Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 197370 |
| ensemblid | ENSG00000169189.17 |
| hgncid | 29897 |
| symbol | NSMCE1 |
| name | NSE1 homolog, SMC5-SMC6 complex component |
| refseq_nuc | NM_145080.4 |
| refseq_prot | NP_659547.2 |
| ensembl_nuc | ENST00000361439.9 |
| ensembl_prot | ENSP00000355077.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 27224994 |
| end | 27268772 |
| strand | - |
| ver | v1.2 |
| region | chr16:27224994-27268772 |
| region5000 | chr16:27219994-27273772 |
| regionname0 | NSMCE1_chr16_27224994_27268772 |
| regionname5000 | NSMCE1_chr16_27219994_27273772 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 266 | 190 | 48 | 32 | 70 | 10 | 28 | 54 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | MQGST others(261): Show |
chr16 | 27219994 | 27273772 |
| a0002 | 0/0 | 266 | 99 | 13 | 14 | 61 | 2 | 9 | 46 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | MQGST others(261): Show |
chr16 | 27219994 | 27273772 |
| a0003 | 0/0 | 266 | 40 | 36 | 4 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | MQGST others(261): Show |
chr16 | 27219994 | 27273772 |
| a0004 | 0/0 | 266 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | MQGST others(261): Show |
chr16 | 27219994 | 27273772 |
| a0005 | 0/0 | 266 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | MQGST others(261): Show |
chr16 | 27219994 | 27273772 |
| a0006 | 0/0 | 266 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | MQGST others(261): Show |
chr16 | 27219994 | 27273772 |
| a0007 | 0/0 | 266 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | MQGST others(261): Show |
chr16 | 27219994 | 27273772 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 798 | 97 | 42 | 18 | 14 | 4 | 17 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0001c0003 | 0/0 | 798 | 92 | 6 | 14 | 55 | 6 | 11 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0001c0009 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0002c0002 | 0/0 | 798 | 97 | 12 | 14 | 60 | 2 | 9 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0002c0010 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0002c0011 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0003c0004 | 0/0 | 798 | 40 | 36 | 4 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0004c0005 | 0/0 | 798 | 2 | 0 | 0 | 2 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0005c0008 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0006c0006 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 | ||
| a0007c0007 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | ATGCA others(793): Show |
chr16 | 27219994 | 27273772 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1042 | 97 | 42 | 18 | 14 | 4 | 17 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0001c0003t0002 | 0/0 | 1042 | 91 | 6 | 14 | 54 | 6 | 11 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0001c0003t0003 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0001c0009t0002 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0002c0002t0001 | 0/0 | 1042 | 96 | 12 | 14 | 59 | 2 | 9 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0002c0002t0002 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0002c0010t0002 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0002c0011t0001 | 0/0 | 1042 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0003c0004t0001 | 0/0 | 1042 | 30 | 26 | 4 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0003c0004t0002 | 0/0 | 1042 | 10 | 10 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0004c0005t0002 | 0/0 | 1042 | 2 | 0 | 0 | 2 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0005c0008t0001 | 0/0 | 1042 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0006c0006t0002 | 0/0 | 1042 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| a0007c0007t0002 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | AAAGG others(1037): Show |
chr16 | 27219994 | 27273772 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0002 | 0/0 | 10 | 0 | 0 | 6 | 3 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0001c0009t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0001 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0010t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0002c0011t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0003c0004t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0004c0005t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0004c0005t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0005c0008t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0006c0006t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| a0007c0007t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0002 | EUR | GBR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0013 | EUR | GBR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0002 | EUR | GBR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0002 | EUR | FIN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00423 | hp2 | a0001 | c0003 | t0002 | g0195 | EAS | CHS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | CHS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00438 | hp2 | a0004 | c0005 | t0002 | g0182 | EAS | CHS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0016 | EAS | CHS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0206 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0018 | EAS | CHS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0279 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00738 | hp1 | a0001 | c0003 | t0002 | g0189 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0283 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0017 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0017 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0232 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0220 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01109 | hp1 | a0003 | c0004 | t0001 | g0140 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0217 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0145 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | PUR | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0219 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0099 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0199 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0092 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0086 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0112 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0221 | AMR | CLM | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0218 | EUR | IBS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01884 | hp1 | a0003 | c0004 | t0001 | g0144 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01891 | hp1 | a0003 | c0004 | t0001 | g0135 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG01993 | hp2 | a0001 | c0003 | t0002 | g0202 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0124 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02027 | hp2 | a0001 | c0003 | t0002 | g0215 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0213 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02129 | hp1 | a0001 | c0003 | t0003 | g0288 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0018 | EAS | KHV | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02145 | hp1 | a0003 | c0004 | t0002 | g0127 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CDX | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0188 | EAS | CDX | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02165 | hp1 | a0001 | c0003 | t0002 | g0153 | EAS | CDX | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CDX | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02257 | hp1 | a0003 | c0004 | t0001 | g0143 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02258 | hp2 | a0003 | c0004 | t0001 | g0276 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02280 | hp1 | a0003 | c0004 | t0001 | g0281 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02451 | hp1 | a0003 | c0004 | t0002 | g0286 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02451 | hp2 | a0003 | c0004 | t0002 | g0272 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0176 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0196 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02615 | hp2 | a0003 | c0004 | t0002 | g0023 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0129 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02630 | hp1 | a0001 | c0003 | t0002 | g0198 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0013 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02717 | hp2 | a0003 | c0004 | t0001 | g0282 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0133 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0203 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02809 | hp2 | a0003 | c0004 | t0002 | g0138 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0285 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0210 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0274 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0132 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02895 | hp2 | a0003 | c0004 | t0002 | g0269 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02897 | hp1 | a0003 | c0004 | t0002 | g0271 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02922 | hp2 | a0002 | c0011 | t0001 | g0088 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0284 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0225 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03041 | hp1 | a0003 | c0004 | t0001 | g0134 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0237 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0142 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0098 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03139 | hp2 | a0003 | c0004 | t0002 | g0287 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03209 | hp2 | a0003 | c0004 | t0001 | g0278 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0131 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0137 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03486 | hp1 | a0005 | c0008 | t0001 | g0174 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0130 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0005 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0207 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0275 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | STU | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0005 | SAS | STU | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0267 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03704 | hp2 | a0001 | c0003 | t0002 | g0177 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0103 | SAS | PJL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0046 | SAS | BEB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0002 | SAS | BEB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03942 | hp1 | a0006 | c0006 | t0002 | g0211 | SAS | BEB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0033 | SAS | BEB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG04184 | hp2 | a0001 | c0003 | t0002 | g0214 | SAS | BEB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | STU | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | STU | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0231 | SAS | STU | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0277 | AFR | YRI | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | CHB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | CHB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | CHB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0128 | AFR | YRI | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18939 | hp2 | a0001 | c0003 | t0002 | g0227 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0238 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0185 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18949 | hp1 | a0001 | c0003 | t0002 | g0180 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18951 | hp2 | a0007 | c0007 | t0002 | g0156 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18952 | hp2 | a0001 | c0003 | t0002 | g0158 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18961 | hp1 | a0001 | c0003 | t0002 | g0157 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18962 | hp2 | a0001 | c0003 | t0002 | g0224 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0201 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18966 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18967 | hp2 | a0001 | c0003 | t0002 | g0216 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18968 | hp1 | a0001 | c0003 | t0002 | g0230 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18969 | hp2 | a0001 | c0009 | t0002 | g0167 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0165 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18973 | hp2 | a0001 | c0003 | t0002 | g0209 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18975 | hp1 | a0002 | c0010 | t0002 | g0079 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18975 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0184 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0208 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18989 | hp1 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18994 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18997 | hp1 | a0001 | c0003 | t0002 | g0197 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0236 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18999 | hp1 | a0001 | c0003 | t0002 | g0191 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19000 | hp1 | a0001 | c0003 | t0002 | g0223 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19002 | hp1 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19011 | hp1 | a0001 | c0003 | t0002 | g0228 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19030 | hp1 | a0003 | c0004 | t0001 | g0273 | AFR | LWK | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0141 | AFR | LWK | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | LWK | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19054 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19055 | hp1 | a0001 | c0003 | t0002 | g0205 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19064 | hp2 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19065 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19077 | hp1 | a0001 | c0003 | t0002 | g0067 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0183 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19080 | hp1 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19082 | hp2 | a0001 | c0003 | t0002 | g0193 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19088 | hp2 | a0004 | c0005 | t0002 | g0147 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19089 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19091 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ASW | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA20129 | hp2 | a0003 | c0004 | t0002 | g0023 | AFR | ASW | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0222 | EUR | TSI | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02109 | hp2 | a0003 | c0004 | t0002 | g0270 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02486 | hp1 | a0003 | c0004 | t0001 | g0139 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG06807 | hp1 | a0003 | c0004 | t0001 | g0280 | AFR | USA | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0204 | AFR | USA | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | USA | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | LWK | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| NA21309 | hp2 | a0003 | c0004 | t0001 | g0136 | AFR | LWK | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0260 | REF | REF | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0119 | REF | REF | NSMCE1_chr16_27219994_27273772 | NSMCE1 | chr16 | 27219994 | 27273772 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:27233113 | G | A | 1 | a0006 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.371C>T | p.Ala124Val | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/8 | 449/1042 | 371/801 | 124/266 | chr16 | 27233113 | |||
