Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81831 |
| ensemblid | ENSG00000171208.10 |
| hgncid | 14644 |
| symbol | NETO2 |
| name | neuropilin and tolloid like 2 |
| refseq_nuc | NM_018092.5 |
| refseq_prot | NP_060562.3 |
| ensembl_nuc | ENST00000562435.6 |
| ensembl_prot | ENSP00000455169.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 47077703 |
| end | 47143945 |
| strand | - |
| ver | v1.2 |
| region | chr16:47077703-47143945 |
| region5000 | chr16:47072703-47148945 |
| regionname0 | NETO2_chr16_47077703_47143945 |
| regionname5000 | NETO2_chr16_47072703_47148945 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 525 | 160 | 75 | 30 | 27 | 6 | 20 | 16 | NETO2_chr16_47072703_47148945 | NETO2 | MALER others(520): Show |
chr16 | 47072703 | 47148945 |
| a0002 | 0/0 | 525 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | MALER others(520): Show |
chr16 | 47072703 | 47148945 |
| a0003 | 0/0 | 525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | MALER others(520): Show |
chr16 | 47072703 | 47148945 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1575 | 160 | 75 | 30 | 27 | 6 | 20 | NETO2_chr16_47072703_47148945 | NETO2 | ATGGC others(1570): Show |
chr16 | 47072703 | 47148945 | ||
| a0002c0002 | 0/0 | 1575 | 7 | 7 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ATGGC others(1570): Show |
chr16 | 47072703 | 47148945 | ||
| a0003c0003 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ATGGC others(1570): Show |
chr16 | 47072703 | 47148945 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7429 | 87 | 26 | 19 | 25 | 5 | 12 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0002 | 0/0 | 7434 | 22 | 18 | 4 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0003 | 0/0 | 7434 | 8 | 8 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0004 | 0/0 | 7434 | 5 | 5 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0005 | 0/0 | 7434 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0007 | 0/0 | 7434 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0008 | 0/1 | 7429 | 3 | 0 | 2 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0009 | 0/0 | 7429 | 3 | 0 | 0 | 0 | 0 | 3 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0010 | 0/0 | 7429 | 3 | 0 | 0 | 0 | 0 | 3 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0012 | 0/0 | 7425 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7420): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0013 | 0/0 | 7429 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0014 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0015 | 0/0 | 7429 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0016 | 0/0 | 7429 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0017 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0018 | 0/0 | 7429 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0019 | 0/0 | 7429 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0020 | 0/0 | 7429 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0021 | 1/0 | 7429 | 1 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0022 | 0/0 | 7429 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0023 | 0/0 | 7429 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0024 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0025 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0026 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0027 | 0/0 | 7429 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0028 | 0/0 | 7429 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0001c0001t0029 | 0/0 | 7429 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| a0002c0002t0006 | 0/0 | 7434 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0002c0002t0011 | 0/0 | 7434 | 3 | 3 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7429): Show |
chr16 | 47072703 | 47148945 |
| a0003c0003t0001 | 0/0 | 7429 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | ACTTC others(7424): Show |
chr16 | 47072703 | 47148945 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0003 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0008g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0009g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0009g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0015g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0016g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0018g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0019g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0020g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0021g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0022g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0023g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0024g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0025g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0026g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0027g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0028g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0001c0001t0029g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0002c0002t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0002c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0002c0002t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0002c0002t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0002c0002t0011g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0002c0002t0011g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00280 | hp2 | a0001 | c0001 | t0029 | g0143 | EUR | FIN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0039 | EAS | CHS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0103 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01074 | hp1 | a0001 | c0001 | t0025 | g0138 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01081 | hp2 | a0001 | c0001 | t0020 | g0099 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01099 | hp1 | a0001 | c0001 | t0018 | g0048 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01358 | hp1 | a0001 | c0001 | t0008 | g0071 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01433 | hp2 | a0001 | c0001 | t0023 | g0079 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01496 | hp2 | a0001 | c0001 | t0024 | g0135 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01884 | hp2 | a0002 | c0002 | t0011 | g0005 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG01891 | hp2 | a0001 | c0001 | t0026 | g0131 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02055 | hp1 | a0002 | c0002 | t0006 | g0018 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02132 | hp1 | a0001 | c0001 | t0019 | g0060 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0016 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02615 | hp1 | a0001 | c0001 | t0027 | g0141 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02683 | hp1 | a0001 | c0001 | t0028 | g0142 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0144 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02735 | hp1 | a0001 | c0001 | t0015 | g0015 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02735 | hp2 | a0001 | c0001 | t0010 | g0056 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02886 | hp2 | a0001 | c0001 | t0022 | g0066 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0033 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0107 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03041 | hp2 | a0002 | c0002 | t0011 | g0022 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0098 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03654 | hp2 | a0001 | c0001 | t0009 | g0007 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0044 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0110 | SAS | BEB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0007 | SAS | BEB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG04204 | hp1 | a0001 | c0001 | t0010 | g0050 | SAS | STU | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0083 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | LWK | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | LWK | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | LWK | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19060 | hp2 | a0001 | c0001 | t0016 | g0055 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA20129 | hp1 | a0002 | c0002 | t0011 | g0005 | AFR | ASW | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02109 | hp1 | a0002 | c0002 | t0006 | g0021 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02486 | hp2 | a0001 | c0001 | t0013 | g0035 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG02559 | hp2 | a0002 | c0002 | t0006 | g0019 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0145 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA20300 | hp1 | a0002 | c0002 | t0006 | g0020 | AFR | USA | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | USA | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0070 | REF | REF | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0021 | g0069 | REF | REF | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:47083433 | A | T | 1 | a0002 | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
missense_variant | MODERATE | c.1366T>A | p.Ser456Thr | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1699/7429 | 1366/1578 | 456/525 | chr16 | 47083433 | |||
