601 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.401-3650C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760601 | |||||||
| chr4:77760610 | A | G | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-3659T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760610 | |||||||
| chr4:77760637 | T | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-3686A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760637 | |||||||
| chr4:77760726 | T | A | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.401-3775A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760726 | |||||||
| chr4:77760860 | C | CTT | 6 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 others(3): Show |
6 | HG00741.hp2 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-3911_401-3910d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTT | 32 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0083 others(29): Show |
32 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.401-3914_401-3910d others(7): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(37): Show |
41 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.401-3915_401-3910d others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT | 14 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0108 others(11): Show |
14 | HG01255.hp2 HG01256.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.401-3916_401-3910d others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0119 others(5): Show |
8 | HG01943.hp1 HG01978.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.401-3918_401-3910d others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0189 a0001c0001t0003g0142 a0001c0001t0003g0198 |
3 | HG01934.hp1 HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.401-3919_401-3910d others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(4): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0210 a0001c0001t0003g0006 others(9): Show |
12 | HG00280.hp1 HG01069.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.401-3920_401-3910d others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0101 a0001c0001t0001g0131 a0001c0001t0001g0140 others(5): Show |
8 | HG00735.hp1 HG00738.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.401-3921_401-3910d others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0016g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.401-3922_401-3910d others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0204 a0001c0001t0005g0175 |
2 | HG01106.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.401-3923_401-3910d others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.401-3925_401-3910d others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0111 a0001c0001t0003g0148 |
2 | HG02135.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.401-3926_401-3910d others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0003g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.401-3930_401-3910d others(23): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CT | C | 13 | a0001c0001t0002g0024 a0001c0001t0002g0030 a0001c0001t0002g0033 others(10): Show |
13 | HG02717.hp1 HG02818.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-3910delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTT | C | 19 | a0001c0001t0002g0014 a0001c0001t0002g0025 a0001c0001t0002g0031 others(16): Show |
19 | HG00673.hp2 HG02109.hp1 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.401-3911_401-3910d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTT | C | 16 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(13): Show |
16 | HG01928.hp1 HG02004.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.401-3912_401-3910d others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTT | C | 17 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0003g0005 others(14): Show |
17 | HG01243.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.401-3915_401-3910d others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTTT | C | 9 | a0001c0001t0001g0150 a0001c0001t0004g0297 a0001c0001t0004g0301 others(6): Show |
9 | HG00639.hp1 HG02809.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.401-3916_401-3910d others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0217 a0001c0001t0001g0224 a0001c0001t0001g0245 others(4): Show |
7 | HG00438.hp2 HG01109.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-3918_401-3910d others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTTT others(3): Show |
C | 84 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(81): Show |
84 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.401-3919_401-3910d others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG00438.hp1 HG02074.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.401-3920_401-3910d others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-3922_401-3910d others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.401-3923_401-3910d others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTTT others(10): Show |
C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | HG03831.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.401-3926_401-3910d others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760860 | CTTTTTTT others(18): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.401-3934_401-3910d others(27): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760860 | |||||||
| chr4:77760946 | G | A | 88 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(85): Show |
88 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.401-3995C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760946 | |||||||
| chr4:77760968 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.401-4017C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77760968 | |||||||
| chr4:77761099 | C | T | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-4148G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77761099 | |||||||
| chr4:77761195 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.401-4244A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77761195 | |||||||
| chr4:77761200 | A | G | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.401-4249T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77761200 | |||||||
| chr4:77761427 | T | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(153): Show |
157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.401-4476A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77761427 | |||||||
| chr4:77761566 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.401-4615A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77761566 | |||||||
| chr4:77761588 | G | A | 83 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(80): Show |
83 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.401-4637C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77761588 | |||||||
| chr4:77761732 | T | C | 1 | a0001c0001t0028g0327 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.401-4781A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77761732 | |||||||
| chr4:77761876 | A | G | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.401-4925T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77761876 | |||||||
| chr4:77762145 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.401-5194A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77762145 | |||||||
| chr4:77762219 | C | G | 4 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(1): Show |
4 | HG00735.hp1 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-5268G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77762219 | |||||||
| chr4:77762485 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.401-5534A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77762485 | |||||||
| chr4:77762719 | C | G | 1 | a0001c0001t0004g0312 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.401-5768G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77762719 | |||||||
| chr4:77762885 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.401-5934A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77762885 | |||||||
| chr4:77763006 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.401-6055T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763006 | |||||||
| chr4:77763057 | C | T | 1 | a0001c0001t0006g0212 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.401-6106G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763057 | |||||||
| chr4:77763173 | A | G | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.401-6222T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763173 | |||||||
| chr4:77763187 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.401-6236C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763187 | |||||||
| chr4:77763338 | C | T | 11 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.401-6387G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763338 | |||||||
| chr4:77763674 | G | A | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.401-6723C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763674 | |||||||
| chr4:77763764 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.401-6813G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763764 | |||||||
| chr4:77763896 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.401-6945A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763896 | |||||||
| chr4:77763927 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.401-6976C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77763927 | |||||||
| chr4:77764092 | C | T | 26 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(23): Show |
26 | HG00673.hp2 HG01928.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.401-7141G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764092 | |||||||
| chr4:77764162 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.401-7211G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764162 | |||||||
| chr4:77764181 | G | A | 1 | a0001c0001t0038g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.401-7230C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764181 | |||||||
| chr4:77764479 | T | C | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.401-7528A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764479 | |||||||
| chr4:77764561 | G | A | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.401-7610C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764561 | |||||||
| chr4:77764681 | G | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.401-7730C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764681 | |||||||
| chr4:77764699 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18953.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.401-7748G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764699 | |||||||
| chr4:77764718 | A | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(302): Show |
306 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.401-7767T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764718 | |||||||
| chr4:77764787 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.401-7836G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764787 | |||||||
| chr4:77764811 | C | T | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.401-7860G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764811 | |||||||
| chr4:77764954 | G | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.401-8003C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77764954 | |||||||
| chr4:77765048 | T | A | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+8033A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765048 | |||||||
| chr4:77765091 | G | A | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.400+7990C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765091 | |||||||
| chr4:77765137 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.400+7944G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765137 | |||||||
| chr4:77765218 | G | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.400+7863C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765218 | |||||||
| chr4:77765292 | A | G | 3 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0205 |
3 | NA18947.hp2 NA18974.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.400+7789T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765292 | |||||||
| chr4:77765369 | T | TA | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(158): Show |
162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.400+7711dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765369 | |||||||
| chr4:77765397 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400+7684T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765397 | |||||||
| chr4:77765749 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0217 a0001c0001t0001g0229 others(3): Show |
6 | HG02129.hp1 NA18939.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+7332G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765749 | |||||||
| chr4:77765908 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.400+7173G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77765908 | |||||||
| chr4:77766015 | T | C | 3 | a0001c0001t0007g0057 a0001c0001t0007g0058 a0001c0001t0007g0059 |
3 | HG00099.hp1 HG00741.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.400+7066A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77766015 | |||||||
| chr4:77766544 | GA | G | 78 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0215 others(75): Show |
78 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.400+6536delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77766544 | |||||||
| chr4:77766605 | ATTTGCAG others(9): Show |
A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400+6460_400+6475d others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77766605 | |||||||
| chr4:77766719 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.400+6362A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77766719 | |||||||
| chr4:77766749 | AAAG | A | 26 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(23): Show |
26 | HG00673.hp2 HG01928.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.400+6329_400+6331d others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77766749 | |||||||
| chr4:77766799 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.400+6282G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77766799 | |||||||
| chr4:77766911 | A | C | 1 | a0001c0001t0002g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400+6170T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77766911 | |||||||
| chr4:77767049 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.400+6032G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767049 | |||||||
| chr4:77767062 | C | CA | 72 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0100 others(69): Show |
73 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.400+6018dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767062 | |||||||
| chr4:77767062 | C | CAA | 12 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0187 others(9): Show |
12 | HG01243.hp1 HG01261.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+6017_400+6018d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767062 | |||||||
| chr4:77767062 | CA | C | 14 | a0001c0001t0001g0133 a0001c0001t0001g0137 a0001c0001t0001g0225 others(11): Show |
14 | HG00323.hp2 HG01169.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.400+6018delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767062 | |||||||
| chr4:77767087 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.400+5994C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767087 | |||||||
| chr4:77767114 | T | TA | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
240 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.400+5966dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767114 | |||||||
| chr4:77767189 | T | G | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.400+5892A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767189 | |||||||
| chr4:77767368 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0205 |
2 | NA18947.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.400+5713G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767368 | |||||||
| chr4:77767584 | GA | G | 10 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.400+5496delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767584 | |||||||
| chr4:77767745 | G | GC | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(153): Show |
157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.400+5335_400+5336i others(3): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767745 | |||||||
| chr4:77767929 | A | C | 1 | a0001c0001t0002g0069 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.400+5152T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767929 | |||||||
| chr4:77767936 | CACCATTG others(1): Show |
C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.400+5137_400+5144d others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767936 | |||||||
| chr4:77767967 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400+5114C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767967 | |||||||
| chr4:77767980 | C | CA | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0085 others(116): Show |
119 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.400+5100dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767980 | |||||||
