Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79612 |
| ensemblid | ENSG00000172766.19 |
| hgncid | 26164 |
| symbol | NAA16 |
| name | N-alpha-acetyltransferase 16, NatA auxiliary subunit |
| refseq_nuc | NM_024561.5 |
| refseq_prot | NP_078837.3 |
| ensembl_nuc | ENST00000379406.8 |
| ensembl_prot | ENSP00000368716.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 41311267 |
| end | 41377030 |
| strand | + |
| ver | v1.2 |
| region | chr13:41311267-41377030 |
| region5000 | chr13:41306267-41382030 |
| regionname0 | NAA16_chr13_41311267_41377030 |
| regionname5000 | NAA16_chr13_41306267_41382030 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 864 | 328 | 63 | 60 | 163 | 11 | 31 | 124 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| a0002 | 0/0 | 864 | 17 | 15 | 2 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| a0003 | 0/0 | 864 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| a0004 | 0/0 | 864 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| a0005 | 0/0 | 864 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| a0006 | 0/0 | 864 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| a0007 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| a0008 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| a0009 | 0/0 | 676 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(671): Show |
chr13 | 41306267 | 41382030 |
| a0010 | 0/0 | 864 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | MPNVL others(859): Show |
chr13 | 41306267 | 41382030 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2592 | 301 | 55 | 57 | 149 | 11 | 29 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0001c0002 | 0/0 | 2592 | 21 | 5 | 3 | 12 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0001c0005 | 0/0 | 2592 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0001c0006 | 0/0 | 2592 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0001c0009 | 0/0 | 2592 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0001c0011 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0001c0013 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0001c0017 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0002c0003 | 0/0 | 2592 | 16 | 14 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0002c0014 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0003c0004 | 0/0 | 2592 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0004c0015 | 0/0 | 2592 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0005c0007 | 0/0 | 2592 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0006c0010 | 0/0 | 2592 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0007c0018 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0008c0012 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 | ||
| a0009c0008 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2560): Show |
chr13 | 41306267 | 41382030 | ||
| a0010c0016 | 0/0 | 2592 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | ATGCC others(2587): Show |
chr13 | 41306267 | 41382030 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4285 | 88 | 9 | 26 | 42 | 2 | 9 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0002 | 0/0 | 4285 | 68 | 10 | 8 | 34 | 5 | 11 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0003 | 0/0 | 4285 | 51 | 1 | 11 | 36 | 1 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0004 | 0/0 | 4285 | 47 | 7 | 5 | 27 | 1 | 7 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0006 | 0/0 | 4285 | 13 | 10 | 3 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0008 | 0/0 | 4285 | 10 | 9 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0010 | 0/0 | 4285 | 5 | 5 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0011 | 0/0 | 4285 | 4 | 0 | 0 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0012 | 0/0 | 4288 | 3 | 0 | 0 | 3 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4283): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0013 | 0/0 | 4285 | 3 | 0 | 2 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0017 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0018 | 0/0 | 4285 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0019 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0020 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0021 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0022 | 0/0 | 4285 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0023 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0024 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0001t0025 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0002t0007 | 0/0 | 4285 | 12 | 0 | 0 | 12 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0002t0009 | 0/0 | 4285 | 9 | 5 | 3 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0005t0001 | 0/0 | 4285 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0006t0001 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0009t0002 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0011t0014 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0013t0015 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0001c0017t0006 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0002c0003t0005 | 0/0 | 4285 | 16 | 14 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0002c0014t0005 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0003c0004t0003 | 0/0 | 4285 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0004c0015t0003 | 0/0 | 4285 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0005c0007t0003 | 0/0 | 4285 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0006c0010t0002 | 0/0 | 4285 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0007c0018t0008 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0008c0012t0001 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| a0009c0008t0026 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4253): Show |
chr13 | 41306267 | 41382030 |
| a0010c0016t0016 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | GCAGT others(4280): Show |
chr13 | 41306267 | 41382030 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0001 | 0/0 | 7 | 2 | 1 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0012g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0013g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0013g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0013g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0017g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0018g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0019g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0020g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0021g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0022g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0023g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0024g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0001t0025g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0007g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0009g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0009g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0002t0009g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0009t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0011t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0013t0015g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0001c0017t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0003t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0002c0014t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0003c0004t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0003c0004t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0004c0015t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0005c0007t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0006c0010t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0007c0018t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0008c0012t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0009c0008t0026g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| a0010c0016t0016g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0256 | EUR | GBR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | GBR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00140 | hp2 | a0004 | c0015 | t0003 | g0148 | EUR | GBR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0219 | EUR | FIN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00423 | hp1 | a0001 | c0002 | t0007 | g0157 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00597 | hp2 | a0001 | c0001 | t0025 | g0270 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00639 | hp1 | a0005 | c0007 | t0003 | g0003 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00673 | hp1 | a0003 | c0004 | t0003 | g0095 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01071 | hp1 | a0001 | c0001 | t0022 | g0009 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01109 | hp2 | a0002 | c0003 | t0005 | g0038 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01167 | hp2 | a0006 | c0010 | t0002 | g0232 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01175 | hp1 | a0001 | c0002 | t0009 | g0169 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0028 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0258 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01243 | hp2 | a0002 | c0003 | t0005 | g0036 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01361 | hp2 | a0001 | c0002 | t0009 | g0016 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0055 | EUR | IBS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0257 | EUR | IBS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01884 | hp2 | a0001 | c0002 | t0009 | g0168 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01891 | hp1 | a0002 | c0003 | t0005 | g0045 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0145 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG01993 | hp2 | a0001 | c0002 | t0009 | g0016 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02055 | hp1 | a0001 | c0002 | t0009 | g0312 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02129 | hp1 | a0001 | c0009 | t0002 | g0284 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02129 | hp2 | a0001 | c0006 | t0001 | g0205 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02135 | hp2 | a0001 | c0002 | t0007 | g0159 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0142 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02145 | hp2 | a0002 | c0003 | t0005 | g0034 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CDX | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CDX | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02280 | hp1 | a0002 | c0003 | t0005 | g0041 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02300 | hp2 | a0001 | c0001 | t0013 | g0182 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0086 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0137 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0092 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0073 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02622 | hp2 | a0002 | c0003 | t0005 | g0047 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02717 | hp2 | a0001 | c0001 | t0017 | g0214 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02723 | hp1 | a0002 | c0003 | t0005 | g0046 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0083 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02809 | hp1 | a0001 | c0002 | t0009 | g0166 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02809 | hp2 | a0002 | c0003 | t0005 | g0043 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02818 | hp1 | a0002 | c0003 | t0005 | g0042 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0084 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02886 | hp2 | a0002 | c0003 | t0005 | g0049 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02922 | hp1 | a0002 | c0003 | t0005 | g0039 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02965 | hp1 | a0002 | c0014 | t0005 | g0037 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02970 | hp1 | a0001 | c0017 | t0006 | g0091 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02970 | hp2 | a0002 | c0003 | t0005 | g0048 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0138 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03041 | hp2 | a0001 | c0013 | t0015 | g0153 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03098 | hp2 | a0001 | c0011 | t0014 | g0154 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03139 | hp2 | a0001 | c0001 | t0020 | g0140 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03453 | hp2 | a0002 | c0003 | t0005 | g0050 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03486 | hp1 | a0001 | c0002 | t0009 | g0165 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03540 | hp1 | a0002 | c0003 | t0005 | g0044 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03688 | hp2 | a0009 | c0008 | t0026 | g0078 | SAS | STU | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03831 | hp1 | a0001 | c0005 | t0001 | g0248 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0151 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03927 | hp1 | a0001 | c0002 | t0009 | g0164 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | STU | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0013 | SAS | STU | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18522 | hp2 | a0002 | c0003 | t0005 | g0040 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0087 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18944 | hp2 | a0001 | c0001 | t0012 | g0110 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18948 | hp1 | a0001 | c0001 | t0011 | g0104 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18957 | hp2 | a0001 | c0001 | t0019 | g0268 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18964 | hp1 | a0001 | c0001 | t0012 | g0014 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18965 | hp1 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18965 | hp2 | a0001 | c0002 | t0007 | g0161 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18967 | hp1 | a0001 | c0002 | t0007 | g0163 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18970 | hp2 | a0001 | c0001 | t0023 | g0265 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18971 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18984 | hp1 | a0001 | c0001 | t0011 | g0118 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18990 | hp1 | a0001 | c0001 | t0011 | g0119 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18990 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18992 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19000 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19002 | hp2 | a0001 | c0002 | t0007 | g0158 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19010 | hp2 | a0001 | c0002 | t0007 | g0162 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19030 | hp2 | a0001 | c0001 | t0021 | g0299 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0152 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0135 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19055 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19059 | hp2 | a0010 | c0016 | t0016 | g0160 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19080 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19081 | hp1 | a0003 | c0004 | t0003 | g0098 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19091 | hp2 | a0001 | c0001 | t0011 | g0105 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19240 | hp1 | a0001 | c0001 | t0024 | g0141 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0136 | AFR | ASW | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ASW | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA20752 | hp1 | a0001 | c0001 | t0013 | g0019 | EUR | TSI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | TSI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA20805 | hp2 | a0001 | c0001 | t0018 | g0129 | EUR | TSI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02109 | hp2 | a0007 | c0018 | t0008 | g0088 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0144 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02486 | hp2 | a0001 | c0002 | t0009 | g0167 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02559 | hp1 | a0002 | c0003 | t0005 | g0035 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG03471 | hp2 | a0008 | c0012 | t0001 | g0243 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | USA | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | USA | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:41325779 | C | G | 1 | a0007 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.619C>G | p.Gln207Glu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/20 | 881/4285 | 619/2595 | 207/864 | chr13 | 41325779 | |||
| chr13:41336653 | A | G | 1 | a0004 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.911A>G | p.Glu304Gly | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/20 | 1173/4285 | 911/2595 | 304/864 | chr13 | 41336653 | |||
| chr13:41355160 | A | G | 1 | a0002 | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
missense_variant | MODERATE | c.1031A>G | p.Glu344Gly | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/20 | 1293/4285 | 1031/2595 | 344/864 | chr13 | 41355160 | |||
| chr13:41358909 | C | G | 1 | a0008 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1357C>G | p.Leu453Val | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/20 | 1619/4285 | 1357/2595 | 453/864 | chr13 | 41358909 | |||
| chr13:41367506 | G | A | 1 | a0005 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1607G>A | p.Arg536His | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/20 | 1869/4285 | 1607/2595 | 536/864 | chr13 | 41367506 | |||
| chr13:41367565 | A | G | 1 | a0006 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.1666A>G | p.Lys556Glu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/20 | 1928/4285 | 1666/2595 | 556/864 | chr13 | 41367565 | |||
| chr13:41372284 | TTAGCATT others(24): Show |
T | 1 | a0009 | 1 | HG03688.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.2032_2056+6delGCAT others(27): Show |
p.Ala678fs | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/20 | 2294/4285 | 2032/2595 | 678/864 | INFO_REALIGN_3_PRIME | chr13 | 41372284 | ||
| chr13:41373693 | C | A | 1 | a0003 | 2 | HG00673.hp1 NA19081.hp1 |
missense_variant | MODERATE | c.2212C>A | p.Gln738Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/20 | 2474/4285 | 2212/2595 | 738/864 | chr13 | 41373693 | |||
| chr13:41375446 | T | G | 1 | a0010 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.2439T>G | p.Phe813Leu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2701/4285 | 2439/2595 | 813/864 | chr13 | 41375446 | |||
| chr13:41375561 | A | C | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2554A>C | p.Asn852His | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2816/4285 | 2554/2595 | 852/864 | chr13 | 41375561 | |||
| chr13:41375575 | T | G | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2568T>G | p.Asn856Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2830/4285 | 2568/2595 | 856/864 | chr13 | 41375575 | |||
| chr13:41375583 | T | A | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2576T>A | p.Val859Asp | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2838/4285 | 2576/2595 | 859/864 | chr13 | 41375583 | |||
| chr13:41375585 | T | A | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2578T>A | p.Leu860Met | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2840/4285 | 2578/2595 | 860/864 | chr13 | 41375585 | |||
| chr13:41375595 | A | C | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2588A>C | p.Glu863Ala | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2850/4285 | 2588/2595 | 863/864 | chr13 | 41375595 | |||
| chr13:41375598 | T | C | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2591T>C | p.Ile864Thr | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2853/4285 | 2591/2595 | 864/864 | chr13 | 41375598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:41325802 | A | G | 1 | a0001c0017 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.642A>G | p.Glu214Glu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/20 | 904/4285 | 642/2595 | 214/864 | chr13 | 41325802 | |||
| chr13:41328803 | T | C | 16 | a0001c0001 a0001c0005 a0001c0006 others(13): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
synonymous_variant | LOW | c.771T>C | p.Asn257Asn | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/20 | 1033/4285 | 771/2595 | 257/864 | chr13 | 41328803 | |||
| chr13:41331317 | G | A | 1 | a0001c0005 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.855G>A | p.Lys285Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/20 | 1117/4285 | 855/2595 | 285/864 | chr13 | 41331317 | |||