| chr16:47083489 | T | A | 1 | a0003 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1310A>T | p.Asp437Val | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1643/7429 | 1310/1578 | 437/525 | chr16 | 47083489 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:47077819 | CTTCT | C | 1 | a0001c0001t0012 | 2 | HG02572.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5398_*5401delAGAA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 5398 | chr16 | 47077819 | ||||||
| chr16:47078669 | A | C | 1 | a0001c0001t0009 | 3 | HG03654.hp2 HG03704.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4552T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 4552 | chr16 | 47078669 | ||||||
| chr16:47078784 | C | A | 1 | a0001c0001t0003 | 8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4437G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 4437 | chr16 | 47078784 | ||||||
| chr16:47079168 | C | G | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4053G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 4053 | chr16 | 47079168 | ||||||
| chr16:47079318 | A | G | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*3903T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 3903 | chr16 | 47079318 | ||||||
| chr16:47079636 | G | A | 1 | a0002c0002t0006 | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3585C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 3585 | chr16 | 47079636 | ||||||
| chr16:47079875 | C | T | 1 | a0001c0001t0020 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3346G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 3346 | chr16 | 47079875 | ||||||
| chr16:47080040 | G | C | 1 | a0001c0001t0026 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3181C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 3181 | chr16 | 47080040 | ||||||
| chr16:47080290 | G | T | 1 | a0001c0001t0019 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2931C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2931 | chr16 | 47080290 | ||||||
| chr16:47080303 | T | C | 1 | a0001c0001t0022 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2918A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2918 | chr16 | 47080303 | ||||||
| chr16:47080345 | T | G | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2876A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2876 | chr16 | 47080345 | ||||||
| chr16:47080431 | T | C | 2 | a0002c0002t0006 a0002c0002t0011 |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2790A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2790 | chr16 | 47080431 | ||||||
| chr16:47080655 | T | C | 1 | a0001c0001t0012 | 2 | HG02572.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2566A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2566 | chr16 | 47080655 | ||||||
| chr16:47080882 | T | G | 1 | a0001c0001t0023 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2339A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2339 | chr16 | 47080882 | ||||||
| chr16:47080976 | A | G | 1 | a0001c0001t0018 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2245T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2245 | chr16 | 47080976 | ||||||
| chr16:47080999 | C | CTTCTG | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(9): Show |
56 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2221_*2222insCAGA others(1): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2221 | chr16 | 47080999 | ||||||
| chr16:47081156 | A | T | 1 | a0001c0001t0016 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065T>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2065 | chr16 | 47081156 | ||||||
| chr16:47081363 | A | C | 1 | a0001c0001t0025 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1858T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1858 | chr16 | 47081363 | ||||||
| chr16:47081865 | T | C | 2 | a0002c0002t0006 a0002c0002t0011 |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1356A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1356 | chr16 | 47081865 | ||||||
| chr16:47082155 | G | A | 1 | a0001c0001t0010 | 3 | HG02735.hp2 HG03831.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1066C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1066 | chr16 | 47082155 | ||||||
| chr16:47082273 | T | G | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(7): Show |
51 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*948A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 948 | chr16 | 47082273 | ||||||
| chr16:47082304 | T | C | 1 | a0001c0001t0007 | 4 | HG02280.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*917A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 917 | chr16 | 47082304 | ||||||
| chr16:47082553 | C | T | 1 | a0001c0001t0024 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*668G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 668 | chr16 | 47082553 | ||||||
| chr16:47082768 | T | C | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0014 others(3): Show |
35 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*453A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 453 | chr16 | 47082768 | ||||||
| chr16:47082951 | C | T | 1 | a0001c0001t0008 | 2 | HG00741.hp2 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*270G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 270 | chr16 | 47082951 | ||||||
| chr16:47083021 | G | C | 1 | a0001c0001t0013 | 2 | HG02486.hp2 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*200C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 200 | chr16 | 47083021 | ||||||
| chr16:47143668 | G | C | 1 | a0001c0001t0027 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | 56 | chr16 | 47143668 | ||||||
| chr16:47143677 | G | A | 1 | a0001c0001t0028 | 1 | HG02683.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-65C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | chr16 | 47143677 | |||||||
| chr16:47143753 | G | C | 1 | a0001c0001t0029 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | 141 | chr16 | 47143753 | ||||||
| chr16:47143780 | G | A | 1 | a0001c0001t0014 | 2 | HG02723.hp1 HG03471.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-168C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | chr16 | 47143780 | |||||||
| chr16:47143908 | A | G | 1 | a0001c0001t0015 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-296T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | 296 | chr16 | 47143908 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:47083897 | T | C | 32 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(29): Show |
35 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.998-96A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47083897 | |||||||
| chr16:47084289 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.998-488C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084289 | |||||||
| chr16:47084405 | CAGG | C | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.998-607_998-605del others(3): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084405 | |||||||
| chr16:47084480 | C | T | 1 | a0002c0002t0011g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.998-679G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084480 | |||||||
| chr16:47084526 | C | G | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.998-725G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084526 | |||||||
| chr16:47084584 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.998-783A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084584 | |||||||
| chr16:47084990 | T | C | 1 | a0001c0001t0014g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.998-1189A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084990 | |||||||
| chr16:47085016 | A | G | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.997+1210T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085016 | |||||||
| chr16:47085238 | A | G | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.997+988T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085238 | |||||||
| chr16:47085309 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.997+917C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085309 | |||||||
| chr16:47085385 | T | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.997+841A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085385 | |||||||
| chr16:47085528 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.997+698G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085528 | |||||||
| chr16:47085626 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.997+600G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085626 | |||||||
| chr16:47085875 | G | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.997+351C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085875 | |||||||
| chr16:47085979 | AC | A | 2 | a0001c0001t0013g0016 a0001c0001t0013g0035 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.997+246delG | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085979 | |||||||
| chr16:47086014 | G | A | 1 | a0001c0001t0017g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.997+212C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47086014 | |||||||
| chr16:47086037 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.997+189G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47086037 | |||||||
| chr16:47086779 | T | C | 7 | a0001c0001t0003g0012 a0001c0001t0003g0092 a0001c0001t0003g0093 others(4): Show |
8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.884-440A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47086779 | |||||||
| chr16:47086906 | A | G | 1 | a0001c0001t0018g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.884-567T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47086906 | |||||||