| chr4:77767980 | C | CAA | 7 | a0001c0001t0001g0224 a0001c0001t0001g0252 a0001c0001t0001g0255 others(4): Show |
7 | HG01993.hp2 HG02015.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+5099_400+5100d others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77767980 | |||||||
| chr4:77768007 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.400+5074A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768007 | |||||||
| chr4:77768033 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.400+5048C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768033 | |||||||
| chr4:77768434 | C | G | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.400+4647G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768434 | |||||||
| chr4:77768470 | A | AATATATA others(3): Show |
1 | a0001c0001t0006g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.400+4610_400+4611i others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768470 | A | AATATATA others(5): Show |
2 | a0001c0001t0006g0213 a0001c0001t0006g0307 |
2 | HG03209.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.400+4610_400+4611i others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768470 | A | AATATATA others(7): Show |
2 | a0001c0001t0006g0268 a0001c0003t0025g0172 |
2 | HG02735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.400+4610_400+4611i others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768470 | A | AATATATA others(9): Show |
1 | a0001c0001t0006g0313 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.400+4610_400+4611i others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768470 | AATAAATA others(13): Show |
A | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.400+4591_400+4610d others(22): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768470 | AATAAATA others(15): Show |
A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0094 a0001c0001t0001g0179 others(4): Show |
7 | HG01169.hp2 HG01243.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+4589_400+4610d others(24): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768470 | AATAAATA others(17): Show |
A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(234): Show |
238 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.400+4587_400+4610d others(26): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768470 | AATAAATA others(19): Show |
A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0228 a0001c0001t0001g0323 |
3 | NA18942.hp1 NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.400+4585_400+4610d others(28): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768470 | AATAAATA others(25): Show |
A | 1 | a0001c0001t0006g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.400+4579_400+4610d others(34): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768470 | |||||||
| chr4:77768474 | A | AATAAATA others(7): Show |
1 | a0001c0001t0002g0029 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.400+4606_400+4607i others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATAAATA others(13): Show |
2 | a0001c0001t0002g0042 a0001c0001t0002g0063 |
2 | HG02895.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.400+4606_400+4607i others(22): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATAT | 6 | a0001c0001t0002g0028 a0001c0001t0002g0052 a0001c0001t0002g0061 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+4601_400+4606d others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(1): Show |
5 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0037 others(2): Show |
5 | HG02004.hp2 HG02273.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+4599_400+4606d others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(3): Show |
7 | a0001c0001t0002g0017 a0001c0001t0002g0030 a0001c0001t0002g0033 others(4): Show |
7 | HG02602.hp1 HG03098.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+4597_400+4606d others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(5): Show |
8 | a0001c0001t0002g0014 a0001c0001t0002g0024 a0001c0001t0002g0031 others(5): Show |
8 | HG00639.hp1 HG00673.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.400+4595_400+4606d others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(7): Show |
5 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0064 others(2): Show |
5 | HG01928.hp1 HG02129.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+4593_400+4606d others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(9): Show |
1 | a0001c0001t0002g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400+4591_400+4606d others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(11): Show |
1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.400+4589_400+4606d others(20): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(13): Show |
2 | a0001c0001t0002g0065 a0001c0001t0002g0069 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.400+4587_400+4606d others(22): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(15): Show |
1 | a0001c0001t0002g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+4585_400+4606d others(24): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | AATATATA others(17): Show |
1 | a0001c0001t0002g0022 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.400+4583_400+4606d others(26): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.400+4606_400+4607i others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | A | T | 8 | a0001c0001t0006g0206 a0001c0001t0006g0212 a0001c0001t0006g0213 others(5): Show |
8 | HG01891.hp2 HG02735.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.400+4607T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | AATATAT | A | 3 | a0001c0001t0002g0049 a0001c0001t0002g0062 a0001c0001t0024g0012 |
3 | HG02717.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.400+4601_400+4606d others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | AATATATA others(13): Show |
A | 1 | a0001c0001t0002g0036 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.400+4587_400+4606d others(22): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | AATATATA others(17): Show |
A | 3 | a0001c0001t0001g0140 a0001c0001t0014g0223 a0001c0001t0014g0269 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.400+4583_400+4606d others(26): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768474 | AATATATA others(19): Show |
A | 1 | a0001c0001t0013g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.400+4581_400+4606d others(28): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768474 | |||||||
| chr4:77768478 | T | A | 1 | a0001c0001t0002g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.400+4603A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768478 | |||||||
| chr4:77768480 | T | A | 1 | a0001c0001t0002g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.400+4601A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768480 | |||||||
| chr4:77768482 | T | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG02602.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.400+4599A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768482 | |||||||
| chr4:77768486 | T | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.400+4595A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768486 | |||||||
| chr4:77768573 | A | C | 2 | a0001c0001t0003g0145 a0001c0001t0003g0211 |
2 | HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.400+4508T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768573 | |||||||
| chr4:77768585 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400+4496A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768585 | |||||||
| chr4:77768776 | CAAAACTT | C | 21 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00323.hp1 HG00438.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.400+4298_400+4304d others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768776 | |||||||
| chr4:77768929 | C | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(243): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.400+4152G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77768929 | |||||||
| chr4:77769604 | A | G | 1 | a0001c0001t0038g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.400+3477T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77769604 | |||||||
| chr4:77769684 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.400+3397G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77769684 | |||||||
| chr4:77769933 | C | T | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.400+3148G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77769933 | |||||||
| chr4:77770189 | A | G | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+2892T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77770189 | |||||||
| chr4:77770616 | C | CCATAT | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.400+2464_400+2465i others(7): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77770616 | |||||||
| chr4:77770681 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.400+2400C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77770681 | |||||||
| chr4:77770735 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.400+2346G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77770735 | |||||||
| chr4:77770860 | A | G | 1 | a0001c0001t0005g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.400+2221T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77770860 | |||||||
| chr4:77771079 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.400+2002T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77771079 | |||||||
| chr4:77771155 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400+1926T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77771155 | |||||||
| chr4:77771182 | G | A | 1 | a0001c0001t0006g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.400+1899C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77771182 | |||||||
| chr4:77771248 | G | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.400+1833C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77771248 | |||||||
| chr4:77771363 | G | A | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.400+1718C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77771363 | |||||||
| chr4:77771381 | A | G | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.400+1700T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77771381 | |||||||
| chr4:77771975 | A | T | 1 | a0001c0001t0001g0247 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.400+1106T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77771975 | |||||||
| chr4:77772157 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.400+924T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772157 | |||||||
| chr4:77772180 | A | G | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.400+901T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772180 | |||||||
| chr4:77772190 | A | G | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.400+891T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772190 | |||||||
| chr4:77772227 | T | C | 1 | a0001c0001t0005g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.400+854A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772227 | |||||||
| chr4:77772263 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.400+818C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772263 | |||||||
| chr4:77772316 | T | A | 1 | a0002c0002t0001g0110 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.400+765A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772316 | |||||||
| chr4:77772372 | A | G | 1 | a0001c0001t0022g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.400+709T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772372 | |||||||
| chr4:77772548 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.400+533T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772548 | |||||||
| chr4:77772718 | C | G | 2 | a0001c0001t0017g0287 a0001c0001t0017g0291 |
2 | NA18992.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.400+363G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772718 | |||||||
| chr4:77772796 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0270 |
2 | HG01069.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.400+285C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772796 | |||||||
| chr4:77772830 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.400+251T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772830 | |||||||
| chr4:77772882 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG02132.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.400+199G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772882 | |||||||
| chr4:77772898 | G | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400+183C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772898 | |||||||
| chr4:77772917 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0193 |
3 | NA18943.hp1 NA18963.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.400+164G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772917 | |||||||
| chr4:77772921 | T | TCAAA | 6 | a0001c0001t0001g0083 a0001c0001t0001g0230 a0001c0001t0001g0239 others(3): Show |
6 | HG00597.hp1 HG01169.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+156_400+159dup others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77772921 | |||||||
| chr4:77773000 | T | C | 3 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.400+81A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77773000 | |||||||
| chr4:77773052 | T | C | 16 | a0001c0001t0001g0179 a0001c0001t0006g0171 a0001c0001t0006g0206 others(13): Show |
16 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.400+29A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | 77773052 | |||||||
| chr4:77773173 | T | A | 1 | a0001c0001t0003g0005 | 1 | NA18989.hp1 | splice_region_variant&intron_variant | LOW | c.315-7A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77773173 | |||||||
| chr4:77773173 | TA | T | 19 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0001g0135 others(16): Show |
19 | HG00639.hp1 HG01891.hp2 HG02451.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.315-8delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77773173 | |||||||
| chr4:77773316 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.315-150T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77773316 | |||||||
| chr4:77773500 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.315-334G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77773500 | |||||||
| chr4:77773738 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0113 others(12): Show |
16 | HG01175.hp1 HG01261.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.315-572A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77773738 | |||||||
| chr4:77773812 | T | C | 1 | a0001c0001t0030g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.315-646A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77773812 | |||||||
| chr4:77773926 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.314+604T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77773926 | |||||||
| chr4:77773984 | T | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.314+546A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77773984 | |||||||
| chr4:77774060 | T | A | 1 | a0001c0001t0001g0294 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.314+470A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77774060 | |||||||
| chr4:77774081 | G | A | 1 | a0002c0002t0001g0110 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.314+449C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77774081 | |||||||
| chr4:77774201 | C | G | 1 | a0001c0001t0001g0284 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.314+329G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77774201 | |||||||
| chr4:77774383 | G | A | 1 | a0001c0001t0006g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.314+147C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 3/11 | chr4 | 77774383 | |||||||
| chr4:77774778 | C | G | 12 | a0001c0001t0002g0017 a0001c0001t0002g0022 a0001c0001t0002g0024 others(9): Show |
12 | HG02080.hp1 HG02129.hp2 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.128-62G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 2/11 | chr4 | 77774778 | |||||||
| chr4:77774803 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128-87C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 2/11 | chr4 | 77774803 | |||||||
| chr4:77774815 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.128-99G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 2/11 | chr4 | 77774815 | |||||||
| chr4:77774845 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.128-129A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 2/11 | chr4 | 77774845 | |||||||
| chr4:77775280 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.128-564G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 2/11 | chr4 | 77775280 | |||||||
| chr4:77775412 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.128-696A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 2/11 | chr4 | 77775412 | |||||||
| chr4:77775725 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.127+546T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 2/11 | chr4 | 77775725 | |||||||
| chr4:77776048 | C | T | 1 | a0001c0001t0007g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127+223G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 2/11 | chr4 | 77776048 | |||||||
