Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4848 |
| ensemblid | ENSG00000111596.14 |
| hgncid | 7878 |
| symbol | CNOT2 |
| name | CCR4-NOT transcription complex subunit 2 |
| refseq_nuc | NM_014515.7 |
| refseq_prot | NP_055330.1 |
| ensembl_nuc | ENST00000229195.8 |
| ensembl_prot | ENSP00000229195.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 70243433 |
| end | 70354993 |
| strand | + |
| ver | v1.2 |
| region | chr12:70243433-70354993 |
| region5000 | chr12:70238433-70359993 |
| regionname0 | CNOT2_chr12_70243433_70354993 |
| regionname5000 | CNOT2_chr12_70238433_70359993 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1620 | 275 | 88 | 60 | 90 | 10 | 25 | CNOT2_chr12_70238433_70359993 | CNOT2 | ATGGT others(1615): Show |
chr12 | 70238433 | 70359993 | ||
| a0001c0002 | 0/0 | 1620 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | ATGGT others(1615): Show |
chr12 | 70238433 | 70359993 | ||
| a0001c0003 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | ATGGT others(1615): Show |
chr12 | 70238433 | 70359993 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2844 | 124 | 48 | 32 | 29 | 4 | 10 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2839): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0002 | 0/0 | 2843 | 49 | 11 | 7 | 25 | 1 | 5 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2838): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0003 | 0/1 | 2845 | 47 | 10 | 10 | 18 | 1 | 7 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2840): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0004 | 0/0 | 2846 | 20 | 5 | 2 | 10 | 1 | 2 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2841): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0005 | 0/0 | 2846 | 8 | 2 | 6 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2841): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0006 | 0/0 | 2845 | 8 | 5 | 0 | 3 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2840): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0007 | 0/0 | 2847 | 6 | 3 | 0 | 2 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2842): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0008 | 0/0 | 2845 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2840): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0009 | 0/0 | 2844 | 2 | 0 | 1 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2839): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0010 | 0/0 | 2843 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2838): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0011 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2841): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0012 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2840): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0013 | 0/0 | 2845 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2840): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0014 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2839): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0015 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2839): Show |
chr12 | 70238433 | 70359993 |
| a0001c0001t0016 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2839): Show |
chr12 | 70238433 | 70359993 |
| a0001c0002t0001 | 0/0 | 2844 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2839): Show |
chr12 | 70238433 | 70359993 |
| a0001c0003t0001 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | GGTGG others(2839): Show |
chr12 | 70238433 | 70359993 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0008g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0009g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0009g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0011g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0012g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0013g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0015g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0016g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0157 | EUR | GBR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0159 | EUR | FIN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0257 | EUR | FIN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | FIN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0230 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0270 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0259 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0253 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0243 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01192 | hp2 | a0001 | c0001 | t0009 | g0151 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01496 | hp2 | a0001 | c0001 | t0012 | g0241 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0231 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0268 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0260 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0242 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0238 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0267 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0250 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02698 | hp2 | a0001 | c0001 | t0015 | g0154 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0236 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0237 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0007 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0029 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | BEB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | BEB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0266 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | CHB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18941 | hp2 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0262 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18977 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18988 | hp1 | a0001 | c0001 | t0006 | g0235 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0240 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ASW | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ASW | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | TSI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0258 | EUR | TSI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | GIH | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0088 | SAS | GIH | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01123 | hp2 | a0001 | c0001 | t0011 | g0229 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0232 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0198 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | USA | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | USA | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | USA | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0213 | REF | REF | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0118 | REF | REF | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:70330452 | G | A | 1 | a0001c0002 | 4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.552G>A | p.Gln184Gln | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/16 | 695/2844 | 552/1623 | 184/540 | chr12 | 70330452 | |||
| chr12:70338700 | G | A | 1 | a0001c0003 | 1 | HG03490.hp2 | synonymous_variant | LOW | c.1056G>A | p.Thr352Thr | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/16 | 1199/2844 | 1056/1623 | 352/540 | chr12 | 70338700 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:70243439 | T | C | 1 | a0001c0001t0009 | 2 | HG00099.hp2 HG01192.hp2 |
5_prime_UTR_variant | MODIFIER | c.-137T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/16 | 34788 | chr12 | 70243439 | ||||||
| chr12:70353913 | T | TA | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(2): Show |
59 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*23dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 24 | INFO_REALIGN_3_PRIME | chr12 | 70353913 | |||||
| chr12:70353913 | T | TAA | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 |
29 | HG00609.hp1 HG01069.hp2 HG01081.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*22_*23dupAA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 24 | INFO_REALIGN_3_PRIME | chr12 | 70353913 | |||||
| chr12:70353913 | T | TAAA | 1 | a0001c0001t0007 | 6 | HG00323.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*21_*23dupAAA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 24 | INFO_REALIGN_3_PRIME | chr12 | 70353913 | |||||
| chr12:70353913 | TA | T | 2 | a0001c0001t0002 a0001c0001t0010 |
51 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*23delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 23 | INFO_REALIGN_3_PRIME | chr12 | 70353913 | |||||
| chr12:70353983 | A | G | 1 | a0001c0001t0008 | 3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 68 | chr12 | 70353983 | ||||||
| chr12:70354053 | C | T | 1 | a0001c0001t0013 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 138 | chr12 | 70354053 | ||||||
| chr12:70354210 | A | C | 1 | a0001c0001t0016 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 295 | chr12 | 70354210 | ||||||
| chr12:70354449 | G | A | 4 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(1): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*534G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 534 | chr12 | 70354449 | ||||||
| chr12:70354471 | T | C | 1 | a0001c0001t0014 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 556 | chr12 | 70354471 | ||||||
| chr12:70354593 | T | C | 4 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(1): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*678T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 678 | chr12 | 70354593 | ||||||
| chr12:70354795 | A | G | 1 | a0001c0001t0015 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 880 | chr12 | 70354795 | ||||||
| chr12:70354820 | A | G | 2 | a0001c0001t0005 a0001c0001t0012 |
9 | HG01099.hp1 HG01192.hp1 HG01255.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*905A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 905 | chr12 | 70354820 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:70243503 | G | A | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-96+23G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243503 | |||||||
| chr12:70243526 | G | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-96+46G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243526 | |||||||
| chr12:70243549 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0003g0273 |
2 | NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-96+69C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243549 | |||||||
| chr12:70243563 | G | T | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+83G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243563 | |||||||
| chr12:70243681 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-96+201G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243681 | |||||||
| chr12:70243736 | C | G | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+256C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243736 | |||||||
| chr12:70243810 | G | C | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+330G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243810 | |||||||
| chr12:70243839 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-96+359C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243839 | |||||||
| chr12:70243920 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+440C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243920 | |||||||
| chr12:70243937 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+457G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243937 | |||||||
| chr12:70244007 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+527A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244007 | |||||||
| chr12:70244032 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-96+552T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244032 | |||||||
| chr12:70244132 | C | A | 1 | a0001c0002t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-96+652C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244132 | |||||||
| chr12:70244355 | A | T | 1 | a0001c0001t0002g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-96+875A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244355 | |||||||
| chr12:70244375 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-96+895C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244375 | |||||||
| chr12:70244404 | T | G | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-96+924T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244404 | |||||||
| chr12:70244592 | C | G | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+1112C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244592 | |||||||
| chr12:70244603 | G | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+1123G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244603 | |||||||
| chr12:70244808 | G | C | 1 | a0001c0001t0002g0022 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-96+1328G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244808 | |||||||
| chr12:70245245 | GA | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0002g0217 |
3 | HG03579.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-96+1772delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70245245 | ||||||
| chr12:70245433 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-96+1953G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245433 | |||||||
| chr12:70245452 | A | T | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-96+1972A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245452 | |||||||
| chr12:70245520 | T | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-96+2040T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245520 | |||||||
| chr12:70245659 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-96+2179G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245659 | |||||||
| chr12:70245662 | A | C | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+2182A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245662 | |||||||
| chr12:70246029 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-96+2549G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246029 | |||||||
| chr12:70246074 | A | C | 36 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-96+2594A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246074 | |||||||
| chr12:70246114 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+2634G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246114 | |||||||
| chr12:70246235 | A | G | 1 | a0001c0001t0005g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-96+2755A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246235 | |||||||
| chr12:70246358 | C | G | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+2878C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246358 | |||||||
| chr12:70246426 | C | G | 1 | a0001c0001t0006g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-96+2946C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246426 | |||||||
| chr12:70246594 | G | T | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-96+3114G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246594 | |||||||
| chr12:70246815 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-96+3335C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246815 | |||||||
| chr12:70247078 | G | T | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-96+3598G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247078 | |||||||
| chr12:70247369 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-96+3889A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247369 | |||||||
| chr12:70247436 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-96+3956A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247436 | |||||||
| chr12:70247448 | G | A | 1 | a0001c0001t0003g0063 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-96+3968G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247448 | |||||||
| chr12:70247471 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-96+3991T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247471 | |||||||
| chr12:70247500 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-96+4020G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247500 | |||||||
| chr12:70247512 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-96+4032A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247512 | |||||||
| chr12:70247585 | T | C | 1 | a0001c0001t0012g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-96+4105T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247585 | |||||||
| chr12:70248328 | A | T | 12 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(9): Show |
12 | HG00741.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.-96+4848A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248328 | |||||||
| chr12:70248459 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+4979C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248459 | |||||||
| chr12:70248538 | T | A | 5 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | NA18954.hp1 NA18987.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+5058T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248538 | |||||||
| chr12:70248781 | A | G | 14 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
14 | HG00438.hp1 HG02015.hp1 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-96+5301A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248781 | |||||||
| chr12:70248790 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-96+5310G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248790 | |||||||
| chr12:70249206 | T | A | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+5726T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70249206 | |||||||
| chr12:70249252 | T | G | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+5772T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70249252 | |||||||
| chr12:70249394 | A | ATTAT | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-96+5917_-96+5918i others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70249394 | ||||||
| chr12:70249524 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-96+6044C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70249524 | |||||||
| chr12:70249850 | T | G | 1 | a0001c0001t0002g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-96+6370T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70249850 | |||||||
| chr12:70250122 | C | G | 1 | a0001c0001t0003g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-96+6642C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250122 | |||||||
| chr12:70250153 | G | A | 1 | a0001c0001t0003g0175 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-96+6673G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250153 | |||||||
| chr12:70250328 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+6848A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250328 | |||||||
| chr12:70250388 | C | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-96+6908C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250388 | |||||||
| chr12:70250506 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-96+7026T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250506 | |||||||
| chr12:70250600 | A | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+7120A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250600 | |||||||
| chr12:70250659 | A | G | 2 | a0001c0002t0001g0020 a0001c0002t0001g0172 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-96+7179A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250659 | |||||||
| chr12:70250763 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-96+7283G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250763 | |||||||
| chr12:70251012 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-96+7532G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251012 | |||||||
| chr12:70251463 | G | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+7983G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251463 | |||||||
| chr12:70251547 | GA | G | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+8075delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70251547 | ||||||
| chr12:70251548 | A | G | 5 | a0001c0001t0003g0207 a0001c0001t0003g0208 a0001c0001t0003g0210 others(2): Show |
5 | HG01256.hp1 HG01261.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+8068A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251548 | |||||||
| chr12:70251612 | C | T | 7 | a0001c0001t0001g0064 a0001c0001t0001g0165 a0001c0001t0001g0166 others(4): Show |
7 | HG00099.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+8132C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251612 | |||||||
| chr12:70251669 | T | C | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-96+8189T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251669 | |||||||
| chr12:70251752 | A | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+8272A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251752 | |||||||
| chr12:70251765 | A | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+8285A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251765 | |||||||
| chr12:70252087 | C | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-96+8607C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252087 | |||||||
| chr12:70252417 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+8937G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252417 | |||||||
| chr12:70252512 | A | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0049 others(4): Show |
7 | HG00408.hp2 HG02040.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+9032A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252512 | |||||||
| chr12:70252555 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-96+9075G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252555 | |||||||
| chr12:70252657 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0163 a0001c0001t0001g0164 |
4 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+9177A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252657 | |||||||
| chr12:70252673 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-96+9193C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252673 | |||||||
| chr12:70252675 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-96+9195G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252675 | |||||||
| chr12:70252808 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+9328C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252808 | |||||||
| chr12:70252871 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-96+9391C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252871 | |||||||
| chr12:70253069 | G | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+9589G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253069 | |||||||
| chr12:70253168 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+9688G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253168 | |||||||
| chr12:70253288 | C | G | 1 | a0001c0001t0003g0212 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-96+9808C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253288 | |||||||
| chr12:70253370 | G | A | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-96+9890G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253370 | |||||||
| chr12:70253464 | A | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | NA18966.hp2 NA18968.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+9984A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253464 | |||||||
| chr12:70253518 | T | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-96+10038T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253518 | |||||||
| chr12:70253702 | A | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-96+10222A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253702 | |||||||
| chr12:70253808 | T | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+10328T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253808 | |||||||
| chr12:70253815 | A | C | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-96+10335A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253815 | |||||||
| chr12:70254020 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+10540C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254020 | |||||||
| chr12:70254065 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+10585C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254065 | |||||||
| chr12:70254213 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+10733G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254213 | |||||||
| chr12:70254237 | CA | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-96+10773delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70254237 | ||||||
| chr12:70254370 | T | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-96+10890T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254370 | |||||||
| chr12:70254467 | A | G | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+10987A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254467 | |||||||
| chr12:70254573 | G | T | 2 | a0001c0001t0001g0108 a0001c0001t0003g0109 |
2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-96+11093G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254573 | |||||||
| chr12:70254896 | G | T | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-96+11416G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254896 | |||||||
| chr12:70254923 | G | A | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+11443G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254923 | |||||||
| chr12:70254980 | C | CA | 19 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(16): Show |
19 | HG00558.hp1 HG01099.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-96+11518dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70254980 | ||||||
| chr12:70254980 | CA | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0024 others(74): Show |
77 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-96+11518delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70254980 | ||||||
| chr12:70254980 | CAAAAA | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
76 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-96+11514_-96+1151 others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70254980 | ||||||
| chr12:70254996 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0190 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+11516A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254996 | |||||||
| chr12:70255044 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-96+11564G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255044 | |||||||
| chr12:70255050 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-96+11570T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255050 | |||||||
| chr12:70255073 | A | C | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+11593A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255073 | |||||||
| chr12:70255087 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-96+11607A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255087 | |||||||
| chr12:70255136 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+11656C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255136 | |||||||
| chr12:70255145 | TTCTC | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+11667_-96+1167 others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70255145 | ||||||
| chr12:70255207 | T | TA | 56 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(53): Show |
56 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.-96+11728dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70255207 | ||||||
| chr12:70255409 | C | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-96+11929C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255409 | |||||||
| chr12:70255464 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-96+11984T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255464 | |||||||
| chr12:70255784 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-96+12304T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255784 | |||||||
| chr12:70255850 | A | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(167): Show |
173 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-96+12370A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255850 | |||||||
| chr12:70256014 | G | T | 1 | a0001c0001t0002g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-96+12534G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256014 | |||||||
| chr12:70256028 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-96+12548C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256028 | |||||||