| chr16:47086973 | T | G | 2 | a0001c0001t0010g0050 a0001c0001t0010g0056 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.884-634A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47086973 | |||||||
| chr16:47087032 | ATT | A | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-695_884-694del others(2): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087032 | |||||||
| chr16:47087078 | G | C | 1 | a0001c0001t0007g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.884-739C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087078 | |||||||
| chr16:47087121 | TG | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0059 others(5): Show |
9 | HG00438.hp2 HG00642.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.884-783delC | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087121 | |||||||
| chr16:47087259 | C | T | 37 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(34): Show |
41 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.884-920G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087259 | |||||||
| chr16:47087831 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.884-1492T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087831 | |||||||
| chr16:47088349 | G | A | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-2010C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47088349 | |||||||
| chr16:47088436 | T | G | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.884-2097A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47088436 | |||||||
| chr16:47088453 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-2114C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47088453 | |||||||
| chr16:47088808 | G | T | 46 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(43): Show |
51 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.884-2469C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47088808 | |||||||
| chr16:47089813 | C | T | 43 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(40): Show |
48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.884-3474G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47089813 | |||||||
| chr16:47089943 | T | A | 1 | a0001c0001t0029g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.884-3604A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47089943 | |||||||
| chr16:47090352 | TCACTGGT others(4): Show |
T | 1 | a0001c0001t0005g0081 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.884-4024_884-4014d others(13): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47090352 | |||||||
| chr16:47090443 | T | C | 43 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(40): Show |
48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.884-4104A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47090443 | |||||||
| chr16:47090729 | C | A | 3 | a0001c0001t0010g0050 a0001c0001t0010g0056 a0001c0001t0010g0110 |
3 | HG02735.hp2 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.884-4390G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47090729 | |||||||
| chr16:47090998 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.884-4659A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47090998 | |||||||
| chr16:47091379 | T | C | 2 | a0001c0001t0012g0030 a0001c0001t0012g0033 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.884-5040A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47091379 | |||||||
| chr16:47091405 | G | T | 1 | a0001c0001t0002g0121 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.884-5066C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47091405 | |||||||
| chr16:47091463 | T | C | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 |
3 | HG02257.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.884-5124A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47091463 | |||||||
| chr16:47091828 | G | A | 44 | a0001c0001t0001g0057 a0001c0001t0002g0004 a0001c0001t0002g0117 others(41): Show |
49 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.884-5489C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47091828 | |||||||
| chr16:47092025 | G | GT | 11 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0051 others(8): Show |
11 | HG00642.hp1 HG01169.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.884-5687dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47092025 | |||||||
| chr16:47092025 | G | T | 1 | a0001c0001t0005g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.884-5686C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47092025 | |||||||
| chr16:47092502 | C | T | 1 | a0001c0001t0012g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.884-6163G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47092502 | |||||||
| chr16:47092542 | G | C | 34 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(31): Show |
38 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.884-6203C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47092542 | |||||||
| chr16:47093068 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-6729G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093068 | |||||||
| chr16:47093466 | A | G | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-7127T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093466 | |||||||
| chr16:47093622 | T | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-7283A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093622 | |||||||
| chr16:47093667 | T | C | 1 | a0001c0001t0023g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.884-7328A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093667 | |||||||
| chr16:47093842 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.884-7503G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093842 | |||||||
| chr16:47093896 | A | G | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-7557T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093896 | |||||||
| chr16:47094041 | A | G | 1 | a0003c0003t0001g0039 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.884-7702T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094041 | |||||||
| chr16:47094193 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.884-7854G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094193 | |||||||
| chr16:47094247 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.884-7908G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094247 | |||||||
| chr16:47094263 | A | AT | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.884-7925dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094263 | |||||||
| chr16:47094263 | A | ATT | 5 | a0001c0001t0002g0134 a0001c0001t0007g0106 a0001c0001t0007g0107 others(2): Show |
5 | HG02280.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-7926_884-7925d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094263 | |||||||
| chr16:47094263 | A | ATTT | 7 | a0001c0001t0002g0121 a0001c0001t0004g0023 a0001c0001t0004g0024 others(4): Show |
7 | HG01361.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-7927_884-7925d others(5): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094263 | |||||||
| chr16:47094403 | T | TTTTA | 37 | a0001c0001t0002g0004 a0001c0001t0002g0118 a0001c0001t0002g0119 others(34): Show |
41 | HG00735.hp2 HG01109.hp2 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.884-8068_884-8065d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094403 | |||||||
| chr16:47094403 | T | TTTTATTT others(1): Show |
4 | a0001c0001t0002g0117 a0001c0001t0002g0121 a0001c0001t0002g0137 others(1): Show |
4 | HG01074.hp1 HG01361.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-8072_884-8065d others(10): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094403 | |||||||
| chr16:47094408 | TTTATTTA others(1): Show |
T | 3 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0021 |
3 | HG02055.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.884-8077_884-8070d others(10): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094408 | |||||||
| chr16:47094416 | C | CTTAT | 2 | a0001c0001t0001g0029 a0001c0001t0001g0057 |
2 | HG00642.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.884-8081_884-8078d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094416 | |||||||
| chr16:47094416 | C | T | 43 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(40): Show |
48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.884-8077G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094416 | |||||||
| chr16:47094437 | T | C | 2 | a0001c0001t0012g0030 a0001c0001t0012g0033 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.884-8098A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094437 | |||||||
| chr16:47094526 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0112 |
2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.884-8187G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094526 | |||||||
| chr16:47094672 | C | T | 1 | a0001c0001t0009g0007 | 2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.884-8333G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094672 | |||||||
| chr16:47095266 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.884-8927T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47095266 | |||||||
| chr16:47095278 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.884-8939T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47095278 | |||||||
| chr16:47095645 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.884-9306C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47095645 | |||||||