| chr4:77776398 | T | TA | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(300): Show |
304 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
splice_region_variant&intron_variant | LOW | c.6-7dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77776398 | |||||||
| chr4:77776411 | G | A | 3 | a0001c0001t0005g0175 a0001c0001t0005g0207 a0001c0001t0005g0208 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.6-19C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77776411 | |||||||
| chr4:77776632 | T | C | 7 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0204 others(4): Show |
7 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-240A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77776632 | |||||||
| chr4:77776636 | A | G | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6-244T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77776636 | |||||||
| chr4:77776764 | G | T | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6-372C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77776764 | |||||||
| chr4:77776874 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-482T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77776874 | |||||||
| chr4:77776948 | A | G | 11 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.6-556T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77776948 | |||||||
| chr4:77777193 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0293 a0001c0001t0001g0326 |
3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6-801T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77777193 | |||||||
| chr4:77777546 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6-1154T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77777546 | |||||||
| chr4:77777690 | A | C | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6-1298T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77777690 | |||||||
| chr4:77777703 | G | C | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6-1311C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77777703 | |||||||
| chr4:77777793 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-1401A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77777793 | |||||||
| chr4:77777907 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6-1515C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77777907 | |||||||
| chr4:77778009 | A | T | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-1617T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778009 | |||||||
| chr4:77778103 | T | C | 18 | a0001c0001t0001g0092 a0001c0001t0005g0175 a0001c0001t0005g0176 others(15): Show |
18 | HG00735.hp1 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.6-1711A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778103 | |||||||
| chr4:77778227 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-1835T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778227 | |||||||
| chr4:77778243 | T | A | 2 | a0001c0001t0001g0095 a0001c0001t0031g0112 |
2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.6-1851A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778243 | |||||||
| chr4:77778404 | C | CT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.6-2013dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778404 | |||||||
| chr4:77778429 | G | C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-2037C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778429 | |||||||
| chr4:77778479 | C | T | 7 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(4): Show |
7 | HG02602.hp2 HG03490.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-2087G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778479 | |||||||
| chr4:77778551 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6-2159C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778551 | |||||||
| chr4:77778660 | C | CTCCCAAA others(18): Show |
1 | a0001c0001t0001g0011 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.6-2293_6-2269dupTG others(23): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778660 | |||||||
| chr4:77778660 | CTCCCAAA others(18): Show |
C | 3 | a0001c0001t0001g0092 a0001c0001t0014g0223 a0001c0001t0014g0269 |
3 | HG02145.hp2 HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6-2293_6-2269delTG others(23): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778660 | |||||||
| chr4:77778681 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6-2289T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778681 | |||||||
| chr4:77778709 | C | A | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6-2317G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778709 | |||||||
| chr4:77778712 | G | T | 1 | a0001c0001t0009g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6-2320C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778712 | |||||||
| chr4:77778974 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6-2582T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778974 | |||||||
| chr4:77778979 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0003g0148 |
2 | HG02135.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.6-2587C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77778979 | |||||||
| chr4:77779046 | C | CA | 77 | a0001c0001t0001g0010 a0001c0001t0001g0215 a0001c0001t0001g0217 others(74): Show |
77 | HG00673.hp2 HG01109.hp1 HG01256.hp2 others(74): Show |
intron_variant | MODIFIER | c.6-2655dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779046 | |||||||
| chr4:77779046 | C | CAA | 14 | a0001c0001t0001g0173 a0001c0001t0001g0218 a0001c0001t0001g0230 others(11): Show |
14 | HG00558.hp2 HG01069.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.6-2656_6-2655dupTT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779046 | |||||||
| chr4:77779046 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.6-2665_6-2655dupTT others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779046 | |||||||
| chr4:77779046 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6-2670_6-2655dupTT others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779046 | |||||||
| chr4:77779046 | CA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(142): Show |
146 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.6-2655delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779046 | |||||||
| chr4:77779059 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-2667T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779059 | |||||||
| chr4:77779062 | AC | A | 10 | a0001c0001t0001g0160 a0001c0001t0006g0212 a0001c0001t0006g0213 others(7): Show |
10 | HG00438.hp1 HG00639.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.6-2671delG | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779062 | |||||||
| chr4:77779063 | C | A | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0136 others(91): Show |
94 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.6-2671G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779063 | |||||||
| chr4:77779064 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-2672T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779064 | |||||||
| chr4:77779069 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-2677T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779069 | |||||||
| chr4:77779073 | AC | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(134): Show |
138 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.6-2682delG | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779073 | |||||||
| chr4:77779074 | C | A | 167 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0136 others(164): Show |
167 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.6-2682G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779074 | |||||||
| chr4:77779075 | A | G | 1 | a0001c0001t0009g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.6-2683T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779075 | |||||||
| chr4:77779076 | C | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0183 a0001c0001t0001g0315 others(1): Show |
4 | HG00738.hp2 HG03688.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-2684G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779076 | |||||||
| chr4:77779199 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6-2807G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779199 | |||||||
| chr4:77779578 | A | C | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-3186T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779578 | |||||||
| chr4:77779722 | G | A | 2 | a0001c0001t0027g0318 a0001c0001t0028g0327 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.6-3330C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779722 | |||||||
| chr4:77779789 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-3397C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779789 | |||||||
| chr4:77779821 | G | A | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-3429C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779821 | |||||||
| chr4:77779833 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-3441C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779833 | |||||||
| chr4:77779858 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6-3466T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779858 | |||||||
| chr4:77779879 | G | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-3487C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779879 | |||||||
| chr4:77779938 | T | C | 1 | a0001c0001t0003g0322 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6-3546A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77779938 | |||||||
| chr4:77780027 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6-3635G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77780027 | |||||||
| chr4:77780135 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0324 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.6-3743C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77780135 | |||||||
| chr4:77780333 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6-3941A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77780333 | |||||||
| chr4:77780424 | T | C | 8 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0121 others(5): Show |
8 | HG00544.hp1 HG00558.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-4032A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77780424 | |||||||
| chr4:77780740 | ATT | A | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-4350_6-4349delAA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77780740 | |||||||
| chr4:77780828 | C | T | 12 | a0001c0001t0001g0108 a0001c0001t0001g0133 a0001c0001t0001g0134 others(9): Show |
12 | HG00323.hp2 HG00597.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.6-4436G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77780828 | |||||||
| chr4:77780925 | T | G | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6-4533A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77780925 | |||||||
| chr4:77781061 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0190 |
3 | HG00544.hp1 HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.6-4669G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77781061 | |||||||
| chr4:77781236 | G | A | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6-4844C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77781236 | |||||||
| chr4:77781254 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6-4862C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77781254 | |||||||
| chr4:77781314 | T | C | 3 | a0001c0001t0001g0273 a0001c0001t0001g0280 a0001c0001t0029g0251 |
3 | NA18947.hp1 NA18959.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.6-4922A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77781314 | |||||||
| chr4:77781657 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.6-5265C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77781657 | |||||||
| chr4:77781673 | C | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6-5281G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77781673 | |||||||
| chr4:77781942 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.6-5550G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77781942 | |||||||
| chr4:77782408 | T | C | 1 | a0001c0001t0003g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.6-6016A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782408 | |||||||
| chr4:77782509 | A | AT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.6-6118dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782509 | |||||||
| chr4:77782561 | G | A | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6-6169C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782561 | |||||||
| chr4:77782605 | C | T | 2 | a0001c0001t0015g0250 a0001c0001t0015g0281 |
2 | NA18980.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.6-6213G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782605 | |||||||
| chr4:77782641 | C | CT | 7 | a0001c0001t0007g0050 a0001c0001t0007g0054 a0001c0001t0019g0310 others(4): Show |
7 | HG02280.hp1 HG02738.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-6250dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782641 | |||||||
| chr4:77782641 | CT | C | 19 | a0001c0001t0002g0016 a0001c0001t0002g0037 a0001c0001t0002g0044 others(16): Show |
19 | HG00639.hp1 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.6-6250delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782641 | |||||||
| chr4:77782641 | CTTT | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(152): Show |
156 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.6-6252_6-6250delAA others(1): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782641 | |||||||
| chr4:77782641 | CTTTT | C | 87 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(84): Show |
87 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6-6253_6-6250delAA others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782641 | |||||||
| chr4:77782772 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-6380T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77782772 | |||||||
| chr4:77783131 | C | T | 1 | a0002c0002t0001g0110 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-6739G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783131 | |||||||
| chr4:77783150 | C | CA | 14 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0103 others(11): Show |
14 | HG01256.hp1 HG02602.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.6-6759dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783150 | |||||||
| chr4:77783150 | C | CAA | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(207): Show |
211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.6-6760_6-6759dupTT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783150 | |||||||
| chr4:77783150 | C | CAAA | 23 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0001t0001g0108 others(20): Show |
23 | HG01109.hp1 HG01169.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.6-6761_6-6759dupTT others(1): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783150 | |||||||
| chr4:77783171 | C | A | 2 | a0001c0001t0001g0265 a0001c0001t0003g0145 |
2 | HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.6-6779G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783171 | |||||||
| chr4:77783175 | T | C | 4 | a0001c0001t0001g0265 a0001c0001t0003g0145 a0001c0001t0014g0223 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-6783A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783175 | |||||||
| chr4:77783187 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.6-6795C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783187 | |||||||
| chr4:77783191 | AG | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0224 a0001c0001t0001g0293 others(1): Show |
4 | HG02922.hp1 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-6800delC | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783191 | |||||||
| chr4:77783235 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6-6843C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783235 | |||||||
| chr4:77783349 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6-6957G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783349 | |||||||
| chr4:77783365 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-6973T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783365 | |||||||
| chr4:77783806 | C | T | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-7414G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783806 | |||||||
| chr4:77783875 | T | TTATTAAA others(26): Show |
1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6-7516_6-7484dupTT others(31): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783875 | |||||||
| chr4:77783939 | A | G | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.6-7547T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77783939 | |||||||
| chr4:77784285 | C | T | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6-7893G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784285 | |||||||
| chr4:77784500 | A | AT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(134): Show |
138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.6-8109dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784500 | |||||||
| chr4:77784500 | A | ATT | 6 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(3): Show |
6 | HG00741.hp1 HG01346.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-8110_6-8109dupAA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784500 | |||||||