| chr12:70256125 | C | G | 1 | a0001c0001t0002g0022 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-96+12645C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256125 | |||||||
| chr12:70256169 | T | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+12689T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256169 | |||||||
| chr12:70256172 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-96+12692A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256172 | |||||||
| chr12:70256476 | A | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+12996A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256476 | |||||||
| chr12:70256582 | T | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01243.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-96+13102T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256582 | |||||||
| chr12:70256582 | T | TA | 97 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(94): Show |
100 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.-96+13123dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70256582 | ||||||
| chr12:70256582 | T | TAA | 16 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(13): Show |
16 | HG00621.hp2 HG01123.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-96+13122_-96+1312 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70256582 | ||||||
| chr12:70256582 | T | TAAA | 29 | a0001c0001t0003g0202 a0001c0001t0003g0248 a0001c0001t0003g0263 others(26): Show |
30 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-96+13121_-96+1312 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70256582 | ||||||
| chr12:70256626 | A | G | 1 | a0001c0001t0013g0159 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-96+13146A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256626 | |||||||
| chr12:70256939 | A | G | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-96+13459A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256939 | |||||||
| chr12:70256953 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-96+13473G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256953 | |||||||
| chr12:70257026 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-96+13546A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257026 | |||||||
| chr12:70257033 | AT | A | 12 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(9): Show |
12 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.-96+13563delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257033 | ||||||
| chr12:70257043 | T | C | 1 | a0001c0001t0012g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-96+13563T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257043 | |||||||
| chr12:70257162 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+13682G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257162 | |||||||
| chr12:70257243 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+13763A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257243 | |||||||
| chr12:70257285 | A | G | 5 | a0001c0001t0003g0263 a0001c0001t0004g0261 a0001c0001t0004g0264 others(2): Show |
5 | NA18977.hp1 NA18980.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.-96+13805A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257285 | |||||||
| chr12:70257309 | G | A | 1 | a0001c0001t0005g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-96+13829G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257309 | |||||||
| chr12:70257354 | C | CT | 8 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0116 others(5): Show |
8 | HG01106.hp2 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-96+13892dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | ||||||
| chr12:70257354 | C | CTT | 7 | a0001c0001t0003g0248 a0001c0001t0004g0246 a0001c0001t0004g0247 others(4): Show |
7 | HG01069.hp2 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+13891_-96+1389 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | ||||||
| chr12:70257354 | C | CTTT | 21 | a0001c0001t0003g0263 a0001c0001t0004g0251 a0001c0001t0004g0254 others(18): Show |
22 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.-96+13890_-96+1389 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | ||||||
| chr12:70257354 | C | CTTTTTT | 6 | a0001c0001t0006g0235 a0001c0001t0006g0236 a0001c0001t0006g0237 others(3): Show |
6 | HG02257.hp1 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+13887_-96+1389 others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | ||||||
| chr12:70257354 | C | CTTTTTTT | 6 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0008g0005 others(3): Show |
7 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+13886_-96+1389 others(11): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | ||||||
| chr12:70257354 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0026 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-96+13883_-96+1389 others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | ||||||
| chr12:70257354 | CT | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0077 others(38): Show |
43 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-96+13892delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | ||||||
| chr12:70257355 | T | C | 10 | a0001c0001t0001g0049 a0001c0001t0001g0183 a0001c0001t0002g0191 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+13875T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257355 | |||||||
| chr12:70257360 | TTTTTTTT others(6): Show |
T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+13886_-96+1389 others(17): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257360 | ||||||
| chr12:70257373 | C | T | 60 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(57): Show |
62 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.-96+13893C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257373 | |||||||
| chr12:70257391 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-96+13911C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257391 | |||||||
| chr12:70257417 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-96+13937G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257417 | |||||||
| chr12:70257461 | C | T | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-96+13981C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257461 | |||||||
| chr12:70257536 | AT | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(2): Show |
5 | HG00639.hp1 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+14067delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257536 | ||||||
| chr12:70257657 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-96+14177G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257657 | |||||||
| chr12:70257687 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-96+14207T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257687 | |||||||
| chr12:70257696 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-96+14216C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257696 | |||||||
| chr12:70257737 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+14257A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257737 | |||||||
| chr12:70257881 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-96+14401A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257881 | |||||||
| chr12:70258081 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-96+14601C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70258081 | |||||||
| chr12:70258231 | C | A | 1 | a0001c0001t0006g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-96+14751C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70258231 | |||||||
| chr12:70258306 | T | TA | 6 | a0001c0001t0006g0230 a0001c0001t0006g0235 a0001c0001t0006g0240 others(3): Show |
7 | HG00621.hp2 HG01123.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+14827dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70258306 | ||||||
| chr12:70258315 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-96+14835A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70258315 | |||||||
| chr12:70258702 | T | G | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+15222T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70258702 | |||||||
| chr12:70259028 | C | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-96+15548C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259028 | |||||||
| chr12:70259033 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-96+15553A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259033 | |||||||
| chr12:70259039 | T | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0077 others(35): Show |
40 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-96+15559T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259039 | |||||||
| chr12:70259056 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0003g0062 |
2 | NA18969.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-96+15576C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259056 | |||||||
| chr12:70259123 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-96+15643A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259123 | |||||||
| chr12:70259132 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-96+15652C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259132 | |||||||
| chr12:70259315 | A | AT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-96+15844dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70259315 | ||||||
| chr12:70259403 | G | A | 1 | a0001c0001t0004g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-96+15923G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259403 | |||||||
| chr12:70259786 | C | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-96+16306C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259786 | |||||||
| chr12:70259799 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-96+16319C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259799 | |||||||
| chr12:70259874 | T | G | 1 | a0001c0001t0002g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-96+16394T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259874 | |||||||
| chr12:70259925 | G | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
82 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-96+16445G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259925 | |||||||
| chr12:70260192 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-96+16712C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260192 | |||||||
| chr12:70260278 | C | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+16798C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260278 | |||||||
| chr12:70260402 | G | T | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+16922G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260402 | |||||||
| chr12:70260409 | T | C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+16929T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260409 | |||||||
| chr12:70260449 | T | C | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-96+16969T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260449 | |||||||
| chr12:70260471 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-96+16991G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260471 | |||||||
| chr12:70260603 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-96+17123T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260603 | |||||||
| chr12:70260613 | AGTT | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-96+17139_-96+1714 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70260613 | ||||||
| chr12:70260718 | C | T | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+17238C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260718 | |||||||
| chr12:70260853 | A | AT | 33 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0053 others(30): Show |
33 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-95-17265dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70260853 | ||||||
| chr12:70260853 | A | ATT | 42 | a0001c0001t0002g0060 a0001c0001t0003g0248 a0001c0001t0003g0263 others(39): Show |
44 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.-95-17266_-95-1726 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70260853 | ||||||
| chr12:70260853 | A | ATTT | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-17267_-95-1726 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70260853 | ||||||
| chr12:70260956 | A | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(184): Show |
191 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-95-17176A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260956 | |||||||
| chr12:70261008 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-95-17124T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261008 | |||||||
| chr12:70261027 | C | G | 1 | a0001c0001t0006g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-95-17105C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261027 | |||||||
| chr12:70261129 | TTGAGATG others(4): Show |
T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-95-17000_-95-1699 others(15): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261129 | ||||||
| chr12:70261281 | T | A | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-95-16851T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261281 | |||||||
| chr12:70261305 | C | CT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0019 others(74): Show |
80 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-95-16800dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | ||||||
| chr12:70261305 | C | CTT | 17 | a0001c0001t0001g0028 a0001c0001t0001g0043 a0001c0001t0002g0017 others(14): Show |
17 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-95-16801_-95-1680 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | ||||||
| chr12:70261305 | C | CTTTT | 5 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-95-16803_-95-1680 others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | ||||||
| chr12:70261305 | CT | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0021 others(61): Show |
66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-95-16800delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | ||||||
| chr12:70261305 | CTT | C | 8 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG00733.hp1 HG00738.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-16801_-95-1680 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | ||||||
| chr12:70261305 | CTTTTTT | C | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-95-16805_-95-1680 others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | ||||||
| chr12:70261338 | G | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-16794G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261338 | |||||||
| chr12:70261415 | C | T | 1 | a0001c0001t0003g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-95-16717C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261415 | |||||||
| chr12:70261416 | G | A | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-16716G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261416 | |||||||
| chr12:70261460 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-16672G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261460 | |||||||
| chr12:70261526 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0003g0141 |
2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-95-16606C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261526 | |||||||
| chr12:70261656 | T | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-16476T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261656 | |||||||
| chr12:70261834 | A | AT | 9 | a0001c0001t0001g0097 a0001c0001t0001g0120 a0001c0001t0002g0080 others(6): Show |
9 | HG00408.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-16282dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261834 | ||||||
| chr12:70261880 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-95-16252C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261880 | |||||||
| chr12:70261887 | C | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-95-16245C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261887 | |||||||
| chr12:70261928 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-95-16204C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261928 | |||||||
| chr12:70262057 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0167 |
2 | HG01074.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-95-16075C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262057 | |||||||
| chr12:70262263 | T | C | 4 | a0001c0001t0004g0244 a0001c0001t0004g0258 a0001c0001t0004g0259 others(1): Show |
4 | HG00323.hp1 HG01081.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-15869T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262263 | |||||||
| chr12:70262334 | C | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-95-15798C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262334 | |||||||
| chr12:70262405 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-95-15727C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262405 | |||||||
| chr12:70262571 | G | A | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-95-15561G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262571 | |||||||
| chr12:70262588 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-15544A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262588 | |||||||
| chr12:70262592 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-95-15540T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262592 | |||||||
| chr12:70262662 | TA | T | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-15469delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262662 | |||||||
| chr12:70262730 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-95-15402G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262730 | |||||||
| chr12:70262760 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-95-15372A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262760 | |||||||
| chr12:70262932 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-15200C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262932 | |||||||
| chr12:70262933 | A | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-15199A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262933 | |||||||
| chr12:70262934 | A | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-15198A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262934 | |||||||
| chr12:70262996 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-15136G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262996 | |||||||
| chr12:70263075 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-95-15057C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263075 | |||||||
| chr12:70263157 | A | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-14975A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263157 | |||||||
| chr12:70263158 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-95-14974C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263158 | |||||||
| chr12:70263213 | ACT | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-95-14916_-95-1491 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70263213 | ||||||
| chr12:70263478 | G | A | 1 | a0001c0001t0006g0235 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-95-14654G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263478 | |||||||
| chr12:70263740 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-95-14392A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263740 | |||||||
| chr12:70264007 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-95-14125A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264007 | |||||||
| chr12:70264096 | A | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-14036A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264096 | |||||||
| chr12:70264369 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-13763C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264369 | |||||||
| chr12:70264583 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-13549C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264583 | |||||||
| chr12:70264682 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-95-13450C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264682 | |||||||
| chr12:70264802 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-95-13330G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264802 | |||||||
| chr12:70264857 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-13275C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264857 | |||||||
| chr12:70265048 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-13084G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265048 | |||||||
| chr12:70265055 | A | T | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0059 |
3 | NA18941.hp1 NA19003.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-95-13077A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265055 | |||||||
| chr12:70265189 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-12943A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265189 | |||||||
| chr12:70265271 | G | GTCTCTTC others(8): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG03098.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-12860_-95-1285 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265271 | ||||||
| chr12:70265271 | G | GTCTCTTC others(18): Show |
1 | a0001c0001t0001g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-95-12860_-95-1285 others(29): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265271 | ||||||
| chr12:70265273 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(2): Show |
5 | HG00639.hp1 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-95-12859T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265273 | |||||||
| chr12:70265273 | T | TTCTTC | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0024 others(61): Show |
66 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.-95-12809_-95-1280 others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | T | TTCTTCTC others(3): Show |
49 | a0001c0001t0001g0015 a0001c0001t0001g0053 a0001c0001t0001g0054 others(46): Show |
51 | HG00280.hp2 HG00733.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.-95-12814_-95-1280 others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | T | TTCTTCTC others(8): Show |
1 | a0001c0001t0002g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-95-12846_-95-1284 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | T | TTCTTCTC others(13): Show |
5 | a0001c0001t0002g0191 a0001c0001t0002g0193 a0001c0001t0002g0194 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-12846_-95-1284 others(24): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | T | TTCTTCTC others(8): Show |
27 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0028 others(24): Show |
27 | HG00438.hp2 HG00558.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.-95-12819_-95-1280 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | T | TTCTTCTC others(13): Show |
4 | a0001c0001t0001g0064 a0001c0001t0001g0143 a0001c0001t0001g0170 others(1): Show |
4 | HG01256.hp1 HG01433.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95-12824_-95-1280 others(24): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | T | TTCTTCTC others(18): Show |
1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-95-12829_-95-1280 others(29): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | T | TTCTTCTC others(33): Show |
1 | a0001c0001t0001g0206 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-95-12844_-95-1280 others(44): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | TTCTTC | T | 21 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0027 others(18): Show |
21 | HG01099.hp2 HG01109.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-95-12809_-95-1280 others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | TTCTTCTC others(3): Show |
T | 11 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0115 others(8): Show |
11 | HG02055.hp1 HG02056.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-95-12814_-95-1280 others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | TTCTTCTC others(8): Show |
T | 1 | a0001c0001t0001g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-95-12819_-95-1280 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265273 | TTCTTCTC others(18): Show |
T | 1 | a0001c0001t0003g0098 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-95-12829_-95-1280 others(29): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | ||||||
| chr12:70265277 | T | TCTCTTCT others(13): Show |
1 | a0001c0001t0002g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-95-12846_-95-1284 others(24): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265277 | ||||||
| chr12:70265297 | T | C | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-95-12835T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265297 | |||||||
| chr12:70265321 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-95-12811T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265321 | |||||||
| chr12:70265321 | T | TTCTCG | 4 | a0001c0001t0004g0247 a0001c0001t0004g0261 a0001c0001t0005g0242 others(1): Show |
4 | HG01952.hp2 HG03195.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-12807_-95-1280 others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265321 | ||||||
| chr12:70265321 | T | TTCTCTTC others(3): Show |
16 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(13): Show |
17 | HG00323.hp1 HG01099.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-95-12805_-95-1280 others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265321 | ||||||
| chr12:70265321 | T | TTCTCTTC others(8): Show |
9 | a0001c0001t0004g0245 a0001c0001t0004g0249 a0001c0001t0004g0256 others(6): Show |
9 | HG00609.hp1 HG01069.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-12805_-95-1280 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265321 | ||||||
| chr12:70265321 | T | TTCTCTTC others(13): Show |
4 | a0001c0001t0004g0246 a0001c0001t0004g0251 a0001c0001t0004g0259 others(1): Show |
4 | HG01081.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-12805_-95-1280 others(24): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265321 | ||||||
| chr12:70265323 | C | CTCTT | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-12799_-95-1279 others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265323 | ||||||
| chr12:70265384 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.-95-12748G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265384 | |||||||
| chr12:70265421 | A | G | 3 | a0001c0001t0003g0063 a0001c0001t0003g0086 a0001c0001t0003g0095 |
3 | HG00438.hp2 HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-95-12711A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265421 | |||||||
| chr12:70265908 | T | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-95-12224T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265908 | |||||||
| chr12:70265964 | T | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-95-12168T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265964 | |||||||
| chr12:70266003 | C | CT | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(115): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-95-12114dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266003 | ||||||
| chr12:70266003 | CT | C | 39 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(36): Show |
40 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-95-12114delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266003 | ||||||
| chr12:70266023 | G | T | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-12109G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266023 | |||||||
| chr12:70266099 | G | GTAT | 9 | a0001c0001t0002g0022 a0001c0001t0002g0191 a0001c0001t0002g0192 others(6): Show |
9 | HG00438.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-95-12013_-95-1201 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266099 | ||||||
| chr12:70266180 | C | G | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-95-11952C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266180 | |||||||
| chr12:70266277 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-11855C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266277 | |||||||
| chr12:70266359 | G | C | 1 | a0001c0002t0001g0121 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-95-11773G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266359 | |||||||
| chr12:70266512 | T | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-95-11620T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266512 | |||||||
| chr12:70266763 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-95-11369C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266763 | |||||||