| chr13:41355191 | A | G | 1 | a0001c0013 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1062A>G | p.Lys354Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/20 | 1324/4285 | 1062/2595 | 354/864 | chr13 | 41355191 | |||
| chr13:41358435 | C | T | 1 | a0002c0014 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1219C>T | p.Leu407Leu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 11/20 | 1481/4285 | 1219/2595 | 407/864 | chr13 | 41358435 | |||
| chr13:41362060 | T | C | 1 | a0001c0006 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1440T>C | p.Asn480Asn | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/20 | 1702/4285 | 1440/2595 | 480/864 | chr13 | 41362060 | |||
| chr13:41367465 | A | G | 2 | a0001c0011 a0001c0013 |
2 | HG03041.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1566A>G | p.Gln522Gln | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/20 | 1828/4285 | 1566/2595 | 522/864 | chr13 | 41367465 | |||
| chr13:41367633 | A | G | 1 | a0001c0009 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.1734A>G | p.Lys578Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/20 | 1996/4285 | 1734/2595 | 578/864 | chr13 | 41367633 | |||
| chr13:41375557 | A | T | 1 | a0009c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2550A>T | p.Ala850Ala | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2812/4285 | 2550/2595 | 850/864 | chr13 | 41375557 | |||
| chr13:41375578 | T | C | 1 | a0009c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2571T>C | p.Tyr857Tyr | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2833/4285 | 2571/2595 | 857/864 | chr13 | 41375578 | |||
| chr13:41375584 | C | G | 1 | a0009c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2577C>G | p.Val859Val | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2839/4285 | 2577/2595 | 859/864 | chr13 | 41375584 | |||
| chr13:41375587 | G | A | 1 | a0009c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2580G>A | p.Leu860Leu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2842/4285 | 2580/2595 | 860/864 | chr13 | 41375587 | |||
| chr13:41375590 | A | C | 1 | a0009c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2583A>C | p.Ala861Ala | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2845/4285 | 2583/2595 | 861/864 | chr13 | 41375590 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:41311280 | A | ACCG | 1 | a0001c0001t0012 | 3 | NA18944.hp2 NA18964.hp1 NA18965.hp1 |
5_prime_UTR_variant | MODIFIER | c.-235_-233dupCGC | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/20 | 232 | INFO_REALIGN_3_PRIME | chr13 | 41311280 | |||||
| chr13:41311329 | C | T | 1 | a0001c0001t0013 | 3 | HG01243.hp1 HG02300.hp2 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-200C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/20 | 200 | chr13 | 41311329 | ||||||
| chr13:41311365 | T | C | 2 | a0001c0011t0014 a0001c0013t0015 |
2 | HG03041.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-164T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/20 | 164 | chr13 | 41311365 | ||||||
| chr13:41375603 | A | T | 1 | a0009c0008t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 1 | chr13 | 41375603 | ||||||
| chr13:41375611 | A | C | 1 | a0009c0008t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 9 | chr13 | 41375611 | ||||||
| chr13:41375618 | A | C | 1 | a0009c0008t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 16 | chr13 | 41375618 | ||||||
| chr13:41375620 | A | C | 1 | a0001c0001t0025 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*18A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 18 | chr13 | 41375620 | ||||||
| chr13:41375627 | T | G | 1 | a0009c0008t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 25 | chr13 | 41375627 | ||||||
| chr13:41375668 | G | T | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(31): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
3_prime_UTR_variant | MODIFIER | c.*66G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 66 | chr13 | 41375668 | ||||||
| chr13:41375689 | A | C | 1 | a0001c0001t0024 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 87 | chr13 | 41375689 | ||||||
| chr13:41375717 | A | G | 1 | a0001c0001t0023 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 115 | chr13 | 41375717 | ||||||
| chr13:41375743 | T | G | 1 | a0010c0016t0016 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 141 | chr13 | 41375743 | ||||||
| chr13:41375785 | T | G | 1 | a0010c0016t0016 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 183 | chr13 | 41375785 | ||||||
| chr13:41375823 | A | T | 1 | a0010c0016t0016 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*221A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 221 | chr13 | 41375823 | ||||||
| chr13:41375825 | C | T | 2 | a0001c0001t0004 a0009c0008t0026 |
48 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*223C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 223 | chr13 | 41375825 | ||||||
| chr13:41375826 | G | A | 1 | a0001c0001t0011 | 4 | NA18948.hp1 NA18984.hp1 NA18990.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*224G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 224 | chr13 | 41375826 | ||||||
| chr13:41375968 | C | T | 2 | a0002c0003t0005 a0002c0014t0005 |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*366C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 366 | chr13 | 41375968 | ||||||
| chr13:41375990 | A | G | 1 | a0001c0001t0022 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 388 | chr13 | 41375990 | ||||||
| chr13:41376016 | G | A | 1 | a0001c0001t0017 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 414 | chr13 | 41376016 | ||||||
| chr13:41376087 | C | T | 1 | a0001c0001t0021 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*485C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 485 | chr13 | 41376087 | ||||||
| chr13:41376089 | A | T | 1 | a0010c0016t0016 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 487 | chr13 | 41376089 | ||||||
| chr13:41376142 | T | C | 9 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0011 others(6): Show |
77 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*540T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 540 | chr13 | 41376142 | ||||||
| chr13:41376317 | T | C | 1 | a0001c0011t0014 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 715 | chr13 | 41376317 | ||||||
| chr13:41376395 | T | C | 1 | a0001c0001t0010 | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*793T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 793 | chr13 | 41376395 | ||||||
| chr13:41376402 | G | C | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0013 others(11): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*800G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 800 | chr13 | 41376402 | ||||||
| chr13:41376403 | G | T | 7 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(4): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*801G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 801 | chr13 | 41376403 | ||||||
| chr13:41376424 | G | A | 1 | a0001c0001t0020 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 822 | chr13 | 41376424 | ||||||
| chr13:41376426 | A | G | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(31): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
3_prime_UTR_variant | MODIFIER | c.*824A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 824 | chr13 | 41376426 | ||||||
| chr13:41376507 | A | C | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(33): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*905A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 905 | chr13 | 41376507 | ||||||
| chr13:41376660 | A | G | 1 | a0001c0001t0018 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1058A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 1058 | chr13 | 41376660 | ||||||
| chr13:41376786 | T | C | 1 | a0001c0001t0019 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1184T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 1184 | chr13 | 41376786 | ||||||
| chr13:41376877 | G | C | 8 | a0001c0001t0001 a0001c0001t0019 a0001c0001t0022 others(5): Show |
95 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1275G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 1275 | chr13 | 41376877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:41311618 | C | T | 1 | a0001c0002t0009g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+36C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311618 | |||||||
| chr13:41311622 | G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.54+40G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311622 | |||||||
| chr13:41311714 | G | T | 158 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.54+132G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311714 | |||||||
| chr13:41311779 | G | T | 1 | a0001c0001t0002g0311 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.54+197G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311779 | |||||||
| chr13:41311783 | C | T | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+201C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311783 | |||||||
| chr13:41311933 | G | T | 2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG00544.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.54+351G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311933 | |||||||
| chr13:41311967 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.54+385C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311967 | |||||||
| chr13:41312016 | G | C | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+434G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312016 | |||||||
| chr13:41312031 | C | T | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.54+449C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312031 | |||||||
| chr13:41312067 | G | C | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+485G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312067 | |||||||
| chr13:41312105 | T | C | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+523T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312105 | |||||||
| chr13:41312119 | C | T | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.54+537C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312119 | |||||||
| chr13:41312144 | A | G | 1 | a0001c0001t0004g0151 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.54+562A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312144 | |||||||
| chr13:41312207 | G | A | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+625G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312207 | |||||||
| chr13:41312403 | C | T | 8 | a0001c0002t0009g0016 a0001c0002t0009g0164 a0001c0002t0009g0165 others(5): Show |
9 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.54+821C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312403 | |||||||
| chr13:41312432 | A | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.54+850A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312432 | |||||||
| chr13:41312484 | T | TC | 3 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0002g0176 |
3 | HG01255.hp1 NA19055.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.54+904dupC | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41312484 | ||||||
| chr13:41312558 | A | C | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54+976A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312558 | |||||||
| chr13:41312570 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.54+988T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312570 | |||||||
| chr13:41312745 | A | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0002g0302 others(7): Show |
10 | HG00621.hp1 HG03492.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+1163A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312745 | |||||||
| chr13:41312785 | G | A | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+1203G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312785 | |||||||
| chr13:41312922 | C | T | 5 | a0001c0002t0007g0002 a0001c0002t0007g0161 a0001c0002t0007g0162 others(2): Show |
10 | NA18965.hp2 NA18967.hp1 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+1340C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312922 | |||||||
| chr13:41313233 | C | A | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.54+1651C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313233 | |||||||
| chr13:41313279 | C | G | 9 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0002g0022 others(6): Show |
11 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+1697C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313279 | |||||||
| chr13:41313290 | C | G | 1 | a0001c0001t0002g0295 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.54+1708C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313290 | |||||||
| chr13:41313653 | C | G | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+2071C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313653 | |||||||
| chr13:41313755 | G | A | 38 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(35): Show |
47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.54+2173G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313755 | |||||||
| chr13:41313865 | C | CT | 202 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.54+2297dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41313865 | ||||||
| chr13:41313960 | G | C | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.54+2378G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313960 | |||||||
| chr13:41313962 | TTC | T | 5 | a0001c0002t0007g0002 a0001c0002t0007g0161 a0001c0002t0007g0162 others(2): Show |
10 | NA18965.hp2 NA18967.hp1 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+2383_54+2384del others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41313962 | ||||||
| chr13:41314168 | GTAAA | G | 4 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(1): Show |
4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+2590_54+2593del others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41314168 | ||||||
| chr13:41314272 | T | G | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-2574T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314272 | |||||||
| chr13:41314475 | C | G | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.55-2371C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314475 | |||||||
| chr13:41314481 | G | GCAGAATC others(16): Show |
16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.55-2360_55-2338dup others(23): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41314481 | ||||||
| chr13:41314536 | T | C | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55-2310T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314536 | |||||||
| chr13:41314644 | T | C | 1 | a0001c0001t0001g0017 | 2 | NA18747.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.55-2202T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314644 | |||||||
| chr13:41314729 | G | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.55-2117G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314729 | |||||||
| chr13:41314759 | G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55-2087G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314759 | |||||||
| chr13:41314797 | C | CCAACATA others(1): Show |
16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.55-2048_55-2041dup others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41314797 | ||||||
| chr13:41314846 | A | T | 2 | a0001c0001t0003g0133 a0001c0001t0003g0134 |
2 | HG01496.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.55-2000A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314846 | |||||||
| chr13:41315023 | A | T | 1 | a0001c0001t0002g0294 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.55-1823A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315023 | |||||||
| chr13:41315191 | G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55-1655G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315191 | |||||||
| chr13:41315347 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55-1499A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315347 | |||||||
| chr13:41315361 | A | G | 199 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.55-1485A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315361 | |||||||
| chr13:41315534 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.55-1312C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315534 | |||||||
| chr13:41315660 | T | TTG | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-1172_55-1171dup others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41315660 | ||||||
| chr13:41315880 | C | A | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.55-966C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315880 | |||||||
| chr13:41316105 | G | A | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.55-741G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316105 | |||||||
| chr13:41316305 | A | AT | 65 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(62): Show |
69 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.55-522dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41316305 | ||||||
| chr13:41316324 | T | G | 1 | a0001c0001t0013g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.55-522T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316324 | |||||||
| chr13:41316346 | T | G | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.55-500T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316346 | |||||||
| chr13:41316402 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.55-444G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316402 | |||||||
| chr13:41316412 | T | G | 1 | a0001c0001t0004g0052 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.55-434T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316412 | |||||||
| chr13:41316453 | C | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55-393C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316453 | |||||||
| chr13:41316495 | C | T | 1 | a0001c0001t0002g0309 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.55-351C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316495 | |||||||
| chr13:41316543 | G | A | 6 | a0001c0001t0006g0090 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-303G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316543 | |||||||
| chr13:41316787 | G | A | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.55-59G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316787 | |||||||
| chr13:41317034 | C | T | 38 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(35): Show |
47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.139+104C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317034 | |||||||
| chr13:41317036 | A | G | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.139+106A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317036 | |||||||
| chr13:41317115 | T | C | 3 | a0001c0001t0002g0022 a0001c0001t0002g0296 a0001c0001t0002g0297 |
4 | HG00140.hp1 HG01192.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+185T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317115 | |||||||
| chr13:41317135 | G | A | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.139+205G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317135 | |||||||
| chr13:41317143 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.139+213C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317143 | |||||||
| chr13:41317220 | A | G | 1 | a0001c0001t0003g0132 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.139+290A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317220 | |||||||
| chr13:41317338 | TG | T | 9 | a0001c0001t0006g0025 a0001c0001t0006g0026 a0001c0001t0006g0027 others(6): Show |
9 | HG01192.hp1 HG01891.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139+409delG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317338 | |||||||
| chr13:41317368 | A | G | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.139+438A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317368 | |||||||
| chr13:41317518 | C | T | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.139+588C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317518 | |||||||
| chr13:41317883 | T | G | 6 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 others(3): Show |
6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-923T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317883 | |||||||
| chr13:41317905 | C | G | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.140-901C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317905 | |||||||
| chr13:41317939 | G | A | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.140-867G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317939 | |||||||
| chr13:41318001 | C | T | 201 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.140-805C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318001 | |||||||