| chr4:77784500 | A | ATTT | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.6-8111_6-8109dupAA others(1): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784500 | |||||||
| chr4:77784500 | AT | A | 7 | a0001c0001t0002g0065 a0001c0001t0004g0302 a0001c0001t0019g0310 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-8109delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784500 | |||||||
| chr4:77784584 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6-8192T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784584 | |||||||
| chr4:77784616 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6-8224C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784616 | |||||||
| chr4:77784737 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-8345C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784737 | |||||||
| chr4:77784782 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0149 a0001c0001t0001g0192 |
3 | HG02970.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6-8390G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784782 | |||||||
| chr4:77784822 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6-8430A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784822 | |||||||
| chr4:77784856 | G | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(81): Show |
84 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.6-8464C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784856 | |||||||
| chr4:77784863 | A | G | 26 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(23): Show |
26 | HG00673.hp2 HG01928.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.6-8471T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784863 | |||||||
| chr4:77784907 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.6-8515G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77784907 | |||||||
| chr4:77785023 | T | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-8631A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77785023 | |||||||
| chr4:77785168 | T | C | 1 | a0001c0001t0007g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.6-8776A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77785168 | |||||||
| chr4:77785303 | C | A | 1 | a0001c0001t0010g0170 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6-8911G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77785303 | |||||||
| chr4:77785450 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0123 |
2 | HG02080.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.6-9058G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77785450 | |||||||
| chr4:77785577 | T | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-9185A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77785577 | |||||||
| chr4:77785629 | G | A | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6-9237C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77785629 | |||||||
| chr4:77785702 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0324 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.6-9310A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77785702 | |||||||
| chr4:77785772 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG00642.hp2 HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.6-9380C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77785772 | |||||||
| chr4:77786006 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.6-9614A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786006 | |||||||
| chr4:77786009 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.6-9617C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786009 | |||||||
| chr4:77786184 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6-9792G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786184 | |||||||
| chr4:77786264 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.6-9872C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786264 | |||||||
| chr4:77786279 | T | TA | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(258): Show |
262 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.6-9888dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786279 | |||||||
| chr4:77786470 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.6-10078T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786470 | |||||||
| chr4:77786485 | T | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-10093A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786485 | |||||||
| chr4:77786576 | G | C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-10184C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786576 | |||||||
| chr4:77786794 | G | C | 1 | a0001c0001t0002g0022 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.6-10402C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786794 | |||||||
| chr4:77786999 | C | T | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-10607G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77786999 | |||||||
| chr4:77787003 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6-10611G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787003 | |||||||
| chr4:77787111 | CA | C | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.6-10720delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787111 | |||||||
| chr4:77787239 | C | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0083 others(42): Show |
46 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.6-10847G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787239 | |||||||
| chr4:77787252 | T | G | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6-10860A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787252 | |||||||
| chr4:77787256 | ACT | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(149): Show |
153 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.6-10866_6-10865del others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787256 | |||||||
| chr4:77787542 | A | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(138): Show |
142 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.6-11150T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787542 | |||||||
| chr4:77787638 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6-11246G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787638 | |||||||
| chr4:77787727 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6-11335C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787727 | |||||||
| chr4:77787950 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.6-11558A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77787950 | |||||||
| chr4:77788091 | A | G | 19 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0005g0175 others(16): Show |
19 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.6-11699T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77788091 | |||||||
| chr4:77788153 | G | T | 1 | a0001c0001t0002g0033 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6-11761C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77788153 | |||||||
| chr4:77788194 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-11802T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77788194 | |||||||
| chr4:77788377 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0263 |
2 | NA19004.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.6-11985A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77788377 | |||||||
| chr4:77788461 | C | T | 1 | a0001c0001t0014g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6-12069G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77788461 | |||||||
| chr4:77788621 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-12229T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77788621 | |||||||
| chr4:77789055 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6-12663A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789055 | |||||||
| chr4:77789090 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6-12698C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789090 | |||||||
| chr4:77789141 | G | A | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.6-12749C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789141 | |||||||
| chr4:77789172 | A | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0019 a0001c0001t0008g0035 |
3 | NA18964.hp1 NA19004.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.6-12780T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789172 | |||||||
| chr4:77789185 | A | C | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6-12793T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789185 | |||||||
| chr4:77789290 | A | AGCTCCCC others(4): Show |
2 | a0001c0001t0001g0161 a0001c0001t0001g0163 |
2 | HG00323.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-12909_6-12899dup others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789290 | |||||||
| chr4:77789384 | C | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(81): Show |
84 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.6-12992G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789384 | |||||||
| chr4:77789408 | A | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0083 others(42): Show |
46 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.6-13016T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789408 | |||||||
| chr4:77789594 | A | T | 1 | a0001c0001t0001g0270 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6-13202T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789594 | |||||||
| chr4:77789657 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0037g0182 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.6-13265G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789657 | |||||||
| chr4:77789679 | G | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6-13287C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789679 | |||||||
| chr4:77789707 | T | C | 4 | a0001c0001t0001g0214 a0001c0001t0001g0224 a0001c0001t0001g0293 others(1): Show |
4 | HG02922.hp1 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-13315A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789707 | |||||||
| chr4:77789829 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6-13437A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789829 | |||||||
| chr4:77789925 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.6-13533C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789925 | |||||||
| chr4:77789934 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0325 |
2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.6-13542T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789934 | |||||||
| chr4:77789945 | C | CA | 14 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0027 others(11): Show |
14 | HG02132.hp1 HG02738.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.6-13554dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789945 | |||||||
| chr4:77789945 | CA | C | 17 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(14): Show |
17 | HG01109.hp2 HG01928.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.6-13554delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789945 | |||||||
| chr4:77789945 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.6-13564_6-13554del others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789945 | |||||||
| chr4:77789945 | CAAAAAAA others(5): Show |
C | 12 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(9): Show |
12 | HG01109.hp1 HG02015.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.6-13565_6-13554del others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789945 | |||||||
| chr4:77789945 | CAAAAAAA others(6): Show |
C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(219): Show |
223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.6-13566_6-13554del others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789945 | |||||||
| chr4:77789945 | CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0119 others(6): Show |
9 | HG00738.hp2 HG02015.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.6-13567_6-13554del others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789945 | |||||||
| chr4:77789945 | CAAAAAAA others(8): Show |
C | 14 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(11): Show |
14 | HG01891.hp2 HG02280.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.6-13568_6-13554del others(15): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789945 | |||||||
| chr4:77789945 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0006g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6-13569_6-13554del others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77789945 | |||||||
| chr4:77790074 | C | T | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6-13682G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790074 | |||||||
| chr4:77790552 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(253): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.6-14160C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790552 | |||||||
| chr4:77790577 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6-14185A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790577 | |||||||
| chr4:77790805 | C | T | 19 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0005g0175 others(16): Show |
19 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.6-14413G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790805 | |||||||
| chr4:77790815 | A | AT | 51 | a0001c0001t0001g0092 a0001c0001t0001g0139 a0001c0001t0001g0209 others(48): Show |
51 | HG00639.hp1 HG00673.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.6-14424dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790815 | |||||||
| chr4:77790815 | AT | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(82): Show |
85 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.6-14424delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790815 | |||||||
| chr4:77790895 | C | T | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6-14503G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790895 | |||||||
| chr4:77790907 | G | A | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.6-14515C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790907 | |||||||
| chr4:77790938 | G | C | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6-14546C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77790938 | |||||||
| chr4:77791006 | G | A | 19 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0006 others(16): Show |
19 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.6-14614C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791006 | |||||||
| chr4:77791014 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG00741.hp1 HG01346.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.6-14622T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791014 | |||||||
| chr4:77791049 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-14657C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791049 | |||||||
| chr4:77791086 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(121): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.6-14694A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791086 | |||||||
| chr4:77791131 | A | G | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-14739T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791131 | |||||||
| chr4:77791270 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0205 |
3 | NA18947.hp2 NA18974.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.6-14878G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791270 | |||||||
| chr4:77791284 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6-14892G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791284 | |||||||
| chr4:77791319 | T | C | 4 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0249 others(1): Show |
4 | HG02523.hp2 NA18963.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-14927A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791319 | |||||||
| chr4:77791413 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6-15021C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791413 | |||||||
| chr4:77791451 | T | C | 1 | a0001c0001t0006g0268 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6-15059A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791451 | |||||||
| chr4:77791514 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6-15122T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791514 | |||||||
| chr4:77791544 | T | A | 1 | a0001c0001t0005g0220 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6-15152A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791544 | |||||||
| chr4:77791571 | A | G | 1 | a0001c0001t0040g0018 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.6-15179T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791571 | |||||||
| chr4:77791630 | T | G | 2 | a0001c0001t0004g0290 a0001c0001t0004g0311 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6-15238A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791630 | |||||||
| chr4:77791853 | T | A | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6-15461A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791853 | |||||||
| chr4:77791894 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6-15502A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791894 | |||||||
| chr4:77791905 | A | G | 7 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0143 others(4): Show |