| chr12:70266794 | GTA | G | 19 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(16): Show |
19 | HG00558.hp1 HG01099.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-95-11334_-95-1133 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266794 | ||||||
| chr12:70266830 | G | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-11302G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266830 | |||||||
| chr12:70266839 | C | CT | 25 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0001g0219 others(22): Show |
26 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-95-11285dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266839 | ||||||
| chr12:70266963 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-95-11169A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266963 | |||||||
| chr12:70266978 | CAT | C | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-11153_-95-1115 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266978 | |||||||
| chr12:70267065 | T | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-11067T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267065 | |||||||
| chr12:70267085 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-95-11047A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267085 | |||||||
| chr12:70267269 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-95-10863C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267269 | |||||||
| chr12:70267470 | C | T | 5 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0194 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-10662C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267470 | |||||||
| chr12:70267564 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-10568A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267564 | |||||||
| chr12:70268038 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-95-10094A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268038 | |||||||
| chr12:70268100 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-95-10032G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268100 | |||||||
| chr12:70268594 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-9538C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268594 | |||||||
| chr12:70268627 | AT | A | 32 | a0001c0001t0002g0034 a0001c0001t0003g0248 a0001c0001t0003g0263 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-95-9492delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70268627 | ||||||
| chr12:70268628 | T | A | 3 | a0001c0001t0001g0023 a0001c0001t0004g0245 a0001c0001t0014g0007 |
3 | HG03486.hp1 HG06807.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-95-9504T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268628 | |||||||
| chr12:70268629 | T | A | 31 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(28): Show |
32 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-95-9503T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268629 | |||||||
| chr12:70268646 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-9486T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268646 | |||||||
| chr12:70268875 | T | C | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-9257T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268875 | |||||||
| chr12:70269025 | G | A | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-9107G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269025 | |||||||
| chr12:70269217 | C | T | 5 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0194 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-8915C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269217 | |||||||
| chr12:70269275 | CT | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0101 others(15): Show |
18 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-95-8846delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70269275 | ||||||
| chr12:70269290 | CT | C | 25 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(22): Show |
26 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.-95-8829delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70269290 | ||||||
| chr12:70269488 | A | G | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-8644A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269488 | |||||||
| chr12:70269545 | A | C | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-95-8587A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269545 | |||||||
| chr12:70269862 | C | T | 5 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0194 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-8270C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269862 | |||||||
| chr12:70269870 | T | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-95-8262T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269870 | |||||||
| chr12:70269995 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-8137C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269995 | |||||||
| chr12:70270040 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-8092A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70270040 | |||||||
| chr12:70270410 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0002g0013 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-95-7722T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70270410 | |||||||
| chr12:70270576 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-7556A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70270576 | |||||||
| chr12:70270878 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-95-7254A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70270878 | |||||||
| chr12:70271085 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-7047T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271085 | |||||||
| chr12:70271203 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-95-6929A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271203 | |||||||
| chr12:70271264 | C | A | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-6868C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271264 | |||||||
| chr12:70271341 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-95-6791G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271341 | |||||||
| chr12:70271375 | C | CT | 34 | a0001c0001t0001g0019 a0001c0001t0001g0113 a0001c0001t0001g0114 others(31): Show |
35 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-95-6735dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | ||||||
| chr12:70271375 | C | CTT | 7 | a0001c0001t0001g0023 a0001c0001t0001g0112 a0001c0001t0004g0256 others(4): Show |
7 | HG00609.hp1 HG01081.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-6736_-95-6735d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | ||||||
| chr12:70271375 | CT | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.-95-6735delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | ||||||
| chr12:70271375 | CTT | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0185 a0001c0001t0001g0215 others(6): Show |
9 | HG01167.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-6736_-95-6735d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | ||||||
| chr12:70271375 | CTTT | C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-95-6737_-95-6735d others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | ||||||
| chr12:70271405 | G | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-6727G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271405 | |||||||
| chr12:70271420 | C | T | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-6712C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271420 | |||||||
| chr12:70271437 | A | G | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-95-6695A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271437 | |||||||
| chr12:70271443 | A | G | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-95-6689A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271443 | |||||||
| chr12:70271509 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-6623G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271509 | |||||||
| chr12:70271517 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-95-6615G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271517 | |||||||
| chr12:70271852 | C | T | 10 | a0001c0001t0006g0230 a0001c0001t0006g0235 a0001c0001t0006g0236 others(7): Show |
11 | HG00621.hp2 HG01123.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-95-6280C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271852 | |||||||
| chr12:70271918 | C | CA | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-6208dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271918 | ||||||
| chr12:70272215 | G | C | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-5917G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272215 | |||||||
| chr12:70272246 | G | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-5886G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272246 | |||||||
| chr12:70272429 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-5703A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272429 | |||||||
| chr12:70272509 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-95-5623G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272509 | |||||||
| chr12:70272565 | A | T | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-5567A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272565 | |||||||
| chr12:70272579 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-95-5553G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272579 | |||||||
| chr12:70273301 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-95-4831A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273301 | |||||||
| chr12:70273313 | C | CT | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-4809dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70273313 | ||||||
| chr12:70273472 | T | C | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-4660T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273472 | |||||||
| chr12:70273777 | A | T | 1 | a0001c0002t0001g0121 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-95-4355A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273777 | |||||||
| chr12:70273851 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-4281A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273851 | |||||||
| chr12:70273957 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-95-4175T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273957 | |||||||
| chr12:70274167 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-95-3965A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274167 | |||||||
| chr12:70274274 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-3858A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274274 | |||||||
| chr12:70274470 | A | G | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-3662A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274470 | |||||||
| chr12:70274690 | A | G | 2 | a0001c0001t0008g0005 a0001c0001t0008g0234 |
3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-95-3442A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274690 | |||||||
| chr12:70274777 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
100 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.-95-3355C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274777 | |||||||
| chr12:70274929 | G | A | 10 | a0001c0001t0006g0230 a0001c0001t0006g0235 a0001c0001t0006g0236 others(7): Show |
11 | HG00621.hp2 HG01123.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-95-3203G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274929 | |||||||
| chr12:70275155 | T | G | 2 | a0001c0001t0001g0014 a0001c0001t0002g0013 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-95-2977T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275155 | |||||||
| chr12:70275184 | T | C | 4 | a0001c0001t0002g0192 a0001c0001t0002g0194 a0001c0001t0002g0195 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-2948T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275184 | |||||||
| chr12:70275196 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-95-2936C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275196 | |||||||
| chr12:70275341 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-95-2791G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275341 | |||||||
| chr12:70275484 | G | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG01099.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-2648G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275484 | |||||||
| chr12:70275671 | G | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-2461G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275671 | |||||||
| chr12:70275768 | G | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(39): Show |
42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-95-2364G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275768 | |||||||
| chr12:70276089 | A | G | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-2043A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276089 | |||||||
| chr12:70276153 | G | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(268): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-95-1979G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276153 | |||||||
| chr12:70276261 | A | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-95-1871A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276261 | |||||||
| chr12:70276298 | T | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-95-1834T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276298 | |||||||
| chr12:70276412 | G | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-1720G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276412 | |||||||
| chr12:70276413 | C | T | 2 | a0001c0001t0003g0205 a0001c0001t0003g0209 |
2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.-95-1719C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276413 | |||||||
| chr12:70276447 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-1685A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276447 | |||||||
| chr12:70276566 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-1566C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276566 | |||||||
| chr12:70276567 | G | T | 1 | a0001c0001t0009g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-95-1565G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276567 | |||||||
| chr12:70276806 | G | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-95-1326G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276806 | |||||||
| chr12:70276821 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-1311G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276821 | |||||||
| chr12:70276877 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-1255T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276877 | |||||||
| chr12:70277366 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-95-766A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277366 | |||||||
| chr12:70277447 | T | G | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-95-685T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277447 | |||||||
| chr12:70277489 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-95-643A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277489 | |||||||
| chr12:70277580 | A | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-95-552A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277580 | |||||||
| chr12:70277643 | G | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-95-489G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277643 | |||||||
| chr12:70277677 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-95-455G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277677 | |||||||
| chr12:70277680 | G | A | 8 | a0001c0001t0003g0248 a0001c0001t0004g0246 a0001c0001t0004g0247 others(5): Show |
8 | HG01069.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-452G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277680 | |||||||
| chr12:70277689 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-443A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277689 | |||||||
| chr12:70277864 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-95-268T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277864 | |||||||
| chr12:70277916 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-216A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277916 | |||||||
| chr12:70277981 | C | T | 1 | a0001c0001t0006g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-95-151C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277981 | |||||||
| chr12:70277988 | G | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(17): Show |
20 | HG00741.hp2 HG01109.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-95-144G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277988 | |||||||
| chr12:70277995 | T | C | 1 | a0001c0001t0006g0237 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-95-137T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277995 | |||||||
| chr12:70278015 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-95-117G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70278015 | |||||||
| chr12:70278032 | T | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-100T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70278032 | |||||||
| chr12:70278369 | T | A | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.48+95T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278369 | |||||||
| chr12:70278537 | A | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(39): Show |
42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.48+263A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278537 | |||||||
| chr12:70278677 | A | G | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+403A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278677 | |||||||
| chr12:70278770 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.48+496C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278770 | |||||||
| chr12:70278820 | T | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.48+546T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278820 | |||||||
| chr12:70278992 | G | A | 8 | a0001c0001t0003g0248 a0001c0001t0004g0246 a0001c0001t0004g0247 others(5): Show |
8 | HG01069.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+718G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278992 | |||||||
| chr12:70279007 | T | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+733T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279007 | |||||||
| chr12:70279068 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+794T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279068 | |||||||
| chr12:70279136 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+862T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279136 | |||||||
| chr12:70279548 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.48+1274T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279548 | |||||||
| chr12:70279705 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.48+1431A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279705 | |||||||
| chr12:70279723 | T | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.48+1449T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279723 | |||||||
| chr12:70279799 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.48+1525A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279799 | |||||||
| chr12:70279844 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+1570G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279844 | |||||||
| chr12:70279857 | CTTTCTAC others(20): Show |
C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0142 a0001c0001t0001g0150 others(2): Show |
5 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+1585_48+1611del others(27): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70279857 | ||||||
| chr12:70279887 | A | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.48+1613A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279887 | |||||||
| chr12:70280003 | A | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.48+1729A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280003 | |||||||
| chr12:70280102 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0002g0217 |
3 | HG03579.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.48+1828G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280102 | |||||||
| chr12:70280348 | G | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+2074G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280348 | |||||||
| chr12:70280377 | T | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0120 others(2): Show |
5 | HG01109.hp1 HG02486.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+2103T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280377 | |||||||
| chr12:70280753 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+2479T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280753 | |||||||
| chr12:70280803 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18961.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.48+2529T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280803 | |||||||
| chr12:70280808 | T | C | 3 | a0001c0001t0006g0237 a0001c0001t0006g0238 a0001c0001t0006g0239 |
3 | HG02257.hp1 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.48+2534T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280808 | |||||||
| chr12:70280820 | C | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+2546C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280820 | |||||||
| chr12:70280875 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+2601C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280875 | |||||||
| chr12:70280915 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+2641C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280915 | |||||||
| chr12:70281084 | C | CT | 16 | a0001c0001t0001g0108 a0001c0001t0001g0177 a0001c0001t0003g0109 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.48+2825dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70281084 | ||||||
| chr12:70281084 | CT | C | 49 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(46): Show |
50 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.48+2825delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70281084 | ||||||
| chr12:70281100 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.48+2826C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281100 | |||||||
| chr12:70281137 | G | T | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+2863G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281137 | |||||||
| chr12:70281157 | T | C | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+2883T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281157 | |||||||
| chr12:70281194 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+2920C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281194 | |||||||
| chr12:70281260 | T | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.48+2986T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281260 | |||||||
| chr12:70281318 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+3044C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281318 | |||||||
| chr12:70281319 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+3045G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281319 | |||||||
| chr12:70281453 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.48+3179C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281453 | |||||||
| chr12:70281685 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.48+3411C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281685 | |||||||
| chr12:70281816 | T | TTAAATTT others(18): Show |
21 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0206 others(18): Show |
22 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+3575_48+3599dup others(25): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70281816 | ||||||
| chr12:70281816 | T | TTAAATTT others(43): Show |
12 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(9): Show |
12 | HG01256.hp1 HG01261.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.48+3550_48+3599dup others(50): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70281816 | ||||||
| chr12:70281922 | A | G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0142 a0001c0001t0001g0150 others(2): Show |
5 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+3648A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281922 | |||||||
| chr12:70281932 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.48+3658T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281932 | |||||||
| chr12:70282102 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.48+3828C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282102 | |||||||
| chr12:70282243 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+3969C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282243 | |||||||
| chr12:70282250 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+3976G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282250 | |||||||
| chr12:70282332 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.48+4058G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282332 | |||||||
| chr12:70282400 | A | G | 1 | a0001c0001t0003g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.48+4126A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282400 | |||||||
| chr12:70282884 | C | CT | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.48+4612dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70282884 | ||||||
| chr12:70283106 | A | G | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.48+4832A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283106 | |||||||
| chr12:70283111 | T | C | 3 | a0001c0002t0001g0020 a0001c0002t0001g0121 a0001c0002t0001g0172 |
3 | HG02970.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.48+4837T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283111 | |||||||
| chr12:70283333 | A | C | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+5059A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283333 | |||||||
| chr12:70283365 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.48+5091C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283365 | |||||||
| chr12:70283366 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0167 a0001c0001t0001g0190 |
3 | HG01074.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+5092G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283366 | |||||||
| chr12:70283420 | A | AGG | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+5146_48+5147ins others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283420 | |||||||
| chr12:70283467 | T | TGATA | 52 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0023 others(49): Show |
52 | HG00558.hp1 HG00609.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.48+5232_48+5235dup others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | ||||||
| chr12:70283467 | T | TGATAGAT others(1): Show |
113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(110): Show |
114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.48+5228_48+5235dup others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | ||||||
| chr12:70283467 | T | TGATAGAT others(5): Show |
35 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0054 others(32): Show |
37 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.48+5224_48+5235dup others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | ||||||
| chr12:70283467 | T | TGATAGAT others(9): Show |
5 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0077 others(2): Show |
5 | HG03225.hp2 HG03710.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+5220_48+5235dup others(16): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | ||||||
| chr12:70283467 | TGATA | T | 32 | a0001c0001t0001g0021 a0001c0001t0001g0065 a0001c0001t0001g0067 others(29): Show |
33 | HG00609.hp1 HG00621.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+5232_48+5235del others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | ||||||
| chr12:70283467 | TGATAGAT others(1): Show |
T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0206 a0001c0001t0002g0013 others(2): Show |
5 | HG00733.hp2 HG01070.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+5228_48+5235del others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | ||||||
| chr12:70283561 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+5287A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283561 | |||||||
| chr12:70283570 | A | T | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.48+5296A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283570 | |||||||