| chr13:41318040 | A | G | 3 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0308 |
3 | HG03492.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.140-766A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318040 | |||||||
| chr13:41318196 | T | C | 1 | a0001c0002t0007g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.140-610T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318196 | |||||||
| chr13:41318205 | AT | A | 32 | a0001c0001t0001g0177 a0001c0001t0002g0185 a0001c0001t0002g0311 others(29): Show |
32 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.140-584delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr13 | 41318205 | ||||||
| chr13:41318390 | C | T | 8 | a0001c0001t0001g0283 a0001c0001t0002g0005 a0001c0001t0002g0280 others(5): Show |
11 | HG02129.hp1 NA18942.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.140-416C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318390 | |||||||
| chr13:41318421 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0278 a0001c0001t0001g0279 |
4 | HG02071.hp1 HG02080.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.140-385C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318421 | |||||||
| chr13:41318438 | A | G | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.140-368A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318438 | |||||||
| chr13:41318443 | C | G | 8 | a0001c0001t0001g0283 a0001c0001t0002g0005 a0001c0001t0002g0280 others(5): Show |
11 | HG02129.hp1 NA18942.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.140-363C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318443 | |||||||
| chr13:41318459 | C | T | 1 | a0001c0001t0021g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.140-347C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318459 | |||||||
| chr13:41318480 | G | T | 6 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 others(3): Show |
6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-326G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318480 | |||||||
| chr13:41318495 | C | T | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.140-311C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318495 | |||||||
| chr13:41318529 | A | T | 1 | a0001c0001t0002g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140-277A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318529 | |||||||
| chr13:41318543 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.140-263T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318543 | |||||||
| chr13:41318571 | T | C | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.140-235T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318571 | |||||||
| chr13:41318711 | G | A | 1 | a0001c0001t0002g0309 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140-95G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318711 | |||||||
| chr13:41318969 | T | G | 200 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(197): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.244+59T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41318969 | |||||||
| chr13:41318984 | G | A | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+74G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41318984 | |||||||
| chr13:41319000 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.244+90C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319000 | |||||||
| chr13:41319044 | C | G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.244+134C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319044 | |||||||
| chr13:41319397 | A | G | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.244+487A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319397 | |||||||
| chr13:41319437 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.244+527A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319437 | |||||||
| chr13:41319516 | T | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0187 |
3 | HG00099.hp2 HG00735.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.244+606T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319516 | |||||||
| chr13:41319620 | G | A | 3 | a0001c0002t0009g0016 a0001c0002t0009g0164 a0001c0002t0009g0169 |
4 | HG01175.hp1 HG01361.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+710G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319620 | |||||||
| chr13:41319677 | T | C | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.244+767T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319677 | |||||||
| chr13:41319784 | T | G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.244+874T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319784 | |||||||
| chr13:41319847 | A | G | 1 | a0001c0001t0008g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.245-820A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319847 | |||||||
| chr13:41319863 | A | AT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0273 a0001c0001t0001g0274 others(3): Show |
7 | HG00738.hp2 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-791dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr13 | 41319863 | ||||||
| chr13:41319863 | AT | A | 17 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(14): Show |
23 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.245-791delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr13 | 41319863 | ||||||
| chr13:41320080 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.245-587A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320080 | |||||||
| chr13:41320130 | C | T | 4 | a0001c0001t0008g0087 a0001c0001t0008g0089 a0001c0001t0008g0092 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-537C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320130 | |||||||
| chr13:41320155 | A | G | 6 | a0001c0001t0006g0090 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-512A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320155 | |||||||
| chr13:41320203 | AT | A | 6 | a0001c0001t0006g0090 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-462delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr13 | 41320203 | ||||||
| chr13:41320296 | G | A | 2 | a0001c0001t0004g0055 a0001c0001t0004g0151 |
2 | HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.245-371G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320296 | |||||||
| chr13:41320461 | C | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0181 others(9): Show |
15 | HG00597.hp2 HG02015.hp2 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.245-206C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320461 | |||||||
| chr13:41320501 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.245-166C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320501 | |||||||
| chr13:41320618 | A | G | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245-49A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320618 | |||||||
| chr13:41320951 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.402+127C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41320951 | |||||||
| chr13:41321023 | G | C | 1 | a0001c0001t0003g0102 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.402+199G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321023 | |||||||
| chr13:41321024 | G | T | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+200G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321024 | |||||||
| chr13:41321030 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.402+206T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321030 | |||||||
| chr13:41321041 | T | G | 203 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(200): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.402+217T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321041 | |||||||
| chr13:41321084 | G | C | 1 | a0001c0001t0002g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.402+260G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321084 | |||||||
| chr13:41321124 | G | C | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.402+300G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321124 | |||||||
| chr13:41321130 | G | T | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+306G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321130 | |||||||
| chr13:41321468 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0276 |
3 | HG02622.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.402+644C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321468 | |||||||
| chr13:41321675 | C | A | 2 | a0001c0001t0003g0093 a0001c0001t0003g0103 |
2 | NA18951.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.402+851C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321675 | |||||||
| chr13:41321717 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.402+893A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321717 | |||||||
| chr13:41321769 | TCTTA | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.402+954_402+957del others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr13 | 41321769 | ||||||
| chr13:41321824 | A | G | 1 | a0001c0001t0002g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.402+1000A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321824 | |||||||
| chr13:41321843 | C | G | 5 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(2): Show |
5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+1019C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321843 | |||||||
| chr13:41321843 | C | T | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.402+1019C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321843 | |||||||
| chr13:41321852 | T | C | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.402+1028T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321852 | |||||||
| chr13:41321914 | G | C | 1 | a0002c0003t0005g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.402+1090G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321914 | |||||||
| chr13:41322017 | C | T | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.403-1039C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322017 | |||||||
| chr13:41322119 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.403-937C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322119 | |||||||
| chr13:41322169 | G | T | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403-887G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322169 | |||||||
| chr13:41322226 | AAGG | A | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.403-827_403-825del others(3): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr13 | 41322226 | ||||||
| chr13:41322316 | T | G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.403-740T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322316 | |||||||
| chr13:41322367 | T | C | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.403-689T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322367 | |||||||
| chr13:41322636 | GCTGTGTC others(4): Show |
G | 1 | a0001c0001t0011g0104 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.403-410_403-400del others(11): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr13 | 41322636 | ||||||
| chr13:41322739 | A | T | 1 | a0001c0017t0006g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.403-317A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322739 | |||||||
| chr13:41323353 | C | CTT | 8 | a0001c0001t0002g0019 a0001c0001t0002g0256 a0001c0001t0002g0257 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.537+175_537+176dup others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41323353 | ||||||
| chr13:41323412 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.537+222A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323412 | |||||||
| chr13:41323424 | T | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.537+234T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323424 | |||||||
| chr13:41323425 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.537+235G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323425 | |||||||
| chr13:41323431 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.537+241A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323431 | |||||||
| chr13:41323526 | A | G | 1 | a0001c0001t0004g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.537+336A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323526 | |||||||
| chr13:41323555 | T | C | 52 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
60 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.537+365T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323555 | |||||||
| chr13:41323566 | A | G | 3 | a0001c0001t0003g0096 a0001c0001t0003g0130 a0001c0001t0018g0129 |
3 | HG00733.hp1 HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.537+376A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323566 | |||||||
| chr13:41323594 | C | T | 3 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0002g0255 |
3 | HG02109.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.537+404C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323594 | |||||||
| chr13:41323635 | A | T | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.537+445A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323635 | |||||||
| chr13:41323647 | C | T | 6 | a0001c0001t0006g0090 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+457C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323647 | |||||||
| chr13:41323674 | G | A | 22 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.537+484G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323674 | |||||||
| chr13:41324009 | T | C | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.537+819T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324009 | |||||||
| chr13:41324011 | T | G | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.537+821T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324011 | |||||||
| chr13:41324038 | T | C | 1 | a0001c0001t0020g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.537+848T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324038 | |||||||
| chr13:41324204 | G | T | 4 | a0001c0001t0004g0054 a0001c0001t0004g0080 a0001c0001t0004g0081 others(1): Show |
4 | NA18977.hp1 NA19043.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+1014G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324204 | |||||||
| chr13:41324255 | A | G | 1 | a0001c0013t0015g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.537+1065A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324255 | |||||||
| chr13:41324269 | A | G | 58 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(55): Show |
62 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.537+1079A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324269 | |||||||
| chr13:41324321 | C | G | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.537+1131C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324321 | |||||||
| chr13:41324322 | A | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.537+1132A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324322 | |||||||
| chr13:41324363 | CTTTT | C | 6 | a0001c0001t0006g0090 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+1200_537+1203d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324363 | ||||||
| chr13:41324363 | CTTTTT | C | 15 | a0001c0001t0001g0252 a0001c0001t0001g0271 a0001c0001t0001g0279 others(12): Show |
15 | HG01069.hp1 HG01175.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.537+1199_537+1203d others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324363 | ||||||
| chr13:41324363 | CTTTTTT | C | 181 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(178): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.537+1198_537+1203d others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324363 | ||||||
| chr13:41324363 | CTTTTTTT | C | 96 | a0001c0001t0001g0190 a0001c0001t0001g0213 a0001c0001t0003g0003 others(93): Show |
109 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.537+1197_537+1203d others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324363 | ||||||
| chr13:41324367 | T | C | 2 | a0001c0001t0008g0085 a0001c0002t0009g0312 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.537+1177T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324367 | |||||||
| chr13:41324374 | T | C | 2 | a0001c0001t0004g0056 a0001c0001t0004g0057 |
2 | NA18964.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.537+1184T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324374 | |||||||
| chr13:41324377 | T | C | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.537+1187T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324377 | |||||||
| chr13:41324415 | G | T | 1 | a0001c0001t0003g0126 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.537+1225G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324415 | |||||||
| chr13:41324433 | T | C | 1 | a0001c0001t0002g0296 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.537+1243T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324433 | |||||||
| chr13:41324564 | C | T | 1 | a0001c0002t0009g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.538-1134C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324564 | |||||||
| chr13:41324664 | G | A | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.538-1034G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324664 | |||||||
| chr13:41324870 | C | T | 3 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0308 |
3 | HG03492.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.538-828C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324870 | |||||||
| chr13:41324879 | G | GT | 13 | a0001c0001t0001g0210 a0001c0001t0006g0025 a0001c0001t0006g0026 others(10): Show |
13 | HG01192.hp1 HG01891.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.538-807dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324879 | ||||||
| chr13:41324881 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.538-817T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324881 | |||||||
| chr13:41324957 | G | GT | 245 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(242): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.538-723dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324957 | ||||||
| chr13:41324957 | G | GTT | 46 | a0001c0001t0001g0250 a0001c0001t0001g0264 a0001c0001t0001g0288 others(43): Show |
55 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.538-724_538-723dup others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324957 | ||||||
| chr13:41324957 | GT | G | 16 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(13): Show |
22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.538-723delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324957 | ||||||
| chr13:41325060 | C | T | 2 | a0001c0001t0004g0073 a0001c0001t0004g0083 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.538-638C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325060 | |||||||
| chr13:41325139 | A | G | 1 | a0001c0001t0004g0072 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.538-559A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325139 | |||||||
| chr13:41325236 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.538-462T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325236 | |||||||
| chr13:41325267 | A | G | 11 | a0001c0001t0006g0010 a0001c0001t0006g0024 a0001c0001t0006g0025 others(8): Show |
12 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.538-431A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325267 | |||||||
| chr13:41325286 | AATT | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.538-411_538-409del others(3): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325286 | |||||||
| chr13:41325399 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.538-299A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325399 | |||||||
| chr13:41325584 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.538-114G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325584 | |||||||
| chr13:41325934 | A | T | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.691+83A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41325934 | |||||||
| chr13:41325951 | G | A | 1 | a0001c0001t0004g0060 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.691+100G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41325951 | |||||||
| chr13:41326013 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.691+162A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326013 | |||||||
| chr13:41326033 | A | G | 1 | a0001c0002t0007g0159 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.691+182A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326033 | |||||||
| chr13:41326154 | T | C | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.691+303T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326154 | |||||||
| chr13:41326164 | G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.691+313G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326164 | |||||||