7 | HG01358.hp1 HG01361.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-15513T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791905 | |||||||
| chr4:77791944 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.6-15552C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791944 | |||||||
| chr4:77791961 | C | A | 1 | a0001c0001t0001g0237 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6-15569G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77791961 | |||||||
| chr4:77792100 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6-15708G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792100 | |||||||
| chr4:77792141 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.6-15749G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792141 | |||||||
| chr4:77792294 | C | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG02083.hp1 NA18945.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.6-15902G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792294 | |||||||
| chr4:77792310 | T | C | 11 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
11 | HG00741.hp1 HG01346.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.6-15918A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792310 | |||||||
| chr4:77792636 | G | A | 10 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.6-16244C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792636 | |||||||
| chr4:77792725 | T | TA | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(223): Show |
227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.6-16334dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792725 | |||||||
| chr4:77792725 | T | TAA | 8 | a0001c0001t0001g0219 a0001c0001t0001g0260 a0001c0001t0001g0265 others(5): Show |
8 | HG01934.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-16335_6-16334dup others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792725 | |||||||
| chr4:77792764 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.6-16372C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792764 | |||||||
| chr4:77792865 | G | A | 1 | a0001c0001t0006g0307 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6-16473C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77792865 | |||||||
| chr4:77793114 | C | T | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6-16722G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793114 | |||||||
| chr4:77793570 | C | T | 2 | a0001c0001t0027g0318 a0001c0001t0028g0327 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.6-17178G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793570 | |||||||
| chr4:77793573 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6-17181G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793573 | |||||||
| chr4:77793579 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0036g0274 |
2 | HG02165.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.6-17187A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793579 | |||||||
| chr4:77793598 | T | TGAGGACA others(6): Show |
5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-17219_6-17207dup others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793598 | |||||||
| chr4:77793657 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | NA18964.hp2 NA18965.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.6-17265A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793657 | |||||||
| chr4:77793747 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-17355A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793747 | |||||||
| chr4:77793762 | C | T | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-17370G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793762 | |||||||
| chr4:77793776 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.6-17384T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793776 | |||||||
| chr4:77793836 | T | C | 2 | a0001c0001t0005g0220 a0001c0001t0005g0240 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.6-17444A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793836 | |||||||
| chr4:77793921 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0149 a0001c0001t0001g0192 |
3 | HG02970.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6-17529G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793921 | |||||||
| chr4:77793923 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.6-17531C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77793923 | |||||||
| chr4:77794007 | C | T | 1 | a0001c0001t0004g0303 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6-17615G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794007 | |||||||
| chr4:77794109 | A | G | 4 | a0001c0001t0006g0222 a0001c0001t0006g0268 a0001c0001t0006g0307 others(1): Show |
4 | HG00639.hp1 HG02735.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-17717T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794109 | |||||||
| chr4:77794110 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(152): Show |
156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.6-17718G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794110 | |||||||
| chr4:77794150 | C | CA | 34 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0192 others(31): Show |
34 | HG00639.hp2 HG01069.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.6-17759dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794150 | |||||||
| chr4:77794150 | C | CAA | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(171): Show |
175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.6-17760_6-17759dup others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794150 | |||||||
| chr4:77794150 | C | CAAA | 54 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0092 others(51): Show |
54 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.6-17761_6-17759dup others(3): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794150 | |||||||
| chr4:77794150 | C | CAAAA | 8 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0104 others(5): Show |
8 | HG00642.hp2 HG01361.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-17762_6-17759dup others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794150 | |||||||
| chr4:77794178 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6-17786T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794178 | |||||||
| chr4:77794205 | T | C | 11 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.6-17813A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794205 | |||||||
| chr4:77794241 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-17849C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794241 | |||||||
| chr4:77794278 | C | G | 89 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(86): Show |
89 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-17886G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794278 | |||||||
| chr4:77794656 | C | G | 5 | a0001c0001t0001g0288 a0001c0001t0001g0296 a0001c0001t0001g0309 others(2): Show |
5 | HG00544.hp2 HG00673.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.6-18264G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794656 | |||||||
| chr4:77794789 | A | G | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6-18397T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794789 | |||||||
| chr4:77794957 | C | CA | 14 | a0001c0001t0001g0108 a0001c0001t0001g0133 a0001c0001t0001g0134 others(11): Show |
14 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.6-18566dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794957 | |||||||
| chr4:77794998 | G | A | 88 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(85): Show |
88 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-18606C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77794998 | |||||||
| chr4:77795021 | C | CT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(136): Show |
140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.6-18630dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77795021 | |||||||
| chr4:77795021 | C | CTT | 8 | a0001c0001t0001g0117 a0001c0001t0001g0188 a0001c0001t0001g0189 others(5): Show |
8 | HG00597.hp2 HG01106.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-18631_6-18630dup others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77795021 | |||||||
| chr4:77795120 | A | G | 11 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.6-18728T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77795120 | |||||||
| chr4:77795261 | C | T | 1 | a0001c0001t0039g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6-18869G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77795261 | |||||||
| chr4:77795692 | C | A | 1 | a0001c0001t0014g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6-19300G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77795692 | |||||||
| chr4:77795898 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.6-19506G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77795898 | |||||||
| chr4:77795951 | G | GT | 12 | a0001c0001t0001g0296 a0001c0001t0005g0175 a0001c0001t0005g0176 others(9): Show |
12 | HG00735.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.6-19560dupA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77795951 | |||||||
| chr4:77795972 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6-19580C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77795972 | |||||||
| chr4:77796117 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6-19725A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796117 | |||||||
| chr4:77796122 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6-19730A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796122 | |||||||
| chr4:77796127 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.6-19735A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796127 | |||||||
| chr4:77796160 | AT | A | 24 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
24 | HG00639.hp1 HG01891.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.6-19769delA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796160 | |||||||
| chr4:77796381 | G | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0201 a0001c0001t0001g0210 |
3 | HG03927.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.6-19989C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796381 | |||||||
| chr4:77796384 | A | T | 13 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(10): Show |
13 | HG02145.hp1 HG02258.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.6-19992T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796384 | |||||||
| chr4:77796394 | C | T | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-20002G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796394 | |||||||
| chr4:77796447 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.6-20055C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796447 | |||||||
| chr4:77796448 | A | T | 1 | a0001c0001t0001g0296 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.6-20056T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796448 | |||||||
| chr4:77796449 | T | G | 1 | a0001c0001t0001g0296 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.6-20057A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796449 | |||||||
| chr4:77796621 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.6-20229C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796621 | |||||||
| chr4:77796787 | A | C | 1 | a0001c0001t0005g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-20395T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796787 | |||||||
| chr4:77796967 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6-20575A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77796967 | |||||||
| chr4:77797051 | G | A | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-20659C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797051 | |||||||
| chr4:77797102 | C | CA | 22 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0017 others(19): Show |
22 | HG00099.hp1 HG02129.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.6-20711dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797102 | |||||||
| chr4:77797102 | C | CAA | 11 | a0001c0001t0002g0033 a0001c0001t0002g0070 a0001c0001t0006g0206 others(8): Show |
11 | HG00741.hp2 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.6-20712_6-20711dup others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797102 | |||||||
| chr4:77797102 | C | CAAA | 24 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0001g0104 others(21): Show |
24 | HG00639.hp1 HG00642.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.6-20713_6-20711dup others(3): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797102 | |||||||
| chr4:77797102 | C | CAAAA | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0080 others(108): Show |
112 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.6-20714_6-20711dup others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797102 | |||||||
| chr4:77797102 | C | CAAAAA | 99 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0101 others(96): Show |
99 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.6-20715_6-20711dup others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797102 | |||||||
| chr4:77797102 | C | CAAAAAA | 15 | a0001c0001t0001g0159 a0001c0001t0001g0193 a0001c0001t0001g0199 others(12): Show |
15 | HG00642.hp1 HG01255.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.6-20716_6-20711dup others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797102 | |||||||
| chr4:77797102 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6-20720_6-20711dup others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797102 | |||||||
| chr4:77797158 | TCTAA | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-20770_6-20767del others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797158 | |||||||
| chr4:77797233 | TA | T | 10 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.6-20842delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797233 | |||||||
| chr4:77797384 | C | A | 1 | a0001c0001t0001g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6-20992G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797384 | |||||||
| chr4:77797734 | T | C | 8 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0121 others(5): Show |
8 | HG00544.hp1 HG00558.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-21342A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77797734 | |||||||
| chr4:77798114 | C | T | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5+21190G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77798114 | |||||||
| chr4:77798144 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5+21160A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77798144 | |||||||
| chr4:77798230 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.5+21074C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77798230 | |||||||
| chr4:77798330 | T | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0204 others(1): Show |
4 | HG00323.hp1 HG01106.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+20974A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77798330 | |||||||
| chr4:77798701 | C | T | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5+20603G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77798701 | |||||||
| chr4:77798789 | G | C | 3 | a0001c0001t0004g0297 a0001c0001t0004g0298 a0001c0001t0004g0303 |
3 | HG01891.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5+20515C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77798789 | |||||||
| chr4:77798821 | T | TA | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
240 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.5+20482dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77798821 | |||||||
| chr4:77799262 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0217 a0001c0001t0001g0229 others(3): Show |
6 | HG02129.hp1 NA18939.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+20042A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799262 | |||||||
| chr4:77799508 | T | C | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.5+19796A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799508 | |||||||
| chr4:77799567 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5+19737A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799567 | |||||||
| chr4:77799595 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.5+19709A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799595 | |||||||
| chr4:77799665 | T | C | 1 | a0001c0001t0008g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5+19639A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799665 | |||||||
| chr4:77799704 | C | CA | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(136): Show |
140 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.5+19599dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799704 | |||||||
| chr4:77799704 | C | CAA | 22 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0105 others(19): Show |
22 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.5+19598_5+19599dup others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799704 | |||||||
| chr4:77799704 | CA | C | 8 | a0001c0001t0001g0275 a0001c0001t0001g0296 a0001c0001t0002g0017 others(5): Show |
8 | HG02895.hp2 HG02896.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.5+19599delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799704 | |||||||
| chr4:77799829 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5+19475G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799829 | |||||||