| chr12:70283611 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.48+5337A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283611 | |||||||
| chr12:70283647 | T | TA | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.48+5393dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283647 | ||||||
| chr12:70283647 | TA | T | 19 | a0001c0001t0001g0161 a0001c0001t0001g0199 a0001c0001t0001g0200 others(16): Show |
20 | HG01123.hp2 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.48+5393delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283647 | ||||||
| chr12:70283653 | A | C | 5 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0194 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+5379A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283653 | |||||||
| chr12:70283658 | A | AG | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+5384_48+5385ins others(1): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283658 | |||||||
| chr12:70283686 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(108): Show |
113 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.48+5412A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283686 | |||||||
| chr12:70283707 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+5433C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283707 | |||||||
| chr12:70283846 | T | C | 1 | a0001c0002t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.48+5572T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283846 | |||||||
| chr12:70283853 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0144 a0001c0001t0001g0147 others(3): Show |
7 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+5579A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283853 | |||||||
| chr12:70283902 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0092 |
4 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+5628C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283902 | |||||||
| chr12:70283930 | A | AT | 28 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0054 others(25): Show |
28 | HG00438.hp1 HG01109.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.48+5679dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283930 | ||||||
| chr12:70283930 | A | ATT | 12 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0112 others(9): Show |
12 | HG02145.hp2 HG02451.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.48+5678_48+5679dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283930 | ||||||
| chr12:70283930 | A | ATTT | 28 | a0001c0001t0002g0195 a0001c0001t0003g0248 a0001c0001t0003g0263 others(25): Show |
29 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.48+5677_48+5679dup others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283930 | ||||||
| chr12:70283930 | A | ATTTT | 5 | a0001c0001t0001g0023 a0001c0001t0004g0245 a0001c0001t0004g0270 others(2): Show |
5 | HG01069.hp2 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+5676_48+5679dup others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283930 | ||||||
| chr12:70284030 | C | T | 1 | a0001c0003t0001g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.48+5756C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284030 | |||||||
| chr12:70284314 | C | T | 34 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0248 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+6040C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284314 | |||||||
| chr12:70284575 | CCT | C | 3 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0003g0063 |
3 | HG00438.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.48+6302_48+6303del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284575 | |||||||
| chr12:70284575 | CCTT | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
68 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.48+6302_48+6304del others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284575 | |||||||
| chr12:70284576 | C | CTT | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+6320_48+6321dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70284576 | ||||||
| chr12:70284576 | CT | C | 43 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(40): Show |
43 | HG00323.hp1 HG00609.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.48+6321delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70284576 | ||||||
| chr12:70284576 | CTT | C | 9 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(6): Show |
9 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.48+6320_48+6321del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70284576 | ||||||
| chr12:70284642 | T | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+6368T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284642 | |||||||
| chr12:70284694 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.48+6420C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284694 | |||||||
| chr12:70284916 | T | C | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.48+6642T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284916 | |||||||
| chr12:70284994 | G | A | 1 | a0001c0001t0004g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.48+6720G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284994 | |||||||
| chr12:70285191 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.48+6917A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285191 | |||||||
| chr12:70285216 | G | GT | 7 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0120 others(4): Show |
7 | HG01109.hp1 HG02896.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+6954dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70285216 | ||||||
| chr12:70285216 | G | T | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+6942G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285216 | |||||||
| chr12:70285221 | T | TG | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+6947_48+6948ins others(1): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285221 | |||||||
| chr12:70285222 | T | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0165 a0001c0001t0001g0166 others(4): Show |
7 | HG00099.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+6948T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285222 | |||||||
| chr12:70285272 | T | C | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+6998T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285272 | |||||||
| chr12:70285289 | A | G | 2 | a0001c0001t0003g0205 a0001c0001t0003g0209 |
2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.48+7015A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285289 | |||||||
| chr12:70285331 | T | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+7057T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285331 | |||||||
| chr12:70285384 | AT | A | 59 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(56): Show |
61 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.48+7123delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70285384 | ||||||
| chr12:70285384 | ATT | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+7122_48+7123del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70285384 | ||||||
| chr12:70285407 | G | A | 1 | a0001c0001t0007g0267 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.48+7133G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285407 | |||||||
| chr12:70285492 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+7218A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285492 | |||||||
| chr12:70285496 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+7222G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285496 | |||||||
| chr12:70285498 | G | A | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+7224G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285498 | |||||||
| chr12:70285638 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.48+7364A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285638 | |||||||
| chr12:70285692 | CAA | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+7420_48+7421del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70285692 | ||||||
| chr12:70285810 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.48+7536G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285810 | |||||||
| chr12:70286084 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+7810G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286084 | |||||||
| chr12:70286106 | T | TCATATTT others(304): Show |
29 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(26): Show |
30 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.48+7841_48+7842ins others(311): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286106 | ||||||
| chr12:70286106 | T | TCATATTT others(305): Show |
3 | a0001c0001t0004g0245 a0001c0001t0005g0268 a0001c0001t0007g0262 |
3 | HG01928.hp1 NA18977.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.48+7841_48+7842ins others(312): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286106 | ||||||
| chr12:70286106 | T | TCATATTT others(320): Show |
1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.48+7841_48+7842ins others(327): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286106 | ||||||
| chr12:70286106 | T | TCATATTT others(324): Show |
1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.48+7841_48+7842ins others(331): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286106 | ||||||
| chr12:70286155 | C | A | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.48+7881C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286155 | |||||||
| chr12:70286212 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+7938C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286212 | |||||||
| chr12:70286239 | G | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+7965G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286239 | |||||||
| chr12:70286280 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+8006A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286280 | |||||||
| chr12:70286359 | A | ATTC | 156 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.48+8089_48+8091dup others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286359 | ||||||
| chr12:70286439 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.48+8165G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286439 | |||||||
| chr12:70286613 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.48+8339A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286613 | |||||||
| chr12:70286759 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+8485C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286759 | |||||||
| chr12:70286822 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+8548C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286822 | |||||||
| chr12:70286950 | T | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.48+8676T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286950 | |||||||
| chr12:70286969 | T | C | 1 | a0001c0001t0002g0017 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.48+8695T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286969 | |||||||
| chr12:70287153 | A | AT | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.48+8887dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70287153 | ||||||
| chr12:70287213 | AT | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(143): Show |
150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.48+8946delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70287213 | ||||||
| chr12:70287302 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.48+9028C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287302 | |||||||
| chr12:70287481 | G | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+9207G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287481 | |||||||
| chr12:70287509 | T | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+9235T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287509 | |||||||
| chr12:70287725 | G | A | 1 | a0001c0001t0005g0268 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.48+9451G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287725 | |||||||
| chr12:70287824 | T | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.48+9550T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287824 | |||||||
| chr12:70288034 | C | T | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.48+9760C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288034 | |||||||
| chr12:70288056 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+9782T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288056 | |||||||
| chr12:70288136 | C | CT | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.48+9886dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | ||||||
| chr12:70288136 | C | CTT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0102 others(6): Show |
9 | HG00438.hp2 HG02486.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+9885_48+9886dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | ||||||
| chr12:70288136 | CT | C | 57 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0043 others(54): Show |
58 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.48+9886delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | ||||||
| chr12:70288136 | CTTTTTT | C | 32 | a0001c0001t0001g0023 a0001c0001t0002g0195 a0001c0001t0003g0248 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+9881_48+9886del others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | ||||||
| chr12:70288136 | CTTTTTTT | C | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+9880_48+9886del others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | ||||||
| chr12:70288136 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.48+9877_48+9886del others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | ||||||
| chr12:70288136 | CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0002g0076 a0001c0001t0002g0123 a0001c0001t0002g0124 others(3): Show |
6 | HG01099.hp2 HG01123.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+9872_48+9886del others(15): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | ||||||
| chr12:70288149 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+9875T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288149 | |||||||
| chr12:70288399 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.48+10125G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288399 | |||||||
| chr12:70288652 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+10378C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288652 | |||||||
| chr12:70289965 | T | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(39): Show |
42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.48+11691T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70289965 | |||||||
| chr12:70290009 | T | G | 1 | a0001c0001t0003g0063 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.48+11735T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290009 | |||||||
| chr12:70290226 | C | CT | 11 | a0001c0001t0001g0025 a0001c0001t0002g0191 a0001c0001t0002g0192 others(8): Show |
11 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.48+11962dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70290226 | ||||||
| chr12:70290282 | A | C | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+12008A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290282 | |||||||
| chr12:70290485 | A | T | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+12211A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290485 | |||||||
| chr12:70290577 | A | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(186): Show |
193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.48+12303A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290577 | |||||||
| chr12:70290640 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+12366C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290640 | |||||||
| chr12:70290657 | C | CTT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(217): Show |
224 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.48+12383_48+12384i others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290657 | |||||||
| chr12:70290713 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+12439A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290713 | |||||||
| chr12:70290875 | C | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+12601C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290875 | |||||||
| chr12:70291201 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(213): Show |
220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.48+12927C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291201 | |||||||
| chr12:70291378 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.48+13104G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291378 | |||||||
| chr12:70291484 | G | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0196 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48+13210G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291484 | |||||||
| chr12:70291492 | A | G | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+13218A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291492 | |||||||
| chr12:70291547 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48+13273C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291547 | |||||||
| chr12:70291708 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+13434C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291708 | |||||||
| chr12:70291733 | C | T | 4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
4 | HG02486.hp1 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13459C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291733 | |||||||
| chr12:70291797 | C | T | 1 | a0001c0001t0009g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.48+13523C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291797 | |||||||
| chr12:70291863 | G | A | 3 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0001t0002g0197 |
3 | HG02109.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.48+13589G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291863 | |||||||
| chr12:70291869 | G | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+13595G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291869 | |||||||
| chr12:70291945 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0002g0217 |
3 | HG03579.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.48+13671A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291945 | |||||||
| chr12:70291989 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+13715A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291989 | |||||||
| chr12:70291990 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+13716C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291990 | |||||||
| chr12:70292283 | C | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.48+14009C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292283 | |||||||
| chr12:70292370 | C | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0003g0221 |
3 | HG01167.hp2 HG01169.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.48+14096C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292370 | |||||||
| chr12:70292379 | T | C | 1 | a0001c0001t0004g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.48+14105T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292379 | |||||||
| chr12:70292399 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+14125G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292399 | |||||||
| chr12:70292449 | G | A | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.48+14175G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292449 | |||||||
| chr12:70292455 | T | G | 1 | a0001c0001t0004g0256 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.48+14181T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292455 | |||||||
| chr12:70292557 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.48+14283G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292557 | |||||||
| chr12:70292764 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+14490A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292764 | |||||||
| chr12:70292780 | T | C | 2 | a0001c0001t0003g0263 a0001c0001t0004g0269 |
2 | NA18986.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.48+14506T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292780 | |||||||
| chr12:70293051 | A | T | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.48+14777A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293051 | |||||||
| chr12:70293094 | T | C | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.48+14820T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293094 | |||||||
| chr12:70293124 | G | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+14850G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293124 | |||||||
| chr12:70293130 | A | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+14856A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293130 | |||||||
| chr12:70293161 | C | CT | 53 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(50): Show |
54 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.48+14903dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293161 | ||||||
| chr12:70293161 | CT | C | 26 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(23): Show |
27 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.48+14903delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293161 | ||||||
| chr12:70293236 | A | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(217): Show |
224 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.48+14962A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293236 | |||||||
| chr12:70293361 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48+15087G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293361 | |||||||
| chr12:70293373 | G | C | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+15099G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293373 | |||||||
| chr12:70293552 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.48+15278C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293552 | |||||||
| chr12:70293579 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+15305A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293579 | |||||||
| chr12:70293634 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0003g0003 |
2 | NA18970.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.48+15360A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293634 | |||||||
| chr12:70293794 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.48+15520G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293794 | |||||||
| chr12:70293811 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0002g0057 |
2 | NA18942.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.48+15537G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293811 | |||||||
| chr12:70293850 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.48+15576A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293850 | |||||||
| chr12:70293914 | C | CT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0130 others(4): Show |
7 | HG00738.hp1 HG01109.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+15666dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293914 | ||||||
| chr12:70293914 | C | CTTT | 7 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(4): Show |
7 | HG01070.hp1 HG01256.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+15664_48+15666d others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293914 | ||||||
| chr12:70293914 | CT | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(117): Show |
122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.48+15666delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293914 | ||||||
| chr12:70293914 | CTT | C | 50 | a0001c0001t0001g0023 a0001c0001t0002g0036 a0001c0001t0002g0061 others(47): Show |
52 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.48+15665_48+15666d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293914 | ||||||
| chr12:70294150 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.48+15876G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294150 | |||||||
| chr12:70294608 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-16287A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294608 | |||||||
| chr12:70294667 | A | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-16228A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294667 | |||||||
| chr12:70294834 | T | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-16061T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294834 | |||||||
| chr12:70294932 | A | G | 24 | a0001c0001t0003g0263 a0001c0001t0004g0244 a0001c0001t0004g0245 others(21): Show |
25 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.49-15963A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294932 | |||||||
| chr12:70294941 | C | T | 1 | a0001c0001t0013g0159 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.49-15954C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294941 | |||||||
| chr12:70295033 | C | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.49-15862C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295033 | |||||||
| chr12:70295075 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49-15820A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295075 | |||||||
| chr12:70295219 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49-15676C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295219 | |||||||
| chr12:70295333 | AG | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-15561delG | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295333 | |||||||
| chr12:70295340 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-15555C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295340 | |||||||
| chr12:70295357 | T | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-15538T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295357 | |||||||
| chr12:70295378 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.49-15517A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295378 | |||||||
| chr12:70295689 | C | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-15206C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295689 | |||||||
| chr12:70295736 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.49-15159G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295736 | |||||||
| chr12:70296305 | G | A | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-14590G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296305 | |||||||
| chr12:70296308 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-14587T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296308 | |||||||
| chr12:70296313 | A | G | 3 | a0001c0001t0003g0083 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02040.hp1 NA18945.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.49-14582A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296313 | |||||||
| chr12:70296408 | G | A | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.49-14487G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296408 | |||||||
| chr12:70296616 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-14279A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296616 | |||||||
| chr12:70296654 | G | GT | 8 | a0001c0001t0001g0011 a0001c0001t0001g0200 a0001c0001t0001g0215 others(5): Show |
8 | HG02486.hp2 HG03098.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-14228dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296654 | ||||||
| chr12:70296654 | GT | G | 15 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(12): Show |
15 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-14228delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296654 | ||||||
| chr12:70296654 | GTT | G | 53 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(50): Show |
55 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.49-14229_49-14228d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296654 | ||||||
| chr12:70296757 | G | GCC | 14 | a0001c0001t0003g0263 a0001c0001t0004g0254 a0001c0001t0004g0256 others(11): Show |
15 | HG00609.hp1 HG01099.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.49-14129_49-14128d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296757 | ||||||
| chr12:70296757 | GC | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0021 others(67): Show |
73 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49-14128delC | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296757 | ||||||
| chr12:70296822 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.49-14073C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296822 | |||||||
| chr12:70296831 | A | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-14064A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296831 | |||||||
