Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 65110 |
| ensemblid | ENSG00000169062.15 |
| hgncid | 20332 |
| symbol | UPF3A |
| name | UPF3A regulator of nonsense mediated mRNA decay |
| refseq_nuc | NM_023011.4 |
| refseq_prot | NP_075387.1 |
| ensembl_nuc | ENST00000375299.8 |
| ensembl_prot | ENSP00000364448.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 114281601 |
| end | 114305817 |
| strand | + |
| ver | v1.2 |
| region | chr13:114281601-114305817 |
| region5000 | chr13:114276601-114310817 |
| regionname0 | UPF3A_chr13_114281601_114305817 |
| regionname5000 | UPF3A_chr13_114276601_114310817 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 476 | 299 | 26 | 58 | 173 | 14 | 26 | 130 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0002 | 0/0 | 476 | 102 | 50 | 18 | 18 | 0 | 16 | 14 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0003 | 0/0 | 476 | 23 | 1 | 1 | 17 | 0 | 4 | 17 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0004 | 0/0 | 476 | 11 | 8 | 3 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0005 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0006 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0007 | 0/0 | 475 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(470): Show |
chr13 | 114276601 | 114310817 |
| a0008 | 0/0 | 476 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0009 | 0/0 | 476 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0010 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0011 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0012 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0013 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(470): Show |
chr13 | 114276601 | 114310817 |
| a0014 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0015 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| a0016 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | MRSEK others(471): Show |
chr13 | 114276601 | 114310817 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1428 | 295 | 26 | 57 | 171 | 13 | 26 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0001c0007 | 0/0 | 1428 | 2 | 0 | 1 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0001c0016 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0001c0019 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0002c0002 | 0/0 | 1428 | 102 | 50 | 18 | 18 | 0 | 16 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0003c0003 | 0/0 | 1428 | 23 | 1 | 1 | 17 | 0 | 4 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0004c0004 | 0/0 | 1428 | 11 | 8 | 3 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0005c0006 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0006c0008 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0007c0005 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1420): Show |
chr13 | 114276601 | 114310817 | ||
| a0008c0012 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0009c0010 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0010c0013 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0011c0009 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0012c0017 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0013c0011 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1420): Show |
chr13 | 114276601 | 114310817 | ||
| a0014c0015 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0015c0018 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 | ||
| a0016c0014 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | ATGCG others(1423): Show |
chr13 | 114276601 | 114310817 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2370 | 287 | 21 | 57 | 168 | 13 | 26 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0001c0001t0004 | 0/0 | 2370 | 3 | 3 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0001c0001t0005 | 0/0 | 2370 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0001c0001t0007 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0001c0001t0012 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0001c0001t0013 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0001c0007t0001 | 0/0 | 2370 | 2 | 0 | 1 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0001c0016t0001 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0001c0019t0001 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0002c0002t0001 | 0/0 | 2370 | 100 | 49 | 17 | 18 | 0 | 16 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0002c0002t0008 | 0/0 | 2370 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0002c0002t0010 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0003c0003t0001 | 0/0 | 2370 | 22 | 0 | 1 | 17 | 0 | 4 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0003c0003t0009 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0004c0004t0002 | 0/0 | 2370 | 6 | 4 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0004c0004t0003 | 0/0 | 2367 | 5 | 4 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2362): Show |
chr13 | 114276601 | 114310817 |
| a0005c0006t0006 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2362): Show |
chr13 | 114276601 | 114310817 |
| a0006c0008t0001 | 0/0 | 2370 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0007c0005t0001 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2362): Show |
chr13 | 114276601 | 114310817 |
| a0008c0012t0001 | 0/0 | 2370 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0009c0010t0001 | 0/0 | 2370 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0010c0013t0001 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0011c0009t0014 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0012c0017t0011 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0013c0011t0001 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2362): Show |
chr13 | 114276601 | 114310817 |
| a0014c0015t0001 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0015c0018t0001 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| a0016c0014t0001 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | GTCGG others(2365): Show |
chr13 | 114276601 | 114310817 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0036 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0316 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0007g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0001t0013g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0007t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0016t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0001c0019t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0008g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0002c0002t0010g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0003c0003t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0004c0004t0002g0006 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0004c0004t0002g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0004c0004t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0004c0004t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0004c0004t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0004c0004t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0004c0004t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0004c0004t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0005c0006t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0005c0006t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0006c0008t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0006c0008t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0007c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0007c0005t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0008c0012t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0009c0010t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0010c0013t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0011c0009t0014g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0012c0017t0011g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0013c0011t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0014c0015t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0015c0018t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| a0016c0014t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | GBR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | GBR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00140 | hp1 | a0001 | c0007 | t0001 | g0032 | EUR | GBR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | GBR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | FIN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0360 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0359 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0365 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00733 | hp1 | a0008 | c0012 | t0001 | g0310 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01069 | hp1 | a0004 | c0004 | t0002 | g0006 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01071 | hp1 | a0004 | c0004 | t0002 | g0006 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0361 | AMR | PUR | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0129 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01257 | hp2 | a0002 | c0002 | t0008 | g0362 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01346 | hp1 | a0001 | c0007 | t0001 | g0032 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0376 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01433 | hp1 | a0009 | c0010 | t0001 | g0375 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01496 | hp2 | a0004 | c0004 | t0003 | g0188 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0312 | EUR | IBS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | IBS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | IBS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0317 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02129 | hp2 | a0010 | c0013 | t0001 | g0035 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0370 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CDX | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02257 | hp1 | a0011 | c0009 | t0014 | g0346 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02258 | hp1 | a0004 | c0004 | t0002 | g0006 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02280 | hp1 | a0012 | c0017 | t0011 | g0334 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02280 | hp2 | a0004 | c0004 | t0002 | g0378 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0367 | EAS | KHV | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02572 | hp2 | a0005 | c0006 | t0006 | g0219 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0195 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0356 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0363 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0358 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0128 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0197 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0373 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0233 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0371 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0354 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02922 | hp2 | a0004 | c0004 | t0003 | g0189 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0318 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02970 | hp2 | a0004 | c0004 | t0003 | g0116 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0353 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03041 | hp1 | a0003 | c0003 | t0009 | g0191 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0357 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0226 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0366 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0331 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0232 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0347 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03516 | hp2 | a0004 | c0004 | t0002 | g0377 | AFR | ESN | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0221 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03579 | hp1 | a0006 | c0008 | t0001 | g0134 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0350 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0348 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0209 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0208 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0217 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0211 | SAS | BEB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0204 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0222 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0120 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0368 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | STU | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0351 | AFR | YRI | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | YRI | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18906 | hp1 | a0005 | c0006 | t0006 | g0218 | AFR | YRI | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | YRI | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18948 | hp1 | a0001 | c0001 | t0012 | g0164 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18951 | hp1 | a0013 | c0011 | t0001 | g0253 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18951 | hp2 | a0014 | c0015 | t0001 | g0274 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18956 | hp2 | a0015 | c0018 | t0001 | g0025 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18960 | hp1 | a0001 | c0001 | t0013 | g0115 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0117 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0196 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0291 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18970 | hp2 | a0001 | c0019 | t0001 | g0161 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0364 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0200 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18989 | hp2 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0126 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19006 | hp1 | a0003 | c0003 | t0001 | g0206 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | LWK | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19043 | hp1 | a0006 | c0008 | t0001 | g0133 | AFR | LWK | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19043 | hp2 | a0004 | c0004 | t0003 | g0190 | AFR | LWK | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19062 | hp2 | a0007 | c0005 | t0001 | g0205 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19067 | hp2 | a0003 | c0003 | t0001 | g0194 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19072 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19082 | hp2 | a0007 | c0005 | t0001 | g0192 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19083 | hp2 | a0001 | c0016 | t0001 | g0270 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | YRI | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | YRI | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ASW | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | ASW | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | GIH | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0349 | SAS | GIH | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02109 | hp2 | a0004 | c0004 | t0003 | g0187 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0352 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG02559 | hp2 | a0004 | c0004 | t0002 | g0006 | AFR | ACB | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | MSL | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0369 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA20300 | hp1 | a0002 | c0002 | t0010 | g0355 | AFR | USA | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | USA | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | LWK | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| NA21309 | hp2 | a0016 | c0014 | t0001 | g0374 | AFR | LWK | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0316 | REF | REF | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0036 | REF | REF | UPF3A_chr13_114276601_114310817 | UPF3A | chr13 | 114276601 | 114310817 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114281680 | C | T | 1 | a0006 | 2 | HG03579.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.41C>T | p.Ala14Val | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/10 | 80/2370 | 41/1431 | 14/476 | chr13 | 114281680 | |||
| chr13:114281830 | G | A | 6 | a0002 a0003 a0005 others(3): Show |
132 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(129): Show |
missense_variant | MODERATE | c.191G>A | p.Arg64Lys | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/10 | 230/2370 | 191/1431 | 64/476 | chr13 | 114281830 | |||
| chr13:114281835 | G | T | 1 | a0015 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.196G>T | p.Ala66Ser | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/10 | 235/2370 | 196/1431 | 66/476 | chr13 | 114281835 | |||
| chr13:114282868 | A | G | 1 | a0009 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.346A>G | p.Ile116Val | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/10 | 385/2370 | 346/1431 | 116/476 | chr13 | 114282868 | |||
| chr13:114286609 | C | T | 1 | a0012 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.611C>T | p.Ala204Val | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/10 | 650/2370 | 611/1431 | 204/476 | chr13 | 114286609 | |||
| chr13:114291661 | CGGA | C | 2 | a0007 a0013 |
3 | NA18951.hp1 NA19062.hp2 NA19082.hp2 |
disruptive_inframe_deletion | MODERATE | c.723_725delGAG | p.Arg242del | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/10 | 762/2370 | 723/1431 | 241/476 | INFO_REALIGN_3_PRIME | chr13 | 114291661 | ||
| chr13:114298948 | G | A | 5 | a0003 a0007 a0008 others(2): Show |
28 | HG00733.hp1 HG01255.hp1 HG01433.hp1 others(25): Show |
missense_variant | MODERATE | c.955G>A | p.Ala319Thr | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/10 | 994/2370 | 955/1431 | 319/476 | chr13 | 114298948 | |||
| chr13:114298969 | A | G | 2 | a0004 a0005 |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
missense_variant | MODERATE | c.976A>G | p.Met326Val | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/10 | 1015/2370 | 976/1431 | 326/476 | chr13 | 114298969 | |||
| chr13:114301843 | G | A | 1 | a0010 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.1120G>A | p.Glu374Lys | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/10 | 1159/2370 | 1120/1431 | 374/476 | chr13 | 114301843 | |||
| chr13:114301916 | A | G | 1 | a0011 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1193A>G | p.Lys398Arg | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/10 | 1232/2370 | 1193/1431 | 398/476 | chr13 | 114301916 | |||
| chr13:114301982 | G | A | 1 | a0016 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1259G>A | p.Cys420Tyr | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/10 | 1298/2370 | 1259/1431 | 420/476 | chr13 | 114301982 | |||
| chr13:114304855 | A | G | 1 | a0014 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1369A>G | p.Arg457Gly | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 1408/2370 | 1369/1431 | 457/476 | chr13 | 114304855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114281687 | C | T | 1 | a0001c0019 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.48C>T | p.Ala16Ala | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/10 | 87/2370 | 48/1431 | 16/476 | chr13 | 114281687 | |||
| chr13:114281780 | T | C | 2 | a0004c0004 a0011c0009 |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
synonymous_variant | LOW | c.141T>C | p.Thr47Thr | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/10 | 180/2370 | 141/1431 | 47/476 | chr13 | 114281780 | |||
| chr13:114291780 | A | G | 1 | a0001c0016 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.834A>G | p.Glu278Glu | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/10 | 873/2370 | 834/1431 | 278/476 | chr13 | 114291780 | |||
| chr13:114301944 | G | A | 1 | a0001c0007 | 2 | HG00140.hp1 HG01346.hp1 |
synonymous_variant | LOW | c.1221G>A | p.Pro407Pro | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/10 | 1260/2370 | 1221/1431 | 407/476 | chr13 | 114301944 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114281629 | G | A | 1 | a0001c0001t0007 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/10 | 11 | chr13 | 114281629 | ||||||
| chr13:114281639 | C | G | 3 | a0004c0004t0002 a0004c0004t0003 a0011c0009t0014 |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-1C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/10 | 1 | chr13 | 114281639 | ||||||
| chr13:114304943 | G | T | 2 | a0001c0001t0004 a0004c0004t0002 |
9 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*26G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 26 | chr13 | 114304943 | ||||||
| chr13:114304951 | A | G | 2 | a0004c0004t0003 a0005c0006t0006 |
7 | HG01496.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*34A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 34 | chr13 | 114304951 | ||||||
| chr13:114304995 | AAGG | A | 2 | a0004c0004t0003 a0005c0006t0006 |
7 | HG01496.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*81_*83delGAG | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 81 | INFO_REALIGN_3_PRIME | chr13 | 114304995 | |||||
| chr13:114305076 | G | A | 1 | a0002c0002t0008 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 159 | chr13 | 114305076 | ||||||
| chr13:114305208 | A | T | 1 | a0001c0001t0013 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*291A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 291 | chr13 | 114305208 | ||||||
| chr13:114305291 | C | T | 1 | a0001c0001t0012 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*374C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 374 | chr13 | 114305291 | ||||||
| chr13:114305321 | C | T | 1 | a0001c0001t0013 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 404 | chr13 | 114305321 | ||||||
| chr13:114305346 | A | G | 4 | a0004c0004t0002 a0004c0004t0003 a0005c0006t0006 others(1): Show |
14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*429A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 429 | chr13 | 114305346 | ||||||
| chr13:114305610 | T | C | 3 | a0004c0004t0002 a0004c0004t0003 a0005c0006t0006 |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*693T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 693 | chr13 | 114305610 | ||||||