| chr16:27234228 | G | A | 1 | a0007 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.296C>T | p.Thr99Met | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/8 | 374/1042 | 296/801 | 99/266 | chr16 | 27234228 | |||
| chr16:27234244 | T | C | 1 | a0005 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.280A>G | p.Ile94Val | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/8 | 358/1042 | 280/801 | 94/266 | chr16 | 27234244 | |||
| chr16:27235250 | A | C | 1 | a0004 | 2 | HG00438.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.186T>G | p.Ser62Arg | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/8 | 264/1042 | 186/801 | 62/266 | chr16 | 27235250 | |||
| chr16:27235296 | T | C | 1 | a0002 | 99 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(96): Show |
missense_variant | MODERATE | c.140A>G | p.Asn47Ser | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/8 | 218/1042 | 140/801 | 47/266 | chr16 | 27235296 | |||
| chr16:27257458 | G | C | 1 | a0003 | 40 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
missense_variant | MODERATE | c.113C>G | p.Thr38Arg | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/8 | 191/1042 | 113/801 | 38/266 | chr16 | 27257458 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:27226762 | G | A | 1 | a0002c0011 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.558C>T | p.Asp186Asp | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/8 | 636/1042 | 558/801 | 186/266 | chr16 | 27226762 | |||
| chr16:27226789 | C | T | 6 | a0001c0003 a0001c0009 a0002c0010 others(3): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
synonymous_variant | LOW | c.531G>A | p.Glu177Glu | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/8 | 609/1042 | 531/801 | 177/266 | chr16 | 27226789 | |||
| chr16:27235268 | G | A | 1 | a0001c0009 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.168C>T | p.Phe56Phe | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/8 | 246/1042 | 168/801 | 56/266 | chr16 | 27235268 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:27225082 | G | A | 9 | a0001c0003t0002 a0001c0003t0003 a0001c0009t0002 others(6): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*75C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 8/8 | 75 | chr16 | 27225082 | ||||||
| chr16:27268712 | G | A | 1 | a0001c0003t0003 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/8 | 11142 | chr16 | 27268712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:27225358 | C | A | 9 | a0001c0001t0001g0159 a0003c0004t0001g0273 a0003c0004t0002g0023 others(6): Show |
10 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.722-122G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 7/7 | chr16 | 27225358 | |||||||
| chr16:27225434 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.722-198C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 7/7 | chr16 | 27225434 | |||||||
| chr16:27225448 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.722-212G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 7/7 | chr16 | 27225448 | |||||||
| chr16:27225537 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.721+189A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 7/7 | chr16 | 27225537 | |||||||
| chr16:27225674 | C | T | 3 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0145 |
3 | HG01243.hp1 HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.721+52G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 7/7 | chr16 | 27225674 | |||||||
| chr16:27226034 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.601-188G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/7 | chr16 | 27226034 | |||||||
| chr16:27226081 | A | G | 82 | a0001c0001t0001g0115 a0001c0003t0002g0002 a0001c0003t0002g0004 others(79): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.601-235T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/7 | chr16 | 27226081 | |||||||
| chr16:27226181 | CA | C | 10 | a0002c0002t0001g0039 a0003c0004t0002g0023 a0003c0004t0002g0127 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.601-336delT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/7 | chr16 | 27226181 | |||||||
| chr16:27226251 | G | GTGTA | 65 | a0001c0003t0002g0002 a0001c0003t0002g0004 a0001c0003t0002g0005 others(62): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.601-409_601-406dup others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/7 | chr16 | 27226251 | |||||||
| chr16:27226491 | T | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+229A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/7 | chr16 | 27226491 | |||||||
| chr16:27226523 | G | A | 2 | a0001c0003t0002g0092 a0001c0003t0002g0124 |
2 | HG01358.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.600+197C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/7 | chr16 | 27226523 | |||||||
| chr16:27226649 | G | A | 1 | a0001c0003t0002g0224 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.600+71C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/7 | chr16 | 27226649 | |||||||
| chr16:27226713 | C | T | 78 | a0001c0003t0002g0002 a0001c0003t0002g0004 a0001c0003t0002g0005 others(75): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
splice_region_variant&intron_variant | LOW | c.600+7G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 6/7 | chr16 | 27226713 | |||||||
| chr16:27226920 | C | T | 1 | a0002c0002t0001g0169 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.484-84G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27226920 | |||||||
| chr16:27226969 | G | A | 3 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0145 |
3 | HG01243.hp1 HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.484-133C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27226969 | |||||||
| chr16:27226975 | G | A | 1 | a0002c0002t0001g0264 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.484-139C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27226975 | |||||||
| chr16:27227067 | C | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-231G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227067 | |||||||
| chr16:27227189 | C | T | 1 | a0003c0004t0001g0276 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.484-353G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227189 | |||||||
| chr16:27227260 | GTGCCTCC others(9): Show |
G | 1 | a0001c0003t0002g0216 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.484-440_484-425del others(16): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227260 | |||||||
| chr16:27227273 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.484-437G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227273 | |||||||
| chr16:27227314 | C | T | 2 | a0001c0001t0001g0159 a0003c0004t0001g0273 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.484-478G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227314 | |||||||
| chr16:27227359 | G | A | 12 | a0003c0004t0001g0135 a0003c0004t0001g0137 a0003c0004t0001g0285 others(9): Show |
13 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-523C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227359 | |||||||
| chr16:27227416 | G | A | 78 | a0001c0003t0002g0002 a0001c0003t0002g0004 a0001c0003t0002g0005 others(75): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.484-580C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227416 | |||||||
| chr16:27227493 | G | A | 1 | a0003c0004t0002g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.484-657C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227493 | |||||||
| chr16:27227557 | C | T | 2 | a0001c0003t0002g0092 a0001c0003t0002g0124 |
2 | HG01358.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.484-721G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227557 | |||||||
| chr16:27227589 | C | T | 4 | a0001c0003t0002g0217 a0001c0003t0002g0218 a0001c0003t0002g0220 others(1): Show |
4 | HG01106.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-753G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227589 | |||||||
| chr16:27227642 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.484-806G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227642 | |||||||
| chr16:27227778 | CTTTTCTT others(3): Show |
C | 78 | a0001c0001t0001g0181 a0001c0001t0001g0229 a0001c0003t0002g0002 others(75): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.484-952_484-943del others(10): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227778 | |||||||
| chr16:27227778 | CTTTTCTT others(4): Show |
C | 2 | a0001c0003t0002g0201 a0001c0003t0002g0213 |
2 | HG02056.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.484-953_484-943del others(11): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227778 | |||||||
| chr16:27227783 | C | CT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0259 a0002c0002t0001g0014 others(3): Show |
8 | HG01243.hp1 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-948dupA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227783 | |||||||
| chr16:27227783 | CT | C | 9 | a0001c0001t0001g0058 a0001c0001t0001g0243 a0002c0002t0001g0010 others(6): Show |
9 | HG01070.hp1 HG02897.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.484-948delA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227783 | |||||||
| chr16:27227788 | T | C | 6 | a0001c0001t0001g0104 a0003c0004t0001g0144 a0003c0004t0001g0274 others(3): Show |
6 | HG01884.hp1 HG02135.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-952A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227788 | |||||||
| chr16:27227974 | A | G | 80 | a0001c0001t0001g0181 a0001c0001t0001g0229 a0001c0003t0002g0002 others(77): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.484-1138T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27227974 | |||||||
| chr16:27228065 | G | A | 77 | a0001c0003t0002g0002 a0001c0003t0002g0004 a0001c0003t0002g0005 others(74): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.484-1229C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228065 | |||||||
| chr16:27228074 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.484-1238G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228074 | |||||||
| chr16:27228092 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.484-1256C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228092 | |||||||
| chr16:27228126 | A | T | 1 | a0002c0002t0001g0044 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.484-1290T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228126 | |||||||
| chr16:27228193 | C | G | 115 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0108 others(112): Show |
136 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.484-1357G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228193 | |||||||
| chr16:27228326 | A | G | 80 | a0001c0001t0001g0181 a0001c0001t0001g0229 a0001c0003t0002g0002 others(77): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.484-1490T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228326 | |||||||
| chr16:27228370 | G | C | 87 | a0001c0001t0001g0108 a0002c0002t0001g0001 a0002c0002t0001g0003 others(84): Show |
107 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.484-1534C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228370 | |||||||
| chr16:27228389 | C | T | 1 | a0001c0003t0002g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.484-1553G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228389 | |||||||
| chr16:27228495 | GCCTCCCC others(49): Show |
G | 1 | a0001c0001t0001g0007 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.484-1715_484-1660d others(58): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228495 | |||||||
| chr16:27228846 | G | C | 80 | a0001c0001t0001g0181 a0001c0001t0001g0229 a0001c0003t0002g0002 others(77): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.484-2010C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228846 | |||||||
| chr16:27228856 | A | AC | 4 | a0001c0003t0002g0175 a0001c0003t0002g0180 a0001c0003t0002g0231 others(1): Show |
4 | HG03098.hp2 HG04204.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-2021dupG | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228856 | |||||||
| chr16:27228868 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.484-2032G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228868 | |||||||
| chr16:27228960 | T | TGCTCTCT others(30): Show |
1 | a0002c0002t0001g0039 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.484-2161_484-2125d others(39): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27228960 | |||||||
| chr16:27229001 | C | T | 2 | a0001c0003t0002g0016 a0001c0003t0002g0191 |
3 | HG00597.hp2 NA18952.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.484-2165G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27229001 | |||||||
| chr16:27229090 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.484-2254C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27229090 | |||||||
| chr16:27229307 | C | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02280.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.484-2471G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27229307 | |||||||
| chr16:27229584 | A | T | 1 | a0003c0004t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.484-2748T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27229584 | |||||||
| chr16:27229606 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.484-2770G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27229606 | |||||||
| chr16:27229817 | G | T | 1 | a0001c0003t0002g0202 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.484-2981C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27229817 | |||||||
| chr16:27230011 | C | T | 78 | a0001c0003t0002g0002 a0001c0003t0002g0004 a0001c0003t0002g0005 others(75): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.483+2990G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230011 | |||||||
| chr16:27230131 | G | A | 3 | a0003c0004t0001g0135 a0003c0004t0001g0137 a0003c0004t0001g0285 |
3 | HG01891.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.483+2870C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230131 | |||||||
| chr16:27230154 | C | T | 6 | a0001c0001t0001g0101 a0001c0001t0001g0161 a0001c0001t0001g0163 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.483+2847G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230154 | |||||||
| chr16:27230204 | T | A | 1 | a0002c0002t0001g0039 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.483+2797A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230204 | |||||||
| chr16:27230224 | G | A | 7 | a0003c0004t0001g0128 a0003c0004t0001g0132 a0003c0004t0001g0133 others(4): Show |
7 | HG01109.hp1 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+2777C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230224 | |||||||
| chr16:27230268 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.483+2733A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230268 | |||||||
| chr16:27230270 | G | A | 2 | a0001c0001t0001g0159 a0003c0004t0001g0273 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.483+2731C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230270 | |||||||
| chr16:27230287 | T | C | 79 | a0001c0001t0001g0108 a0001c0001t0001g0181 a0001c0001t0001g0186 others(76): Show |
98 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.483+2714A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230287 | |||||||
| chr16:27230447 | C | T | 1 | a0002c0002t0001g0044 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.483+2554G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230447 | |||||||