| chr12:70296879 | A | G | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-14016A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296879 | |||||||
| chr12:70297134 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-13761G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297134 | |||||||
| chr12:70297167 | G | A | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-13728G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297167 | |||||||
| chr12:70297172 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01261.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.49-13723T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297172 | |||||||
| chr12:70297201 | G | A | 1 | a0001c0001t0004g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.49-13694G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297201 | |||||||
| chr12:70297525 | C | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.49-13370C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297525 | |||||||
| chr12:70297543 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-13352A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297543 | |||||||
| chr12:70297546 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-13349A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297546 | |||||||
| chr12:70297685 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0002g0047 others(1): Show |
4 | HG00408.hp2 HG02040.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-13210T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297685 | |||||||
| chr12:70297893 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-13002C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297893 | |||||||
| chr12:70298071 | C | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-12824C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298071 | |||||||
| chr12:70298123 | G | A | 1 | a0001c0001t0004g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.49-12772G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298123 | |||||||
| chr12:70298257 | T | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-12638T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298257 | |||||||
| chr12:70298264 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-12631C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298264 | |||||||
| chr12:70298288 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-12607A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298288 | |||||||
| chr12:70298326 | C | T | 1 | a0001c0002t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49-12569C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298326 | |||||||
| chr12:70298361 | T | C | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-12534T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298361 | |||||||
| chr12:70298409 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.49-12486C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298409 | |||||||
| chr12:70298465 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-12430A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298465 | |||||||
| chr12:70298552 | A | G | 1 | a0001c0001t0004g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.49-12343A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298552 | |||||||
| chr12:70298626 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-12269G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298626 | |||||||
| chr12:70298695 | A | AT | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-12196dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70298695 | ||||||
| chr12:70299009 | T | C | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-11886T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299009 | |||||||
| chr12:70299040 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-11855C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299040 | |||||||
| chr12:70299135 | C | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-11760C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299135 | |||||||
| chr12:70299136 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-11759G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299136 | |||||||
| chr12:70299140 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(143): Show |
150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.49-11755C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299140 | |||||||
| chr12:70299146 | G | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-11749G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299146 | |||||||
| chr12:70299148 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-11747G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299148 | |||||||
| chr12:70299213 | A | ATT | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-11673_49-11672d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70299213 | ||||||
| chr12:70299336 | T | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-11559T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299336 | |||||||
| chr12:70299362 | GTCCCTCC others(7): Show |
G | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-11532_49-11519d others(16): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299362 | |||||||
| chr12:70299374 | T | C | 1 | a0001c0001t0003g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.49-11521T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299374 | |||||||
| chr12:70299374 | T | TC | 8 | a0001c0001t0001g0008 a0001c0001t0001g0112 a0001c0001t0001g0190 others(5): Show |
8 | HG00741.hp2 HG01099.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-11515dupC | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70299374 | ||||||
| chr12:70299380 | C | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-11515C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299380 | |||||||
| chr12:70299381 | AC | A | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.49-11508delC | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70299381 | ||||||
| chr12:70299386 | C | A | 1 | a0001c0001t0002g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.49-11509C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299386 | |||||||
| chr12:70299491 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-11404G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299491 | |||||||
| chr12:70299738 | C | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-11157C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299738 | |||||||
| chr12:70299839 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0003g0109 |
2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.49-11056A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299839 | |||||||
| chr12:70299840 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0003g0109 |
2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.49-11055G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299840 | |||||||
| chr12:70299923 | T | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-10972T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299923 | |||||||
| chr12:70300021 | T | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-10874T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300021 | |||||||
| chr12:70300045 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-10850G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300045 | |||||||
| chr12:70300065 | T | G | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.49-10830T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300065 | |||||||
| chr12:70300181 | C | T | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-10714C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300181 | |||||||
| chr12:70300190 | G | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-10705G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300190 | |||||||
| chr12:70300247 | G | T | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-10648G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300247 | |||||||
| chr12:70300256 | G | A | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-10639G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300256 | |||||||
| chr12:70300301 | A | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-10594A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300301 | |||||||
| chr12:70300327 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-10568T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300327 | |||||||
| chr12:70300412 | T | G | 5 | a0001c0001t0003g0063 a0001c0001t0003g0084 a0001c0001t0003g0086 others(2): Show |
5 | HG00438.hp2 HG02015.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-10483T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300412 | |||||||
| chr12:70300501 | G | A | 13 | a0001c0001t0003g0263 a0001c0001t0004g0261 a0001c0001t0004g0264 others(10): Show |
14 | HG01099.hp1 HG01192.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.49-10394G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300501 | |||||||
| chr12:70300555 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-10340C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300555 | |||||||
| chr12:70300617 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-10278C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300617 | |||||||
| chr12:70300623 | C | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-10272C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300623 | |||||||
| chr12:70300652 | G | A | 1 | a0001c0001t0003g0110 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.49-10243G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300652 | |||||||
| chr12:70300685 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49-10210A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300685 | |||||||
| chr12:70300724 | AACTTTAA others(3): Show |
A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-10169_49-10160d others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70300724 | ||||||
| chr12:70300779 | G | T | 1 | a0001c0001t0002g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.49-10116G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300779 | |||||||
| chr12:70300827 | C | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0088 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.49-10068C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300827 | |||||||
| chr12:70300834 | G | A | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-10061G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300834 | |||||||
| chr12:70300846 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-10049G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300846 | |||||||
| chr12:70300847 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-10048T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300847 | |||||||
| chr12:70300856 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-10039G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300856 | |||||||
| chr12:70300880 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-10015T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300880 | |||||||
| chr12:70300919 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.49-9976T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300919 | |||||||
| chr12:70301067 | T | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-9828T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301067 | |||||||
| chr12:70301096 | A | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-9799A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301096 | |||||||
| chr12:70301097 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-9798T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301097 | |||||||
| chr12:70301182 | T | C | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.49-9713T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301182 | |||||||
| chr12:70301269 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.49-9626T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301269 | |||||||
| chr12:70301378 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-9517A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301378 | |||||||
| chr12:70301407 | T | G | 1 | a0001c0001t0004g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.49-9488T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301407 | |||||||
| chr12:70301464 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.49-9431A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301464 | |||||||
| chr12:70301484 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01261.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.49-9411C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301484 | |||||||
| chr12:70301485 | GT | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
214 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.49-9402delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70301485 | ||||||
| chr12:70301486 | T | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01261.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.49-9409T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301486 | |||||||
| chr12:70301522 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-9373G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301522 | |||||||
| chr12:70301534 | T | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-9361T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301534 | |||||||
| chr12:70301535 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-9360C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301535 | |||||||
| chr12:70301536 | T | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-9359T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301536 | |||||||
| chr12:70301559 | C | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-9336C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301559 | |||||||
| chr12:70301636 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.49-9259G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301636 | |||||||
| chr12:70301696 | C | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-9199C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301696 | |||||||
| chr12:70301770 | T | G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0220 others(8): Show |
11 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.49-9125T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301770 | |||||||
| chr12:70301773 | T | C | 1 | a0001c0001t0006g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.49-9122T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301773 | |||||||
| chr12:70301784 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.49-9111C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301784 | |||||||
| chr12:70301797 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.49-9098A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301797 | |||||||
| chr12:70301807 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.49-9088C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301807 | |||||||
| chr12:70301878 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-9017T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301878 | |||||||
| chr12:70301884 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.49-9011C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301884 | |||||||
| chr12:70301961 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-8934T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301961 | |||||||
| chr12:70302199 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.49-8696T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302199 | |||||||
| chr12:70302209 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-8686A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302209 | |||||||
| chr12:70302232 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.49-8663T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302232 | |||||||
| chr12:70302283 | C | T | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-8612C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302283 | |||||||
| chr12:70302430 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49-8465G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302430 | |||||||
| chr12:70302485 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.49-8410T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302485 | |||||||
| chr12:70302521 | A | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-8374A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302521 | |||||||
| chr12:70302543 | T | C | 2 | a0001c0001t0003g0078 a0001c0001t0003g0088 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.49-8352T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302543 | |||||||
| chr12:70302570 | G | C | 3 | a0001c0001t0003g0063 a0001c0001t0003g0086 a0001c0001t0003g0095 |
3 | HG00438.hp2 HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.49-8325G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302570 | |||||||
| chr12:70302709 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.49-8186A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302709 | |||||||
| chr12:70302734 | A | C | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-8161A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302734 | |||||||
| chr12:70302871 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.49-8024A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302871 | |||||||
| chr12:70302959 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-7936A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302959 | |||||||
| chr12:70302992 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-7903A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302992 | |||||||
| chr12:70303010 | T | C | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-7885T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303010 | |||||||
| chr12:70303029 | G | A | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-7866G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303029 | |||||||
| chr12:70303175 | G | T | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-7720G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303175 | |||||||
| chr12:70303215 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-7680C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303215 | |||||||
| chr12:70303271 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49-7624G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303271 | |||||||
| chr12:70303274 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49-7621G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303274 | |||||||
| chr12:70303283 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.49-7612C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303283 | |||||||
| chr12:70303392 | G | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.49-7503G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303392 | |||||||
| chr12:70303395 | A | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-7500A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303395 | |||||||
| chr12:70303425 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49-7470G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303425 | |||||||
| chr12:70303482 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49-7413G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303482 | |||||||
| chr12:70303538 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-7357A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303538 | |||||||
| chr12:70303574 | G | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.49-7321G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303574 | |||||||
| chr12:70303576 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
78 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.49-7319C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303576 | |||||||
| chr12:70303638 | A | C | 1 | a0001c0001t0001g0054 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.49-7257A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303638 | |||||||
| chr12:70303661 | A | C | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-7234A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303661 | |||||||
| chr12:70303699 | C | A | 17 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0002g0038 others(14): Show |
18 | HG00621.hp2 HG01123.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-7196C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303699 | |||||||
| chr12:70303739 | A | G | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-7156A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303739 | |||||||
| chr12:70303754 | A | C | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-7141A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303754 | |||||||
| chr12:70303803 | C | G | 5 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-7092C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303803 | |||||||
| chr12:70303837 | G | A | 36 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0186 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.49-7058G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303837 | |||||||
| chr12:70303938 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.49-6957C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303938 | |||||||
| chr12:70303958 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.49-6937G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303958 | |||||||
| chr12:70303967 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-6928C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303967 | |||||||
| chr12:70304023 | C | T | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-6872C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304023 | |||||||
| chr12:70304025 | C | T | 1 | a0001c0001t0006g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.49-6870C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304025 | |||||||
| chr12:70304032 | G | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-6863G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304032 | |||||||
| chr12:70304047 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.49-6848G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304047 | |||||||
| chr12:70304096 | C | G | 2 | a0001c0001t0008g0005 a0001c0001t0008g0234 |
3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.49-6799C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304096 | |||||||
| chr12:70304102 | G | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-6793G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304102 | |||||||
| chr12:70304134 | T | C | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-6761T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304134 | |||||||
| chr12:70304136 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-6759C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304136 | |||||||
| chr12:70304202 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-6693C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304202 | |||||||
| chr12:70304218 | G | C | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.49-6677G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304218 | |||||||
| chr12:70304219 | G | GTCCAGCT others(66): Show |
6 | a0001c0001t0002g0076 a0001c0001t0002g0123 a0001c0001t0002g0124 others(3): Show |
6 | HG01099.hp2 HG01123.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-6670_49-6598dup others(73): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70304219 | ||||||
| chr12:70304398 | G | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0003g0109 |
3 | HG01081.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.49-6497G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304398 | |||||||
| chr12:70304440 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | HG02056.hp1 NA18961.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-6455G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304440 | |||||||
| chr12:70304627 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49-6268C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304627 | |||||||
| chr12:70304680 | A | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0077 others(35): Show |
40 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-6215A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304680 | |||||||
| chr12:70304681 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-6214A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304681 | |||||||
| chr12:70304777 | G | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-6118G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304777 | |||||||
| chr12:70304829 | G | A | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-6066G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304829 | |||||||
| chr12:70304879 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
201 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.49-6016A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304879 | |||||||
| chr12:70304950 | C | T | 1 | a0001c0001t0003g0110 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.49-5945C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304950 | |||||||
| chr12:70304956 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-5939C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304956 | |||||||
| chr12:70304980 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-5915G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304980 | |||||||
| chr12:70305011 | C | T | 1 | a0001c0001t0007g0262 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49-5884C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305011 | |||||||
| chr12:70305067 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-5828G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305067 | |||||||
| chr12:70305146 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-5749C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305146 | |||||||
| chr12:70305192 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49-5703C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305192 | |||||||
| chr12:70305222 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-5673C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305222 | |||||||
| chr12:70305298 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.49-5597C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305298 | |||||||
| chr12:70305388 | C | G | 1 | a0001c0001t0004g0255 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.49-5507C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305388 | |||||||
| chr12:70305402 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.49-5493C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305402 | |||||||
| chr12:70305403 | G | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-5492G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305403 | |||||||
| chr12:70305408 | G | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-5487G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305408 | |||||||
| chr12:70305482 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-5413G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305482 | |||||||
| chr12:70305490 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.49-5405G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305490 | |||||||
| chr12:70305685 | G | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0196 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.49-5210G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305685 | |||||||
| chr12:70305771 | G | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-5124G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305771 | |||||||
| chr12:70305873 | G | GT | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(153): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.49-5001dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | ||||||
| chr12:70305873 | G | GTT | 42 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0019 others(39): Show |
42 | HG00438.hp1 HG00609.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.49-5002_49-5001dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | ||||||
| chr12:70305873 | G | GTTT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(15): Show |
18 | HG00408.hp2 HG00621.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.49-5003_49-5001dup others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | ||||||
| chr12:70305873 | G | GTTTT | 10 | a0001c0001t0001g0018 a0001c0001t0001g0200 a0001c0001t0001g0220 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-5004_49-5001dup others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | ||||||
| chr12:70305873 | GT | G | 28 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(25): Show |
29 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.49-5001delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | ||||||