| chr16:47096150 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.884-9811T>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096150 | |||||||
| chr16:47096154 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.884-9815G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096154 | |||||||
| chr16:47096271 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.884-9932G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096271 | |||||||
| chr16:47096322 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.884-9983A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096322 | |||||||
| chr16:47096881 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.884-10542C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096881 | |||||||
| chr16:47096912 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
19 | HG00735.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.884-10573G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096912 | |||||||
| chr16:47097140 | C | A | 2 | a0001c0001t0008g0071 a0001c0001t0008g0103 |
2 | HG00741.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.884-10801G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097140 | |||||||
| chr16:47097141 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-10802G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097141 | |||||||
| chr16:47097365 | G | C | 1 | a0001c0001t0004g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.884-11026C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097365 | |||||||
| chr16:47097535 | A | G | 1 | a0001c0001t0017g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.884-11196T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097535 | |||||||
| chr16:47097549 | T | C | 1 | a0001c0001t0004g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.884-11210A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097549 | |||||||
| chr16:47097864 | A | G | 5 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-11525T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097864 | |||||||
| chr16:47097928 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883+11555T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097928 | |||||||
| chr16:47098318 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.883+11165A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098318 | |||||||
| chr16:47098371 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0027g0141 |
3 | HG01884.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883+11112G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098371 | |||||||
| chr16:47098888 | T | G | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+10595A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098888 | |||||||
| chr16:47098951 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.883+10532C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098951 | |||||||
| chr16:47098984 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.883+10499G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098984 | |||||||
| chr16:47099328 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.883+10155C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47099328 | |||||||
| chr16:47099450 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.883+10033G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47099450 | |||||||
| chr16:47099581 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.883+9902T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47099581 | |||||||
| chr16:47101022 | C | A | 1 | a0001c0001t0004g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.883+8461G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47101022 | |||||||
| chr16:47101039 | G | C | 31 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(28): Show |
35 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.883+8444C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47101039 | |||||||
| chr16:47101622 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.883+7861T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47101622 | |||||||
| chr16:47102034 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.883+7449A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102034 | |||||||
| chr16:47102253 | C | T | 1 | a0001c0001t0005g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.883+7230G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102253 | |||||||
| chr16:47102607 | A | AC | 26 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(23): Show |
29 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.883+6875dupG | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102607 | |||||||
| chr16:47102607 | A | C | 16 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0004g0014 others(13): Show |
18 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.883+6876T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102607 | |||||||
| chr16:47102611 | C | A | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.883+6872G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102611 | |||||||
| chr16:47102756 | C | T | 29 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(26): Show |
32 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.883+6727G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102756 | |||||||
| chr16:47102838 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.883+6645A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102838 | |||||||
| chr16:47102844 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.883+6639C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102844 | |||||||
| chr16:47102883 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.883+6600C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102883 | |||||||
| chr16:47103082 | C | T | 1 | a0001c0001t0012g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.883+6401G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47103082 | |||||||
| chr16:47103929 | C | T | 1 | a0001c0001t0017g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.883+5554G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47103929 | |||||||
| chr16:47104737 | T | C | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.883+4746A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47104737 | |||||||
| chr16:47105025 | T | TTTTC | 46 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(43): Show |
51 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.883+4457_883+4458i others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47105025 | |||||||
| chr16:47106069 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0115 |
2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.883+3414A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106069 | |||||||
| chr16:47106109 | ACATGGAT others(17): Show |
A | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+3350_883+3373d others(26): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106109 | |||||||
| chr16:47106287 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.883+3196T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106287 | |||||||
| chr16:47106729 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.883+2754A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106729 | |||||||
| chr16:47106927 | G | A | 7 | a0001c0001t0003g0012 a0001c0001t0003g0092 a0001c0001t0003g0093 others(4): Show |
8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.883+2556C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106927 | |||||||
| chr16:47107303 | C | G | 43 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(40): Show |
48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.883+2180G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47107303 | |||||||
| chr16:47107589 | C | T | 1 | a0001c0001t0004g0014 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.883+1894G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47107589 | |||||||
| chr16:47107621 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.883+1862A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47107621 | |||||||
| chr16:47108375 | T | A | 1 | a0001c0001t0004g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.883+1108A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108375 | |||||||
| chr16:47108560 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0005g0077 |
2 | HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.883+923A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108560 | |||||||
| chr16:47108597 | G | T | 3 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 |
3 | HG01891.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.883+886C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108597 | |||||||
| chr16:47108792 | G | C | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 |
3 | HG02257.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.883+691C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108792 | |||||||
| chr16:47109381 | AAC | A | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+100_883+101del others(2): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47109381 | |||||||
| chr16:47109470 | ATTAT | A | 2 | a0001c0001t0001g0017 a0001c0001t0013g0016 |
2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.883+9_883+12delATA others(1): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47109470 | |||||||
| chr16:47109762 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.655-51T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47109762 | |||||||