| chr16:27230448 | T | C | 1 | a0002c0002t0001g0044 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.483+2553A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230448 | |||||||
| chr16:27230459 | G | A | 3 | a0003c0004t0001g0135 a0003c0004t0001g0137 a0003c0004t0001g0285 |
3 | HG01891.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.483+2542C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230459 | |||||||
| chr16:27230500 | G | A | 1 | a0001c0003t0002g0215 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.483+2501C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230500 | |||||||
| chr16:27230621 | C | T | 2 | a0001c0001t0001g0148 a0005c0008t0001g0174 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.483+2380G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230621 | |||||||
| chr16:27230693 | C | A | 2 | a0003c0004t0001g0135 a0003c0004t0001g0137 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.483+2308G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230693 | |||||||
| chr16:27230723 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.483+2278C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230723 | |||||||
| chr16:27230779 | G | A | 1 | a0002c0002t0001g0014 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.483+2222C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230779 | |||||||
| chr16:27230990 | C | T | 7 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.483+2011G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27230990 | |||||||
| chr16:27231273 | T | C | 1 | a0003c0004t0001g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.483+1728A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231273 | |||||||
| chr16:27231320 | G | A | 7 | a0003c0004t0001g0128 a0003c0004t0001g0132 a0003c0004t0001g0133 others(4): Show |
7 | HG01109.hp1 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+1681C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231320 | |||||||
| chr16:27231335 | C | T | 2 | a0001c0001t0001g0159 a0003c0004t0001g0273 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.483+1666G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231335 | |||||||
| chr16:27231388 | G | C | 14 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(11): Show |
14 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.483+1613C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231388 | |||||||
| chr16:27231512 | T | C | 3 | a0002c0002t0001g0009 a0002c0002t0001g0036 a0002c0002t0001g0062 |
4 | HG01175.hp2 HG01258.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1489A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231512 | |||||||
| chr16:27231559 | T | C | 199 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(196): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.483+1442A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231559 | |||||||
| chr16:27231574 | T | C | 1 | a0003c0004t0002g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.483+1427A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231574 | |||||||
| chr16:27231637 | T | TA | 85 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(82): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.483+1363dupT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231637 | |||||||
| chr16:27231637 | TA | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0105 a0001c0001t0001g0243 others(4): Show |
7 | HG02897.hp2 HG03491.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+1363delT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231637 | |||||||
| chr16:27231656 | G | A | 9 | a0003c0004t0002g0023 a0003c0004t0002g0127 a0003c0004t0002g0138 others(6): Show |
10 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+1345C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231656 | |||||||
| chr16:27231672 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.483+1329C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231672 | |||||||
| chr16:27231675 | C | T | 13 | a0001c0001t0001g0029 a0001c0001t0001g0146 a0001c0001t0001g0149 others(10): Show |
13 | HG00735.hp2 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.483+1326G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231675 | |||||||
| chr16:27231748 | G | A | 3 | a0002c0002t0001g0011 a0002c0002t0001g0070 a0002c0002t0001g0072 |
4 | HG01261.hp1 HG02698.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1253C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231748 | |||||||
| chr16:27231811 | G | A | 11 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(8): Show |
11 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.483+1190C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231811 | |||||||
| chr16:27231837 | C | T | 1 | a0001c0003t0002g0217 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.483+1164G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231837 | |||||||
| chr16:27231928 | C | T | 7 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.483+1073G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231928 | |||||||
| chr16:27231929 | G | A | 1 | a0001c0003t0002g0214 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.483+1072C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27231929 | |||||||
| chr16:27232106 | G | A | 11 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(8): Show |
11 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.483+895C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232106 | |||||||
| chr16:27232199 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.483+802C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232199 | |||||||
| chr16:27232591 | G | A | 1 | a0001c0003t0002g0177 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.483+410C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232591 | |||||||
| chr16:27232702 | T | A | 1 | a0003c0004t0001g0283 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.483+299A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232702 | |||||||
| chr16:27232787 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0192 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.483+214A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232787 | |||||||
| chr16:27232808 | C | T | 67 | a0001c0001t0001g0186 a0002c0002t0001g0001 a0002c0002t0001g0008 others(64): Show |
82 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.483+193G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232808 | |||||||
| chr16:27232852 | G | A | 1 | a0002c0002t0001g0265 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.483+149C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232852 | |||||||
| chr16:27232867 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.483+134T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232867 | |||||||
| chr16:27232998 | T | C | 1 | a0002c0002t0001g0065 | 1 | NA19070.hp1 | splice_region_variant&intron_variant | LOW | c.483+3A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 5/7 | chr16 | 27232998 | |||||||
| chr16:27233227 | A | G | 199 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(196): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.337-80T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27233227 | |||||||
| chr16:27233360 | C | T | 4 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG03017.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-213G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27233360 | |||||||
| chr16:27233414 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.337-267G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27233414 | |||||||
| chr16:27233500 | C | T | 11 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(8): Show |
11 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-353G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27233500 | |||||||
| chr16:27233606 | G | A | 78 | a0001c0003t0002g0002 a0001c0003t0002g0004 a0001c0003t0002g0005 others(75): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.337-459C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27233606 | |||||||
| chr16:27233765 | G | T | 210 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(207): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.336+423C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27233765 | |||||||
| chr16:27233831 | G | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0108 others(109): Show |
133 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.336+357C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27233831 | |||||||
| chr16:27234070 | A | G | 5 | a0003c0004t0001g0144 a0003c0004t0001g0274 a0003c0004t0001g0275 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.336+118T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27234070 | |||||||
| chr16:27234165 | G | A | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.336+23C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 4/7 | chr16 | 27234165 | |||||||
| chr16:27234284 | C | A | 2 | a0001c0001t0001g0029 a0003c0004t0001g0278 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.259-19G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234284 | |||||||
| chr16:27234308 | G | A | 6 | a0003c0004t0001g0144 a0003c0004t0001g0274 a0003c0004t0001g0275 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-43C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234308 | |||||||
| chr16:27234320 | G | A | 3 | a0003c0004t0001g0135 a0003c0004t0001g0137 a0003c0004t0001g0285 |
3 | HG01891.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.259-55C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234320 | |||||||
| chr16:27234391 | C | T | 78 | a0001c0003t0002g0002 a0001c0003t0002g0004 a0001c0003t0002g0005 others(75): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.259-126G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234391 | |||||||
| chr16:27234397 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.259-132C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234397 | |||||||
| chr16:27234459 | C | G | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259-194G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234459 | |||||||
| chr16:27234460 | T | C | 1 | a0002c0002t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.259-195A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234460 | |||||||
| chr16:27234470 | G | A | 1 | a0003c0004t0001g0276 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259-205C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234470 | |||||||
| chr16:27234494 | T | A | 114 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0108 others(111): Show |
135 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.259-229A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234494 | |||||||
| chr16:27234939 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258+239C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234939 | |||||||
| chr16:27234946 | C | A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0159 a0001c0001t0001g0161 others(3): Show |
6 | HG02486.hp2 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+232G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 3/7 | chr16 | 27234946 | |||||||
| chr16:27235448 | T | C | 23 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0159 others(20): Show |
23 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.137-149A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27235448 | |||||||
| chr16:27235457 | GCTT | G | 2 | a0001c0003t0002g0017 a0001c0003t0002g0199 |
3 | HG01070.hp2 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.137-161_137-159del others(3): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27235457 | |||||||
| chr16:27235507 | G | A | 1 | a0003c0004t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.137-208C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27235507 | |||||||
| chr16:27235617 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0029 others(33): Show |
38 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.137-318T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27235617 | |||||||
| chr16:27235649 | C | T | 1 | a0002c0011t0001g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.137-350G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27235649 | |||||||
| chr16:27235650 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.137-351C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27235650 | |||||||
| chr16:27235980 | C | G | 7 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-681G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27235980 | |||||||
| chr16:27236158 | A | G | 120 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0146 others(117): Show |
143 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(140): Show |
intron_variant | MODIFIER | c.137-859T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236158 | |||||||
| chr16:27236217 | G | A | 1 | a0004c0005t0002g0147 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.137-918C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236217 | |||||||
| chr16:27236292 | CT | C | 12 | a0001c0001t0001g0096 a0001c0001t0001g0243 a0001c0003t0002g0178 others(9): Show |
12 | HG01261.hp1 HG02027.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.137-994delA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236292 | |||||||
| chr16:27236292 | CTT | C | 191 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(188): Show |
231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.137-995_137-994del others(2): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236292 | |||||||
| chr16:27236292 | CTTT | C | 10 | a0001c0003t0002g0153 a0001c0003t0002g0196 a0001c0003t0002g0230 others(7): Show |
10 | HG01884.hp1 HG02165.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-996_137-994del others(3): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236292 | |||||||
| chr16:27236292 | CTTTT | C | 10 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(7): Show |
10 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-997_137-994del others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236292 | |||||||
| chr16:27236340 | T | A | 223 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(220): Show |
263 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.137-1041A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236340 | |||||||
| chr16:27236360 | A | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0085 others(4): Show |
9 | HG02258.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.137-1061T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236360 | |||||||
| chr16:27236539 | C | T | 1 | a0003c0004t0002g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.137-1240G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236539 | |||||||
| chr16:27236641 | CACT | C | 223 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(220): Show |
263 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.137-1345_137-1343d others(5): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236641 | |||||||
| chr16:27236737 | T | C | 16 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.137-1438A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236737 | |||||||
| chr16:27236895 | T | C | 2 | a0001c0003t0002g0203 a0001c0003t0002g0218 |
2 | HG01516.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.137-1596A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236895 | |||||||
| chr16:27236939 | AGATT | A | 5 | a0003c0004t0001g0144 a0003c0004t0001g0274 a0003c0004t0001g0275 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-1644_137-1641d others(6): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236939 | |||||||
| chr16:27236952 | T | TA | 13 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(10): Show |
13 | HG01109.hp1 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-1654dupT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236952 | |||||||
| chr16:27236996 | T | C | 13 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(10): Show |