| chr12:70305878 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-5017T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305878 | |||||||
| chr12:70305954 | T | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-4941T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305954 | |||||||
| chr12:70306055 | G | A | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.49-4840G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306055 | |||||||
| chr12:70306126 | T | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-4769T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306126 | |||||||
| chr12:70306160 | T | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(14): Show |
18 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-4735T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306160 | |||||||
| chr12:70306203 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.49-4692A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306203 | |||||||
| chr12:70306258 | C | A | 1 | a0001c0001t0010g0231 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.49-4637C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306258 | |||||||
| chr12:70306467 | T | G | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-4428T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306467 | |||||||
| chr12:70306508 | G | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-4387G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306508 | |||||||
| chr12:70306515 | T | TGTCTTGA others(6): Show |
1 | a0001c0001t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49-4377_49-4365dup others(13): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70306515 | ||||||
| chr12:70306566 | T | A | 1 | a0001c0001t0001g0055 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.49-4329T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306566 | |||||||
| chr12:70306584 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.49-4311A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306584 | |||||||
| chr12:70306598 | TA | T | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.49-4288delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70306598 | ||||||
| chr12:70306634 | G | A | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-4261G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306634 | |||||||
| chr12:70306756 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.49-4139G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306756 | |||||||
| chr12:70306891 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.49-4004T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306891 | |||||||
| chr12:70306950 | C | T | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-3945C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306950 | |||||||
| chr12:70306967 | T | C | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-3928T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306967 | |||||||
| chr12:70307061 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-3834C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307061 | |||||||
| chr12:70307062 | G | A | 1 | a0001c0001t0002g0057 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.49-3833G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307062 | |||||||
| chr12:70307126 | A | T | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-3769A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307126 | |||||||
| chr12:70307224 | C | G | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-3671C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307224 | |||||||
| chr12:70307234 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.49-3661C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307234 | |||||||
| chr12:70307307 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0077 others(35): Show |
40 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-3588G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307307 | |||||||
| chr12:70307452 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
201 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.49-3443G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307452 | |||||||
| chr12:70307557 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-3338C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307557 | |||||||
| chr12:70307578 | A | ACCAAATT others(347): Show |
1 | a0001c0001t0001g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49-3302_49-3301ins others(354): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70307578 | ||||||
| chr12:70307681 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-3214C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307681 | |||||||
| chr12:70307873 | A | G | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-3022A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307873 | |||||||
| chr12:70307899 | T | TA | 11 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG01069.hp2 HG01109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.49-2982dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70307899 | ||||||
| chr12:70307899 | TA | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.49-2982delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70307899 | ||||||
| chr12:70307932 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-2963T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307932 | |||||||
| chr12:70307990 | C | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49-2905C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307990 | |||||||
| chr12:70308002 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-2893C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308002 | |||||||
| chr12:70308032 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-2863A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308032 | |||||||
| chr12:70308047 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.49-2848A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308047 | |||||||
| chr12:70308365 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
201 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.49-2530T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308365 | |||||||
| chr12:70308555 | T | TTC | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0215 others(3): Show |
6 | HG01192.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-2311_49-2310dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308555 | ||||||
| chr12:70308555 | T | TTCTTTC | 27 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0246 others(24): Show |
28 | HG00609.hp1 HG01069.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.49-2337_49-2336ins others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308555 | ||||||
| chr12:70308555 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-2337_49-2336ins others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308555 | ||||||
| chr12:70308555 | TTC | T | 29 | a0001c0001t0001g0018 a0001c0001t0001g0171 a0001c0001t0001g0206 others(26): Show |
29 | HG00733.hp1 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.49-2311_49-2310del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308555 | ||||||
| chr12:70308558 | T | G | 1 | a0001c0001t0009g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.49-2337T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308558 | |||||||
| chr12:70308559 | C | T | 4 | a0001c0001t0004g0244 a0001c0001t0004g0245 a0001c0001t0004g0255 others(1): Show |
4 | HG00323.hp1 HG01891.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-2336C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308559 | |||||||
| chr12:70308582 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0181 |
3 | HG02647.hp1 HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-2313T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308582 | |||||||
| chr12:70308582 | TCTCA | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49-2311_49-2308del others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308582 | ||||||
| chr12:70308584 | T | A | 38 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
39 | HG00609.hp1 HG00733.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.49-2311T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308584 | |||||||
| chr12:70308584 | T | TCA | 7 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0115 others(4): Show |
7 | HG01099.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-2288_49-2287dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308584 | T | TCACA | 78 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.49-2290_49-2287dup others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308584 | T | TCACACA | 30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(27): Show |
30 | HG00408.hp1 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.49-2292_49-2287dup others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308584 | T | TCTCA | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-2310_49-2309ins others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308584 | T | TCTCTCTC others(3): Show |
10 | a0001c0001t0006g0230 a0001c0001t0006g0235 a0001c0001t0006g0236 others(7): Show |
10 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-2310_49-2309ins others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308584 | T | TCTCTCTC others(7): Show |
3 | a0001c0001t0003g0202 a0001c0001t0008g0005 a0001c0001t0008g0234 |
3 | HG02055.hp1 NA18941.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.49-2310_49-2309ins others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308584 | T | TCTCTCTC others(9): Show |
1 | a0001c0001t0008g0005 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.49-2310_49-2309ins others(16): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308584 | T | TCTCTCTC others(21): Show |
1 | a0001c0001t0001g0026 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49-2310_49-2309ins others(28): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308584 | T | TCTCTCTC others(19): Show |
1 | a0001c0001t0001g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49-2310_49-2309ins others(26): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | ||||||
| chr12:70308586 | A | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG03486.hp1 HG03579.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-2309A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308586 | |||||||
| chr12:70308867 | A | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-2028A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308867 | |||||||
| chr12:70309020 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49-1875C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309020 | |||||||
| chr12:70309224 | A | G | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-1671A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309224 | |||||||
| chr12:70309278 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.49-1617T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309278 | |||||||
| chr12:70309300 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.49-1595G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309300 | |||||||
| chr12:70309607 | A | C | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-1288A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309607 | |||||||
| chr12:70309623 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-1272C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309623 | |||||||
| chr12:70309893 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.49-1002G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309893 | |||||||
| chr12:70309917 | A | G | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.49-978A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309917 | |||||||
| chr12:70309958 | A | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-937A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309958 | |||||||
| chr12:70310025 | G | A | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-870G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310025 | |||||||
| chr12:70310061 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.49-834A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310061 | |||||||
| chr12:70310185 | T | C | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-710T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310185 | |||||||
| chr12:70310228 | A | C | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-667A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310228 | |||||||
| chr12:70310468 | G | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0003g0202 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-427G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310468 | |||||||
| chr12:70310589 | CTATG | C | 4 | a0001c0002t0001g0020 a0001c0002t0001g0121 a0001c0002t0001g0152 others(1): Show |
4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-301_49-298delTA others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70310589 | ||||||
| chr12:70310722 | C | T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0066 |
3 | NA18954.hp1 NA19057.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.49-173C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310722 | |||||||
| chr12:70310761 | G | T | 1 | a0001c0001t0006g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.49-134G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310761 | |||||||
| chr12:70311382 | A | G | 1 | a0001c0001t0003g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.171+365A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311382 | |||||||
| chr12:70311383 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.171+366C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311383 | |||||||
| chr12:70311567 | T | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+550T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311567 | |||||||
| chr12:70311751 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.171+734T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311751 | |||||||
| chr12:70311831 | A | G | 1 | a0001c0001t0004g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.171+814A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311831 | |||||||
| chr12:70312061 | A | C | 1 | a0001c0002t0001g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.171+1044A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312061 | |||||||
| chr12:70312189 | T | C | 1 | a0001c0001t0003g0089 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.171+1172T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312189 | |||||||
| chr12:70312212 | A | C | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171+1195A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312212 | |||||||
| chr12:70312249 | T | A | 1 | a0001c0001t0003g0109 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+1232T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312249 | |||||||
| chr12:70312585 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.171+1568C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312585 | |||||||
| chr12:70312755 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.171+1738A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312755 | |||||||
| chr12:70312884 | G | A | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.171+1867G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312884 | |||||||
| chr12:70312925 | A | G | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171+1908A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312925 | |||||||
| chr12:70313076 | A | T | 2 | a0001c0001t0001g0043 a0001c0001t0002g0030 |
2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.171+2059A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313076 | |||||||
| chr12:70313174 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.171+2157A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313174 | |||||||
| chr12:70313236 | C | T | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.171+2219C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313236 | |||||||
| chr12:70313374 | AATTAAAT others(3): Show |
A | 1 | a0001c0001t0004g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.171+2360_171+2369d others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70313374 | ||||||
| chr12:70313489 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.171+2472A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313489 | |||||||
| chr12:70313566 | G | C | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.171+2549G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313566 | |||||||
| chr12:70313582 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.171+2565C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313582 | |||||||
| chr12:70313803 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.171+2786G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313803 | |||||||
| chr12:70313819 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+2802C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313819 | |||||||
| chr12:70313925 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.171+2908C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313925 | |||||||
| chr12:70314023 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.171+3006T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314023 | |||||||
| chr12:70314072 | T | C | 2 | a0001c0001t0003g0072 a0001c0001t0003g0073 |
2 | HG02257.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.171+3055T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314072 | |||||||
| chr12:70314076 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.171+3059G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314076 | |||||||
| chr12:70314081 | G | C | 2 | a0001c0001t0003g0205 a0001c0001t0003g0209 |
2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.171+3064G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314081 | |||||||
| chr12:70314251 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.171+3234T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314251 | |||||||
| chr12:70314349 | C | G | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+3332C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314349 | |||||||
| chr12:70314439 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.171+3422C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314439 | |||||||
| chr12:70314443 | A | G | 4 | a0001c0001t0002g0076 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG01099.hp2 HG01952.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+3426A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314443 | |||||||
| chr12:70314794 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.171+3777A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314794 | |||||||
| chr12:70314829 | C | G | 1 | a0001c0001t0015g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.171+3812C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314829 | |||||||
| chr12:70314837 | C | CTTGT | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0067 others(17): Show |
20 | HG01099.hp2 HG01123.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.171+3847_171+3850d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70314837 | ||||||
| chr12:70314837 | CTTGT | C | 56 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(53): Show |
58 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.171+3847_171+3850d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70314837 | ||||||
| chr12:70314902 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.171+3885T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314902 | |||||||
| chr12:70314925 | A | G | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.171+3908A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314925 | |||||||
| chr12:70314949 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.171+3932C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314949 | |||||||
| chr12:70315127 | G | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+4110G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70315127 | |||||||
| chr12:70315153 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.171+4136C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70315153 | |||||||
| chr12:70315910 | GTAT | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-3383_172-3381d others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70315910 | ||||||
| chr12:70315912 | A | G | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.172-3386A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70315912 | |||||||
| chr12:70316246 | T | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-3052T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316246 | |||||||
| chr12:70316264 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.172-3034A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316264 | |||||||
| chr12:70316568 | C | G | 24 | a0001c0001t0003g0263 a0001c0001t0004g0244 a0001c0001t0004g0245 others(21): Show |
25 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.172-2730C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316568 | |||||||
| chr12:70316665 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172-2633C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316665 | |||||||
| chr12:70316687 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.172-2611G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316687 | |||||||
| chr12:70316756 | G | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2542G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316756 | |||||||
| chr12:70316794 | T | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-2504T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316794 | |||||||
| chr12:70316845 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.172-2453C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316845 | |||||||
| chr12:70316901 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.172-2397G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316901 | |||||||
| chr12:70316905 | G | A | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.172-2393G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316905 | |||||||
| chr12:70316926 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.172-2372A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316926 | |||||||
| chr12:70316975 | A | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2323A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316975 | |||||||
| chr12:70317021 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.172-2277G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317021 | |||||||
| chr12:70317465 | A | C | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.172-1833A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317465 | |||||||
| chr12:70317513 | G | A | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.172-1785G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317513 | |||||||
| chr12:70317575 | A | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.172-1723A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317575 | |||||||
| chr12:70317611 | A | AT | 21 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0077 others(18): Show |
21 | HG00408.hp1 HG01123.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.172-1662dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | ||||||
| chr12:70317611 | A | ATT | 5 | a0001c0001t0003g0075 a0001c0001t0004g0070 a0001c0001t0016g0198 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1663_172-1662d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | ||||||
| chr12:70317611 | AT | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(53): Show |
57 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.172-1662delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | ||||||
| chr12:70317611 | ATT | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0133 a0001c0001t0001g0168 others(9): Show |
12 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-1663_172-1662d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | ||||||
| chr12:70317611 | ATTTTT | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.172-1666_172-1662d others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | ||||||
| chr12:70317816 | A | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-1482A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317816 | |||||||
| chr12:70317867 | G | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1431G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317867 | |||||||
| chr12:70317868 | G | A | 2 | a0001c0001t0003g0084 a0001c0001t0004g0081 |
2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.172-1430G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317868 | |||||||
| chr12:70317958 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.172-1340C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317958 | |||||||
| chr12:70317959 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.172-1339C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317959 | |||||||
| chr12:70318084 | G | C | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.172-1214G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318084 | |||||||
| chr12:70318170 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.172-1128C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318170 | |||||||
| chr12:70318219 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1079A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318219 | |||||||
| chr12:70318253 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.172-1045C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318253 | |||||||
| chr12:70318516 | C | T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.172-782C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318516 | |||||||
| chr12:70318641 | A | G | 2 | a0001c0001t0009g0151 a0001c0001t0009g0157 |
2 | HG00099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.172-657A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318641 | |||||||
| chr12:70318860 | T | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
210 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.172-438T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318860 | |||||||
| chr12:70318924 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.172-374A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318924 | |||||||
| chr12:70319028 | G | T | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.172-270G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70319028 | |||||||
| chr12:70319116 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.172-182C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70319116 | |||||||
| chr12:70319209 | T | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.172-89T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70319209 | |||||||
| chr12:70319438 | C | G | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.238+74C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319438 | |||||||
| chr12:70319519 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.238+155A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319519 | |||||||
| chr12:70319720 | C | CTG | 35 | a0001c0001t0001g0026 a0001c0001t0002g0196 a0001c0001t0003g0248 others(32): Show |
36 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.238+374_238+375dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70319720 | ||||||
| chr12:70319720 | CTG | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.238+374_238+375del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70319720 | ||||||
| chr12:70319743 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
215 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.238+379T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319743 | |||||||
| chr12:70319875 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.238+511G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319875 | |||||||
| chr12:70319964 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+600G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319964 | |||||||
| chr12:70320036 | T | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.238+672T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320036 | |||||||
| chr12:70320221 | T | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+857T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320221 | |||||||
| chr12:70320615 | CT | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+1252delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320615 | |||||||
| chr12:70320891 | G | A | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.238+1527G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320891 | |||||||
| chr12:70320925 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238+1561A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320925 | |||||||