| chr16:47110006 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0059 others(5): Show |
9 | HG00438.hp2 HG00642.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.655-295A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47110006 | |||||||
| chr16:47110385 | A | G | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-674T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47110385 | |||||||
| chr16:47110391 | C | G | 1 | a0001c0001t0028g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.655-680G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47110391 | |||||||
| chr16:47110637 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0023g0079 |
3 | HG00642.hp2 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.655-926A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47110637 | |||||||
| chr16:47111538 | T | G | 1 | a0001c0001t0001g0028 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655-1827A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111538 | |||||||
| chr16:47111586 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.655-1875G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111586 | |||||||
| chr16:47111597 | C | A | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.655-1886G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111597 | |||||||
| chr16:47111708 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655-1997C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111708 | |||||||
| chr16:47111771 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.655-2060C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111771 | |||||||
| chr16:47111822 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.655-2111C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111822 | |||||||
| chr16:47112381 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.655-2670G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112381 | |||||||
| chr16:47112428 | G | A | 1 | a0001c0001t0029g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.655-2717C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112428 | |||||||
| chr16:47112526 | T | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-2815A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112526 | |||||||
| chr16:47112807 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
19 | HG00735.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.655-3096T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112807 | |||||||
| chr16:47112836 | G | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-3125C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112836 | |||||||
| chr16:47112869 | ATT | A | 2 | a0001c0001t0001g0013 a0001c0001t0027g0141 |
3 | HG01884.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.655-3160_655-3159d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112869 | |||||||
| chr16:47112869 | ATTGT | A | 2 | a0001c0001t0012g0030 a0001c0001t0012g0033 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.655-3162_655-3159d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112869 | |||||||
| chr16:47112976 | T | C | 1 | a0001c0001t0020g0099 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.655-3265A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112976 | |||||||
| chr16:47113212 | T | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-3501A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113212 | |||||||
| chr16:47113216 | A | C | 1 | a0001c0001t0007g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.655-3505T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113216 | |||||||
| chr16:47113386 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-3675G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113386 | |||||||
| chr16:47113560 | C | T | 1 | a0001c0001t0022g0066 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.655-3849G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113560 | |||||||
| chr16:47113585 | C | CT | 14 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0080 others(11): Show |
15 | HG01255.hp1 HG01884.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.655-3875dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113585 | |||||||
| chr16:47113585 | CT | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0116 a0001c0001t0002g0132 others(1): Show |
5 | HG00280.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-3875delA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113585 | |||||||
| chr16:47113753 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.655-4042C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113753 | |||||||
| chr16:47114085 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655-4374G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114085 | |||||||
| chr16:47114207 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0139 |
3 | HG03098.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.655-4496A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114207 | |||||||
| chr16:47114365 | C | CT | 20 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0002g0132 others(17): Show |
22 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.655-4655dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114365 | |||||||
| chr16:47114365 | C | CTT | 25 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(22): Show |
28 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.655-4656_655-4655d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114365 | |||||||
| chr16:47114379 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.655-4668A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114379 | |||||||
| chr16:47114439 | C | CT | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(9): Show |
12 | HG00438.hp1 HG00642.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.655-4729dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114439 | |||||||
| chr16:47114439 | CT | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0074 others(33): Show |
43 | HG00280.hp1 HG01074.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.655-4729delA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114439 | |||||||
| chr16:47114439 | CTT | C | 10 | a0001c0001t0002g0134 a0001c0001t0003g0092 a0001c0001t0004g0014 others(7): Show |
11 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.655-4730_655-4729d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114439 | |||||||
| chr16:47114448 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.655-4737A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114448 | |||||||
| chr16:47114532 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.655-4821C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114532 | |||||||
| chr16:47114600 | G | A | 6 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0113 others(3): Show |
6 | HG00438.hp2 HG00642.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-4889C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114600 | |||||||
| chr16:47114851 | A | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-5140T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114851 | |||||||
| chr16:47114946 | C | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-5235G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114946 | |||||||
| chr16:47115236 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
140 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.655-5525T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115236 | |||||||
| chr16:47115590 | C | T | 43 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(40): Show |
48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.655-5879G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115590 | |||||||
| chr16:47115697 | T | TTATATAT others(25): Show |
1 | a0001c0001t0002g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.655-5987_655-5986i others(34): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115697 | |||||||
| chr16:47115700 | T | TATATATA others(7): Show |
4 | a0001c0001t0007g0106 a0001c0001t0007g0107 a0001c0001t0007g0108 others(1): Show |
4 | HG02280.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-6003_655-5990d others(16): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115700 | |||||||
| chr16:47115701 | A | ATATATAT others(27): Show |
1 | a0001c0001t0010g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.655-6024_655-5991d others(36): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115701 | |||||||
| chr16:47115714 | C | CATATATA others(25): Show |
2 | a0002c0002t0006g0019 a0002c0002t0006g0021 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.655-6004_655-6003i others(34): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | |||||||
| chr16:47115714 | C | CATATATA others(27): Show |
1 | a0002c0002t0006g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.655-6004_655-6003i others(36): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | |||||||
| chr16:47115714 | C | CATATATA others(49): Show |
1 | a0002c0002t0006g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.655-6004_655-6003i others(58): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | |||||||
| chr16:47115714 | C | CATATATA others(43): Show |
1 | a0002c0002t0011g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.655-6004_655-6003i others(52): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | |||||||
| chr16:47115714 | CATAT | C | 5 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0005g0081 others(2): Show |