13 | HG01109.hp1 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-1697A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27236996 | |||||||
| chr16:27237001 | C | T | 1 | a0003c0004t0001g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137-1702G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237001 | |||||||
| chr16:27237004 | T | G | 1 | a0001c0001t0001g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.137-1705A>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237004 | |||||||
| chr16:27237215 | C | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0108 others(77): Show |
100 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.137-1916G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237215 | |||||||
| chr16:27237254 | G | T | 5 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-1955C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237254 | |||||||
| chr16:27237273 | G | A | 2 | a0001c0001t0001g0148 a0005c0008t0001g0174 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.137-1974C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237273 | |||||||
| chr16:27237456 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG00738.hp2 HG01517.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.137-2157G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237456 | |||||||
| chr16:27237633 | C | CCT | 224 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(221): Show |
264 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.137-2336_137-2335d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237633 | |||||||
| chr16:27237747 | G | C | 2 | a0002c0002t0001g0034 a0002c0002t0001g0066 |
2 | HG02080.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.137-2448C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237747 | |||||||
| chr16:27237922 | T | C | 94 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(91): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.137-2623A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237922 | |||||||
| chr16:27237953 | C | A | 1 | a0002c0002t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.137-2654G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27237953 | |||||||
| chr16:27238060 | G | A | 81 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(78): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.137-2761C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238060 | |||||||
| chr16:27238151 | G | T | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-2852C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238151 | |||||||
| chr16:27238159 | A | G | 11 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(8): Show |
11 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-2860T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238159 | |||||||
| chr16:27238226 | C | G | 6 | a0001c0003t0002g0013 a0001c0003t0002g0112 a0001c0003t0002g0124 others(3): Show |
7 | HG00099.hp2 HG01361.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-2927G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238226 | |||||||
| chr16:27238259 | G | A | 3 | a0002c0002t0001g0011 a0002c0002t0001g0070 a0002c0002t0001g0072 |
4 | HG01261.hp1 HG02698.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-2960C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238259 | |||||||
| chr16:27238299 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.137-3000C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238299 | |||||||
| chr16:27238463 | G | A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0159 a0001c0001t0001g0161 others(3): Show |
6 | HG02486.hp2 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-3164C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238463 | |||||||
| chr16:27238524 | G | C | 12 | a0003c0004t0001g0135 a0003c0004t0001g0137 a0003c0004t0001g0283 others(9): Show |
13 | HG00741.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.137-3225C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238524 | |||||||
| chr16:27238532 | C | T | 3 | a0002c0002t0001g0059 a0002c0002t0001g0063 a0002c0002t0001g0065 |
3 | NA18961.hp2 NA19012.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.137-3233G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238532 | |||||||
| chr16:27238543 | T | TTTC | 223 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(220): Show |
263 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.137-3245_137-3244i others(5): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238543 | |||||||
| chr16:27238556 | A | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 |
3 | HG02559.hp2 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.137-3257T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238556 | |||||||
| chr16:27238581 | G | A | 1 | a0003c0004t0001g0278 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.137-3282C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238581 | |||||||
| chr16:27238872 | A | AT | 31 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(28): Show |
31 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.137-3574dupA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238872 | |||||||
| chr16:27238886 | T | TC | 3 | a0003c0004t0001g0128 a0003c0004t0001g0132 a0003c0004t0001g0140 |
3 | HG01109.hp1 HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137-3588_137-3587i others(3): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238886 | |||||||
| chr16:27238955 | C | T | 224 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(221): Show |
264 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.137-3656G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27238955 | |||||||
| chr16:27239166 | A | G | 94 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(91): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.137-3867T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239166 | |||||||
| chr16:27239185 | C | T | 81 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(78): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.137-3886G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239185 | |||||||
| chr16:27239236 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.137-3937C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239236 | |||||||
| chr16:27239337 | A | T | 94 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(91): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.137-4038T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239337 | |||||||
| chr16:27239483 | T | C | 8 | a0003c0004t0001g0128 a0003c0004t0001g0130 a0003c0004t0001g0132 others(5): Show |
8 | HG01109.hp1 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-4184A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239483 | |||||||
| chr16:27239536 | T | C | 1 | a0003c0004t0001g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.137-4237A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239536 | |||||||
| chr16:27239585 | C | T | 13 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(10): Show |
13 | HG01109.hp1 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-4286G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239585 | |||||||
| chr16:27239643 | G | A | 1 | a0003c0004t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.137-4344C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239643 | |||||||
| chr16:27239660 | C | T | 1 | a0003c0004t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.137-4361G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239660 | |||||||
| chr16:27239767 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.137-4468T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239767 | |||||||
| chr16:27239885 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(221): Show |
264 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.137-4586T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239885 | |||||||
| chr16:27239956 | T | TGCCA | 93 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(90): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.137-4661_137-4658d others(6): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239956 | |||||||
| chr16:27239982 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.137-4683G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27239982 | |||||||
| chr16:27240437 | C | T | 1 | a0001c0003t0002g0208 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.137-5138G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27240437 | |||||||
| chr16:27240633 | T | TGGCAA | 3 | a0002c0002t0001g0045 a0002c0002t0001g0055 a0002c0002t0001g0089 |
3 | HG02071.hp2 NA18946.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.137-5339_137-5335d others(7): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27240633 | |||||||
| chr16:27240682 | A | C | 1 | a0001c0003t0002g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.137-5383T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27240682 | |||||||
| chr16:27240718 | G | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0085 others(4): Show |
9 | HG02258.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.137-5419C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27240718 | |||||||
| chr16:27240842 | G | A | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.137-5543C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27240842 | |||||||
| chr16:27241590 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0162 |
2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.137-6291C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27241590 | |||||||
| chr16:27241695 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0192 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.137-6396C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27241695 | |||||||
| chr16:27241738 | G | A | 281 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0019 others(278): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.137-6439C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27241738 | |||||||
| chr16:27241928 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-6629T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27241928 | |||||||
| chr16:27242074 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | HG02559.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-6775T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27242074 | |||||||
| chr16:27242342 | G | A | 4 | a0001c0003t0002g0217 a0001c0003t0002g0218 a0001c0003t0002g0220 others(1): Show |
4 | HG01106.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-7043C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27242342 | |||||||
| chr16:27242378 | A | AAGAAGTT others(10): Show |
3 | a0003c0004t0001g0283 a0003c0004t0001g0284 a0003c0004t0001g0285 |
3 | HG00741.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.137-7096_137-7080d others(19): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27242378 | |||||||
| chr16:27242536 | G | C | 1 | a0002c0002t0001g0170 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.137-7237C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27242536 | |||||||
| chr16:27242748 | A | G | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.137-7449T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27242748 | |||||||
| chr16:27242810 | C | T | 191 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0071 others(188): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.137-7511G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27242810 | |||||||
| chr16:27242858 | C | T | 4 | a0003c0004t0001g0278 a0003c0004t0001g0279 a0003c0004t0001g0280 others(1): Show |
4 | HG00735.hp2 HG02280.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-7559G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27242858 | |||||||
| chr16:27243007 | T | C | 213 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(210): Show |
251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.137-7708A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243007 | |||||||
| chr16:27243074 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.137-7775G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243074 | |||||||
| chr16:27243364 | T | C | 2 | a0002c0002t0001g0039 a0002c0002t0001g0040 |
2 | NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.137-8065A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243364 | |||||||
| chr16:27243397 | T | C | 1 | a0002c0002t0001g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.137-8098A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243397 | |||||||
| chr16:27243534 | C | T | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-8235G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243534 | |||||||
| chr16:27243557 | A | G | 3 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0145 |
3 | HG01243.hp1 HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.137-8258T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243557 | |||||||
| chr16:27243592 | C | T | 3 | a0001c0003t0002g0178 a0001c0003t0002g0195 a0001c0003t0002g0209 |
3 | HG00423.hp2 NA18973.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.137-8293G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243592 | |||||||
| chr16:27243639 | C | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0071 others(77): Show |
99 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.137-8340G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243639 | |||||||
| chr16:27243681 | C | T | 120 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0071 others(117): Show |
140 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.137-8382G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243681 | |||||||
| chr16:27243785 | G | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-8486C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27243785 | |||||||
| chr16:27244028 | T | C | 120 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0071 others(117): Show |
140 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.137-8729A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244028 | |||||||
| chr16:27244033 | C | T | 1 | a0001c0003t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.137-8734G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244033 | |||||||
| chr16:27244236 | G | A | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-8937C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244236 | |||||||
| chr16:27244302 | G | T | 4 | a0001c0003t0002g0217 a0001c0003t0002g0218 a0001c0003t0002g0220 others(1): Show |
4 | HG01106.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-9003C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244302 | |||||||
| chr16:27244316 | G | A | 2 | a0003c0004t0002g0127 a0003c0004t0002g0138 |
2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137-9017C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244316 | |||||||
| chr16:27244392 | G | A | 1 | a0003c0004t0001g0282 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137-9093C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244392 | |||||||
| chr16:27244396 | T | A | 1 | a0002c0002t0001g0063 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.137-9097A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244396 | |||||||
| chr16:27244538 | C | T | 1 | a0002c0002t0001g0052 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.137-9239G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244538 | |||||||
| chr16:27244655 | CA | C | 71 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(68): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.137-9357delT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244655 | |||||||
| chr16:27244786 | C | A | 1 | a0003c0004t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.137-9487G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244786 | |||||||
| chr16:27244808 | C | T | 71 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(68): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.137-9509G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244808 | |||||||