| chr13:114305616 | G | A | 3 | a0004c0004t0002 a0004c0004t0003 a0005c0006t0006 |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*699G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 699 | chr13 | 114305616 | ||||||
| chr13:114305640 | A | G | 4 | a0004c0004t0002 a0004c0004t0003 a0005c0006t0006 others(1): Show |
14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*723A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 723 | chr13 | 114305640 | ||||||
| chr13:114305657 | G | T | 1 | a0002c0002t0010 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*740G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 740 | chr13 | 114305657 | ||||||
| chr13:114305717 | T | C | 1 | a0001c0001t0005 | 2 | HG01891.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*800T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 800 | chr13 | 114305717 | ||||||
| chr13:114305769 | C | T | 1 | a0003c0003t0009 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*852C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 10/10 | 852 | chr13 | 114305769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114281851 | G | A | 1 | a0002c0002t0001g0046 | 1 | HG00733.hp2 | splice_region_variant&intron_variant | LOW | c.207+5G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | chr13 | 114281851 | |||||||
| chr13:114281895 | T | TGAGGGGA others(11): Show |
1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.207+52_207+53insGG others(16): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281895 | ||||||
| chr13:114281895 | T | TGAGTGGA others(2): Show |
3 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 |
6 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+53_207+61dupTG others(7): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281895 | ||||||
| chr13:114281899 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.207+53T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | chr13 | 114281899 | |||||||
| chr13:114281899 | T | TGGAGGGA others(2): Show |
113 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0023 others(110): Show |
131 | HG00280.hp1 HG00621.hp2 HG00733.hp2 others(128): Show |
intron_variant | MODIFIER | c.207+74_207+82dupAG others(7): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281899 | ||||||
| chr13:114281899 | T | TGGAGGGA others(11): Show |
71 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(68): Show |
83 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.207+65_207+82dupAG others(16): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281899 | ||||||
| chr13:114281899 | T | TGGAGGGA others(20): Show |
11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
12 | HG01106.hp2 HG01192.hp1 HG03942.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+56_207+82dupAG others(25): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281899 | ||||||
| chr13:114281899 | T | TGGAGGGA others(29): Show |
15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
16 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.207+82_207+83insAG others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281899 | ||||||
| chr13:114281899 | T | TGGAGGGA others(38): Show |
2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02071.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.207+82_207+83insAG others(43): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281899 | ||||||
| chr13:114281899 | T | TGGAGGGA others(47): Show |
1 | a0001c0001t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.207+82_207+83insAG others(52): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281899 | ||||||
| chr13:114281899 | TGGAGGGA others(2): Show |
T | 8 | a0001c0001t0001g0045 a0001c0001t0001g0371 a0001c0001t0001g0372 others(5): Show |
11 | HG01358.hp2 HG01433.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+74_207+82delAG others(7): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 114281899 | ||||||
| chr13:114281917 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.207+71G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | chr13 | 114281917 | |||||||
| chr13:114281989 | C | T | 123 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(120): Show |
144 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.208-32C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 1/9 | chr13 | 114281989 | |||||||
| chr13:114282145 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314+18G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282145 | |||||||
| chr13:114282178 | G | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.314+51G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282178 | |||||||
| chr13:114282190 | C | G | 2 | a0001c0001t0001g0336 a0001c0001t0013g0115 |
2 | HG01346.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.314+63C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282190 | |||||||
| chr13:114282225 | A | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
351 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(348): Show |
intron_variant | MODIFIER | c.314+98A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282225 | |||||||
| chr13:114282277 | C | A | 9 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.314+150C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282277 | |||||||
| chr13:114282277 | C | T | 1 | a0002c0002t0001g0029 | 2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.314+150C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282277 | |||||||
| chr13:114282330 | G | T | 9 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.314+203G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282330 | |||||||
| chr13:114282349 | C | G | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.314+222C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282349 | |||||||
| chr13:114282436 | G | T | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.314+309G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282436 | |||||||
| chr13:114282484 | C | G | 1 | a0001c0001t0001g0039 | 2 | HG01496.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.315-353C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282484 | |||||||
| chr13:114282537 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.315-300C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282537 | |||||||
| chr13:114282551 | G | C | 44 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0062 others(41): Show |
48 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.315-286G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282551 | |||||||
| chr13:114282693 | C | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(78): Show |
99 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.315-144C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282693 | |||||||
| chr13:114282725 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.315-112C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282725 | |||||||
| chr13:114282760 | A | G | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.315-77A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282760 | |||||||
| chr13:114282762 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.315-75A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282762 | |||||||
| chr13:114282828 | T | C | 1 | a0002c0002t0001g0350 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.315-9T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 2/9 | chr13 | 114282828 | |||||||
| chr13:114283093 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+150G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283093 | |||||||