| chr13:41326337 | C | T | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691+486C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326337 | |||||||
| chr13:41326375 | A | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.691+524A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326375 | |||||||
| chr13:41326429 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.691+578C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326429 | |||||||
| chr13:41326436 | A | G | 156 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.691+585A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326436 | |||||||
| chr13:41326589 | T | TA | 6 | a0001c0001t0006g0090 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+739dupA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41326589 | ||||||
| chr13:41326793 | T | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.691+942T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326793 | |||||||
| chr13:41326803 | C | T | 1 | a0001c0001t0013g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.691+952C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326803 | |||||||
| chr13:41326933 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.691+1082A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326933 | |||||||
| chr13:41327134 | G | A | 1 | a0001c0001t0023g0265 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.691+1283G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327134 | |||||||
| chr13:41327160 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.691+1309T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327160 | |||||||
| chr13:41327250 | ATAAT | A | 16 | a0001c0001t0002g0293 a0002c0003t0005g0035 a0002c0003t0005g0036 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.691+1403_691+1406d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327250 | ||||||
| chr13:41327458 | T | TA | 265 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(262): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.692-1255dupA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327458 | ||||||
| chr13:41327718 | C | T | 3 | a0001c0001t0003g0100 a0001c0001t0003g0122 a0001c0001t0003g0125 |
3 | NA18977.hp2 NA18987.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.692-1006C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327718 | |||||||
| chr13:41327719 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.692-1005A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327719 | |||||||
| chr13:41327735 | T | TGTTTAAA others(304): Show |
1 | a0002c0014t0005g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.692-977_692-976ins others(311): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(321): Show |
1 | a0002c0003t0005g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.692-977_692-976ins others(328): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(322): Show |
3 | a0002c0003t0005g0039 a0002c0003t0005g0040 a0002c0003t0005g0041 |
3 | HG02280.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.692-977_692-976ins others(329): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(323): Show |
4 | a0002c0003t0005g0042 a0002c0003t0005g0043 a0002c0003t0005g0044 others(1): Show |
4 | HG01891.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.692-977_692-976ins others(330): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(324): Show |
2 | a0002c0003t0005g0036 a0002c0003t0005g0048 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.692-977_692-976ins others(331): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(327): Show |
2 | a0002c0003t0005g0034 a0002c0003t0005g0046 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.692-977_692-976ins others(334): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(329): Show |
1 | a0002c0003t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.692-977_692-976ins others(336): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(331): Show |
1 | a0002c0003t0005g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.692-977_692-976ins others(338): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(337): Show |
1 | a0002c0003t0005g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.692-977_692-976ins others(344): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327735 | T | TGTTTAAA others(346): Show |
1 | a0002c0003t0005g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.692-977_692-976ins others(353): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | ||||||
| chr13:41327807 | C | G | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.692-917C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327807 | |||||||
| chr13:41327811 | C | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0251 |
2 | NA18940.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.692-913C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327811 | |||||||
| chr13:41327937 | T | C | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.692-787T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327937 | |||||||
| chr13:41328012 | T | G | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.692-712T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328012 | |||||||
| chr13:41328104 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.692-620C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328104 | |||||||
| chr13:41328157 | G | T | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.692-567G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328157 | |||||||
| chr13:41328528 | A | G | 6 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 others(3): Show |
6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-196A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328528 | |||||||
| chr13:41328543 | A | G | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.692-181A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328543 | |||||||
| chr13:41328590 | C | A | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.692-134C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328590 | |||||||
| chr13:41328617 | A | G | 1 | a0001c0013t0015g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.692-107A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328617 | |||||||
| chr13:41328647 | A | T | 1 | a0001c0001t0006g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.692-77A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328647 | |||||||
| chr13:41328911 | A | C | 1 | a0001c0001t0010g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.811+68A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41328911 | |||||||
| chr13:41329259 | T | C | 1 | a0001c0001t0010g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.811+416T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329259 | |||||||
| chr13:41329278 | G | T | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.811+435G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329278 | |||||||
| chr13:41329506 | AT | A | 28 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0220 others(25): Show |
28 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.811+681delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr13 | 41329506 | ||||||
| chr13:41329555 | T | C | 1 | a0001c0001t0008g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.811+712T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329555 | |||||||
| chr13:41329556 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.811+713A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329556 | |||||||
| chr13:41329573 | C | T | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.811+730C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329573 | |||||||
| chr13:41329593 | A | G | 1 | a0001c0001t0008g0092 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.811+750A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329593 | |||||||
| chr13:41329722 | A | G | 1 | a0001c0001t0008g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.811+879A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329722 | |||||||
| chr13:41329919 | T | C | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.811+1076T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329919 | |||||||
| chr13:41330026 | AT | A | 302 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.811+1194delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr13 | 41330026 | ||||||
| chr13:41330133 | T | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.812-1141T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330133 | |||||||
| chr13:41330173 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0192 others(3): Show |
9 | HG01109.hp1 HG01167.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.812-1101G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330173 | |||||||
| chr13:41330286 | G | A | 6 | a0001c0001t0006g0090 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.812-988G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330286 | |||||||
| chr13:41330480 | T | C | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.812-794T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330480 | |||||||
| chr13:41330928 | C | T | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.812-346C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330928 | |||||||
| chr13:41331103 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.812-171T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41331103 | |||||||
| chr13:41331177 | C | T | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.812-97C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41331177 | |||||||
| chr13:41331571 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0137 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.907+202A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331571 | |||||||
| chr13:41331583 | A | C | 6 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.907+214A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331583 | |||||||
| chr13:41331726 | T | G | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.907+357T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331726 | |||||||
| chr13:41331766 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.907+397A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331766 | |||||||
| chr13:41331804 | G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.907+435G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331804 | |||||||
| chr13:41331872 | G | T | 2 | a0001c0001t0003g0099 a0001c0001t0003g0121 |
2 | NA18963.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.907+503G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331872 | |||||||
| chr13:41331953 | A | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.907+584A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331953 | |||||||
| chr13:41332014 | A | G | 6 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 others(3): Show |
6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.907+645A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41332014 | |||||||
| chr13:41332132 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.907+763A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41332132 | |||||||
| chr13:41332797 | TTGAC | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.907+1434_907+1437d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41332797 | ||||||
| chr13:41332880 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0137 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.907+1511A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41332880 | |||||||
| chr13:41333247 | T | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
93 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.907+1878T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333247 | |||||||
| chr13:41333336 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.907+1967A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333336 | |||||||
| chr13:41333502 | G | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.907+2133G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333502 | |||||||
| chr13:41333643 | GCTT | G | 6 | a0001c0001t0002g0230 a0001c0001t0002g0253 a0001c0001t0002g0254 others(3): Show |
6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.907+2278_907+2280d others(5): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41333643 | ||||||
| chr13:41333690 | A | G | 61 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(58): Show |
65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.907+2321A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333690 | |||||||
| chr13:41333714 | C | T | 18 | a0001c0001t0008g0084 a0002c0003t0005g0034 a0002c0003t0005g0035 others(15): Show |
18 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.907+2345C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333714 | |||||||
| chr13:41333879 | G | A | 1 | a0001c0001t0008g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.907+2510G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333879 | |||||||
| chr13:41333957 | G | A | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.907+2588G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333957 | |||||||
| chr13:41333994 | G | A | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.907+2625G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333994 | |||||||
| chr13:41334586 | C | G | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.908-2064C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41334586 | |||||||
| chr13:41334622 | T | C | 1 | a0001c0017t0006g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.908-2028T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41334622 | |||||||
| chr13:41334751 | A | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0244 a0008c0012t0001g0243 |
3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.908-1899A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41334751 | |||||||
| chr13:41334906 | AC | A | 302 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.908-1736delC | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41334906 | ||||||
| chr13:41335064 | C | T | 2 | a0001c0001t0004g0055 a0001c0001t0004g0151 |
2 | HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.908-1586C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335064 | |||||||
| chr13:41335161 | G | A | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.908-1489G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335161 | |||||||
| chr13:41335225 | G | GAAGAT | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.908-1421_908-1420i others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41335225 | ||||||
| chr13:41335306 | T | C | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.908-1344T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335306 | |||||||
| chr13:41335435 | G | A | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.908-1215G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335435 | |||||||
| chr13:41335533 | G | A | 1 | a0001c0001t0003g0109 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.908-1117G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335533 | |||||||
| chr13:41335613 | T | G | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.908-1037T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335613 | |||||||
| chr13:41335683 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0209 a0001c0001t0001g0289 |
3 | NA18956.hp2 NA18993.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.908-967A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335683 | |||||||
| chr13:41335817 | C | T | 5 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(2): Show |
5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.908-833C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335817 | |||||||
| chr13:41335859 | GT | G | 241 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(238): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.908-778delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41335859 | ||||||
| chr13:41335859 | GTT | G | 60 | a0001c0001t0002g0230 a0001c0001t0003g0003 a0001c0001t0003g0006 others(57): Show |
64 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.908-779_908-778del others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41335859 | ||||||
| chr13:41335872 | T | C | 47 | a0001c0001t0002g0242 a0001c0001t0002g0263 a0001c0001t0004g0001 others(44): Show |
56 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.908-778T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335872 | |||||||
| chr13:41335922 | T | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.908-728T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335922 | |||||||
| chr13:41336041 | G | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.908-609G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336041 | |||||||
| chr13:41336103 | A | G | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.908-547A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336103 | |||||||
| chr13:41336162 | TA | T | 20 | a0001c0001t0001g0266 a0001c0001t0004g0052 a0001c0001t0008g0143 others(17): Show |
20 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.908-479delA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41336162 | ||||||
| chr13:41336169 | A | T | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.908-481A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336169 | |||||||
| chr13:41336171 | A | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(286): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.908-479A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336171 | |||||||
| chr13:41336351 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.908-299T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336351 | |||||||
| chr13:41336373 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.908-277G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336373 | |||||||
| chr13:41336495 | T | C | 8 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0231 others(5): Show |
10 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.908-155T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336495 | |||||||
| chr13:41336556 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0180 others(15): Show |
20 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.908-94A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336556 | |||||||
| chr13:41336932 | G | T | 1 | a0001c0001t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1014+176G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41336932 | |||||||
| chr13:41337034 | T | C | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1014+278T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337034 | |||||||
| chr13:41337044 | T | G | 1 | a0001c0001t0003g0100 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1014+288T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337044 | |||||||
| chr13:41337096 | A | G | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1014+340A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337096 | |||||||
| chr13:41337357 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1014+601C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337357 | |||||||
| chr13:41337415 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+659C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337415 | |||||||
| chr13:41337491 | C | T | 5 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(2): Show |
5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+735C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337491 | |||||||
| chr13:41337497 | C | T | 3 | a0001c0001t0002g0189 a0001c0001t0002g0241 a0001c0001t0002g0263 |
3 | HG01358.hp2 HG02280.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1014+741C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337497 | |||||||
| chr13:41337530 | G | A | 1 | a0001c0001t0006g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1014+774G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337530 | |||||||
| chr13:41337542 | C | CA | 283 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(280): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1014+803dupA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337542 | ||||||
| chr13:41337542 | C | CAA | 12 | a0001c0001t0001g0288 a0001c0001t0001g0290 a0001c0001t0002g0221 others(9): Show |
12 | HG00621.hp2 HG00735.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014+802_1014+803d others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337542 | ||||||
| chr13:41337600 | A | G | 1 | a0001c0001t0003g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1014+844A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337600 | |||||||
| chr13:41337676 | GT | G | 22 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1014+922delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337676 | ||||||