5 | HG01496.hp2 HG01891.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-6007_655-6004d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | |||||||
| chr16:47115716 | T | TATATATA others(5): Show |
2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-6006_655-6005i others(14): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | |||||||
| chr16:47115716 | T | TATATATA others(157): Show |
1 | a0001c0001t0004g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655-6006_655-6005i others(166): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | |||||||
| chr16:47115716 | T | TATATATA others(23): Show |
2 | a0001c0001t0002g0121 a0001c0001t0003g0101 |
2 | HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.655-6006_655-6005i others(32): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | |||||||
| chr16:47115716 | T | TATATATA others(53): Show |
1 | a0001c0001t0002g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.655-6006_655-6005i others(62): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | |||||||
| chr16:47115716 | T | TATATATA others(23): Show |
17 | a0001c0001t0002g0004 a0001c0001t0002g0118 a0001c0001t0002g0119 others(14): Show |
20 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.655-6006_655-6005i others(32): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | |||||||
| chr16:47115716 | T | TATATATA others(55): Show |
4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0130 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-6006_655-6005i others(64): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | |||||||
| chr16:47115716 | T | TATATATA others(25): Show |
1 | a0001c0001t0002g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.655-6006_655-6005i others(34): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | |||||||
| chr16:47115716 | T | TATATATA others(170): Show |
1 | a0001c0001t0004g0014 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.655-6006_655-6005i others(179): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | |||||||
| chr16:47115717 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.655-6006T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115717 | |||||||
| chr16:47115718 | T | C | 1 | a0001c0001t0005g0083 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655-6007A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115718 | |||||||
| chr16:47115718 | T | TATATATA others(21): Show |
3 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0096 |
3 | HG02922.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.655-6008_655-6007i others(30): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115718 | |||||||
| chr16:47115718 | T | TATATATA others(17): Show |
1 | a0001c0001t0017g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.655-6008_655-6007i others(26): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115718 | |||||||
| chr16:47115732 | C | T | 43 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(40): Show |
48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.655-6021G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115732 | |||||||
| chr16:47115734 | T | TATATATG others(75): Show |
1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.655-6024_655-6023i others(84): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115734 | |||||||
| chr16:47115785 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.655-6074C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115785 | |||||||
| chr16:47115919 | CTGATA | C | 2 | a0001c0001t0001g0100 a0001c0001t0029g0143 |
2 | HG00280.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.655-6213_655-6209d others(7): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115919 | |||||||
| chr16:47116014 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0023g0079 |
3 | HG00642.hp2 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.655-6303A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116014 | |||||||
| chr16:47116031 | T | C | 1 | a0001c0001t0001g0006 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.655-6320A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116031 | |||||||
| chr16:47116140 | C | G | 1 | a0001c0001t0007g0109 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.655-6429G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116140 | |||||||
| chr16:47116142 | G | GTT | 6 | a0001c0001t0007g0106 a0002c0002t0006g0018 a0002c0002t0006g0019 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-6433_655-6432d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116142 | |||||||
| chr16:47116142 | GT | G | 26 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(23): Show |
29 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.655-6432delA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116142 | |||||||
| chr16:47116346 | G | C | 7 | a0001c0001t0003g0012 a0001c0001t0003g0092 a0001c0001t0003g0093 others(4): Show |
8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+6311C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116346 | |||||||
| chr16:47116945 | G | T | 36 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(33): Show |
40 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.654+5712C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116945 | |||||||
| chr16:47116964 | C | G | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+5693G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116964 | |||||||
| chr16:47117028 | T | C | 1 | a0001c0001t0002g0004 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.654+5629A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117028 | |||||||
| chr16:47117146 | C | G | 2 | a0001c0001t0014g0144 a0001c0001t0014g0145 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.654+5511G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117146 | |||||||
| chr16:47117341 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.654+5316A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117341 | |||||||
| chr16:47117422 | T | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+5235A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117422 | |||||||
| chr16:47117763 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.654+4894C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117763 | |||||||
| chr16:47117917 | T | C | 40 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(37): Show |
44 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.654+4740A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117917 | |||||||
| chr16:47118003 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.654+4654G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47118003 | |||||||
| chr16:47118195 | CTTTG | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+4458_654+4461d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47118195 | |||||||
| chr16:47118510 | A | C | 2 | a0001c0001t0007g0107 a0001c0001t0007g0108 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.654+4147T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47118510 | |||||||
| chr16:47118723 | CTTATT | C | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.654+3929_654+3933d others(7): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47118723 | |||||||
| chr16:47119276 | T | C | 1 | a0001c0001t0015g0015 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.654+3381A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119276 | |||||||
| chr16:47119297 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.654+3360C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119297 | |||||||
| chr16:47119376 | T | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+3281A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119376 | |||||||
| chr16:47119714 | G | T | 1 | a0001c0001t0019g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.654+2943C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119714 | |||||||
| chr16:47119741 | A | G | 32 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(29): Show |
35 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.654+2916T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119741 | |||||||
| chr16:47121021 | T | A | 7 | a0001c0001t0003g0012 a0001c0001t0003g0092 a0001c0001t0003g0093 others(4): Show |
8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+1636A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47121021 | |||||||
| chr16:47121380 | G | T | 1 | a0001c0001t0017g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.654+1277C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47121380 | |||||||
| chr16:47121456 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.654+1201C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47121456 | |||||||
| chr16:47121730 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.654+927G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47121730 | |||||||
| chr16:47122098 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.654+559A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47122098 | |||||||
| chr16:47122239 | G | C | 1 | a0002c0002t0011g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.654+418C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47122239 | |||||||
| chr16:47122359 | T | C | 38 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(35): Show |
42 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.654+298A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47122359 | |||||||
| chr16:47122637 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.654+20C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47122637 | |||||||