| chr13:114283099 | C | T | 7 | a0001c0001t0001g0045 a0001c0001t0001g0184 a0001c0001t0001g0185 others(4): Show |
8 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+156C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283099 | |||||||
| chr13:114283129 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421+186C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283129 | |||||||
| chr13:114283198 | G | T | 9 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.421+255G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283198 | |||||||
| chr13:114283386 | G | A | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.421+443G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283386 | |||||||
| chr13:114283388 | A | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(78): Show |
99 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.421+445A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283388 | |||||||
| chr13:114283413 | A | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.421+470A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283413 | |||||||
| chr13:114283478 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.421+535A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283478 | |||||||
| chr13:114283555 | C | T | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.421+612C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283555 | |||||||
| chr13:114283560 | G | A | 7 | a0001c0001t0001g0045 a0001c0001t0001g0184 a0001c0001t0001g0185 others(4): Show |
8 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+617G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283560 | |||||||
| chr13:114283636 | C | T | 9 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.421+693C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283636 | |||||||
| chr13:114283714 | C | T | 26 | a0002c0002t0001g0012 a0002c0002t0001g0013 a0002c0002t0001g0028 others(23): Show |
31 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.421+771C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283714 | |||||||
| chr13:114283745 | T | C | 45 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0062 others(42): Show |
49 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.421+802T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283745 | |||||||
| chr13:114283823 | A | G | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.421+880A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283823 | |||||||
| chr13:114283849 | G | C | 1 | a0001c0001t0001g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421+906G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283849 | |||||||
| chr13:114283850 | C | A | 1 | a0002c0002t0001g0011 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.421+907C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114283850 | |||||||
| chr13:114284049 | G | C | 9 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.421+1106G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284049 | |||||||
| chr13:114284109 | A | AT | 4 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(1): Show |
4 | HG01361.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+1167dupT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114284109 | ||||||
| chr13:114284135 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.421+1192G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284135 | |||||||
| chr13:114284293 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.421+1350C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284293 | |||||||
| chr13:114284383 | A | ATG | 78 | a0001c0001t0001g0284 a0002c0002t0001g0011 a0002c0002t0001g0012 others(75): Show |
92 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1454_421+1455d others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114284383 | ||||||
| chr13:114284383 | ATG | A | 37 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0062 others(34): Show |
41 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.421+1454_421+1455d others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114284383 | ||||||
| chr13:114284477 | AGTTGAGG others(6): Show |
A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG00639.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+1538_421+1550d others(15): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114284477 | ||||||
| chr13:114284529 | T | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0238 others(10): Show |
16 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.421+1586T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284529 | |||||||
| chr13:114284534 | T | TA | 12 | a0001c0001t0001g0040 a0001c0001t0001g0175 a0001c0001t0001g0176 others(9): Show |
13 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+1606dupA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114284534 | ||||||
| chr13:114284534 | TAAAAA | T | 9 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.421+1602_421+1606d others(7): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114284534 | ||||||
| chr13:114284566 | A | G | 9 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.421+1623A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284566 | |||||||
| chr13:114284580 | T | A | 3 | a0002c0002t0001g0013 a0002c0002t0001g0359 a0002c0002t0001g0360 |
5 | HG00408.hp1 HG00423.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+1637T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284580 | |||||||
| chr13:114284623 | C | T | 7 | a0002c0002t0001g0044 a0002c0002t0001g0228 a0002c0002t0001g0229 others(4): Show |
8 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-1679C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284623 | |||||||
| chr13:114284624 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.422-1678G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284624 | |||||||
| chr13:114284698 | CA | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0173 a0001c0001t0001g0247 others(13): Show |
17 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.422-1591delA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114284698 | ||||||
| chr13:114284789 | AGTC | A | 1 | a0002c0002t0001g0014 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.422-1509_422-1507d others(5): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114284789 | ||||||
| chr13:114284794 | T | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 |
3 | HG01109.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.422-1508T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284794 | |||||||
| chr13:114284804 | C | T | 2 | a0003c0003t0001g0072 a0003c0003t0001g0206 |
2 | NA19006.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.422-1498C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284804 | |||||||
| chr13:114284909 | C | T | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.422-1393C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284909 | |||||||
| chr13:114284915 | A | C | 3 | a0002c0002t0001g0064 a0002c0002t0001g0132 a0002c0002t0001g0226 |
3 | HG02145.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.422-1387A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284915 | |||||||
| chr13:114284951 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.422-1351G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114284951 | |||||||
| chr13:114285155 | A | T | 2 | a0002c0002t0001g0046 a0002c0002t0001g0225 |
2 | HG00733.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.422-1147A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285155 | |||||||