| chr13:41337787 | A | G | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1014+1031A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337787 | |||||||
| chr13:41337809 | G | A | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1014+1053G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337809 | |||||||
| chr13:41337854 | A | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0193 a0001c0001t0001g0206 others(8): Show |
12 | HG00609.hp1 HG02056.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014+1098A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337854 | |||||||
| chr13:41337934 | A | AG | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1014+1179dupG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337934 | ||||||
| chr13:41337955 | T | TA | 6 | a0001c0001t0002g0260 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+1207dupA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337955 | ||||||
| chr13:41337964 | C | T | 1 | a0001c0001t0002g0292 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1014+1208C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337964 | |||||||
| chr13:41337974 | C | T | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014+1218C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337974 | |||||||
| chr13:41338054 | T | G | 72 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(69): Show |
77 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1014+1298T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338054 | |||||||
| chr13:41338111 | T | G | 1 | a0001c0001t0012g0110 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1014+1355T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338111 | |||||||
| chr13:41338204 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
92 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1014+1448T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338204 | |||||||
| chr13:41338244 | G | A | 16 | a0002c0003t0005g0035 a0002c0003t0005g0036 a0002c0003t0005g0038 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014+1488G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338244 | |||||||
| chr13:41338268 | T | C | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1014+1512T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338268 | |||||||
| chr13:41338359 | A | G | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1014+1603A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338359 | |||||||
| chr13:41338519 | A | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+1763A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338519 | |||||||
| chr13:41338724 | A | T | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+1968A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338724 | |||||||
| chr13:41338758 | A | T | 2 | a0001c0001t0004g0075 a0009c0008t0026g0078 |
2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1014+2002A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338758 | |||||||
| chr13:41338838 | C | G | 1 | a0001c0001t0002g0305 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1014+2082C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338838 | |||||||
| chr13:41338878 | T | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1014+2122T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338878 | |||||||
| chr13:41338995 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+2239C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338995 | |||||||
| chr13:41339120 | T | TTTG | 233 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1014+2376_1014+237 others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41339120 | ||||||
| chr13:41339132 | GT | G | 65 | a0001c0001t0001g0208 a0001c0001t0003g0003 a0001c0001t0003g0006 others(62): Show |
69 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1014+2379delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41339132 | ||||||
| chr13:41339193 | T | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+2437T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339193 | |||||||
| chr13:41339429 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1014+2673G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339429 | |||||||
| chr13:41339441 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1014+2685A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339441 | |||||||
| chr13:41339455 | A | C | 1 | a0001c0017t0006g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1014+2699A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339455 | |||||||
| chr13:41339481 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0251 |
2 | NA18940.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1014+2725G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339481 | |||||||
| chr13:41339531 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0244 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1014+2775A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339531 | |||||||
| chr13:41339618 | T | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+2862T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339618 | |||||||
| chr13:41339870 | G | A | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+3114G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339870 | |||||||
| chr13:41340052 | T | C | 2 | a0001c0001t0003g0097 a0001c0001t0003g0111 |
2 | HG02523.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1014+3296T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340052 | |||||||
| chr13:41340447 | G | C | 202 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1014+3691G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340447 | |||||||
| chr13:41340495 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0181 others(8): Show |
14 | HG00597.hp2 HG02015.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014+3739T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340495 | |||||||
| chr13:41340539 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+3783C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340539 | |||||||
| chr13:41340647 | G | GTTTTTTT others(5): Show |
1 | a0001c0002t0009g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1014+3924_1014+393 others(16): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340647 | GTTTT | G | 4 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0159 others(1): Show |
9 | HG00423.hp1 HG02135.hp2 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.1014+3932_1014+393 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340647 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0004g0075 a0009c0008t0026g0078 |
2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1014+3923_1014+393 others(17): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340647 | GTTTTTTT others(7): Show |
G | 9 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0271 others(6): Show |
9 | HG01981.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1014+3922_1014+393 others(18): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340647 | GTTTTTTT others(8): Show |
G | 84 | a0001c0001t0001g0017 a0001c0001t0001g0175 a0001c0001t0001g0212 others(81): Show |
89 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1014+3921_1014+393 others(19): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340647 | GTTTTTTT others(9): Show |
G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(173): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1014+3920_1014+393 others(20): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340647 | GTTTTTTT others(10): Show |
G | 31 | a0001c0001t0001g0180 a0001c0001t0001g0220 a0001c0001t0001g0222 others(28): Show |
31 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1014+3919_1014+393 others(21): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340647 | GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1014+3918_1014+393 others(22): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340647 | GTTTTTTT others(14): Show |
G | 1 | a0002c0003t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1014+3915_1014+393 others(25): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | ||||||
| chr13:41340671 | T | G | 2 | a0001c0001t0006g0026 a0001c0001t0006g0027 |
2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1014+3915T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340671 | |||||||
| chr13:41340674 | T | G | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1014+3918T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340674 | |||||||
| chr13:41340690 | T | C | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1014+3934T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340690 | |||||||
| chr13:41340691 | T | C | 37 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0276 others(34): Show |
38 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1014+3935T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340691 | |||||||
| chr13:41340778 | G | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+4022G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340778 | |||||||
| chr13:41340822 | G | A | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+4066G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340822 | |||||||
| chr13:41340831 | C | T | 1 | a0001c0001t0004g0057 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1014+4075C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340831 | |||||||
| chr13:41340837 | C | T | 71 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(68): Show |
76 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1014+4081C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340837 | |||||||
| chr13:41340853 | T | C | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1014+4097T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340853 | |||||||
| chr13:41340880 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1014+4124C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340880 | |||||||
| chr13:41340928 | A | G | 38 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(35): Show |
47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1014+4172A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340928 | |||||||
| chr13:41341267 | A | G | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1014+4511A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341267 | |||||||
| chr13:41341788 | A | G | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014+5032A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341788 | |||||||
| chr13:41341820 | T | C | 1 | a0001c0001t0008g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1014+5064T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341820 | |||||||
| chr13:41341836 | C | CT | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1014+5093dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41341836 | ||||||
| chr13:41341836 | C | CTT | 21 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(18): Show |
21 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1014+5092_1014+509 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41341836 | ||||||
| chr13:41341980 | C | T | 4 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(1): Show |
4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+5224C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341980 | |||||||
| chr13:41341984 | A | G | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1014+5228A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341984 | |||||||
| chr13:41341988 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0181 others(9): Show |
15 | HG00597.hp2 HG02015.hp2 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.1014+5232T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341988 | |||||||
| chr13:41341998 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1014+5242A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341998 | |||||||
| chr13:41342010 | T | C | 4 | a0001c0001t0011g0104 a0001c0001t0011g0105 a0001c0001t0011g0118 others(1): Show |
4 | NA18948.hp1 NA18984.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+5254T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342010 | |||||||
| chr13:41342067 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+5311C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342067 | |||||||
| chr13:41342074 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1014+5318C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342074 | |||||||
| chr13:41342130 | CCTCT | C | 3 | a0001c0001t0008g0142 a0001c0001t0008g0145 a0001c0001t0024g0141 |
3 | HG01981.hp2 HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1014+5385_1014+538 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41342130 | ||||||
| chr13:41342143 | C | CT | 7 | a0001c0001t0001g0283 a0001c0001t0002g0005 a0001c0001t0002g0280 others(4): Show |
10 | NA18942.hp1 NA18943.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014+5399dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41342143 | ||||||
| chr13:41342177 | G | A | 1 | a0001c0001t0010g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1014+5421G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342177 | |||||||
| chr13:41342323 | A | G | 2 | a0001c0001t0003g0115 a0001c0001t0003g0116 |
2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1014+5567A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342323 | |||||||
| chr13:41342378 | T | A | 1 | a0001c0002t0009g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1014+5622T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342378 | |||||||
| chr13:41342557 | G | A | 3 | a0001c0001t0008g0143 a0001c0001t0008g0144 a0001c0001t0020g0140 |
3 | HG02486.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1014+5801G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342557 | |||||||
| chr13:41342769 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1014+6013T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342769 | |||||||
| chr13:41342815 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1014+6059A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342815 | |||||||
| chr13:41343001 | CAG | C | 71 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(68): Show |
76 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1014+6248_1014+624 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41343001 | ||||||
| chr13:41343043 | A | G | 1 | a0001c0001t0003g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1014+6287A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343043 | |||||||
| chr13:41343169 | A | G | 2 | a0001c0001t0001g0250 a0001c0001t0002g0238 |
2 | HG00597.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1014+6413A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343169 | |||||||
| chr13:41343171 | C | T | 1 | a0001c0001t0003g0114 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1014+6415C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343171 | |||||||
| chr13:41343229 | T | TGAGTA | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1014+6476_1014+648 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41343229 | ||||||
| chr13:41343432 | A | G | 202 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1014+6676A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343432 | |||||||
| chr13:41343461 | C | A | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1014+6705C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343461 | |||||||
| chr13:41343511 | A | T | 5 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(2): Show |
5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+6755A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343511 | |||||||
| chr13:41343637 | C | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+6881C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343637 | |||||||
| chr13:41343653 | C | T | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+6897C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343653 | |||||||
| chr13:41343667 | C | G | 2 | a0002c0003t0005g0035 a0002c0003t0005g0049 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1014+6911C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343667 | |||||||
| chr13:41344074 | T | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+7318T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344074 | |||||||
| chr13:41344082 | GTTA | G | 7 | a0002c0003t0005g0036 a0002c0003t0005g0039 a0002c0003t0005g0041 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1014+7333_1014+733 others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41344082 | ||||||
| chr13:41344088 | A | G | 1 | a0001c0001t0010g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1014+7332A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344088 | |||||||
| chr13:41344167 | A | G | 1 | a0002c0003t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1014+7411A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344167 | |||||||
| chr13:41344257 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1014+7501T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344257 | |||||||
| chr13:41344344 | G | A | 60 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(57): Show |
64 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1014+7588G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344344 | |||||||
| chr13:41344421 | C | T | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+7665C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344421 | |||||||
| chr13:41344426 | T | C | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1014+7670T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344426 | |||||||
| chr13:41344507 | G | C | 1 | a0001c0001t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1014+7751G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344507 | |||||||
| chr13:41344544 | G | A | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+7788G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344544 | |||||||
| chr13:41344666 | T | C | 6 | a0001c0001t0006g0090 a0001c0001t0008g0086 a0001c0001t0008g0087 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+7910T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344666 | |||||||
| chr13:41344774 | A | G | 1 | a0002c0003t0005g0048 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1014+8018A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344774 | |||||||
| chr13:41344793 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1014+8037A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344793 | |||||||
| chr13:41344828 | A | G | 11 | a0001c0001t0006g0010 a0001c0001t0006g0024 a0001c0001t0006g0025 others(8): Show |
12 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014+8072A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344828 | |||||||
| chr13:41345025 | T | C | 5 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(2): Show |
5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+8269T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345025 | |||||||
| chr13:41345068 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1014+8312G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345068 | |||||||
| chr13:41345235 | T | G | 4 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(1): Show |
4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+8479T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345235 | |||||||
| chr13:41345450 | G | A | 1 | a0003c0004t0003g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1014+8694G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345450 | |||||||
| chr13:41345530 | T | C | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014+8774T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345530 | |||||||
| chr13:41345562 | G | T | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014+8806G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345562 | |||||||
| chr13:41345692 | C | T | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014+8936C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345692 | |||||||
| chr13:41345739 | T | A | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1014+8983T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345739 | |||||||
| chr13:41345763 | C | G | 8 | a0001c0001t0001g0283 a0001c0001t0002g0005 a0001c0001t0002g0280 others(5): Show |
11 | HG02129.hp1 NA18942.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+9007C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345763 | |||||||
| chr13:41345784 | G | A | 4 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(1): Show |
4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+9028G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345784 | |||||||
| chr13:41345789 | G | T | 8 | a0001c0001t0003g0006 a0001c0001t0003g0015 a0001c0001t0003g0131 others(5): Show |
11 | HG00642.hp2 HG01074.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+9033G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345789 | |||||||
| chr13:41345853 | C | T | 38 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(35): Show |