| chr12:70321193 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.238+1829T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321193 | |||||||
| chr12:70321230 | A | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+1866A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321230 | |||||||
| chr12:70321694 | C | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+2330C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321694 | |||||||
| chr12:70321710 | C | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.238+2346C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321710 | |||||||
| chr12:70321792 | C | CAAGAAAG others(308): Show |
1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+2443_238+2444i others(317): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70321792 | ||||||
| chr12:70321975 | A | G | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.238+2611A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321975 | |||||||
| chr12:70321986 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.238+2622C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321986 | |||||||
| chr12:70321989 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.238+2625G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321989 | |||||||
| chr12:70322191 | A | T | 12 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(9): Show |
12 | HG00741.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+2827A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322191 | |||||||
| chr12:70322222 | A | C | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+2858A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322222 | |||||||
| chr12:70322225 | A | G | 2 | a0001c0001t0010g0231 a0001c0001t0010g0232 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.238+2861A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322225 | |||||||
| chr12:70322522 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+3158A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322522 | |||||||
| chr12:70322584 | G | T | 1 | a0001c0001t0003g0110 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.238+3220G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322584 | |||||||
| chr12:70322678 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.238+3314C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322678 | |||||||
| chr12:70322699 | G | A | 6 | a0001c0001t0002g0076 a0001c0001t0002g0123 a0001c0001t0002g0124 others(3): Show |
6 | HG01099.hp2 HG01123.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+3335G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322699 | |||||||
| chr12:70322797 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.238+3433A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322797 | |||||||
| chr12:70322839 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.238+3475C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322839 | |||||||
| chr12:70322976 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0014g0007 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.238+3612C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322976 | |||||||
| chr12:70323091 | G | A | 3 | a0001c0001t0006g0233 a0001c0001t0010g0231 a0001c0001t0010g0232 |
3 | HG01884.hp2 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.238+3727G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323091 | |||||||
| chr12:70323166 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+3802C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323166 | |||||||
| chr12:70323240 | A | G | 1 | a0001c0001t0004g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.238+3876A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323240 | |||||||
| chr12:70323280 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.238+3916G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323280 | |||||||
| chr12:70323287 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.238+3923C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323287 | |||||||
| chr12:70323451 | T | C | 58 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(55): Show |
60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.238+4087T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323451 | |||||||
| chr12:70323456 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.238+4092T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323456 | |||||||
| chr12:70323809 | C | A | 1 | a0001c0001t0004g0256 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.238+4445C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323809 | |||||||
| chr12:70323892 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+4528C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323892 | |||||||
| chr12:70323901 | GAC | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.238+4542_238+4543d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70323901 | ||||||
| chr12:70323912 | A | G | 1 | a0001c0001t0004g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.238+4548A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323912 | |||||||
| chr12:70324098 | A | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+4734A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324098 | |||||||
| chr12:70324265 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.238+4901A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324265 | |||||||
| chr12:70324305 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.238+4941A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324305 | |||||||
| chr12:70324344 | G | GGA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.238+4995_238+4996d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70324344 | ||||||
| chr12:70324367 | G | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+5003G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324367 | |||||||
| chr12:70324513 | T | A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-4910T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324513 | |||||||
| chr12:70324657 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.239-4766C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324657 | |||||||
| chr12:70324819 | A | G | 24 | a0001c0001t0003g0263 a0001c0001t0004g0244 a0001c0001t0004g0245 others(21): Show |
25 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.239-4604A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324819 | |||||||
| chr12:70324825 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.239-4598C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324825 | |||||||
| chr12:70324914 | T | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(211): Show |
218 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.239-4509T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324914 | |||||||
| chr12:70324935 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.239-4488T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324935 | |||||||
| chr12:70324981 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.239-4442A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324981 | |||||||
| chr12:70325014 | C | T | 14 | a0001c0001t0003g0202 a0001c0001t0006g0230 a0001c0001t0006g0233 others(11): Show |
15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-4409C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325014 | |||||||
| chr12:70325175 | GAGAAAGA | G | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-4237_239-4231d others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70325175 | ||||||
| chr12:70325215 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.239-4208G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325215 | |||||||
| chr12:70325565 | T | C | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-3858T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325565 | |||||||
| chr12:70325785 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-3638A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325785 | |||||||
| chr12:70325876 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-3547T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325876 | |||||||
| chr12:70325974 | G | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-3449G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325974 | |||||||
| chr12:70326044 | ATTC | A | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-3376_239-3374d others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70326044 | ||||||
| chr12:70326055 | G | C | 1 | a0001c0001t0003g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-3368G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70326055 | |||||||
| chr12:70326222 | T | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-3201T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70326222 | |||||||
| chr12:70326340 | T | G | 2 | a0001c0001t0003g0001 a0001c0001t0003g0092 |
4 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-3083T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70326340 | |||||||
| chr12:70326404 | GTT | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.239-3016_239-3015d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70326404 | ||||||
| chr12:70326454 | C | CT | 38 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0190 others(35): Show |
39 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.239-2960dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70326454 | ||||||
| chr12:70326454 | C | CTT | 20 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(17): Show |
21 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.239-2961_239-2960d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70326454 | ||||||
| chr12:70326752 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.239-2671A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70326752 | |||||||
| chr12:70327023 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
206 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.239-2400T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327023 | |||||||
| chr12:70327182 | T | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-2241T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327182 | |||||||
| chr12:70327245 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-2178A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327245 | |||||||
| chr12:70327270 | GAA | G | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-2151_239-2150d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70327270 | ||||||
| chr12:70327331 | C | T | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.239-2092C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327331 | |||||||
| chr12:70327396 | A | G | 73 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(70): Show |
75 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.239-2027A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327396 | |||||||
| chr12:70327417 | T | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0002g0052 others(3): Show |
6 | HG02015.hp1 NA18942.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-2006T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327417 | |||||||
| chr12:70327824 | T | TATC | 42 | a0001c0001t0001g0023 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.239-1597_239-1596i others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70327824 | ||||||
| chr12:70327862 | C | T | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.239-1561C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327862 | |||||||
| chr12:70327898 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.239-1525A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327898 | |||||||
| chr12:70327959 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.239-1464T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327959 | |||||||
| chr12:70327990 | T | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-1433T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327990 | |||||||
| chr12:70328109 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.239-1314A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328109 | |||||||
| chr12:70328218 | A | T | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-1205A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328218 | |||||||
| chr12:70328359 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-1064T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328359 | |||||||
| chr12:70328368 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239-1055C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328368 | |||||||
| chr12:70328394 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.239-1029T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328394 | |||||||
| chr12:70328626 | A | C | 3 | a0001c0001t0001g0002 a0001c0001t0002g0002 a0001c0001t0002g0218 |
3 | HG02056.hp2 NA19084.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.239-797A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328626 | |||||||
| chr12:70328742 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-681T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328742 | |||||||
| chr12:70328956 | A | T | 78 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(75): Show |
80 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.239-467A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328956 | |||||||
| chr12:70329021 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.239-402C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70329021 | |||||||
| chr12:70329697 | T | C | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.386+127T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70329697 | |||||||
| chr12:70329980 | C | T | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.387-307C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70329980 | |||||||
| chr12:70329989 | A | T | 68 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.387-298A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70329989 | |||||||
| chr12:70330201 | C | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-86C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70330201 | |||||||
| chr12:70330227 | A | T | 68 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0026 others(65): Show |
70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.387-60A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70330227 | |||||||
| chr12:70330273 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.387-14G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70330273 | |||||||
| chr12:70330477 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | splice_region_variant&intron_variant | LOW | c.569+8G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70330477 | |||||||
| chr12:70330500 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.569+31G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70330500 | |||||||
| chr12:70330590 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.569+121A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70330590 | |||||||
| chr12:70330939 | C | A | 1 | a0001c0001t0002g0044 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.569+470C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70330939 | |||||||
| chr12:70331021 | T | G | 1 | a0001c0001t0003g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.569+552T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331021 | |||||||
| chr12:70331025 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.569+556C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331025 | |||||||
| chr12:70331028 | A | G | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.569+559A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331028 | |||||||
| chr12:70331030 | A | G | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+561A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331030 | |||||||
| chr12:70331144 | C | CA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.569+676dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 70331144 | ||||||
| chr12:70331185 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.569+716C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331185 | |||||||
| chr12:70331210 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.569+741T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331210 | |||||||
| chr12:70331341 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0084 a0001c0001t0003g0086 others(2): Show |
5 | HG00438.hp2 HG02015.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+872C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331341 | |||||||
| chr12:70331584 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.569+1115T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331584 | |||||||
| chr12:70331890 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.570-877T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331890 | |||||||
| chr12:70332079 | A | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(39): Show |
42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.570-688A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70332079 | |||||||
| chr12:70332293 | G | A | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.570-474G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70332293 | |||||||
| chr12:70332340 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.570-427A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70332340 | |||||||
| chr12:70333050 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.649+204G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70333050 | |||||||
| chr12:70333092 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.649+246C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70333092 | |||||||
| chr12:70333094 | G | A | 5 | a0001c0001t0003g0207 a0001c0001t0003g0208 a0001c0001t0003g0210 others(2): Show |
5 | HG01256.hp1 HG01261.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+248G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70333094 | |||||||
| chr12:70333874 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.649+1028A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70333874 | |||||||
| chr12:70334108 | A | G | 2 | a0001c0001t0008g0005 a0001c0001t0008g0234 |
3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.649+1262A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334108 | |||||||
| chr12:70334123 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.649+1277A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334123 | |||||||
| chr12:70334144 | T | C | 5 | a0001c0001t0001g0064 a0001c0001t0001g0165 a0001c0001t0001g0167 others(2): Show |
5 | HG00099.hp1 HG01074.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-1294T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334144 | |||||||
| chr12:70334161 | A | G | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.650-1277A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334161 | |||||||
| chr12:70334274 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.650-1164G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334274 | |||||||
| chr12:70334297 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.650-1141C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334297 | |||||||
| chr12:70334484 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.650-954T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334484 | |||||||
| chr12:70334627 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0003g0248 a0001c0001t0003g0263 others(31): Show |
35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.650-811A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334627 | |||||||
| chr12:70334647 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.650-791T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334647 | |||||||
| chr12:70334751 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0163 a0001c0001t0001g0164 |
4 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.650-687T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334751 | |||||||
| chr12:70334899 | C | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(129): Show |
134 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.650-539C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334899 | |||||||
| chr12:70334903 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.650-535C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334903 | |||||||
| chr12:70335040 | A | G | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.650-398A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335040 | |||||||
| chr12:70335061 | A | G | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.650-377A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335061 | |||||||
| chr12:70335105 | G | A | 1 | a0001c0001t0004g0245 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.650-333G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335105 | |||||||
| chr12:70335190 | T | G | 1 | a0001c0002t0001g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.650-248T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335190 | |||||||
| chr12:70335269 | A | G | 28 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0025 others(25): Show |
29 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.650-169A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335269 | |||||||
| chr12:70335323 | C | T | 1 | a0001c0001t0004g0265 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.650-115C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335323 | |||||||
| chr12:70335346 | G | A | 1 | a0001c0002t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.650-92G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335346 | |||||||
| chr12:70335816 | G | T | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+253G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70335816 | |||||||
| chr12:70335985 | A | G | 7 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.775+422A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70335985 | |||||||
| chr12:70335988 | T | TCCA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.775+427_775+429dup others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 70335988 | ||||||
| chr12:70336035 | T | C | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.775+472T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336035 | |||||||
| chr12:70336036 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(15): Show |
18 | HG00099.hp1 HG00639.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.775+473G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336036 | |||||||
| chr12:70336063 | T | A | 39 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0032 others(36): Show |
41 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.775+500T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336063 | |||||||
| chr12:70336101 | A | G | 3 | a0001c0001t0003g0202 a0001c0001t0007g0250 a0001c0001t0007g0252 |
3 | HG02055.hp1 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.775+538A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336101 | |||||||
| chr12:70336345 | A | T | 1 | a0001c0001t0009g0151 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.775+782A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336345 | |||||||
| chr12:70336349 | G | A | 1 | a0001c0001t0005g0260 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.775+786G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336349 | |||||||
| chr12:70336421 | G | A | 17 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(14): Show |
18 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.775+858G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336421 | |||||||
| chr12:70336561 | T | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.776-828T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336561 | |||||||
| chr12:70336659 | C | A | 1 | a0001c0001t0004g0255 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.776-730C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336659 | |||||||
| chr12:70336668 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.776-721T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336668 | |||||||
| chr12:70336759 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.776-630G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336759 | |||||||
| chr12:70336940 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0002g0040 |
2 | NA18612.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.776-449A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336940 | |||||||
| chr12:70337022 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.776-367T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70337022 | |||||||
| chr12:70337264 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.776-125C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70337264 | |||||||
| chr12:70337343 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.776-46A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70337343 | |||||||
| chr12:70337367 | C | T | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.776-22C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70337367 | |||||||
| chr12:70337531 | G | T | 1 | a0001c0001t0007g0267 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.900+18G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | chr12 | 70337531 | |||||||
| chr12:70337960 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.900+447G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | chr12 | 70337960 | |||||||
| chr12:70337967 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.900+454A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | chr12 | 70337967 | |||||||
| chr12:70338061 | C | T | 13 | a0001c0001t0003g0263 a0001c0001t0004g0261 a0001c0001t0004g0264 others(10): Show |
14 | HG01099.hp1 HG01192.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.901-382C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | chr12 | 70338061 | |||||||
| chr12:70338171 | AT | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(76): Show |
81 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.901-261delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 70338171 | ||||||
| chr12:70338965 | T | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1178+143T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70338965 | |||||||
| chr12:70339014 | A | ATG | 16 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0069 others(13): Show |
16 | HG00733.hp2 HG01070.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1178+227_1178+228d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | ||||||
| chr12:70339014 | A | ATGTG | 19 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(16): Show |
19 | HG01109.hp1 HG01256.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1178+225_1178+228d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | ||||||
| chr12:70339014 | A | ATGTGTG | 12 | a0001c0001t0001g0021 a0001c0001t0001g0101 a0001c0001t0001g0102 others(9): Show |
12 | HG01261.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1178+223_1178+228d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | ||||||
| chr12:70339014 | ATG | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0139 a0001c0001t0001g0143 others(12): Show |
15 | HG01175.hp2 HG01192.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1178+227_1178+228d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | ||||||
| chr12:70339014 | ATGTG | A | 62 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
64 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1178+225_1178+228d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | ||||||
| chr12:70339014 | ATGTGTG | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0185 others(2): Show |
5 | HG01069.hp2 HG01167.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1178+223_1178+228d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | ||||||
| chr12:70339014 | ATGTGTGT others(1): Show |
A | 12 | a0001c0001t0001g0107 a0001c0001t0001g0219 a0001c0001t0003g0248 others(9): Show |
12 | HG01081.hp2 HG01192.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178+221_1178+228d others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | ||||||
| chr12:70339014 | ATGTGTGT others(3): Show |
A | 8 | a0001c0001t0001g0087 a0001c0001t0002g0191 a0001c0001t0002g0192 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+219_1178+228d others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | ||||||
| chr12:70339047 | T | C | 1 | a0001c0001t0004g0081 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1178+225T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339047 | |||||||
| chr12:70339049 | T | C | 6 | a0001c0001t0002g0035 a0001c0001t0003g0063 a0001c0001t0003g0084 others(3): Show |
6 | HG00438.hp2 HG02015.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1178+227T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339049 | |||||||