| chr13:114285268 | GCTCT | G | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.422-1031_422-1028d others(6): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114285268 | ||||||
| chr13:114285324 | A | T | 1 | a0002c0002t0001g0370 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.422-978A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285324 | |||||||
| chr13:114285446 | C | T | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.422-856C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285446 | |||||||
| chr13:114285504 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.422-798C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285504 | |||||||
| chr13:114285518 | A | T | 1 | a0001c0001t0001g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.422-784A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285518 | |||||||
| chr13:114285519 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.422-783T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285519 | |||||||
| chr13:114285550 | C | CA | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(78): Show |
99 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.422-743dupA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 114285550 | ||||||
| chr13:114285582 | A | G | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.422-720A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285582 | |||||||
| chr13:114285592 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.422-710G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285592 | |||||||
| chr13:114285674 | C | T | 1 | a0002c0002t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.422-628C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285674 | |||||||
| chr13:114285705 | A | G | 1 | a0007c0005t0001g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.422-597A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285705 | |||||||
| chr13:114285881 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.422-421G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285881 | |||||||
| chr13:114285978 | A | C | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.422-324A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114285978 | |||||||
| chr13:114286196 | C | T | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.422-106C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114286196 | |||||||
| chr13:114286245 | C | T | 2 | a0001c0001t0004g0177 a0001c0001t0004g0178 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.422-57C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 3/9 | chr13 | 114286245 | |||||||
| chr13:114286428 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.520+28G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 4/9 | chr13 | 114286428 | |||||||
| chr13:114286438 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.520+38A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 4/9 | chr13 | 114286438 | |||||||
| chr13:114286513 | G | A | 1 | a0003c0003t0001g0206 | 1 | NA19006.hp1 | splice_region_variant&intron_variant | LOW | c.521-6G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 4/9 | chr13 | 114286513 | |||||||
| chr13:114286656 | T | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.631+27T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114286656 | |||||||
| chr13:114286920 | C | T | 3 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 |
6 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+291C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114286920 | |||||||
| chr13:114286965 | C | T | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631+336C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114286965 | |||||||
| chr13:114287132 | A | G | 9 | a0001c0001t0001g0304 a0002c0002t0001g0073 a0002c0002t0001g0207 others(6): Show |
9 | HG02451.hp2 HG03491.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+503A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287132 | |||||||
| chr13:114287144 | T | C | 1 | a0002c0002t0001g0022 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.631+515T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287144 | |||||||
| chr13:114287153 | TTACTTCC others(14): Show |
T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0172 |
3 | HG01123.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.631+547_631+567del others(21): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114287153 | ||||||
| chr13:114287184 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.631+555G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287184 | |||||||
| chr13:114287236 | C | G | 1 | a0001c0001t0001g0345 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.631+607C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287236 | |||||||
| chr13:114287344 | T | C | 8 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
10 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.631+715T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287344 | |||||||
| chr13:114287384 | C | G | 3 | a0001c0001t0001g0179 a0001c0001t0004g0331 a0002c0002t0001g0224 |
3 | HG02622.hp1 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.631+755C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287384 | |||||||
| chr13:114287449 | G | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0344 a0003c0003t0001g0072 |
6 | HG01993.hp1 NA18992.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+820G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287449 | |||||||
| chr13:114287450 | G | A | 2 | a0002c0002t0001g0213 a0002c0002t0001g0214 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.631+821G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287450 | |||||||
| chr13:114287451 | C | CA | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0138 others(3): Show |
8 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+823dupA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114287451 | ||||||
| chr13:114287458 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
187 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.631+829G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287458 | |||||||
| chr13:114287459 | T | TG | 5 | a0001c0001t0001g0372 a0001c0001t0004g0177 a0001c0001t0004g0178 others(2): Show |
5 | HG01243.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+831dupG | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114287459 | ||||||
| chr13:114287463 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
205 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.631+834T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287463 | |||||||
| chr13:114287480 | A | G | 1 | a0002c0002t0001g0354 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.631+851A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287480 | |||||||
| chr13:114287653 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0139 |
2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.631+1024T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287653 | |||||||
| chr13:114287680 | T | C | 53 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0138 others(50): Show |
64 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.631+1051T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287680 | |||||||
| chr13:114287693 | G | A | 1 | a0003c0003t0001g0129 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.631+1064G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287693 | |||||||