| chr16:47123001 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.482-89A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123001 | |||||||
| chr16:47123011 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0118 |
2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.482-99T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123011 | |||||||
| chr16:47123024 | T | C | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.482-112A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123024 | |||||||
| chr16:47123062 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.482-150C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123062 | |||||||
| chr16:47123459 | C | T | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-547G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123459 | |||||||
| chr16:47123573 | T | G | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-661A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123573 | |||||||
| chr16:47123993 | G | A | 1 | a0001c0001t0003g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-1081C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123993 | |||||||
| chr16:47124682 | A | T | 7 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0005g0081 others(4): Show |
7 | HG01496.hp2 HG01891.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-1770T>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47124682 | |||||||
| chr16:47124955 | G | A | 30 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(27): Show |
33 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.482-2043C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47124955 | |||||||
| chr16:47125007 | AAAGT | A | 22 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(19): Show |
24 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-2099_482-2096d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125007 | |||||||
| chr16:47125064 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.482-2152T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125064 | |||||||
| chr16:47125211 | G | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-2299C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125211 | |||||||
| chr16:47125349 | G | GT | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-2438dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125349 | |||||||
| chr16:47125364 | C | A | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 |
3 | HG02257.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.482-2452G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125364 | |||||||
| chr16:47125535 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0023g0079 |
3 | HG00642.hp2 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.482-2623C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125535 | |||||||
| chr16:47125556 | G | T | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 |
3 | HG02257.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.482-2644C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125556 | |||||||
| chr16:47125760 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.481+2565T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125760 | |||||||
| chr16:47126821 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.481+1504C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47126821 | |||||||
| chr16:47126892 | A | C | 1 | a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.481+1433T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47126892 | |||||||
| chr16:47126900 | C | A | 36 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(33): Show |
40 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.481+1425G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47126900 | |||||||
| chr16:47127338 | C | T | 1 | a0001c0001t0013g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.481+987G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127338 | |||||||
| chr16:47127434 | TAC | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.481+889_481+890del others(2): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127434 | |||||||
| chr16:47127436 | C | G | 1 | a0001c0001t0005g0083 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.481+889G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127436 | |||||||
| chr16:47127555 | G | T | 29 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(26): Show |
32 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.481+770C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127555 | |||||||
| chr16:47127588 | T | C | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.481+737A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127588 | |||||||
| chr16:47128745 | C | T | 1 | a0001c0001t0004g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.233-172G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 3/8 | chr16 | 47128745 | |||||||
| chr16:47129380 | C | A | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-16G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47129380 | |||||||
| chr16:47129404 | A | G | 14 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(11): Show |
16 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-40T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47129404 | |||||||
| chr16:47129814 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.92-450G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47129814 | |||||||
| chr16:47129963 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.92-599G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47129963 | |||||||
| chr16:47130417 | G | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(3): Show |
9 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-1053C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130417 | |||||||
| chr16:47130456 | A | ATAAC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(3): Show |
9 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-1093_92-1092ins others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130456 | |||||||
| chr16:47130469 | T | A | 1 | a0001c0001t0007g0106 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-1105A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130469 | |||||||
| chr16:47130668 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91+1301C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130668 | |||||||
| chr16:47130938 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+1031C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130938 | |||||||
| chr16:47131074 | G | GA | 5 | a0001c0001t0001g0100 a0001c0001t0004g0014 a0001c0001t0004g0105 others(2): Show |
6 | HG00280.hp2 HG01496.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+894dupT | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47131074 | |||||||
| chr16:47131092 | T | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0104 |
3 | HG02071.hp2 NA18948.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.91+877A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47131092 | |||||||
| chr16:47131455 | T | C | 1 | a0001c0001t0019g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.91+514A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47131455 | |||||||
| chr16:47131935 | A | G | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.91+34T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47131935 | |||||||
| chr16:47132447 | G | A | 3 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 |
3 | HG02818.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.35-422C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47132447 | |||||||
| chr16:47132506 | C | A | 1 | a0001c0001t0002g0120 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.35-481G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47132506 | |||||||
| chr16:47132792 | C | T | 4 | a0001c0001t0007g0106 a0001c0001t0007g0107 a0001c0001t0007g0108 others(1): Show |
4 | HG02280.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-767G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47132792 | |||||||
| chr16:47133558 | C | G | 3 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 |
3 | HG01891.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.35-1533G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133558 | |||||||
| chr16:47133604 | C | A | 1 | a0001c0001t0029g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.35-1579G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133604 | C | CATAAA | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0102 others(4): Show |
9 | HG00741.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.35-1584_35-1580dup others(5): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133604 | C | CATAAAAT others(3): Show |
1 | a0001c0001t0001g0072 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.35-1589_35-1580dup others(10): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133604 | C | CATAAAAT others(18): Show |
3 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 |
3 | HG02818.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.35-1604_35-1580dup others(25): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133604 | CATAAA | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.35-1584_35-1580del others(5): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133604 | CATAAAAT others(3): Show |
C | 20 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0076 others(17): Show |