47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1014+9097C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345853 | |||||||
| chr13:41345920 | A | G | 8 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(5): Show |
13 | HG00423.hp1 HG02135.hp2 NA18965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1014+9164A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345920 | |||||||
| chr13:41346120 | A | G | 8 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(5): Show |
13 | HG00423.hp1 HG02135.hp2 NA18965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-9024A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346120 | |||||||
| chr13:41346206 | C | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015-8938C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346206 | |||||||
| chr13:41346237 | C | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-8907C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346237 | |||||||
| chr13:41346296 | G | T | 2 | a0001c0001t0003g0133 a0001c0001t0003g0134 |
2 | HG01496.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1015-8848G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346296 | |||||||
| chr13:41346389 | G | T | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1015-8755G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346389 | |||||||
| chr13:41346538 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-8606A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346538 | |||||||
| chr13:41346898 | A | C | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015-8246A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346898 | |||||||
| chr13:41346900 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-8244T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346900 | |||||||
| chr13:41346941 | G | A | 1 | a0001c0001t0023g0265 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1015-8203G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346941 | |||||||
| chr13:41347067 | A | C | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-8077A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347067 | |||||||
| chr13:41347202 | G | A | 1 | a0001c0001t0003g0114 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1015-7942G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347202 | |||||||
| chr13:41347210 | G | A | 7 | a0001c0001t0004g0011 a0001c0001t0004g0052 a0001c0001t0004g0056 others(4): Show |
8 | HG00621.hp2 HG02080.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1015-7934G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347210 | |||||||
| chr13:41347222 | AAAAAAC | A | 160 | a0001c0001t0001g0213 a0001c0001t0001g0244 a0001c0001t0002g0219 others(157): Show |
174 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1015-7904_1015-789 others(10): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41347222 | ||||||
| chr13:41347223 | AAAAAC | A | 6 | a0001c0001t0002g0221 a0001c0001t0003g0106 a0001c0001t0003g0128 others(3): Show |
6 | HG00621.hp2 HG01192.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1015-7916_1015-791 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41347223 | ||||||
| chr13:41347224 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1015-7920A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347224 | |||||||
| chr13:41347225 | A | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
61 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1015-7919A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347225 | |||||||
| chr13:41347227 | ACAAAAAC | A | 134 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1015-7916_1015-791 others(11): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347227 | |||||||
| chr13:41347234 | C | A | 18 | a0001c0001t0001g0213 a0001c0001t0001g0244 a0001c0001t0002g0219 others(15): Show |
18 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1015-7910C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347234 | |||||||
| chr13:41347240 | C | A | 9 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0231 others(6): Show |
11 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-7904C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347240 | |||||||
| chr13:41347320 | T | A | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1015-7824T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347320 | |||||||
| chr13:41347321 | A | C | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1015-7823A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347321 | |||||||
| chr13:41347359 | TTTTAGGA others(16): Show |
T | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-7783_1015-776 others(27): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41347359 | ||||||
| chr13:41347750 | T | C | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1015-7394T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347750 | |||||||
| chr13:41347752 | C | A | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1015-7392C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347752 | |||||||
| chr13:41347752 | C | G | 16 | a0002c0003t0005g0035 a0002c0003t0005g0036 a0002c0003t0005g0038 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1015-7392C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347752 | |||||||
| chr13:41347792 | A | G | 38 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(35): Show |
47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1015-7352A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347792 | |||||||
| chr13:41347797 | G | A | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1015-7347G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347797 | |||||||
| chr13:41348043 | G | A | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-7101G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348043 | |||||||
| chr13:41348108 | T | A | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1015-7036T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348108 | |||||||
| chr13:41348109 | T | A | 145 | a0001c0001t0001g0204 a0001c0001t0003g0003 a0001c0001t0003g0006 others(142): Show |
159 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1015-7035T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348109 | |||||||
| chr13:41348174 | AT | A | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-6960delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41348174 | ||||||
| chr13:41348231 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-6913A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348231 | |||||||
| chr13:41348248 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG02080.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1015-6896A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348248 | |||||||
| chr13:41348558 | T | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-6586T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348558 | |||||||
| chr13:41348563 | A | C | 15 | a0002c0003t0005g0035 a0002c0003t0005g0036 a0002c0003t0005g0038 others(12): Show |
15 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1015-6581A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348563 | |||||||
| chr13:41348588 | A | T | 1 | a0001c0001t0002g0302 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1015-6556A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348588 | |||||||
| chr13:41348680 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1015-6464C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348680 | |||||||
| chr13:41348693 | G | A | 2 | a0001c0001t0003g0146 a0004c0015t0003g0148 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1015-6451G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348693 | |||||||
| chr13:41348694 | G | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0180 others(15): Show |
20 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1015-6450G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348694 | |||||||
| chr13:41348805 | T | C | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-6339T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348805 | |||||||
| chr13:41348811 | T | A | 2 | a0001c0001t0003g0120 a0001c0001t0004g0065 |
2 | NA19010.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1015-6333T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348811 | |||||||
| chr13:41348932 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-6212C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348932 | |||||||
| chr13:41348983 | T | C | 311 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(308): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1015-6161T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348983 | |||||||
| chr13:41349100 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-6044C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349100 | |||||||
| chr13:41349190 | T | A | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-5954T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349190 | |||||||
| chr13:41349277 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0264 |
2 | HG01433.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1015-5867T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349277 | |||||||
| chr13:41349325 | A | G | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1015-5819A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349325 | |||||||
| chr13:41349336 | C | T | 1 | a0001c0001t0004g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1015-5808C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349336 | |||||||
| chr13:41349463 | C | G | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1015-5681C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349463 | |||||||
| chr13:41349486 | C | CT | 302 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1015-5649dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41349486 | ||||||
| chr13:41349629 | A | T | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5515A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349629 | |||||||
| chr13:41349631 | T | A | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5513T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349631 | |||||||
| chr13:41349680 | C | T | 1 | a0001c0001t0004g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1015-5464C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349680 | |||||||
| chr13:41349689 | G | C | 1 | a0001c0001t0004g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1015-5455G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349689 | |||||||
| chr13:41349702 | C | T | 201 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1015-5442C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349702 | |||||||
| chr13:41349767 | C | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1015-5377C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349767 | |||||||
| chr13:41349835 | G | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-5309G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349835 | |||||||
| chr13:41349845 | C | A | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5299C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349845 | |||||||
| chr13:41349869 | G | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-5275G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349869 | |||||||
| chr13:41349888 | G | A | 2 | a0001c0001t0004g0055 a0001c0001t0004g0151 |
2 | HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1015-5256G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349888 | |||||||
| chr13:41349888 | G | T | 1 | a0001c0001t0003g0128 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1015-5256G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349888 | |||||||
| chr13:41349927 | T | C | 1 | a0001c0001t0004g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1015-5217T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349927 | |||||||
| chr13:41349959 | T | C | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5185T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349959 | |||||||
| chr13:41349960 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5184C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349960 | |||||||
| chr13:41349960 | CA | C | 294 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(291): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1015-5168delA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41349960 | ||||||
| chr13:41349961 | A | C | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5183A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349961 | |||||||
| chr13:41349968 | A | T | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5176A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349968 | |||||||
| chr13:41350203 | C | A | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1015-4941C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350203 | |||||||
| chr13:41350297 | GT | G | 298 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1015-4833delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350297 | ||||||
| chr13:41350300 | T | G | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-4844T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350300 | |||||||
| chr13:41350368 | A | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-4776A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350368 | |||||||
| chr13:41350471 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-4673A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350471 | |||||||
| chr13:41350532 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-4612A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350532 | |||||||
| chr13:41350566 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1015-4578G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350566 | |||||||
| chr13:41350603 | TTTTG | T | 6 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0029 others(3): Show |
6 | HG01192.hp1 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1015-4537_1015-453 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350603 | ||||||
| chr13:41350604 | TTTGTTTT others(9): Show |
T | 1 | a0001c0001t0001g0290 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1015-4537_1015-452 others(20): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350604 | ||||||
| chr13:41350607 | G | T | 4 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(1): Show |
5 | HG01069.hp2 HG01071.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1015-4537G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350607 | |||||||
| chr13:41350611 | T | G | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-4533T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350611 | |||||||
| chr13:41350611 | TTTTTTTT others(10): Show |
T | 57 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0266 others(54): Show |
66 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1015-4524_1015-450 others(21): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350611 | ||||||
| chr13:41350612 | TTTTTTTT others(9): Show |
T | 1 | a0001c0001t0004g0056 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1015-4524_1015-450 others(20): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350612 | ||||||
| chr13:41350618 | TTG | T | 207 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(204): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1015-4524_1015-452 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350618 | ||||||
| chr13:41350619 | TG | T | 18 | a0001c0001t0001g0177 a0001c0001t0001g0195 a0001c0001t0001g0207 others(15): Show |
18 | HG01175.hp2 HG01496.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.1015-4524delG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350619 | |||||||
| chr13:41350619 | TGTTTG | T | 3 | a0001c0001t0006g0025 a0001c0001t0006g0026 a0001c0001t0006g0032 |
3 | HG02895.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1015-4524_1015-452 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350619 | |||||||
| chr13:41350620 | G | T | 10 | a0001c0001t0003g0128 a0001c0001t0006g0010 a0001c0001t0006g0027 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-4524G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350620 | |||||||
| chr13:41350622 | T | G | 1 | a0001c0001t0001g0290 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1015-4522T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350622 | |||||||
| chr13:41350623 | T | G | 4 | a0001c0001t0001g0177 a0001c0001t0001g0195 a0001c0001t0001g0229 others(1): Show |
4 | HG01981.hp1 HG03688.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-4521T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350623 | |||||||
| chr13:41350624 | G | T | 19 | a0001c0001t0001g0177 a0001c0001t0001g0195 a0001c0001t0001g0229 others(16): Show |
20 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1015-4520G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350624 | |||||||
| chr13:41350628 | G | T | 242 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(239): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1015-4516G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350628 | |||||||
| chr13:41350656 | C | T | 60 | a0001c0001t0001g0250 a0001c0001t0001g0283 a0001c0001t0002g0005 others(57): Show |
63 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1015-4488C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350656 | |||||||
| chr13:41350755 | G | T | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-4389G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350755 | |||||||
| chr13:41350883 | C | T | 1 | a0001c0001t0008g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1015-4261C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350883 | |||||||
| chr13:41350981 | A | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0203 a0001c0001t0001g0208 |
3 | NA18987.hp1 NA19011.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1015-4163A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350981 | |||||||
| chr13:41351049 | C | T | 1 | a0001c0001t0021g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1015-4095C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351049 | |||||||
| chr13:41351061 | C | T | 38 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(35): Show |
47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1015-4083C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351061 | |||||||
| chr13:41351123 | G | A | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1015-4021G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351123 | |||||||
| chr13:41351148 | A | G | 9 | a0001c0001t0006g0025 a0001c0001t0006g0026 a0001c0001t0006g0027 others(6): Show |
9 | HG01192.hp1 HG01891.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-3996A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351148 | |||||||
| chr13:41351175 | C | T | 9 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0231 others(6): Show |
11 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-3969C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351175 | |||||||
| chr13:41351189 | G | A | 2 | a0001c0001t0004g0073 a0001c0001t0004g0083 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1015-3955G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351189 | |||||||
| chr13:41351258 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-3886C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351258 | |||||||
| chr13:41351288 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-3856C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351288 | |||||||
| chr13:41351569 | G | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-3575G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351569 | |||||||
| chr13:41351632 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1015-3512T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351632 | |||||||
| chr13:41351777 | TG | T | 302 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1015-3363delG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41351777 | ||||||
| chr13:41352064 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-3080A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352064 | |||||||
| chr13:41352127 | C | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1015-3017C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352127 | |||||||
| chr13:41352215 | G | T | 301 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(298): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1015-2929G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352215 | |||||||
| chr13:41352257 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0190 others(7): Show |
13 | HG01109.hp1 HG01167.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-2887G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352257 | |||||||
| chr13:41352366 | A | G | 38 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(35): Show |