| chr13:114287748 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.631+1119G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287748 | |||||||
| chr13:114287830 | T | A | 4 | a0001c0001t0001g0076 a0002c0002t0001g0073 a0002c0002t0001g0348 others(1): Show |
4 | HG03710.hp2 HG03831.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+1201T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287830 | |||||||
| chr13:114287889 | C | T | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631+1260C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287889 | |||||||
| chr13:114287938 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.631+1309C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287938 | |||||||
| chr13:114287954 | C | T | 37 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(34): Show |
40 | HG01255.hp1 HG01433.hp1 HG02257.hp1 others(37): Show |
intron_variant | MODIFIER | c.631+1325C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114287954 | |||||||
| chr13:114288040 | G | A | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.631+1411G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288040 | |||||||
| chr13:114288070 | A | G | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.631+1441A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288070 | |||||||
| chr13:114288309 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.631+1680C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288309 | |||||||
| chr13:114288364 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.631+1735G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288364 | |||||||
| chr13:114288407 | G | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
44 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.631+1778G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288407 | |||||||
| chr13:114288431 | A | T | 1 | a0002c0002t0001g0201 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.631+1802A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288431 | |||||||
| chr13:114288438 | G | A | 7 | a0001c0001t0001g0040 a0001c0001t0001g0298 a0001c0001t0001g0299 others(4): Show |
8 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.631+1809G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288438 | |||||||
| chr13:114288467 | C | T | 1 | a0002c0002t0001g0201 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.631+1838C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288467 | |||||||
| chr13:114288549 | C | G | 1 | a0002c0002t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.631+1920C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288549 | |||||||
| chr13:114288614 | T | C | 1 | a0001c0001t0004g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.631+1985T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288614 | |||||||
| chr13:114288649 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.631+2020C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288649 | |||||||
| chr13:114288660 | CTG | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(10): Show |
17 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.631+2034_631+2035d others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114288660 | ||||||
| chr13:114288699 | G | A | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.631+2070G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288699 | |||||||
| chr13:114288751 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.631+2122A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288751 | |||||||
| chr13:114288809 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(88): Show |
112 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.631+2180A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288809 | |||||||
| chr13:114288973 | A | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0043 others(54): Show |
68 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.631+2344A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288973 | |||||||
| chr13:114288988 | T | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG00735.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.631+2359T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114288988 | |||||||
| chr13:114289382 | G | C | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.632-2107G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289382 | |||||||
| chr13:114289455 | C | T | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-2034C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289455 | |||||||
| chr13:114289473 | A | G | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-2016A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289473 | |||||||
| chr13:114289522 | C | CA | 5 | a0001c0001t0001g0254 a0002c0002t0001g0014 a0002c0002t0001g0217 others(2): Show |
7 | HG02074.hp1 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.632-1947dupA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114289522 | ||||||
| chr13:114289522 | CA | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.632-1947delA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114289522 | ||||||
| chr13:114289654 | G | C | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-1835G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289654 | |||||||
| chr13:114289841 | G | A | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-1648G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289841 | |||||||
| chr13:114289857 | G | T | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-1632G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289857 | |||||||
| chr13:114289881 | G | A | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.632-1608G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289881 | |||||||
| chr13:114289926 | G | T | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-1563G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289926 | |||||||
| chr13:114289936 | C | A | 1 | a0002c0002t0001g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.632-1553C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289936 | |||||||
| chr13:114289954 | C | G | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.632-1535C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289954 | |||||||
| chr13:114289960 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.632-1529C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289960 | |||||||
| chr13:114289989 | C | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG00735.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.632-1500C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114289989 | |||||||
| chr13:114290089 | A | G | 11 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00597.hp2 HG00673.hp1 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-1400A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290089 | |||||||
| chr13:114290094 | A | C | 35 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(32): Show |
38 | HG01255.hp1 HG01433.hp1 HG02257.hp1 others(35): Show |
intron_variant | MODIFIER | c.632-1395A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290094 | |||||||
| chr13:114290207 | G | T | 1 | a0012c0017t0011g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.632-1282G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290207 | |||||||
| chr13:114290311 | T | C | 15 | a0001c0001t0001g0045 a0001c0001t0001g0184 a0001c0001t0001g0185 others(12): Show |
19 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.632-1178T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290311 | |||||||