| chr4:77799870 | T | A | 1 | a0001c0001t0001g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5+19434A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799870 | |||||||
| chr4:77799946 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5+19358G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77799946 | |||||||
| chr4:77800065 | CA | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(148): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.5+19238delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77800065 | |||||||
| chr4:77800065 | CAA | C | 9 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
9 | HG00642.hp2 HG01361.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.5+19237_5+19238del others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77800065 | |||||||
| chr4:77800347 | A | T | 3 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5+18957T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77800347 | |||||||
| chr4:77800348 | T | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(141): Show |
145 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.5+18956A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77800348 | |||||||
| chr4:77800349 | T | A | 2 | a0001c0001t0001g0134 a0001c0001t0009g0088 |
2 | HG02897.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.5+18955A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77800349 | |||||||
| chr4:77800413 | G | A | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.5+18891C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77800413 | |||||||
| chr4:77800546 | A | C | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.5+18758T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77800546 | |||||||
| chr4:77800651 | T | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.5+18653A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77800651 | |||||||
| chr4:77801161 | C | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(81): Show |
84 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.5+18143G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801161 | |||||||
| chr4:77801363 | C | T | 1 | a0001c0001t0026g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.5+17941G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801363 | |||||||
| chr4:77801690 | T | TGG | 69 | a0001c0001t0001g0011 a0001c0001t0001g0094 a0001c0001t0001g0103 others(66): Show |
69 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.5+17612_5+17613dup others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801690 | |||||||
| chr4:77801690 | T | TGGG | 73 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0079 others(70): Show |
73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.5+17611_5+17613dup others(3): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801690 | |||||||
| chr4:77801690 | T | TGGGG | 42 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(39): Show |
42 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.5+17610_5+17613dup others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801690 | |||||||
| chr4:77801690 | T | TGGGGG | 61 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(58): Show |
62 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.5+17609_5+17613dup others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801690 | |||||||
| chr4:77801694 | G | C | 5 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(2): Show |
5 | HG03490.hp2 NA18950.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+17610C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801694 | |||||||
| chr4:77801761 | G | A | 5 | a0001c0001t0005g0175 a0001c0001t0005g0207 a0001c0001t0005g0208 others(2): Show |
5 | HG02572.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+17543C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801761 | |||||||
| chr4:77801850 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.5+17454C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77801850 | |||||||
| chr4:77802900 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5+16404G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77802900 | |||||||
| chr4:77803022 | C | A | 1 | a0001c0001t0036g0274 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5+16282G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803022 | |||||||
| chr4:77803039 | A | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.5+16265T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803039 | |||||||
| chr4:77803119 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5+16185A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803119 | |||||||
| chr4:77803192 | CA | C | 4 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0249 others(1): Show |
4 | HG02523.hp2 NA18963.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+16111delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803192 | |||||||
| chr4:77803267 | A | C | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.5+16037T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803267 | |||||||
| chr4:77803385 | A | T | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.5+15919T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803385 | |||||||
| chr4:77803426 | T | A | 1 | a0001c0001t0001g0205 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5+15878A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803426 | |||||||
| chr4:77803474 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5+15830A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803474 | |||||||
| chr4:77803542 | A | G | 87 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(84): Show |
87 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.5+15762T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803542 | |||||||
| chr4:77803597 | T | C | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG02083.hp1 NA18945.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.5+15707A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803597 | |||||||
| chr4:77803693 | C | T | 2 | a0001c0001t0002g0014 a0001c0001t0002g0034 |
2 | NA18747.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.5+15611G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803693 | |||||||
| chr4:77803696 | C | T | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5+15608G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803696 | |||||||
| chr4:77803737 | C | A | 2 | a0001c0001t0006g0307 a0001c0001t0006g0313 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.5+15567G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803737 | |||||||
| chr4:77803836 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+15468T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803836 | |||||||
| chr4:77803866 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+15438C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803866 | |||||||
| chr4:77803948 | C | T | 5 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0074 others(2): Show |
5 | HG01109.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+15356G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803948 | |||||||
| chr4:77803966 | T | C | 88 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(85): Show |
88 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.5+15338A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803966 | |||||||
| chr4:77803989 | A | AAACACAG others(18): Show |
1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.5+15314_5+15315ins others(25): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803989 | |||||||
| chr4:77803991 | C | T | 1 | a0001c0001t0008g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.5+15313G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77803991 | |||||||
| chr4:77804074 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.5+15230A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804074 | |||||||
| chr4:77804201 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5+15103C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804201 | |||||||
| chr4:77804257 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.5+15047C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804257 | |||||||
| chr4:77804322 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+14982T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804322 | |||||||
| chr4:77804397 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.5+14907G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804397 | |||||||
| chr4:77804428 | C | CA | 8 | a0001c0001t0001g0105 a0001c0001t0002g0049 a0001c0001t0005g0175 others(5): Show |
8 | HG01361.hp1 HG02280.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+14875dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804428 | |||||||
| chr4:77804428 | CA | C | 6 | a0001c0001t0001g0133 a0001c0001t0001g0165 a0001c0001t0001g0188 others(3): Show |
6 | HG02451.hp2 HG02897.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+14875delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804428 | |||||||
| chr4:77804443 | A | G | 4 | a0001c0001t0010g0077 a0001c0001t0010g0168 a0001c0001t0010g0169 others(1): Show |
4 | HG00280.hp2 HG01192.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+14861T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804443 | |||||||
| chr4:77804547 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+14757A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804547 | |||||||
| chr4:77804612 | T | C | 3 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5+14692A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804612 | |||||||
| chr4:77804740 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5+14564A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804740 | |||||||
| chr4:77804855 | A | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | HG02895.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5+14449T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804855 | |||||||
| chr4:77804890 | T | C | 3 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 |
3 | HG02818.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5+14414A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77804890 | |||||||
| chr4:77805130 | G | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+14174C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805130 | |||||||
| chr4:77805164 | A | C | 93 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(90): Show |
93 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.5+14140T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805164 | |||||||
| chr4:77805192 | G | A | 1 | a0001c0001t0039g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5+14112C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805192 | |||||||
| chr4:77805338 | T | C | 1 | a0001c0001t0001g0315 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5+13966A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805338 | |||||||
| chr4:77805378 | G | A | 12 | a0001c0001t0001g0108 a0001c0001t0001g0133 a0001c0001t0001g0134 others(9): Show |
12 | HG00323.hp2 HG00597.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.5+13926C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805378 | |||||||
| chr4:77805439 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0037g0182 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.5+13865T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805439 | |||||||
| chr4:77805616 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5+13688G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805616 | |||||||
| chr4:77805645 | A | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG00438.hp1 HG02074.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.5+13659T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805645 | |||||||
| chr4:77805667 | T | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+13637A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805667 | |||||||
| chr4:77805703 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.5+13601G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805703 | |||||||
| chr4:77805753 | A | G | 1 | a0001c0001t0006g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5+13551T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805753 | |||||||
| chr4:77805789 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(261): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.5+13515C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805789 | |||||||
| chr4:77805835 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5+13469C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805835 | |||||||
| chr4:77805954 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(243): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.5+13350A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77805954 | |||||||
| chr4:77806073 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5+13231A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77806073 | |||||||
| chr4:77806164 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5+13140C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77806164 | |||||||
| chr4:77806281 | C | T | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+13023G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77806281 | |||||||
| chr4:77806293 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5+13011G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77806293 | |||||||
| chr4:77806458 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5+12846G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77806458 | |||||||
| chr4:77806555 | C | G | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.5+12749G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77806555 | |||||||
| chr4:77806745 | A | G | 1 | a0001c0001t0001g0314 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.5+12559T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77806745 | |||||||
| chr4:77807093 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+12211A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807093 | |||||||
| chr4:77807118 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+12186C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807118 | |||||||
| chr4:77807256 | G | A | 1 | a0001c0001t0009g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5+12048C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807256 | |||||||
| chr4:77807276 | C | CA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(110): Show |
114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.5+12027dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAA | 8 | a0001c0001t0001g0105 a0001c0001t0001g0139 a0001c0001t0001g0165 others(5): Show |
8 | HG01361.hp1 HG02083.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.5+12026_5+12027dup others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAA | 15 | a0001c0001t0001g0226 a0001c0001t0001g0284 a0001c0001t0001g0296 others(12): Show |
15 | HG00639.hp1 HG01081.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.5+12025_5+12027dup others(3): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAA | 76 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.5+12024_5+12027dup others(4): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAA | 11 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0238 others(8): Show |
11 | HG01943.hp2 HG02015.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.5+12023_5+12027dup others(5): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0005g0175 a0001c0001t0041g0076 |
2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5+12018_5+12027dup others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0014g0269 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5+12017_5+12027dup others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0014g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5+12016_5+12027dup others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5+12015_5+12027dup others(13): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0214 a0001c0001t0001g0326 |
2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5+12027_5+12028ins others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5+12027_5+12028ins others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0224 a0001c0001t0005g0208 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5+12027_5+12028ins others(23): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0005g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5+12027_5+12028ins others(24): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(18): Show |
4 | a0001c0001t0005g0177 a0001c0001t0005g0178 a0001c0001t0005g0207 others(1): Show |
4 | HG02622.hp2 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+12027_5+12028ins others(25): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(19): Show |
3 | a0001c0001t0005g0202 a0001c0001t0009g0089 a0001c0001t0009g0157 |
3 | HG02630.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5+12027_5+12028ins others(26): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0009g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5+12027_5+12028ins others(27): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(21): Show |
2 | a0001c0001t0005g0240 a0001c0001t0009g0091 |
2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5+12027_5+12028ins others(28): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0179 a0001c0001t0009g0087 |