| chr16:27244823 | G | A | 2 | a0003c0004t0002g0127 a0003c0004t0002g0138 |
2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137-9524C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244823 | |||||||
| chr16:27244834 | C | T | 1 | a0001c0003t0002g0200 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.137-9535G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244834 | |||||||
| chr16:27244902 | T | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-9603A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244902 | |||||||
| chr16:27244998 | T | C | 120 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0071 others(117): Show |
140 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.137-9699A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27244998 | |||||||
| chr16:27245054 | T | C | 2 | a0003c0004t0002g0286 a0003c0004t0002g0287 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.137-9755A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27245054 | |||||||
| chr16:27245217 | C | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-9918G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27245217 | |||||||
| chr16:27245241 | G | A | 8 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(5): Show |
8 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-9942C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27245241 | |||||||
| chr16:27245331 | T | A | 3 | a0003c0004t0001g0283 a0003c0004t0001g0284 a0003c0004t0001g0285 |
3 | HG00741.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.137-10032A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27245331 | |||||||
| chr16:27245427 | T | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-10128A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27245427 | |||||||
| chr16:27245456 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.137-10157C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27245456 | |||||||
| chr16:27245910 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137-10611A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27245910 | |||||||
| chr16:27246042 | G | A | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-10743C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246042 | |||||||
| chr16:27246064 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.137-10765C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246064 | |||||||
| chr16:27246117 | G | A | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.137-10818C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246117 | |||||||
| chr16:27246209 | G | A | 1 | a0001c0003t0002g0207 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.137-10910C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246209 | |||||||
| chr16:27246245 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.137-10946T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246245 | |||||||
| chr16:27246257 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.137-10958G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246257 | |||||||
| chr16:27246262 | C | T | 134 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0071 others(131): Show |
154 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(151): Show |
intron_variant | MODIFIER | c.137-10963G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246262 | |||||||
| chr16:27246413 | C | T | 1 | a0002c0002t0001g0061 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.136+11022G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246413 | |||||||
| chr16:27246489 | T | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+10946A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246489 | |||||||
| chr16:27246620 | C | T | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+10815G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246620 | |||||||
| chr16:27246963 | T | TAAAACTC others(360): Show |
2 | a0003c0004t0001g0129 a0003c0004t0001g0141 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136+10471_136+1047 others(371): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27246963 | T | TAAAACTC others(356): Show |
1 | a0003c0004t0001g0140 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.136+10471_136+1047 others(367): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27246963 | T | TAAAACTC others(356): Show |
1 | a0003c0004t0001g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136+10471_136+1047 others(367): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27246963 | T | TAAAACTC others(355): Show |
3 | a0003c0004t0001g0128 a0003c0004t0001g0135 a0003c0004t0001g0137 |
3 | HG01891.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.136+10471_136+1047 others(366): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27246963 | T | TAAAACTC others(354): Show |
3 | a0003c0004t0001g0130 a0003c0004t0001g0133 a0003c0004t0001g0136 |
3 | HG02723.hp2 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.136+10471_136+1047 others(365): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27246963 | T | TAAAACTC others(352): Show |
1 | a0003c0004t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136+10471_136+1047 others(363): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27246963 | T | TAAAACTC others(353): Show |
2 | a0003c0004t0001g0132 a0003c0004t0001g0134 |
2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.136+10471_136+1047 others(364): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27246963 | T | TAAAACTC others(356): Show |
1 | a0003c0004t0002g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136+10471_136+1047 others(367): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27246963 | T | TAAAACTC others(357): Show |
1 | a0003c0004t0002g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.136+10471_136+1047 others(368): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27246963 | |||||||
| chr16:27247183 | A | T | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+10252T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247183 | |||||||
| chr16:27247265 | T | A | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+10170A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247265 | |||||||
| chr16:27247383 | G | T | 39 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(36): Show |
40 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.136+10052C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247383 | |||||||
| chr16:27247400 | C | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+10035G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247400 | |||||||
| chr16:27247473 | A | C | 1 | a0001c0003t0002g0228 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.136+9962T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247473 | |||||||
| chr16:27247479 | G | A | 1 | a0002c0002t0001g0047 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136+9956C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247479 | |||||||
| chr16:27247560 | A | G | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+9875T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247560 | |||||||
| chr16:27247615 | G | A | 1 | a0001c0003t0002g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.136+9820C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247615 | |||||||
| chr16:27247692 | C | T | 23 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(20): Show |
23 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.136+9743G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247692 | |||||||
| chr16:27247770 | C | T | 28 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(25): Show |
28 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.136+9665G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247770 | |||||||
| chr16:27247863 | G | T | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+9572C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247863 | |||||||
| chr16:27247926 | C | CA | 9 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(6): Show |
9 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+9508dupT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247926 | |||||||
| chr16:27247926 | CA | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+9508delT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247926 | |||||||
| chr16:27247933 | A | C | 2 | a0003c0004t0002g0127 a0003c0004t0002g0138 |
2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.136+9502T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27247933 | |||||||
| chr16:27248031 | T | C | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+9404A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248031 | |||||||
| chr16:27248114 | C | T | 39 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(36): Show |
40 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.136+9321G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248114 | |||||||
| chr16:27248234 | T | C | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+9201A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248234 | |||||||
| chr16:27248276 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136+9159A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248276 | |||||||
| chr16:27248406 | C | CT | 99 | a0001c0001t0001g0024 a0001c0001t0001g0093 a0001c0001t0001g0094 others(96): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.136+9028dupA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248406 | |||||||
| chr16:27248406 | C | CTT | 24 | a0001c0001t0001g0212 a0001c0003t0002g0157 a0001c0003t0002g0178 others(21): Show |
24 | HG00423.hp2 HG01106.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.136+9027_136+9028d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248406 | |||||||
| chr16:27248406 | C | CTTT | 7 | a0001c0003t0002g0208 a0003c0004t0001g0128 a0003c0004t0001g0129 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+9026_136+9028d others(5): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248406 | |||||||
| chr16:27248413 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136+9022A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248413 | |||||||
| chr16:27248503 | C | T | 1 | a0003c0004t0001g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136+8932G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248503 | |||||||
| chr16:27248875 | C | G | 71 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(68): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.136+8560G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27248875 | |||||||
| chr16:27249076 | G | A | 2 | a0002c0002t0001g0064 a0002c0002t0001g0100 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.136+8359C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27249076 | |||||||
| chr16:27249221 | T | C | 2 | a0001c0003t0002g0204 a0001c0003t0002g0210 |
2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.136+8214A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27249221 | |||||||
| chr16:27249509 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+7926G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27249509 | |||||||
| chr16:27249626 | C | G | 3 | a0001c0001t0001g0007 a0002c0002t0001g0031 a0002c0002t0001g0032 |
4 | HG02145.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+7809G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27249626 | |||||||
| chr16:27249633 | T | G | 8 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(5): Show |
8 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+7802A>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27249633 | |||||||
| chr16:27249858 | G | A | 1 | a0001c0003t0002g0177 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.136+7577C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27249858 | |||||||
| chr16:27249863 | C | T | 1 | a0001c0003t0002g0194 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.136+7572G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27249863 | |||||||
| chr16:27250086 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.136+7349T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250086 | |||||||
| chr16:27250126 | T | C | 1 | a0001c0003t0002g0112 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.136+7309A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250126 | |||||||
| chr16:27250358 | G | C | 10 | a0003c0004t0001g0283 a0003c0004t0001g0284 a0003c0004t0001g0285 others(7): Show |
11 | HG00741.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+7077C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250358 | |||||||
| chr16:27250479 | A | AT | 15 | a0001c0001t0001g0111 a0002c0002t0001g0046 a0003c0004t0001g0128 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+6955dupA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250479 | |||||||
| chr16:27250479 | AT | A | 5 | a0001c0001t0001g0254 a0001c0003t0002g0206 a0002c0002t0001g0010 others(2): Show |
6 | HG00639.hp2 HG01070.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+6955delA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250479 | |||||||
| chr16:27250653 | C | A | 8 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(5): Show |
8 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+6782G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250653 | |||||||
| chr16:27250784 | A | G | 1 | a0003c0004t0001g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136+6651T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250784 | |||||||
| chr16:27250842 | TG | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0258 |
3 | HG00735.hp1 HG02300.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.136+6592delC | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250842 | |||||||
| chr16:27250843 | G | GT | 30 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0101 others(27): Show |
30 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.136+6591dupA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250843 | |||||||
| chr16:27250843 | G | GTTT | 19 | a0003c0004t0001g0142 a0003c0004t0001g0144 a0003c0004t0001g0145 others(16): Show |
19 | HG00741.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.136+6589_136+6591d others(5): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250843 | |||||||
| chr16:27250843 | GT | G | 67 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(64): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.136+6591delA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250843 | |||||||
| chr16:27250843 | GTT | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+6590_136+6591d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250843 | |||||||
| chr16:27250844 | T | G | 1 | a0002c0002t0001g0065 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.136+6591A>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250844 | |||||||
| chr16:27250935 | G | A | 1 | a0003c0004t0001g0278 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136+6500C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250935 | |||||||
| chr16:27250959 | G | A | 40 | a0001c0001t0001g0160 a0003c0004t0001g0128 a0003c0004t0001g0129 others(37): Show |
41 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.136+6476C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250959 | |||||||
| chr16:27250996 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.136+6439G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27250996 | |||||||
| chr16:27251076 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0085 others(4): Show |
9 | HG02258.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+6359C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251076 | |||||||
| chr16:27251121 | G | A | 4 | a0001c0003t0002g0067 a0002c0002t0001g0034 a0002c0002t0001g0066 others(1): Show |
4 | HG02080.hp2 NA18989.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+6314C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251121 | |||||||