47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1015-2778A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352366 | |||||||
| chr13:41352426 | G | A | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-2718G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352426 | |||||||
| chr13:41352475 | C | T | 5 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(2): Show |
5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-2669C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352475 | |||||||
| chr13:41352511 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1015-2633C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352511 | |||||||
| chr13:41352624 | C | T | 2 | a0001c0001t0002g0285 a0001c0009t0002g0284 |
2 | HG02129.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1015-2520C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352624 | |||||||
| chr13:41352713 | G | A | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-2431G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352713 | |||||||
| chr13:41352717 | C | T | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1015-2427C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352717 | |||||||
| chr13:41352949 | T | C | 1 | a0001c0001t0004g0074 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1015-2195T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352949 | |||||||
| chr13:41352955 | A | G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015-2189A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352955 | |||||||
| chr13:41352973 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1015-2171C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352973 | |||||||
| chr13:41353113 | T | TCAAAA | 224 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(221): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1015-2008_1015-200 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | ||||||
| chr13:41353113 | T | TCAAAACA others(3): Show |
14 | a0001c0001t0001g0272 a0001c0001t0008g0086 a0001c0001t0008g0087 others(11): Show |
19 | HG02040.hp2 HG02109.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1015-2013_1015-200 others(14): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | ||||||
| chr13:41353113 | T | TCAAAACA others(8): Show |
10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-2018_1015-200 others(19): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | ||||||
| chr13:41353113 | T | TCAAAACA others(13): Show |
3 | a0001c0001t0003g0147 a0001c0001t0003g0171 a0001c0017t0006g0091 |
3 | HG01496.hp1 HG02970.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1015-2023_1015-200 others(24): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | ||||||
| chr13:41353113 | T | TCAAAACA others(18): Show |
1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1015-2028_1015-200 others(29): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | ||||||
| chr13:41353113 | T | TCAAAACA others(13): Show |
55 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(52): Show |
59 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1015-2021_1015-202 others(24): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | ||||||
| chr13:41353113 | T | TCAAAACA others(18): Show |
1 | a0001c0001t0003g0131 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1015-2021_1015-202 others(29): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | ||||||
| chr13:41353113 | T | TCAAAACA others(23): Show |
1 | a0001c0001t0003g0102 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1015-2021_1015-202 others(34): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | ||||||
| chr13:41353149 | A | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-1995A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353149 | |||||||
| chr13:41353482 | A | G | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1015-1662A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353482 | |||||||
| chr13:41353542 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1015-1602A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353542 | |||||||
| chr13:41353600 | TAA | T | 285 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(282): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1015-1528_1015-152 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353600 | ||||||
| chr13:41353600 | TAAA | T | 17 | a0001c0001t0001g0208 a0001c0001t0001g0226 a0001c0001t0001g0266 others(14): Show |
18 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1015-1529_1015-152 others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353600 | ||||||
| chr13:41353727 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0137 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1015-1417A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353727 | |||||||
| chr13:41353768 | T | TAC | 4 | a0001c0001t0001g0215 a0001c0001t0003g0113 a0001c0001t0003g0120 others(1): Show |
4 | HG02922.hp2 NA18947.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-1343_1015-134 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | ||||||
| chr13:41353768 | T | TACAC | 3 | a0001c0001t0003g0108 a0001c0001t0003g0131 a0001c0001t0003g0146 |
3 | HG01433.hp1 HG03017.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1015-1345_1015-134 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | ||||||
| chr13:41353768 | TAC | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
105 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1015-1343_1015-134 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | ||||||
| chr13:41353768 | TACAC | T | 91 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0213 others(88): Show |
95 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1015-1345_1015-134 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | ||||||
| chr13:41353768 | TACACAC | T | 8 | a0001c0001t0002g0176 a0001c0001t0002g0233 a0001c0001t0002g0235 others(5): Show |
8 | HG02015.hp1 HG02027.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.1015-1347_1015-134 others(10): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | ||||||
| chr13:41353768 | TACACACA others(1): Show |
T | 9 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0001t0004g0069 others(6): Show |
9 | HG00738.hp1 HG01261.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-1349_1015-134 others(12): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | ||||||
| chr13:41353768 | TACACACA others(3): Show |
T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(37): Show |
49 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1015-1351_1015-134 others(14): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | ||||||
| chr13:41353768 | TACACACA others(7): Show |
T | 1 | a0001c0001t0004g0072 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1015-1355_1015-134 others(18): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | ||||||
| chr13:41353801 | A | C | 6 | a0001c0001t0001g0225 a0001c0001t0010g0135 a0001c0001t0010g0136 others(3): Show |
6 | HG00280.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1015-1343A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353801 | |||||||
| chr13:41353806 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1015-1338A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353806 | |||||||
| chr13:41353978 | C | T | 1 | a0008c0012t0001g0243 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1015-1166C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353978 | |||||||
| chr13:41354054 | A | C | 1 | a0001c0001t0004g0070 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1015-1090A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354054 | |||||||
| chr13:41354163 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1015-981G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354163 | |||||||
| chr13:41354178 | A | G | 78 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(75): Show |
82 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1015-966A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354178 | |||||||
| chr13:41354339 | T | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-805T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354339 | |||||||
| chr13:41354355 | C | T | 1 | a0001c0001t0004g0059 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1015-789C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354355 | |||||||
| chr13:41354391 | A | T | 8 | a0001c0002t0007g0002 a0001c0002t0007g0157 a0001c0002t0007g0158 others(5): Show |
13 | HG00423.hp1 HG02135.hp2 NA18965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-753A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354391 | |||||||
| chr13:41354457 | T | A | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1015-687T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354457 | |||||||
| chr13:41354468 | G | A | 201 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1015-676G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354468 | |||||||
| chr13:41354603 | C | T | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1015-541C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354603 | |||||||
| chr13:41354612 | A | C | 2 | a0002c0003t0005g0035 a0002c0003t0005g0049 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1015-532A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354612 | |||||||
| chr13:41354668 | A | ATTTTGTA others(47): Show |
1 | a0002c0003t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1015-474_1015-421d others(56): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354668 | ||||||
| chr13:41354886 | A | AT | 22 | a0001c0001t0001g0226 a0001c0001t0001g0278 a0001c0001t0002g0183 others(19): Show |
27 | HG00423.hp1 HG01074.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.1015-239dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | ||||||
| chr13:41354886 | A | ATT | 173 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(170): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1015-240_1015-239d others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | ||||||
| chr13:41354886 | A | ATTT | 109 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0195 others(106): Show |
122 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1015-241_1015-239d others(5): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | ||||||
| chr13:41354886 | A | ATTTT | 6 | a0001c0001t0001g0262 a0001c0001t0003g0106 a0001c0001t0003g0128 others(3): Show |
6 | HG02630.hp2 HG03491.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1015-242_1015-239d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | ||||||
| chr13:41354886 | AT | A | 5 | a0001c0002t0009g0016 a0001c0002t0009g0164 a0001c0002t0009g0167 others(2): Show |
6 | HG01175.hp1 HG01361.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1015-239delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | ||||||
| chr13:41355394 | C | G | 1 | a0001c0001t0003g0109 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1087+178C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355394 | |||||||
| chr13:41355422 | T | G | 1 | a0001c0001t0006g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1087+206T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355422 | |||||||
| chr13:41355574 | C | T | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087+358C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355574 | |||||||
| chr13:41355696 | G | A | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1087+480G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355696 | |||||||
| chr13:41355976 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1087+760G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355976 | |||||||
| chr13:41356005 | T | C | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1087+789T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356005 | |||||||
| chr13:41356174 | T | C | 311 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(308): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1087+958T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356174 | |||||||
| chr13:41356188 | C | CG | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1087+977dupG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr13 | 41356188 | ||||||
| chr13:41356214 | G | C | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1087+998G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356214 | |||||||
| chr13:41356272 | C | T | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1087+1056C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356272 | |||||||
| chr13:41356373 | TATCTTAG others(88): Show |
T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1087+1253_1087+134 others(99): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr13 | 41356373 | ||||||
| chr13:41356711 | A | G | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1087+1495A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356711 | |||||||
| chr13:41356922 | G | A | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1088-1382G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356922 | |||||||
| chr13:41357002 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1088-1302G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357002 | |||||||
| chr13:41357004 | C | T | 2 | a0001c0001t0004g0073 a0001c0001t0004g0083 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1088-1300C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357004 | |||||||
| chr13:41357045 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1088-1259C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357045 | |||||||
| chr13:41357153 | C | T | 311 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(308): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1088-1151C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357153 | |||||||
| chr13:41357371 | T | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1088-933T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357371 | |||||||
| chr13:41357379 | T | TTTC | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1088-923_1088-921d others(5): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr13 | 41357379 | ||||||
| chr13:41357474 | G | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1088-830G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357474 | |||||||
| chr13:41357550 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1088-754A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357550 | |||||||
| chr13:41357727 | A | G | 38 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(35): Show |
47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1088-577A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357727 | |||||||
| chr13:41357902 | A | G | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1088-402A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357902 | |||||||
| chr13:41358197 | T | C | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1088-107T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41358197 | |||||||
| chr13:41358584 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1257+111C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 11/19 | chr13 | 41358584 | |||||||
| chr13:41358701 | G | A | 1 | a0001c0005t0001g0248 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1258-109G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 11/19 | chr13 | 41358701 | |||||||
| chr13:41359091 | TA | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1410+133delA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr13 | 41359091 | ||||||
| chr13:41359328 | T | C | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1410+366T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359328 | |||||||
| chr13:41359501 | A | G | 61 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(58): Show |
65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1410+539A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359501 | |||||||
| chr13:41359610 | G | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0251 |
2 | NA18940.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1410+648G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359610 | |||||||
| chr13:41359612 | T | C | 3 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 |
3 | HG02451.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1410+650T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359612 | |||||||
| chr13:41359731 | T | C | 1 | a0001c0001t0004g0059 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1410+769T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359731 | |||||||
| chr13:41359736 | GA | G | 10 | a0001c0001t0006g0010 a0001c0001t0006g0025 a0001c0001t0006g0026 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1410+778delA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr13 | 41359736 | ||||||
| chr13:41359786 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1410+824A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359786 | |||||||
| chr13:41359807 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1410+845G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359807 | |||||||
| chr13:41360041 | A | G | 1 | a0001c0001t0002g0306 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1410+1079A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360041 | |||||||
| chr13:41360107 | A | G | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1410+1145A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360107 | |||||||
| chr13:41360458 | C | G | 4 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(1): Show |
4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1410+1496C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360458 | |||||||
| chr13:41360476 | G | A | 2 | a0001c0001t0002g0263 a0001c0001t0006g0024 |
2 | HG01358.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1410+1514G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360476 | |||||||
| chr13:41360631 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1411-1400T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360631 | |||||||
| chr13:41360684 | A | G | 1 | a0001c0001t0004g0013 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1411-1347A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360684 | |||||||
| chr13:41360751 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1411-1280A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360751 | |||||||
| chr13:41360795 | A | G | 4 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(1): Show |
4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-1236A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360795 | |||||||
| chr13:41360971 | ATAAC | A | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411-1057_1411-105 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr13 | 41360971 | ||||||
| chr13:41361006 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0192 |
4 | HG01109.hp1 HG01167.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-1025A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361006 | |||||||
| chr13:41361114 | C | A | 61 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(58): Show |
65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1411-917C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361114 | |||||||
| chr13:41361124 | GTGACAAA others(3): Show |
G | 1 | a0001c0001t0010g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1411-903_1411-894d others(12): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr13 | 41361124 | ||||||
| chr13:41361158 | C | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0237 |
2 | HG02015.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1411-873C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361158 | |||||||
| chr13:41361704 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1411-327C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361704 | |||||||
| chr13:41361770 | C | T | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1411-261C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361770 | |||||||
| chr13:41361771 | G | A | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411-260G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361771 | |||||||
| chr13:41361833 | T | G | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1411-198T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361833 | |||||||
| chr13:41361904 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0267 |
2 | HG02015.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1411-127A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361904 | |||||||
| chr13:41362277 | T | C | 2 | a0001c0001t0008g0143 a0001c0001t0008g0144 |
2 | HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1539+118T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362277 | |||||||
| chr13:41362357 | A | C | 1 | a0001c0001t0004g0069 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1539+198A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362357 | |||||||