2 | HG01243.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.5+12027_5+12028ins others(29): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0005g0203 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5+12027_5+12028ins others(30): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0009g0088 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.5+12027_5+12028ins others(31): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5+12027_5+12028ins others(32): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0005g0220 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5+12027_5+12028ins others(35): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807276 | C | CAAAAAAA others(35): Show |
1 | a0001c0001t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5+12027_5+12028ins others(42): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807276 | |||||||
| chr4:77807353 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.5+11951G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807353 | |||||||
| chr4:77807543 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(149): Show |
153 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.5+11761C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807543 | |||||||
| chr4:77807587 | A | C | 1 | a0001c0001t0001g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5+11717T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807587 | |||||||
| chr4:77807774 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0293 a0001c0001t0001g0326 |
3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5+11530A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807774 | |||||||
| chr4:77807784 | C | A | 1 | a0001c0001t0003g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5+11520G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807784 | |||||||
| chr4:77807968 | G | C | 20 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0006 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.5+11336C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77807968 | |||||||
| chr4:77808036 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5+11268A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808036 | |||||||
| chr4:77808040 | GA | G | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.5+11263delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808040 | |||||||
| chr4:77808107 | T | C | 5 | a0001c0001t0001g0261 a0001c0001t0010g0077 a0001c0001t0010g0168 others(2): Show |
5 | HG00280.hp2 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+11197A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808107 | |||||||
| chr4:77808183 | C | T | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5+11121G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808183 | |||||||
| chr4:77808187 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.5+11117G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808187 | |||||||
| chr4:77808204 | G | T | 1 | a0001c0001t0001g0180 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.5+11100C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808204 | |||||||
| chr4:77808277 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5+11027G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808277 | |||||||
| chr4:77808318 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+10986G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808318 | |||||||
| chr4:77808322 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5+10982A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808322 | |||||||
| chr4:77808334 | C | T | 2 | a0001c0001t0003g0003 a0001c0001t0023g0004 |
2 | HG01175.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.5+10970G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808334 | |||||||
| chr4:77808416 | C | T | 15 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(12): Show |
15 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.5+10888G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808416 | |||||||
| chr4:77808462 | C | CA | 21 | a0001c0001t0001g0149 a0001c0001t0001g0199 a0001c0001t0001g0201 others(18): Show |
21 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.5+10841dupT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808462 | |||||||
| chr4:77808462 | CA | C | 13 | a0001c0001t0001g0209 a0001c0001t0001g0228 a0001c0001t0001g0261 others(10): Show |
13 | HG01169.hp1 HG01169.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.5+10841delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808462 | |||||||
| chr4:77808480 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5+10824T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808480 | |||||||
| chr4:77808771 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0229 |
2 | NA18939.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.5+10533A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808771 | |||||||
| chr4:77808895 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0037g0182 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.5+10409A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808895 | |||||||
| chr4:77808915 | T | C | 6 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(3): Show |
6 | HG00735.hp1 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+10389A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808915 | |||||||
| chr4:77808946 | G | A | 1 | a0001c0001t0006g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5+10358C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77808946 | |||||||
| chr4:77809336 | T | G | 1 | a0001c0001t0002g0036 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5+9968A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77809336 | |||||||
| chr4:77809540 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+9764A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77809540 | |||||||
| chr4:77809840 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5+9464G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77809840 | |||||||
| chr4:77809860 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5+9444C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77809860 | |||||||
| chr4:77809865 | T | C | 2 | a0001c0001t0005g0220 a0001c0001t0005g0240 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.5+9439A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77809865 | |||||||
| chr4:77809866 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0229 |
2 | NA18939.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.5+9438T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77809866 | |||||||
| chr4:77809891 | T | C | 1 | a0001c0001t0037g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5+9413A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77809891 | |||||||
| chr4:77809935 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.5+9369G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77809935 | |||||||
| chr4:77810020 | TAATA | T | 13 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(10): Show |
13 | HG02145.hp1 HG02258.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.5+9280_5+9283delTA others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810020 | |||||||
| chr4:77810053 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0002g0037 |
2 | HG02074.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.5+9251C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810053 | |||||||
| chr4:77810063 | T | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.5+9241A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810063 | |||||||
| chr4:77810206 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5+9098A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810206 | |||||||
| chr4:77810243 | A | G | 18 | a0001c0001t0001g0092 a0001c0001t0005g0175 a0001c0001t0005g0176 others(15): Show |
18 | HG00735.hp1 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.5+9061T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810243 | |||||||
| chr4:77810284 | C | T | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+9020G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810284 | |||||||
| chr4:77810328 | A | G | 1 | a0001c0001t0005g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5+8976T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810328 | |||||||
| chr4:77810393 | C | T | 20 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0104 others(17): Show |
20 | HG00323.hp1 HG00438.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.5+8911G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810393 | |||||||
| chr4:77810643 | T | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | NA18964.hp2 NA18965.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.5+8661A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810643 | |||||||
| chr4:77810678 | A | G | 1 | a0001c0001t0037g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5+8626T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810678 | |||||||
| chr4:77810693 | T | C | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+8611A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810693 | |||||||
| chr4:77810830 | T | C | 1 | a0001c0001t0010g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5+8474A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810830 | |||||||
| chr4:77810837 | T | C | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | HG02895.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5+8467A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810837 | |||||||
| chr4:77810951 | C | G | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+8353G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810951 | |||||||
| chr4:77810995 | T | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+8309A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77810995 | |||||||
| chr4:77811239 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5+8065C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811239 | |||||||
| chr4:77811289 | C | T | 1 | a0001c0003t0025g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5+8015G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811289 | |||||||
| chr4:77811310 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+7994C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811310 | |||||||
| chr4:77811395 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5+7909C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811395 | |||||||
| chr4:77811424 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+7880C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811424 | |||||||
| chr4:77811549 | A | G | 1 | a0001c0001t0019g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5+7755T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811549 | |||||||
| chr4:77811676 | T | C | 1 | a0001c0001t0030g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5+7628A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811676 | |||||||
| chr4:77811711 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5+7593G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811711 | |||||||
| chr4:77811795 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5+7509A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811795 | |||||||
| chr4:77811861 | G | T | 11 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
11 | HG00741.hp1 HG01346.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.5+7443C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811861 | |||||||
| chr4:77811874 | TA | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
240 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.5+7429delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811874 | |||||||
| chr4:77811874 | TAA | T | 13 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(10): Show |
13 | HG00738.hp1 HG01433.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.5+7428_5+7429delTT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811874 | |||||||
| chr4:77811874 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0003g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5+7419_5+7429delTT others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811874 | |||||||
| chr4:77811923 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5+7381T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811923 | |||||||
| chr4:77811974 | C | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.5+7330G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77811974 | |||||||
| chr4:77812032 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.5+7272G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812032 | |||||||
| chr4:77812059 | G | A | 5 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+7245C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812059 | |||||||
| chr4:77812112 | A | G | 1 | a0001c0001t0030g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5+7192T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812112 | |||||||
| chr4:77812119 | T | C | 1 | a0001c0001t0005g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5+7185A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812119 | |||||||
| chr4:77812232 | C | T | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+7072G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812232 | |||||||
| chr4:77812322 | C | T | 26 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(23): Show |
26 | HG00673.hp2 HG01928.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.5+6982G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812322 | |||||||
| chr4:77812359 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+6945T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812359 | |||||||
| chr4:77812365 | G | A | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+6939C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812365 | |||||||
| chr4:77812394 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.5+6910A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812394 | |||||||
| chr4:77812417 | G | A | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5+6887C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812417 | |||||||
| chr4:77812421 | G | C | 5 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+6883C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812421 | |||||||
| chr4:77812437 | C | CAAA | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.5+6864_5+6866dupTT others(1): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812437 | |||||||
| chr4:77812464 | A | G | 9 | a0001c0001t0006g0171 a0001c0001t0006g0206 a0001c0001t0006g0212 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.5+6840T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812464 | |||||||
| chr4:77812776 | C | G | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+6528G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812776 | |||||||
| chr4:77812890 | G | A | 1 | a0001c0001t0005g0208 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5+6414C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77812890 | |||||||
| chr4:77813180 | T | A | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5+6124A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813180 | |||||||
| chr4:77813194 | C | CAA | 6 | a0001c0001t0001g0266 a0001c0001t0001g0276 a0001c0001t0001g0283 others(3): Show |
6 | HG02074.hp1 HG02135.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+6108_5+6109dupTT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813194 | |||||||
| chr4:77813289 | T | TTAGA | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(243): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.5+6011_5+6014dupTC others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813289 | |||||||
| chr4:77813325 | A | AATAG | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(243): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.5+5975_5+5978dupCT others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813325 | |||||||
| chr4:77813409 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(158): Show |
162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.5+5895T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813409 | |||||||
| chr4:77813544 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.5+5760T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813544 | |||||||
| chr4:77813620 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5+5684A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813620 | |||||||
| chr4:77813775 | T | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.5+5529A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813775 | |||||||
| chr4:77813877 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5+5427G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77813877 | |||||||
| chr4:77814084 | A | G | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+5220T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814084 | |||||||
| chr4:77814141 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+5163C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814141 | |||||||
| chr4:77814252 | G | A | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+5052C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814252 | |||||||
| chr4:77814267 | G | T | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5+5037C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814267 | |||||||
| chr4:77814515 | C | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+4789G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814515 | |||||||