| chr16:27251132 | C | T | 1 | a0003c0004t0001g0285 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.136+6303G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251132 | |||||||
| chr16:27251159 | A | AAT | 9 | a0001c0001t0001g0111 a0001c0001t0001g0149 a0001c0001t0001g0151 others(6): Show |
9 | HG00642.hp2 HG01258.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+6274_136+6275d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATAT | 10 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0155 others(7): Show |
12 | HG00099.hp2 HG00280.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.136+6272_136+6275d others(6): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATAT | 7 | a0001c0001t0001g0020 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
8 | HG00741.hp2 HG01106.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+6270_136+6275d others(8): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(1): Show |
5 | a0001c0001t0001g0150 a0001c0001t0001g0154 a0001c0003t0002g0158 others(2): Show |
5 | HG02040.hp2 HG02129.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+6268_136+6275d others(10): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(3): Show |
3 | a0001c0001t0001g0253 a0001c0003t0002g0157 a0002c0002t0001g0168 |
3 | HG02683.hp2 NA18961.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.136+6266_136+6275d others(12): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(5): Show |
2 | a0001c0003t0002g0153 a0002c0002t0001g0076 |
2 | HG02165.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.136+6264_136+6275d others(14): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(7): Show |
4 | a0001c0001t0001g0058 a0002c0002t0001g0098 a0002c0002t0001g0266 others(1): Show |
4 | HG03139.hp1 NA18951.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+6262_136+6275d others(16): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(9): Show |
4 | a0001c0001t0001g0261 a0002c0002t0001g0045 a0002c0002t0001g0057 others(1): Show |
4 | HG02071.hp2 HG03831.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+6260_136+6275d others(18): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(11): Show |
1 | a0002c0002t0001g0056 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.136+6258_136+6275d others(20): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(13): Show |
3 | a0002c0002t0001g0034 a0002c0002t0001g0055 a0002c0002t0001g0089 |
3 | NA18946.hp2 NA18998.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.136+6256_136+6275d others(22): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(15): Show |
2 | a0002c0002t0001g0044 a0002c0002t0001g0054 |
2 | NA18964.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.136+6254_136+6275d others(24): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(17): Show |
1 | a0002c0002t0001g0053 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.136+6252_136+6275d others(26): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(19): Show |
1 | a0002c0002t0001g0043 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.136+6250_136+6275d others(28): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | A | AATATATA others(21): Show |
1 | a0002c0002t0001g0052 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.136+6248_136+6275d others(30): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | AAT | A | 10 | a0001c0001t0001g0021 a0001c0001t0001g0104 a0001c0001t0001g0241 others(7): Show |
11 | HG00735.hp1 HG01261.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+6274_136+6275d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251159 | AATAT | A | 3 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0074 |
3 | HG03017.hp2 HG03491.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.136+6272_136+6275d others(6): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251159 | |||||||
| chr16:27251161 | T | TATATATA others(22): Show |
1 | a0001c0001t0001g0105 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.136+6245_136+6273d others(31): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251161 | |||||||
| chr16:27251161 | T | TATATATA others(53): Show |
1 | a0001c0001t0001g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.136+6273_136+6274i others(62): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251161 | |||||||
| chr16:27251163 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.136+6272A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251163 | |||||||
| chr16:27251163 | TATATATA others(21): Show |
T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0085 others(27): Show |
33 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.136+6244_136+6271d others(30): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251163 | |||||||
| chr16:27251165 | TATATATA others(19): Show |
T | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+6244_136+6269d others(28): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251165 | |||||||
| chr16:27251167 | TATATATA others(17): Show |
T | 13 | a0001c0001t0001g0212 a0001c0001t0001g0233 a0001c0001t0001g0234 others(10): Show |
13 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.136+6244_136+6267d others(26): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251167 | |||||||
| chr16:27251169 | T | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(1): Show |
5 | HG00738.hp2 HG01346.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+6266A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251169 | |||||||
| chr16:27251169 | TATATATA others(15): Show |
T | 48 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0229 others(45): Show |
66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.136+6244_136+6265d others(24): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251169 | |||||||
| chr16:27251171 | TATATATA others(13): Show |
T | 2 | a0001c0003t0002g0203 a0001c0003t0002g0225 |
2 | HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.136+6244_136+6263d others(22): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251171 | |||||||
| chr16:27251173 | TATATATA others(11): Show |
T | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.136+6244_136+6261d others(20): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251173 | |||||||
| chr16:27251173 | TATATATA others(29): Show |
T | 1 | a0001c0001t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136+6226_136+6261d others(38): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251173 | |||||||
| chr16:27251179 | TATATATA others(5): Show |
T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+6244_136+6255d others(14): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251179 | |||||||
| chr16:27251179 | TATATATA others(23): Show |
T | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136+6226_136+6255d others(32): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251179 | |||||||
| chr16:27251181 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.136+6244_136+6253d others(12): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251181 | |||||||
| chr16:27251185 | TATATAA | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0173 a0005c0008t0001g0174 |
3 | HG01891.hp2 HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.136+6244_136+6249d others(8): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251185 | |||||||
| chr16:27251187 | TATAAATA others(15): Show |
T | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.136+6226_136+6247d others(24): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251187 | |||||||
| chr16:27251189 | T | A | 2 | a0002c0002t0001g0032 a0002c0002t0001g0074 |
2 | HG02622.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.136+6246A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(3): Show |
4 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0046 others(1): Show |
4 | HG02559.hp1 HG03831.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+6245_136+6246i others(12): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(4): Show |
1 | a0002c0002t0001g0001 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.136+6245_136+6246i others(13): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(5): Show |
13 | a0001c0003t0002g0015 a0002c0002t0001g0001 a0002c0002t0001g0009 others(10): Show |
15 | HG00423.hp1 HG00438.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.136+6245_136+6246i others(14): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0118 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.136+6245_136+6246i others(15): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(7): Show |
14 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0010 others(11): Show |
17 | HG01070.hp1 HG01175.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.136+6245_136+6246i others(16): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(8): Show |
1 | a0002c0002t0001g0033 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.136+6245_136+6246i others(17): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(9): Show |
15 | a0001c0001t0001g0071 a0002c0002t0001g0001 a0002c0002t0001g0008 others(12): Show |
17 | HG01081.hp1 HG01243.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.136+6245_136+6246i others(18): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(10): Show |
1 | a0002c0002t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.136+6245_136+6246i others(19): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(11): Show |
6 | a0001c0001t0001g0007 a0001c0003t0002g0067 a0002c0002t0001g0008 others(3): Show |
7 | HG00642.hp1 HG02145.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+6245_136+6246i others(20): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(13): Show |
4 | a0002c0002t0001g0068 a0002c0002t0001g0086 a0002c0002t0001g0087 others(1): Show |
4 | HG00673.hp2 HG01361.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+6245_136+6246i others(22): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(15): Show |
5 | a0002c0002t0001g0003 a0002c0002t0001g0041 a0002c0002t0001g0048 others(2): Show |
5 | HG02080.hp2 HG03209.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+6245_136+6246i others(24): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(45): Show |
1 | a0001c0001t0001g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.136+6245_136+6246i others(54): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(17): Show |
4 | a0002c0002t0001g0040 a0002c0002t0001g0078 a0002c0002t0001g0091 others(1): Show |
4 | HG02056.hp2 NA18975.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+6245_136+6246i others(26): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(19): Show |
1 | a0002c0002t0001g0080 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.136+6245_136+6246i others(28): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251189 | T | TATATATA others(21): Show |
1 | a0002c0002t0001g0039 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.136+6245_136+6246i others(30): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251189 | |||||||
| chr16:27251191 | A | T | 42 | a0001c0001t0001g0101 a0001c0001t0001g0117 a0001c0001t0001g0123 others(39): Show |
49 | HG00423.hp1 HG00642.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.136+6244T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251191 | |||||||
| chr16:27251205 | T | A | 39 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(36): Show |
40 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.136+6230A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251205 | |||||||
| chr16:27251207 | T | A | 61 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0212 others(58): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.136+6228A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251207 | |||||||
| chr16:27251207 | T | TATATATA others(3): Show |
2 | a0001c0003t0002g0220 a0001c0003t0002g0221 |
2 | HG01106.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.136+6227_136+6228i others(12): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251207 | |||||||
| chr16:27251207 | T | TATATATA others(5): Show |
1 | a0001c0003t0002g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.136+6227_136+6228i others(14): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251207 | |||||||
| chr16:27251208 | A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.136+6226_136+6227i others(17): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251208 | |||||||
| chr16:27251209 | A | T | 14 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(11): Show |
14 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.136+6226T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251209 | |||||||
| chr16:27251210 | A | T | 1 | a0002c0002t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.136+6225T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251210 | |||||||
| chr16:27251309 | T | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+6126A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251309 | |||||||
| chr16:27251465 | C | T | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+5970G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251465 | |||||||
| chr16:27251472 | G | T | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+5963C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251472 | |||||||
| chr16:27251522 | G | A | 39 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(36): Show |
40 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.136+5913C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251522 | |||||||
| chr16:27251541 | C | T | 4 | a0001c0001t0001g0071 a0002c0002t0001g0011 a0002c0002t0001g0070 others(1): Show |
5 | HG01261.hp1 HG01517.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+5894G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251541 | |||||||
| chr16:27251568 | G | A | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+5867C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251568 | |||||||
| chr16:27251638 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.136+5797A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251638 | |||||||
| chr16:27251871 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136+5564G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27251871 | |||||||
| chr16:27252067 | G | A | 1 | a0001c0003t0002g0178 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.136+5368C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252067 | |||||||
| chr16:27252137 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.136+5298T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252137 | |||||||
| chr16:27252391 | T | C | 1 | a0001c0003t0002g0179 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.136+5044A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252391 | |||||||
| chr16:27252452 | T | C | 72 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(69): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.136+4983A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252452 | |||||||
| chr16:27252581 | G | A | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+4854C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252581 | |||||||
| chr16:27252609 | C | T | 1 | a0001c0003t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136+4826G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252609 | |||||||
| chr16:27252650 | G | A | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+4785C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252650 | |||||||
| chr16:27252833 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136+4602G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252833 | |||||||
| chr16:27252897 | C | T | 16 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(13): Show |
16 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+4538G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252897 | |||||||
| chr16:27252968 | G | A | 2 | a0003c0004t0001g0283 a0003c0004t0001g0284 |
2 | HG00741.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.136+4467C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27252968 | |||||||