| chr12:70339066 | A | ATGTGTG | 13 | a0001c0001t0001g0026 a0001c0001t0001g0190 a0001c0001t0006g0230 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1178+250_1178+255d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339066 | ||||||
| chr12:70339066 | A | ATGTGTGT others(1): Show |
8 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+248_1178+255d others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339066 | ||||||
| chr12:70339066 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1178+246_1178+255d others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339066 | ||||||
| chr12:70339066 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1178+255_1178+256i others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339066 | ||||||
| chr12:70339076 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0077 others(41): Show |
46 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1178+254G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339076 | |||||||
| chr12:70339076 | G | GTGTA | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0059 |
3 | NA18941.hp1 NA19003.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1178+255_1178+256i others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339076 | ||||||
| chr12:70339076 | GTA | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0188 a0001c0002t0001g0152 |
3 | HG00558.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1178+269_1178+270d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339076 | ||||||
| chr12:70339078 | A | G | 63 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(60): Show |
65 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1178+256A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339078 | |||||||
| chr12:70339080 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG02647.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1178+258A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339080 | |||||||
| chr12:70339089 | T | C | 16 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(13): Show |
17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1178+267T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339089 | |||||||
| chr12:70339089 | T | TACAC | 9 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0002g0191 others(6): Show |
9 | HG01261.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1178+268_1178+269i others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339089 | ||||||
| chr12:70339091 | T | C | 81 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(78): Show |
83 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.1178+269T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339091 | |||||||
| chr12:70339091 | T | TAC | 66 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
68 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1178+290_1178+291d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339091 | ||||||
| chr12:70339091 | T | TACAC | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG02486.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1178+288_1178+291d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339091 | ||||||
| chr12:70339091 | T | TACACAC | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1178+286_1178+291d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339091 | ||||||
| chr12:70339091 | T | TATAC | 38 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(35): Show |
38 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1178+270_1178+271i others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339091 | ||||||
| chr12:70339093 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0001t0003g0158 |
3 | HG02717.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1178+271C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339093 | |||||||
| chr12:70339113 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1178+291C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339113 | |||||||
| chr12:70339158 | A | AGGAATTT others(185): Show |
1 | a0001c0001t0001g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1178+345_1178+346i others(194): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339158 | ||||||
| chr12:70339190 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1178+368C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339190 | |||||||
| chr12:70339283 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1178+461C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339283 | |||||||
| chr12:70339589 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1178+767A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339589 | |||||||
| chr12:70339882 | A | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1178+1060A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339882 | |||||||
| chr12:70340247 | C | T | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1178+1425C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340247 | |||||||
| chr12:70340276 | T | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1178+1454T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340276 | |||||||
| chr12:70340629 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1179-1478C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340629 | |||||||
| chr12:70340763 | G | T | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179-1344G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340763 | |||||||
| chr12:70340774 | C | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179-1333C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340774 | |||||||
| chr12:70340778 | C | G | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1179-1329C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340778 | |||||||
| chr12:70340813 | C | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0183 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1179-1294C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340813 | |||||||
| chr12:70340872 | G | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1179-1235G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340872 | |||||||
| chr12:70340887 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1179-1220A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340887 | |||||||
| chr12:70340889 | CT | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0019 others(109): Show |
113 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1179-1195delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70340889 | ||||||
| chr12:70340889 | CTT | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
101 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1179-1196_1179-119 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70340889 | ||||||
| chr12:70340889 | CTTT | C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0093 others(19): Show |
22 | HG01256.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1179-1197_1179-119 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70340889 | ||||||
| chr12:70340889 | CTTTT | C | 25 | a0001c0001t0003g0263 a0001c0001t0004g0244 a0001c0001t0004g0245 others(22): Show |
26 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1179-1198_1179-119 others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70340889 | ||||||
| chr12:70340998 | C | T | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179-1109C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340998 | |||||||
| chr12:70340999 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1179-1108G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340999 | |||||||
| chr12:70341005 | C | G | 26 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0112 others(23): Show |
27 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1179-1102C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341005 | |||||||
| chr12:70341138 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1179-969G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341138 | |||||||
| chr12:70341172 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1179-935C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341172 | |||||||
| chr12:70341314 | G | A | 70 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(67): Show |
72 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1179-793G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341314 | |||||||
| chr12:70341416 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0002g0013 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1179-691A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341416 | |||||||
| chr12:70341550 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1179-557T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341550 | |||||||
| chr12:70341717 | T | C | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179-390T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341717 | |||||||
| chr12:70341902 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1179-205T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341902 | |||||||
| chr12:70341953 | G | A | 80 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(77): Show |
82 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.1179-154G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341953 | |||||||
| chr12:70341970 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1179-137T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341970 | |||||||
| chr12:70342333 | A | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1290+26A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342333 | |||||||
| chr12:70342418 | A | T | 2 | a0001c0001t0002g0061 a0001c0001t0003g0062 |
2 | NA18969.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1290+111A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342418 | |||||||
| chr12:70342434 | C | T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1290+127C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342434 | |||||||
| chr12:70342573 | CTTATT | C | 2 | a0001c0001t0001g0272 a0001c0001t0003g0273 |
2 | NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1290+271_1290+275d others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 70342573 | ||||||
| chr12:70342797 | G | A | 9 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0003g0205 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1290+490G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342797 | |||||||
| chr12:70342984 | G | T | 1 | a0001c0001t0002g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1290+677G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342984 | |||||||
| chr12:70343166 | A | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
38 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1290+859A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343166 | |||||||
| chr12:70343332 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1291-796C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343332 | |||||||
| chr12:70343333 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0155 a0001c0001t0003g0141 |
3 | HG02055.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1291-795G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343333 | |||||||
| chr12:70343610 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0219 |
3 | HG01109.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1291-518G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343610 | |||||||
| chr12:70343681 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1291-447C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343681 | |||||||
| chr12:70343726 | T | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1291-402T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343726 | |||||||
| chr12:70343818 | T | A | 71 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(68): Show |
73 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1291-310T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343818 | |||||||
| chr12:70343898 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1291-230A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343898 | |||||||
| chr12:70343943 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1291-185T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343943 | |||||||
| chr12:70344056 | A | C | 1 | a0001c0001t0003g0072 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1291-72A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70344056 | |||||||
| chr12:70344073 | AT | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
83 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1291-53delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 70344073 | ||||||
| chr12:70344343 | T | A | 1 | a0001c0001t0003g0089 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1391+115T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344343 | |||||||
| chr12:70344659 | T | C | 1 | a0001c0001t0009g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1391+431T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344659 | |||||||
| chr12:70344711 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1391+483T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344711 | |||||||
| chr12:70344742 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0155 a0001c0001t0003g0141 |
3 | HG02055.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1391+514A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344742 | |||||||
| chr12:70344839 | T | G | 81 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(78): Show |
83 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.1391+611T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344839 | |||||||
| chr12:70345058 | C | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1391+830C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345058 | |||||||
| chr12:70345310 | C | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1392-870C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345310 | |||||||
| chr12:70345575 | A | C | 24 | a0001c0001t0003g0263 a0001c0001t0004g0244 a0001c0001t0004g0245 others(21): Show |
25 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1392-605A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345575 | |||||||
| chr12:70345617 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1392-563T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345617 | |||||||
| chr12:70345715 | G | C | 71 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(68): Show |
73 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1392-465G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345715 | |||||||
| chr12:70345724 | T | A | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1392-456T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345724 | |||||||
| chr12:70345733 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0142 a0001c0001t0001g0155 others(1): Show |
4 | HG02055.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392-447A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345733 | |||||||
| chr12:70345771 | C | A | 1 | a0001c0001t0002g0066 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1392-409C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345771 | |||||||
| chr12:70346049 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1392-131G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70346049 | |||||||
| chr12:70346096 | C | T | 1 | a0001c0001t0002g0041 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1392-84C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70346096 | |||||||
| chr12:70346110 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1392-70A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70346110 | |||||||
| chr12:70346122 | A | G | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1392-58A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70346122 | |||||||
| chr12:70346414 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
166 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1536+90G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346414 | |||||||
| chr12:70346475 | T | C | 6 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536+151T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346475 | |||||||
| chr12:70346492 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1536+168A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346492 | |||||||
| chr12:70346496 | A | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+172A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346496 | |||||||
| chr12:70346840 | T | C | 24 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(21): Show |
25 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1536+516T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346840 | |||||||
| chr12:70346896 | C | G | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536+572C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346896 | |||||||
| chr12:70346897 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0003g0221 |
3 | HG01167.hp2 HG01169.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1536+573G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346897 | |||||||
| chr12:70346955 | G | C | 70 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(67): Show |
72 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1536+631G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346955 | |||||||
| chr12:70346979 | T | TAGAGAAT others(20): Show |
35 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0003g0248 others(32): Show |
36 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1536+668_1536+694d others(29): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70346979 | ||||||
| chr12:70347059 | ACAACTC | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1536+738_1536+743d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70347059 | ||||||
| chr12:70347216 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1536+892G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347216 | |||||||
| chr12:70347353 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1536+1029C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347353 | |||||||
| chr12:70347598 | A | C | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1536+1274A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347598 | |||||||
| chr12:70347814 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1536+1490G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347814 | |||||||
| chr12:70347828 | T | C | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1536+1504T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347828 | |||||||
| chr12:70347926 | A | G | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1536+1602A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347926 | |||||||
| chr12:70348121 | T | G | 70 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(67): Show |
72 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1536+1797T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348121 | |||||||
| chr12:70348126 | G | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1536+1802G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348126 | |||||||
| chr12:70348161 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1536+1837G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348161 | |||||||
| chr12:70348180 | G | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1536+1856G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348180 | |||||||
| chr12:70348274 | A | G | 7 | a0001c0001t0001g0219 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536+1950A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348274 | |||||||
| chr12:70348320 | A | G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0142 a0001c0001t0001g0150 others(2): Show |
5 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1536+1996A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348320 | |||||||
| chr12:70348464 | TAGGTGAT others(1470): Show |
T | 1 | a0001c0001t0004g0256 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1536+2145_1536+362 others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70348464 | ||||||
| chr12:70348676 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1536+2352A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348676 | |||||||
| chr12:70348697 | C | T | 26 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0112 others(23): Show |
27 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1536+2373C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348697 | |||||||
| chr12:70348821 | G | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1536+2497G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348821 | |||||||
| chr12:70348903 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1536+2579A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348903 | |||||||
| chr12:70348965 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1536+2641T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348965 | |||||||
| chr12:70349120 | A | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1536+2796A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349120 | |||||||
| chr12:70349243 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1536+2919G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349243 | |||||||
| chr12:70349385 | C | T | 1 | a0001c0001t0003g0212 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1536+3061C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349385 | |||||||
| chr12:70349405 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+3081C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349405 | |||||||
| chr12:70349587 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1536+3263G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349587 | |||||||
| chr12:70349619 | T | C | 4 | a0001c0002t0001g0020 a0001c0002t0001g0121 a0001c0002t0001g0152 others(1): Show |
4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536+3295T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349619 | |||||||
| chr12:70349624 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+3300T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349624 | |||||||
| chr12:70349829 | GTC | G | 35 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(32): Show |
36 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1536+3509_1536+351 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70349829 | ||||||
| chr12:70349830 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1536+3506T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349830 | |||||||
| chr12:70349971 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1536+3647A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349971 | |||||||
| chr12:70350004 | T | C | 1 | a0001c0001t0006g0235 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1536+3680T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70350004 | |||||||
| chr12:70350057 | C | T | 8 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1536+3733C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70350057 | |||||||
| chr12:70350059 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1536+3735T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70350059 | |||||||
| chr12:70350768 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1537-3061T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70350768 | |||||||
| chr12:70350889 | AGT | A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1537-2933_1537-293 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70350889 | ||||||
| chr12:70351143 | A | G | 8 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(5): Show |
8 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1537-2686A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351143 | |||||||
| chr12:70351314 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-2515C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351314 | |||||||
| chr12:70351320 | C | T | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1537-2509C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351320 | |||||||
| chr12:70351388 | A | G | 1 | a0001c0001t0003g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1537-2441A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351388 | |||||||
| chr12:70351477 | A | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1537-2352A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351477 | |||||||
| chr12:70351541 | C | T | 1 | a0001c0001t0002g0040 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1537-2288C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351541 | |||||||
| chr12:70351680 | T | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-2149T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351680 | |||||||
| chr12:70351693 | A | G | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1537-2136A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351693 | |||||||
| chr12:70351976 | A | G | 1 | a0001c0001t0014g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1537-1853A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351976 | |||||||
| chr12:70351995 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1537-1834A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351995 | |||||||
| chr12:70352222 | G | T | 1 | a0001c0001t0004g0245 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1537-1607G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352222 | |||||||
| chr12:70352248 | G | A | 1 | a0001c0001t0016g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1537-1581G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352248 | |||||||
| chr12:70352362 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1537-1467T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352362 | |||||||
| chr12:70352394 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1537-1435A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352394 | |||||||
| chr12:70352502 | G | A | 13 | a0001c0001t0006g0230 a0001c0001t0006g0233 a0001c0001t0006g0235 others(10): Show |
14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1537-1327G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352502 | |||||||
| chr12:70352623 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1537-1206A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352623 | |||||||
| chr12:70352633 | T | C | 2 | a0001c0001t0008g0005 a0001c0001t0008g0234 |
3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1537-1196T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352633 | |||||||
| chr12:70352819 | G | T | 1 | a0001c0001t0006g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1537-1010G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352819 | |||||||
| chr12:70352829 | T | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-1000T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352829 | |||||||
| chr12:70353075 | C | CT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(13): Show |
16 | HG00438.hp1 HG01934.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.1537-738dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70353075 | ||||||
| chr12:70353075 | CT | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0222 others(6): Show |
9 | HG00733.hp1 HG00738.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1537-738delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70353075 | ||||||
| chr12:70353079 | T | G | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1537-750T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353079 | |||||||
| chr12:70353096 | G | A | 12 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(9): Show |
12 | HG00741.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1537-733G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353096 | |||||||
| chr12:70353218 | G | A | 32 | a0001c0001t0003g0248 a0001c0001t0003g0263 a0001c0001t0004g0244 others(29): Show |
33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1537-611G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353218 | |||||||
| chr12:70353230 | G | A | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1537-599G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353230 | |||||||
| chr12:70353430 | C | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1537-399C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353430 | |||||||
| chr12:70353463 | A | T | 2 | a0001c0001t0003g0082 a0001c0001t0003g0094 |
2 | HG02080.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1537-366A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353463 | |||||||
| chr12:70353520 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537-309A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353520 | |||||||
| chr12:70353673 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1537-156A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353673 | |||||||
| chr12:70353719 | T | C | 1 | a0001c0001t0002g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1537-110T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353719 |