| chr4:77814517 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+4787T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814517 | |||||||
| chr4:77814741 | G | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(81): Show |
84 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.5+4563C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814741 | |||||||
| chr4:77814813 | A | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+4491T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814813 | |||||||
| chr4:77814873 | T | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(82): Show |
85 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.5+4431A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77814873 | |||||||
| chr4:77815105 | A | G | 11 | a0001c0001t0004g0286 a0001c0001t0004g0290 a0001c0001t0004g0297 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.5+4199T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77815105 | |||||||
| chr4:77815121 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+4183A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77815121 | |||||||
| chr4:77815260 | G | A | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+4044C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77815260 | |||||||
| chr4:77815261 | C | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+4043G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77815261 | |||||||
| chr4:77815817 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5+3487T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77815817 | |||||||
| chr4:77815840 | C | G | 19 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0005g0175 others(16): Show |
19 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.5+3464G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77815840 | |||||||
| chr4:77816071 | C | G | 1 | a0001c0001t0013g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5+3233G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77816071 | |||||||
| chr4:77816105 | A | T | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+3199T>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77816105 | |||||||
| chr4:77816213 | ATC | A | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0321 others(1): Show |
4 | NA18941.hp1 NA18950.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+3089_5+3090delGA | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77816213 | |||||||
| chr4:77816817 | A | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+2487T>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77816817 | |||||||
| chr4:77816928 | G | C | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+2376C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77816928 | |||||||
| chr4:77816935 | C | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(257): Show |
261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.5+2369G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77816935 | |||||||
| chr4:77816982 | T | C | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+2322A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77816982 | |||||||
| chr4:77817002 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5+2302A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77817002 | |||||||
| chr4:77817128 | T | C | 5 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0074 others(2): Show |
5 | HG01109.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+2176A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77817128 | |||||||
| chr4:77817221 | GA | G | 6 | a0001c0001t0001g0083 a0001c0001t0019g0310 a0001c0001t0020g0319 others(3): Show |
6 | HG00597.hp1 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+2082delT | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77817221 | |||||||
| chr4:77817370 | T | A | 2 | a0001c0001t0014g0223 a0001c0001t0014g0269 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5+1934A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77817370 | |||||||
| chr4:77817429 | G | T | 1 | a0001c0001t0041g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5+1875C>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77817429 | |||||||
| chr4:77817552 | GCTCT | G | 88 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0173 others(85): Show |
88 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.5+1748_5+1751delAG others(2): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77817552 | |||||||
| chr4:77817947 | T | C | 3 | a0001c0001t0019g0310 a0001c0001t0020g0319 a0001c0001t0021g0320 |
3 | HG02280.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5+1357A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77817947 | |||||||
| chr4:77818047 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5+1257T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818047 | |||||||
| chr4:77818171 | C | T | 1 | a0001c0001t0027g0318 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5+1133G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818171 | |||||||
| chr4:77818185 | T | G | 1 | a0001c0001t0001g0267 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5+1119A>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818185 | |||||||
| chr4:77818244 | T | C | 1 | a0001c0001t0001g0002 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.5+1060A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818244 | |||||||
| chr4:77818387 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5+917T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818387 | |||||||
| chr4:77818515 | T | A | 1 | a0001c0001t0005g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5+789A>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818515 | |||||||
| chr4:77818549 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5+755C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818549 | |||||||
| chr4:77818624 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0224 a0001c0001t0001g0293 others(1): Show |
4 | HG02922.hp1 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+680G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818624 | |||||||
| chr4:77818737 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.5+567G>A | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818737 | |||||||
| chr4:77818807 | G | A | 1 | a0001c0001t0009g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5+497C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818807 | |||||||
| chr4:77818870 | G | A | 1 | a0001c0001t0005g0203 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5+434C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818870 | |||||||
| chr4:77818912 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0079 others(154): Show |
158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.5+392A>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818912 | |||||||
| chr4:77818933 | A | G | 1 | a0001c0001t0024g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+371T>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818933 | |||||||
| chr4:77818978 | G | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5+326C>G | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77818978 | |||||||
| chr4:77819006 | G | A | 15 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.5+298C>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819006 | |||||||
| chr4:77819015 | C | A | 1 | a0001c0001t0010g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5+289G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819015 | |||||||
| chr4:77819049 | G | GACACACA others(3): Show |
5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+245_5+254dupGTGT others(6): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(16): Show |
1 | a0001c0001t0001g0321 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(5): Show |
90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0083 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.5+243_5+254dupGTGT others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(7): Show |
35 | a0001c0001t0001g0173 a0001c0001t0001g0179 a0001c0001t0001g0180 others(32): Show |
35 | HG00558.hp1 HG00597.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.5+241_5+254dupGTGT others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(9): Show |
6 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0003g0211 others(3): Show |
6 | HG00280.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+239_5+254dupGTGT others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(11): Show |
10 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG01255.hp1 HG01256.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.5+237_5+254dupGTGT others(14): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(13): Show |
19 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(16): Show |
19 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.5+235_5+254dupGTGT others(16): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(15): Show |
19 | a0001c0001t0001g0242 a0001c0001t0001g0244 a0001c0001t0001g0245 others(16): Show |
19 | HG00642.hp1 HG01109.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.5+233_5+254dupGTGT others(18): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(17): Show |
7 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(4): Show |
7 | HG01169.hp2 HG02486.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+231_5+254dupGTGT others(20): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(19): Show |
9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG01069.hp2 HG02132.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5+229_5+254dupGTGT others(22): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(21): Show |
4 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(1): Show |
4 | HG01358.hp2 HG01433.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(24): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(23): Show |
3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0015g0281 |
3 | HG00558.hp2 NA18980.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(26): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(25): Show |
2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18747.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(28): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(27): Show |
3 | a0001c0001t0001g0288 a0001c0001t0017g0287 a0001c0001t0018g0289 |
3 | HG00544.hp2 HG02015.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(30): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(29): Show |
2 | a0001c0001t0001g0292 a0001c0001t0017g0291 |
2 | HG00438.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(32): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(31): Show |
3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02074.hp1 HG06807.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(34): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(33): Show |
1 | a0001c0001t0001g0299 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(36): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(35): Show |
1 | a0001c0001t0001g0304 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(38): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(37): Show |
1 | a0001c0001t0001g0306 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(40): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(45): Show |
2 | a0001c0001t0001g0308 a0001c0001t0006g0307 |
2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(48): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(47): Show |
1 | a0001c0001t0001g0309 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(50): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(49): Show |
1 | a0001c0001t0019g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(52): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(53): Show |
1 | a0001c0001t0006g0313 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(56): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(55): Show |
1 | a0001c0001t0001g0314 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(58): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(65): Show |
1 | a0001c0001t0001g0315 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(68): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(69): Show |
1 | a0001c0001t0001g0316 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(72): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(75): Show |
1 | a0001c0001t0001g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(78): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(91): Show |
1 | a0001c0001t0028g0327 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(94): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(101): Show |
2 | a0001c0001t0020g0319 a0001c0001t0027g0318 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(104): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(105): Show |
1 | a0001c0001t0021g0320 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(108): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(132): Show |
1 | a0001c0001t0001g0296 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(135): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(93): Show |
2 | a0001c0001t0004g0300 a0001c0001t0004g0301 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5+254_5+255insGTGT others(96): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(99): Show |
1 | a0001c0001t0004g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(102): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(109): Show |
1 | a0001c0001t0004g0312 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(112): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(87): Show |
1 | a0001c0001t0004g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(90): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(91): Show |
1 | a0001c0001t0004g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(94): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(109): Show |
1 | a0001c0001t0004g0311 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(112): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(143): Show |
1 | a0001c0001t0004g0286 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(146): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(97): Show |
1 | a0001c0001t0004g0303 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(100): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(93): Show |
1 | a0001c0001t0004g0298 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(96): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819049 | G | GACACACA others(93): Show |
1 | a0001c0001t0004g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5+254_5+255insGTGT others(96): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819049 | |||||||
| chr4:77819074 | A | ACACACAC others(14): Show |
1 | a0001c0001t0001g0010 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.5+229_5+230insGTGT others(17): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819074 | |||||||
| chr4:77819074 | A | ACACACAC others(54): Show |
1 | a0001c0001t0001g0011 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5+229_5+230insGTGT others(57): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819074 | |||||||
| chr4:77819074 | A | ACACACAC others(9): Show |
1 | a0001c0001t0003g0009 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.5+229_5+230insGGTG others(12): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819074 | |||||||
| chr4:77819074 | A | ACACACAC others(7): Show |
1 | a0001c0001t0003g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.5+229_5+230insGGTG others(10): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819074 | |||||||
| chr4:77819074 | A | ACACACAC others(5): Show |
5 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0006 others(2): Show |
5 | HG01069.hp1 HG01175.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+229_5+230insGGTG others(8): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819074 | |||||||
| chr4:77819075 | C | CACACACA others(6): Show |
1 | a0001c0001t0003g0322 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5+228_5+229insTGTG others(9): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819075 | |||||||
| chr4:77819075 | C | CACACACA others(8): Show |
1 | a0001c0001t0001g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5+228_5+229insTGTG others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819075 | |||||||
| chr4:77819075 | C | CACACACA others(16): Show |
2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | HG03688.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.5+228_5+229insTGTG others(19): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819075 | |||||||
| chr4:77819075 | C | CACACACA others(30): Show |
1 | a0001c0001t0001g0325 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5+228_5+229insTGTG others(33): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819075 | |||||||
| chr4:77819077 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5+227G>T | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819077 | |||||||
| chr4:77819091 | C | G | 1 | a0001c0001t0001g0002 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.5+213G>C | CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819091 | |||||||
| chr4:77819111 | T | TCAGCCCC others(8): Show |
1 | a0001c0001t0028g0327 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5+178_5+192dupGGGG others(11): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | 77819111 |