| chr16:27253172 | T | C | 5 | a0003c0004t0001g0274 a0003c0004t0001g0275 a0003c0004t0001g0276 others(2): Show |
5 | HG02258.hp2 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+4263A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27253172 | |||||||
| chr16:27253212 | C | A | 1 | a0002c0011t0001g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.136+4223G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27253212 | |||||||
| chr16:27253621 | C | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0115 others(1): Show |
4 | HG01071.hp1 HG01993.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+3814G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27253621 | |||||||
| chr16:27253927 | G | T | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+3508C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27253927 | |||||||
| chr16:27254002 | G | A | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+3433C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254002 | |||||||
| chr16:27254149 | T | C | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+3286A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254149 | |||||||
| chr16:27254216 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+3219T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254216 | |||||||
| chr16:27254499 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0024 |
3 | HG00280.hp1 HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.136+2936T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254499 | |||||||
| chr16:27254712 | G | A | 16 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.136+2723C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254712 | |||||||
| chr16:27254752 | A | G | 3 | a0003c0004t0001g0283 a0003c0004t0001g0284 a0003c0004t0001g0285 |
3 | HG00741.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.136+2683T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254752 | |||||||
| chr16:27254866 | C | CT | 10 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0114 others(7): Show |
10 | HG00597.hp1 HG00741.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.136+2568dupA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254866 | |||||||
| chr16:27254866 | CT | C | 88 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(85): Show |
106 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.136+2568delA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254866 | |||||||
| chr16:27254866 | CTT | C | 12 | a0001c0003t0002g0166 a0001c0009t0002g0167 a0002c0002t0001g0069 others(9): Show |
13 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.136+2567_136+2568d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254866 | |||||||
| chr16:27254866 | CTTT | C | 9 | a0003c0004t0001g0144 a0003c0004t0001g0145 a0003c0004t0001g0278 others(6): Show |
9 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+2566_136+2568d others(5): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254866 | |||||||
| chr16:27254866 | CTTTTT | C | 9 | a0001c0001t0001g0190 a0001c0001t0001g0234 a0001c0003t0002g0191 others(6): Show |
9 | HG00438.hp2 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+2564_136+2568d others(7): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254866 | |||||||
| chr16:27254866 | CTTTTTT | C | 82 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(79): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.136+2563_136+2568d others(8): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254866 | |||||||
| chr16:27254866 | CTTTTTTT | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0001g0146 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.136+2562_136+2568d others(9): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254866 | |||||||
| chr16:27254903 | ATG | A | 5 | a0001c0003t0002g0015 a0001c0003t0002g0157 a0001c0003t0002g0158 others(2): Show |
6 | NA18942.hp2 NA18951.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+2530_136+2531d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27254903 | |||||||
| chr16:27255496 | G | A | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+1939C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27255496 | |||||||
| chr16:27255730 | G | A | 94 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(91): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.136+1705C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27255730 | |||||||
| chr16:27255792 | T | C | 7 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+1643A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27255792 | |||||||
| chr16:27255856 | C | T | 1 | a0001c0003t0002g0189 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.136+1579G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27255856 | |||||||
| chr16:27255988 | C | T | 118 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(115): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.136+1447G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27255988 | |||||||
| chr16:27256082 | G | A | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+1353C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256082 | |||||||
| chr16:27256098 | G | A | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+1337C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256098 | |||||||
| chr16:27256124 | C | T | 5 | a0003c0004t0001g0274 a0003c0004t0001g0275 a0003c0004t0001g0276 others(2): Show |
5 | HG02258.hp2 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+1311G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256124 | |||||||
| chr16:27256203 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0126 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.136+1232C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256203 | |||||||
| chr16:27256443 | G | A | 1 | a0002c0002t0001g0069 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.136+992C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256443 | |||||||
| chr16:27256551 | C | T | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+884G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256551 | |||||||
| chr16:27256621 | A | C | 7 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+814T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256621 | |||||||
| chr16:27256757 | G | A | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+678C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256757 | |||||||
| chr16:27256898 | A | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+537T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27256898 | |||||||
| chr16:27257038 | C | T | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG02155.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.136+397G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27257038 | |||||||
| chr16:27257060 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+375C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27257060 | |||||||
| chr16:27257241 | A | T | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+194T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27257241 | |||||||
| chr16:27257300 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+135C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27257300 | |||||||
| chr16:27257342 | C | T | 5 | a0003c0004t0001g0274 a0003c0004t0001g0275 a0003c0004t0001g0276 others(2): Show |
5 | HG02258.hp2 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+93G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27257342 | |||||||
| chr16:27257398 | C | T | 16 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.136+37G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27257398 | |||||||
| chr16:27257407 | G | A | 16 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.136+28C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 2/7 | chr16 | 27257407 | |||||||
| chr16:27257633 | G | A | 1 | a0001c0003t0002g0222 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-11-52C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257633 | |||||||
| chr16:27257702 | T | C | 71 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(68): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-11-121A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257702 | |||||||
| chr16:27257760 | T | G | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11-179A>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257760 | |||||||
| chr16:27257787 | G | A | 4 | a0001c0001t0001g0071 a0002c0002t0001g0011 a0002c0002t0001g0070 others(1): Show |
5 | HG01261.hp1 HG01517.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-206C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257787 | |||||||
| chr16:27257793 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0244 others(5): Show |
10 | HG00741.hp2 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-212G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257793 | |||||||
| chr16:27257828 | G | A | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-247C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257828 | |||||||
| chr16:27257829 | T | C | 4 | a0001c0003t0002g0165 a0001c0003t0002g0166 a0001c0009t0002g0167 others(1): Show |
4 | HG02071.hp1 NA18948.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-248A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257829 | |||||||
| chr16:27257914 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-11-333A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257914 | |||||||
| chr16:27257920 | G | A | 12 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-339C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27257920 | |||||||
| chr16:27258653 | T | A | 1 | a0001c0003t0002g0206 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-11-1072A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27258653 | |||||||
| chr16:27258696 | G | A | 12 | a0002c0002t0001g0012 a0002c0002t0001g0035 a0002c0002t0001g0039 others(9): Show |
13 | HG02027.hp1 HG02040.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11-1115C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27258696 | |||||||
| chr16:27258879 | T | C | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11-1298A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27258879 | |||||||
| chr16:27259016 | G | C | 39 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(36): Show |
40 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.-11-1435C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259016 | |||||||
| chr16:27259286 | C | T | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11-1705G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259286 | |||||||
| chr16:27259526 | T | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-1945A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259526 | |||||||
| chr16:27259584 | T | G | 5 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-2003A>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259584 | |||||||
| chr16:27259587 | G | C | 1 | a0001c0003t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-11-2006C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259587 | |||||||
| chr16:27259662 | T | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-2081A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259662 | |||||||
| chr16:27259751 | A | G | 149 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(146): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-11-2170T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259751 | |||||||
| chr16:27259772 | G | T | 1 | a0001c0003t0002g0227 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-11-2191C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259772 | |||||||
| chr16:27259862 | G | A | 5 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(2): Show |
5 | HG01891.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-2281C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259862 | |||||||
| chr16:27259896 | C | G | 149 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(146): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-11-2315G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259896 | |||||||
| chr16:27259924 | G | A | 1 | a0001c0003t0002g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-11-2343C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259924 | |||||||
| chr16:27259926 | G | A | 2 | a0002c0002t0001g0081 a0002c0002t0001g0082 |
2 | NA18940.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-11-2345C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27259926 | |||||||
| chr16:27260042 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-11-2461T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260042 | |||||||
| chr16:27260049 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-11-2468G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260049 | |||||||
| chr16:27260354 | C | A | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-2773G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260354 | |||||||
| chr16:27260375 | G | A | 1 | a0003c0004t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11-2794C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260375 | |||||||
| chr16:27260545 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-11-2964T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260545 | |||||||
| chr16:27260610 | T | C | 33 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(30): Show |
34 | HG01884.hp2 HG01891.hp2 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11-3029A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260610 | |||||||
| chr16:27260824 | A | G | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-3243T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260824 | |||||||
| chr16:27260832 | C | A | 1 | a0002c0002t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-3251G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260832 | |||||||
| chr16:27260858 | C | CA | 9 | a0001c0001t0001g0007 a0001c0001t0001g0258 a0001c0001t0001g0259 others(6): Show |
11 | HG01175.hp2 HG02056.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-3278dupT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260858 | |||||||
| chr16:27260858 | C | CAAAAAAA others(2): Show |
81 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(78): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.-11-3286_-11-3278d others(11): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260858 | |||||||
| chr16:27260858 | C | CAAAAAAA others(3): Show |
26 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0172 others(23): Show |
27 | HG00673.hp1 HG01891.hp2 HG02027.hp2 others(24): Show |
intron_variant | MODIFIER | c.-11-3287_-11-3278d others(12): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260858 | |||||||
| chr16:27260858 | C | CAAAAAAA others(4): Show |
10 | a0003c0004t0001g0128 a0003c0004t0001g0130 a0003c0004t0001g0131 others(7): Show |
10 | HG01891.hp1 HG02723.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-3288_-11-3278d others(13): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260858 | |||||||
| chr16:27260858 | C | CAAAAAAA others(5): Show |
4 | a0003c0004t0001g0129 a0003c0004t0001g0139 a0003c0004t0001g0140 others(1): Show |
4 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-3289_-11-3278d others(14): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260858 | |||||||
| chr16:27260858 | C | CAAAAAAA others(7): Show |
1 | a0003c0004t0002g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-11-3291_-11-3278d others(16): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260858 | |||||||
| chr16:27260858 | CAA | C | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11-3279_-11-3278d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260858 | |||||||
| chr16:27260973 | C | T | 3 | a0003c0004t0001g0283 a0003c0004t0001g0284 a0003c0004t0001g0285 |