| chr13:41362367 | A | G | 1 | a0007c0018t0008g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1539+208A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362367 | |||||||
| chr13:41362449 | C | A | 1 | a0003c0004t0003g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1539+290C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362449 | |||||||
| chr13:41362921 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1539+762C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362921 | |||||||
| chr13:41363226 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1539+1067T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363226 | |||||||
| chr13:41363394 | C | T | 1 | a0001c0001t0002g0305 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1539+1235C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363394 | |||||||
| chr13:41363409 | G | C | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1539+1250G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363409 | |||||||
| chr13:41363449 | C | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1539+1290C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363449 | |||||||
| chr13:41363654 | T | C | 72 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(69): Show |
77 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1539+1495T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363654 | |||||||
| chr13:41364051 | TTAA | T | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1539+1894_1539+189 others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41364051 | ||||||
| chr13:41364067 | A | G | 5 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(2): Show |
5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+1908A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364067 | |||||||
| chr13:41364148 | T | C | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1539+1989T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364148 | |||||||
| chr13:41364163 | G | A | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1539+2004G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364163 | |||||||
| chr13:41364324 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1539+2165T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364324 | |||||||
| chr13:41364657 | A | G | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+2498A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364657 | |||||||
| chr13:41364684 | CTT | C | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1539+2527_1539+252 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41364684 | ||||||
| chr13:41365148 | CTAACTT | C | 6 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 others(3): Show |
6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-2288_1540-228 others(10): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41365148 | ||||||
| chr13:41365360 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1540-2079T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41365360 | |||||||
| chr13:41365464 | C | G | 22 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1540-1975C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41365464 | |||||||
| chr13:41365586 | A | G | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1540-1853A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41365586 | |||||||
| chr13:41365713 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1540-1726C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41365713 | |||||||
| chr13:41366055 | C | CT | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1540-1381dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41366055 | ||||||
| chr13:41366342 | T | G | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1540-1097T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366342 | |||||||
| chr13:41366411 | A | G | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1540-1028A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366411 | |||||||
| chr13:41366441 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1540-998A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366441 | |||||||
| chr13:41366461 | A | G | 61 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(58): Show |
65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1540-978A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366461 | |||||||
| chr13:41366812 | TTGGC | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1540-624_1540-621d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41366812 | ||||||
| chr13:41366990 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-449T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366990 | |||||||
| chr13:41367005 | T | G | 1 | a0001c0001t0002g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1540-434T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41367005 | |||||||
| chr13:41367028 | A | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1540-411A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41367028 | |||||||
| chr13:41367192 | T | C | 1 | a0006c0010t0002g0232 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1540-247T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41367192 | |||||||
| chr13:41367280 | T | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1540-159T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41367280 | |||||||
| chr13:41367687 | A | G | 1 | a0001c0013t0015g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1753+35A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41367687 | |||||||
| chr13:41367777 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1753+125C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41367777 | |||||||
| chr13:41367853 | A | C | 3 | a0001c0001t0008g0143 a0001c0001t0008g0144 a0001c0001t0020g0140 |
3 | HG02486.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1753+201A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41367853 | |||||||
| chr13:41368098 | C | G | 3 | a0001c0001t0008g0143 a0001c0001t0008g0144 a0001c0001t0020g0140 |
3 | HG02486.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1753+446C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368098 | |||||||
| chr13:41368104 | T | A | 6 | a0001c0001t0003g0100 a0001c0001t0003g0114 a0001c0001t0003g0122 others(3): Show |
6 | NA18957.hp1 NA18977.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1753+452T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368104 | |||||||
| chr13:41368173 | C | A | 1 | a0001c0001t0003g0102 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1753+521C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368173 | |||||||
| chr13:41368225 | T | G | 1 | a0001c0001t0002g0238 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1753+573T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368225 | |||||||
| chr13:41368291 | A | G | 1 | a0001c0017t0006g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1753+639A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368291 | |||||||
| chr13:41368333 | A | G | 1 | a0001c0001t0010g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1753+681A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368333 | |||||||
| chr13:41368406 | CAA | C | 3 | a0001c0001t0008g0143 a0001c0001t0008g0144 a0001c0001t0020g0140 |
3 | HG02486.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1754-682_1754-681d others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr13 | 41368406 | ||||||
| chr13:41368443 | G | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0220 others(8): Show |
13 | HG00280.hp2 HG00738.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1754-647G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368443 | |||||||
| chr13:41368576 | C | A | 1 | a0001c0001t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1754-514C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368576 | |||||||
| chr13:41368608 | A | G | 11 | a0001c0001t0006g0010 a0001c0001t0006g0024 a0001c0001t0006g0025 others(8): Show |
12 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1754-482A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368608 | |||||||
| chr13:41368744 | G | A | 7 | a0001c0001t0001g0220 a0001c0001t0001g0228 a0001c0001t0008g0086 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1754-346G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368744 | |||||||
| chr13:41368916 | A | T | 61 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(58): Show |
65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1754-174A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368916 | |||||||
| chr13:41368929 | A | G | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1754-161A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368929 | |||||||
| chr13:41368969 | G | A | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1754-121G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368969 | |||||||
| chr13:41369003 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-87A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41369003 | |||||||
| chr13:41369011 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1754-79A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41369011 | |||||||
| chr13:41369013 | T | G | 1 | a0001c0013t0015g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1754-77T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41369013 | |||||||
| chr13:41369050 | A | C | 1 | a0001c0001t0002g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1754-40A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41369050 | |||||||
| chr13:41369508 | G | A | 22 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1947+225G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369508 | |||||||
| chr13:41369562 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1947+279G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369562 | |||||||
| chr13:41369755 | G | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1947+472G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369755 | |||||||
| chr13:41369763 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1947+480A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369763 | |||||||
| chr13:41369822 | C | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1947+539C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369822 | |||||||
| chr13:41370008 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1947+725G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370008 | |||||||
| chr13:41370311 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1947+1028G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370311 | |||||||
| chr13:41370392 | A | G | 1 | a0001c0001t0002g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1947+1109A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370392 | |||||||
| chr13:41370483 | T | C | 1 | a0001c0001t0002g0277 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1947+1200T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370483 | |||||||
| chr13:41370778 | A | G | 1 | a0001c0001t0004g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-1425A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370778 | |||||||
| chr13:41370847 | A | G | 3 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 |
3 | HG02451.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1948-1356A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370847 | |||||||
| chr13:41370848 | C | T | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0187 others(1): Show |
4 | HG00099.hp2 HG00735.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1948-1355C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370848 | |||||||
| chr13:41371033 | TAAAAG | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0190 others(8): Show |
14 | HG01109.hp1 HG01167.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1948-1168_1948-116 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr13 | 41371033 | ||||||
| chr13:41371113 | C | G | 1 | a0001c0001t0002g0304 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1948-1090C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371113 | |||||||
| chr13:41371153 | G | T | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1948-1050G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371153 | |||||||
| chr13:41371312 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0225 |
3 | HG00280.hp2 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1948-891A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371312 | |||||||
| chr13:41371407 | C | G | 1 | a0002c0003t0005g0048 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1948-796C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371407 | |||||||
| chr13:41371418 | A | G | 1 | a0001c0001t0004g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1948-785A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371418 | |||||||
| chr13:41371470 | A | G | 1 | a0002c0003t0005g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1948-733A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371470 | |||||||
| chr13:41371591 | G | A | 311 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(308): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1948-612G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371591 | |||||||
| chr13:41371614 | T | C | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1948-589T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371614 | |||||||
| chr13:41371620 | A | G | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1948-583A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371620 | |||||||
| chr13:41371953 | T | C | 2 | a0001c0011t0014g0154 a0001c0013t0015g0153 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1948-250T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371953 | |||||||
| chr13:41371983 | T | A | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1948-220T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371983 | |||||||
| chr13:41372340 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2056+29A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/19 | chr13 | 41372340 | |||||||
| chr13:41372458 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2056+147G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/19 | chr13 | 41372458 | |||||||
| chr13:41372462 | G | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2056+151G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/19 | chr13 | 41372462 | |||||||
| chr13:41372502 | T | C | 11 | a0001c0001t0003g0006 a0001c0001t0003g0015 a0001c0001t0003g0107 others(8): Show |
14 | HG00642.hp2 HG01074.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.2056+191T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/19 | chr13 | 41372502 | |||||||
| chr13:41373084 | AAAT | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2155+264_2155+266d others(5): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr13 | 41373084 | ||||||
| chr13:41373297 | G | T | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2156-340G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 17/19 | chr13 | 41373297 | |||||||
| chr13:41373344 | A | T | 17 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0036 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2156-293A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 17/19 | chr13 | 41373344 | |||||||
| chr13:41373418 | C | T | 44 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(41): Show |
53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2156-219C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 17/19 | chr13 | 41373418 | |||||||
| chr13:41373801 | G | A | 1 | a0001c0002t0007g0158 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2299+21G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41373801 | |||||||
| chr13:41373915 | G | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2299+135G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41373915 | |||||||
| chr13:41373955 | G | A | 1 | a0001c0001t0011g0118 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2299+175G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41373955 | |||||||
| chr13:41373989 | A | G | 59 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0014 others(56): Show |
63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.2299+209A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41373989 | |||||||
| chr13:41374015 | T | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2299+235T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374015 | |||||||
| chr13:41374038 | G | T | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2299+258G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374038 | |||||||
| chr13:41374041 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2299+261C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374041 | |||||||
| chr13:41374114 | T | G | 1 | a0010c0016t0016g0160 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2299+334T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374114 | |||||||
| chr13:41374141 | CT | C | 39 | a0001c0001t0004g0001 a0001c0001t0004g0011 a0001c0001t0004g0012 others(36): Show |
48 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.2299+375delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr13 | 41374141 | ||||||
| chr13:41374145 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2299+365T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374145 | |||||||
| chr13:41374233 | T | G | 1 | a0010c0016t0016g0160 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2299+453T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374233 | |||||||
| chr13:41374249 | A | T | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2299+469A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374249 | |||||||
| chr13:41374271 | G | GC | 12 | a0002c0003t0005g0035 a0002c0003t0005g0036 a0002c0003t0005g0038 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2300-470dupC | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr13 | 41374271 | ||||||
| chr13:41374350 | A | G | 1 | a0001c0001t0008g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2300-392A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374350 | |||||||
| chr13:41374457 | C | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2300-285C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374457 | |||||||
| chr13:41374548 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2300-194C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374548 | |||||||
| chr13:41374636 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2300-106C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374636 | |||||||
| chr13:41374683 | T | C | 22 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0001c0001t0010g0137 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2300-59T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374683 | |||||||
| chr13:41374686 | C | G | 1 | a0001c0001t0002g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2300-56C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374686 | |||||||
| chr13:41374843 | A | G | 1 | a0010c0016t0016g0160 | 1 | NA19059.hp2 | splice_region_variant&intron_variant | LOW | c.2397+4A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374843 | |||||||
| chr13:41374844 | G | T | 1 | a0010c0016t0016g0160 | 1 | NA19059.hp2 | splice_region_variant&intron_variant | LOW | c.2397+5G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374844 | |||||||
| chr13:41374882 | C | T | 1 | a0001c0001t0013g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2397+43C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374882 | |||||||
| chr13:41374903 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2397+64G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374903 | |||||||
| chr13:41374955 | C | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2397+116C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374955 | |||||||
| chr13:41374973 | G | A | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2397+134G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374973 | |||||||
| chr13:41374980 | T | C | 5 | a0001c0001t0008g0086 a0001c0001t0008g0087 a0001c0001t0008g0089 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+141T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374980 | |||||||
| chr13:41375085 | C | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2397+246C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41375085 | |||||||
| chr13:41375126 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2398-279A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41375126 | |||||||
| chr13:41375235 | A | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2398-170A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41375235 | |||||||
| chr13:41375312 | T | G | 1 | a0010c0016t0016g0160 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2398-93T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41375312 |