22 | HG00735.hp2 HG01074.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.35-1589_35-1580del others(10): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133604 | CATAAAAT others(8): Show |
C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0080 others(2): Show |
5 | HG01074.hp2 HG01169.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-1594_35-1580del others(15): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133604 | CATAAAAT others(13): Show |
C | 5 | a0001c0001t0002g0119 a0002c0002t0006g0018 a0002c0002t0006g0019 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-1599_35-1580del others(20): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133604 | CATAAAAT others(18): Show |
C | 2 | a0001c0001t0004g0014 a0001c0001t0004g0105 |
3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.35-1604_35-1580del others(25): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | |||||||
| chr16:47133750 | A | G | 39 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(36): Show |
43 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.35-1725T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133750 | |||||||
| chr16:47133897 | C | T | 1 | a0001c0001t0012g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.35-1872G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133897 | |||||||
| chr16:47133994 | C | CA | 6 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(3): Show |
6 | HG01496.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.35-1970dupT | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133994 | |||||||
| chr16:47134233 | T | TA | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0005g0077 |
3 | HG02615.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.35-2209dupT | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47134233 | |||||||
| chr16:47134355 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.35-2330C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47134355 | |||||||
| chr16:47134701 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.35-2676G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47134701 | |||||||
| chr16:47134882 | T | C | 22 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(19): Show |
24 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.35-2857A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47134882 | |||||||
| chr16:47135069 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.35-3044C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47135069 | |||||||
| chr16:47135071 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0005g0077 |
2 | HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.35-3046A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47135071 | |||||||
| chr16:47135690 | G | C | 1 | a0001c0001t0004g0014 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.35-3665C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47135690 | |||||||
| chr16:47136390 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.35-4365A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47136390 | |||||||
| chr16:47136825 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.35-4800A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47136825 | |||||||
| chr16:47136910 | C | T | 1 | a0001c0001t0023g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.35-4885G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47136910 | |||||||
| chr16:47137070 | C | T | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.35-5045G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47137070 | |||||||
| chr16:47137422 | T | C | 71 | a0001c0001t0001g0013 a0001c0001t0001g0080 a0001c0001t0001g0084 others(68): Show |
77 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.35-5397A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47137422 | |||||||
| chr16:47137442 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.35-5417G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47137442 | |||||||
| chr16:47138019 | G | A | 25 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(22): Show |
27 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.34+5560C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138019 | |||||||
| chr16:47138039 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.34+5540C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138039 | |||||||
| chr16:47138128 | G | A | 1 | a0001c0001t0008g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.34+5451C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138128 | |||||||
| chr16:47138192 | A | G | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+5387T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138192 | |||||||
| chr16:47138257 | G | A | 3 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0024g0135 |
3 | HG01496.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.34+5322C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138257 | |||||||
| chr16:47138272 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(1): Show |
4 | HG00408.hp1 HG02071.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+5307G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138272 | |||||||
| chr16:47138324 | T | C | 3 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0024g0135 |
3 | HG01496.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.34+5255A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138324 | |||||||
| chr16:47138591 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.34+4988G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138591 | |||||||
| chr16:47138750 | T | C | 33 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(30): Show |
36 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.34+4829A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138750 | |||||||
| chr16:47138809 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.34+4770A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138809 | |||||||
| chr16:47139067 | T | G | 39 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(36): Show |
43 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.34+4512A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47139067 | |||||||
| chr16:47139103 | G | A | 1 | a0001c0001t0010g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.34+4476C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47139103 | |||||||
| chr16:47139885 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.34+3694A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47139885 | |||||||
| chr16:47140133 | G | C | 6 | a0002c0002t0006g0018 a0002c0002t0006g0019 a0002c0002t0006g0020 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+3446C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47140133 | |||||||
| chr16:47140152 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.34+3427G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47140152 | |||||||
| chr16:47140364 | A | G | 25 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(22): Show |
27 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.34+3215T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47140364 | |||||||
| chr16:47140728 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.34+2851A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47140728 | |||||||
| chr16:47141041 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+2538T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141041 | |||||||
| chr16:47141244 | G | C | 1 | a0001c0001t0004g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.34+2335C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141244 | |||||||
| chr16:47141273 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+2306A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141273 | |||||||
| chr16:47141373 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.34+2206A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141373 | |||||||
| chr16:47141381 | G | C | 1 | a0001c0001t0025g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.34+2198C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141381 | |||||||
| chr16:47141781 | A | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.34+1798T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141781 | |||||||
| chr16:47142140 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.34+1439A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47142140 | |||||||
| chr16:47142413 | A | G | 8 | a0001c0001t0014g0144 a0001c0001t0014g0145 a0002c0002t0006g0018 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.34+1166T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47142413 | |||||||
| chr16:47142447 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0013g0016 |
2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.34+1132G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47142447 | |||||||
| chr16:47142547 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0118 |
2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.34+1032T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47142547 | |||||||
| chr16:47143431 | G | A | 25 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0118 others(22): Show |
27 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.34+148C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47143431 | |||||||
| chr16:47143491 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.34+88C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47143491 | |||||||
| chr16:47143524 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.34+55C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47143524 |