3 | HG00741.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-11-3392G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27260973 | |||||||
| chr16:27261142 | G | A | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-3561C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261142 | |||||||
| chr16:27261151 | A | C | 1 | a0002c0002t0001g0102 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-11-3570T>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261151 | |||||||
| chr16:27261166 | C | CA | 118 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(115): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-11-3586dupT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261166 | |||||||
| chr16:27261166 | C | CAA | 9 | a0001c0003t0002g0217 a0001c0003t0002g0218 a0001c0003t0002g0219 others(6): Show |
9 | HG01081.hp2 HG01106.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11-3587_-11-3586d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261166 | |||||||
| chr16:27261166 | CA | C | 80 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0071 others(77): Show |
99 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.-11-3586delT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261166 | |||||||
| chr16:27261172 | AAAAAAAA others(33): Show |
A | 1 | a0002c0002t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-11-3631_-11-3592d others(42): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261172 | |||||||
| chr16:27261428 | T | C | 2 | a0001c0003t0002g0179 a0001c0003t0002g0224 |
2 | NA18962.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-11-3847A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261428 | |||||||
| chr16:27261432 | C | G | 134 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(131): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-11-3851G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261432 | |||||||
| chr16:27261516 | G | A | 1 | a0003c0004t0001g0283 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-11-3935C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27261516 | |||||||
| chr16:27262105 | G | A | 7 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-4524C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27262105 | |||||||
| chr16:27262115 | G | A | 1 | a0001c0003t0002g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-11-4534C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27262115 | |||||||
| chr16:27262243 | CA | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0071 others(89): Show |
111 | HG00438.hp1 HG00735.hp2 HG01070.hp1 others(108): Show |
intron_variant | MODIFIER | c.-11-4663delT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27262243 | |||||||
| chr16:27262243 | CAA | C | 135 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(132): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-11-4664_-11-4663d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27262243 | |||||||
| chr16:27262403 | C | CCAATGGA others(40): Show |
1 | a0002c0002t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-11-4823_-11-4822i others(49): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27262403 | |||||||
| chr16:27262680 | C | G | 2 | a0002c0002t0001g0039 a0002c0002t0001g0040 |
2 | NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-11-5099G>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27262680 | |||||||
| chr16:27262765 | C | T | 1 | a0003c0004t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-11-5184G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27262765 | |||||||
| chr16:27263190 | C | A | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-12+5516G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27263190 | |||||||
| chr16:27263306 | A | G | 1 | a0003c0004t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12+5400T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27263306 | |||||||
| chr16:27263589 | C | T | 149 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(146): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-12+5117G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27263589 | |||||||
| chr16:27263675 | C | T | 1 | a0004c0005t0002g0182 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-12+5031G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27263675 | |||||||
| chr16:27263722 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-12+4984A>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27263722 | |||||||
| chr16:27263885 | C | A | 5 | a0001c0001t0001g0181 a0001c0001t0001g0229 a0001c0003t0002g0227 others(2): Show |
5 | HG02080.hp1 NA18747.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+4821G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27263885 | |||||||
| chr16:27263927 | G | A | 51 | a0001c0001t0001g0101 a0001c0001t0001g0148 a0001c0001t0001g0154 others(48): Show |
53 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.-12+4779C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27263927 | |||||||
| chr16:27264065 | T | G | 1 | a0001c0001t0001g0261 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12+4641A>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264065 | |||||||
| chr16:27264091 | C | T | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12+4615G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264091 | |||||||
| chr16:27264132 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-12+4574G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264132 | |||||||
| chr16:27264297 | C | T | 4 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+4409G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264297 | |||||||
| chr16:27264419 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0239 |
4 | HG00280.hp1 HG01109.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+4287G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264419 | |||||||
| chr16:27264454 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-12+4252T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264454 | |||||||
| chr16:27264494 | G | A | 3 | a0003c0004t0001g0283 a0003c0004t0001g0284 a0003c0004t0001g0285 |
3 | HG00741.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-12+4212C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264494 | |||||||
| chr16:27264494 | G | C | 15 | a0003c0004t0001g0128 a0003c0004t0001g0129 a0003c0004t0001g0130 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-12+4212C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264494 | |||||||
| chr16:27264518 | T | C | 1 | a0002c0002t0001g0099 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-12+4188A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264518 | |||||||
| chr16:27264816 | A | G | 118 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(115): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-12+3890T>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264816 | |||||||
| chr16:27264974 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG02970.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-12+3732G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264974 | |||||||
| chr16:27264987 | C | T | 1 | a0003c0004t0002g0286 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+3719G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27264987 | |||||||
| chr16:27265050 | T | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+3656A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265050 | |||||||
| chr16:27265142 | G | A | 149 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(146): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-12+3564C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265142 | |||||||
| chr16:27265161 | C | CT | 117 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(114): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-12+3544dupA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265161 | |||||||
| chr16:27265161 | C | CTT | 14 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0181 others(11): Show |
14 | HG01891.hp2 HG02080.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12+3543_-12+3544d others(4): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265161 | |||||||
| chr16:27265161 | C | CTTTTT | 24 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(21): Show |
27 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-12+3540_-12+3544d others(7): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265161 | |||||||
| chr16:27265161 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-12+3521_-12+3544d others(26): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265161 | |||||||
| chr16:27265161 | CT | C | 8 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0002g0023 others(5): Show |
9 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+3544delA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265161 | |||||||
| chr16:27265229 | A | T | 1 | a0002c0002t0001g0033 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-12+3477T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265229 | |||||||
| chr16:27265271 | G | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG02970.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-12+3435C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265271 | |||||||
| chr16:27265289 | C | A | 1 | a0003c0004t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-12+3417G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265289 | |||||||
| chr16:27265290 | C | A | 1 | a0003c0004t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-12+3416G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265290 | |||||||
| chr16:27265330 | G | A | 125 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(122): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-12+3376C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265330 | |||||||
| chr16:27265379 | G | A | 1 | a0002c0002t0001g0100 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12+3327C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265379 | |||||||
| chr16:27265406 | G | A | 24 | a0003c0004t0001g0142 a0003c0004t0001g0143 a0003c0004t0001g0144 others(21): Show |
25 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-12+3300C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265406 | |||||||
| chr16:27265598 | C | T | 1 | a0003c0004t0001g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12+3108G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265598 | |||||||
| chr16:27265735 | G | A | 71 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0190 others(68): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-12+2971C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27265735 | |||||||
| chr16:27266104 | G | A | 103 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(100): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-12+2602C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27266104 | |||||||
| chr16:27266407 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+2299C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27266407 | |||||||
| chr16:27266571 | C | A | 1 | a0001c0003t0002g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-12+2135G>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27266571 | |||||||
| chr16:27266573 | C | T | 7 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+2133G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27266573 | |||||||
| chr16:27266622 | G | GA | 141 | a0001c0001t0001g0101 a0001c0001t0001g0146 a0001c0001t0001g0148 others(138): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.-12+2083dupT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27266622 | |||||||
| chr16:27266668 | T | C | 1 | a0001c0003t0002g0237 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-12+2038A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27266668 | |||||||
| chr16:27266959 | T | C | 1 | a0002c0002t0001g0102 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-12+1747A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27266959 | |||||||
| chr16:27267099 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12+1607A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267099 | |||||||
| chr16:27267123 | G | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+1583C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267123 | |||||||
| chr16:27267200 | TTTA | T | 7 | a0003c0004t0002g0023 a0003c0004t0002g0269 a0003c0004t0002g0270 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+1503_-12+1505d others(5): Show |
NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267200 | |||||||
| chr16:27267248 | T | A | 1 | a0001c0003t0002g0238 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-12+1458A>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267248 | |||||||
| chr16:27267306 | G | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(23): Show |
29 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-12+1400C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267306 | |||||||
| chr16:27267315 | C | T | 1 | a0001c0003t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-12+1391G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267315 | |||||||
| chr16:27267625 | GA | G | 25 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
26 | HG00735.hp2 HG00741.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-12+1080delT | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267625 | |||||||
| chr16:27267728 | A | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+978T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267728 | |||||||
| chr16:27267734 | A | AT | 85 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0058 others(82): Show |
105 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.-12+971dupA | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267734 | |||||||
| chr16:27267801 | TC | T | 3 | a0001c0001t0001g0007 a0002c0002t0001g0031 a0002c0002t0001g0032 |
4 | HG02145.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+904delG | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27267801 | |||||||
| chr16:27268023 | G | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+683C>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268023 | |||||||
| chr16:27268026 | G | A | 20 | a0003c0004t0001g0273 a0003c0004t0001g0274 a0003c0004t0001g0275 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+680C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268026 | |||||||
| chr16:27268109 | G | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+597C>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268109 | |||||||
| chr16:27268141 | A | T | 1 | a0002c0002t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-12+565T>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268141 | |||||||
| chr16:27268176 | G | A | 4 | a0002c0002t0001g0022 a0002c0002t0001g0264 a0002c0002t0001g0265 others(1): Show |
5 | HG02257.hp2 HG02300.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+530C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268176 | |||||||
| chr16:27268205 | C | T | 20 | a0003c0004t0001g0273 a0003c0004t0001g0274 a0003c0004t0001g0275 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+501G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268205 | |||||||
| chr16:27268328 | T | G | 1 | a0002c0002t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-12+378A>C | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268328 | |||||||
| chr16:27268464 | G | A | 1 | a0002c0002t0002g0268 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-12+242C>T | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268464 | |||||||
| chr16:27268497 | T | C | 20 | a0003c0004t0001g0273 a0003c0004t0001g0274 a0003c0004t0001g0275 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+209A>G | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268497 | |||||||
| chr16:27268664 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-12+42G>A | NSMCE1 | ENSG00000169189.17 | transcript | ENST00000361439.9 | protein_coding | 1/7 | chr16 | 27268664 |