| chr13:114290415 | TC | T | 9 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.632-1072delC | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114290415 | ||||||
| chr13:114290508 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.632-981G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290508 | |||||||
| chr13:114290554 | G | A | 1 | a0002c0002t0001g0354 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.632-935G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290554 | |||||||
| chr13:114290734 | C | CT | 8 | a0001c0001t0001g0084 a0001c0001t0001g0114 a0001c0001t0001g0169 others(5): Show |
8 | HG01243.hp1 HG02698.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.632-739dupT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114290734 | ||||||
| chr13:114290734 | CT | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0299 a0001c0001t0001g0309 others(3): Show |
7 | HG02155.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.632-739delT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 114290734 | ||||||
| chr13:114290797 | A | G | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | NA18959.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.632-692A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290797 | |||||||
| chr13:114290818 | C | T | 2 | a0001c0001t0005g0317 a0001c0001t0005g0318 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.632-671C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290818 | |||||||
| chr13:114290827 | G | A | 5 | a0002c0002t0001g0028 a0002c0002t0001g0230 a0002c0002t0001g0231 others(2): Show |
6 | HG01243.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.632-662G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290827 | |||||||
| chr13:114290836 | T | C | 28 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0175 others(25): Show |
33 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.632-653T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290836 | |||||||
| chr13:114290924 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0062 a0002c0002t0001g0202 others(1): Show |
5 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-565G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114290924 | |||||||
| chr13:114291150 | T | G | 1 | a0002c0002t0001g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.632-339T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114291150 | |||||||
| chr13:114291265 | C | G | 35 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(32): Show |
38 | HG01255.hp1 HG01433.hp1 HG02257.hp1 others(35): Show |
intron_variant | MODIFIER | c.632-224C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114291265 | |||||||
| chr13:114291317 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.632-172A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114291317 | |||||||
| chr13:114291363 | A | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0298 |
3 | HG00621.hp1 NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.632-126A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114291363 | |||||||
| chr13:114291460 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.632-29A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 5/9 | chr13 | 114291460 | |||||||
| chr13:114291572 | C | T | 8 | a0002c0002t0001g0073 a0002c0002t0001g0207 a0002c0002t0001g0208 others(5): Show |
8 | HG03491.hp2 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.687+28C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 6/9 | chr13 | 114291572 | |||||||
| chr13:114291574 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.687+30C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 6/9 | chr13 | 114291574 | |||||||
| chr13:114291912 | G | T | 1 | a0002c0002t0001g0014 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.846+120G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114291912 | |||||||
| chr13:114291934 | ATCTT | A | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+149_846+152del others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114291934 | ||||||
| chr13:114291973 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.846+181G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114291973 | |||||||
| chr13:114292063 | G | T | 1 | a0002c0002t0001g0369 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.846+271G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292063 | |||||||
| chr13:114292076 | C | T | 1 | a0002c0002t0001g0232 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.846+284C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292076 | |||||||
| chr13:114292086 | C | T | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+294C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292086 | |||||||
| chr13:114292090 | C | CT | 15 | a0001c0001t0001g0113 a0001c0001t0001g0271 a0001c0001t0007g0291 others(12): Show |
20 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.846+318dupT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114292090 | ||||||
| chr13:114292090 | CT | C | 24 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0087 others(21): Show |
25 | HG00323.hp1 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.846+318delT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114292090 | ||||||
| chr13:114292161 | T | C | 1 | a0001c0001t0001g0344 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.846+369T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292161 | |||||||
| chr13:114292183 | CGCGTACA others(79): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.846+470_846+555del others(86): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114292183 | ||||||
| chr13:114292185 | C | T | 2 | a0002c0002t0001g0208 a0002c0002t0001g0209 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.846+393C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292185 | |||||||
| chr13:114292234 | C | T | 1 | a0011c0009t0014g0346 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.846+442C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292234 | |||||||
| chr13:114292277 | C | T | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+485C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292277 | |||||||
| chr13:114292292 | C | T | 1 | a0001c0001t0001g0020 | 2 | NA18747.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.846+500C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292292 | |||||||
| chr13:114292293 | G | A | 5 | a0002c0002t0001g0044 a0002c0002t0001g0229 a0002c0002t0001g0358 others(2): Show |
6 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.846+501G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292293 | |||||||
| chr13:114292336 | ATGTTCAT others(294): Show |
A | 1 | a0012c0017t0011g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.846+584_846+884del | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114292336 | ||||||
| chr13:114292348 | G | A | 1 | a0002c0002t0001g0361 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.846+556G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292348 | |||||||
| chr13:114292401 | T | G | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+609T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292401 | |||||||
| chr13:114292444 | G | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.846+652G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292444 | |||||||
| chr13:114292450 | G | A | 1 | a0001c0001t0013g0115 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.846+658G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292450 | |||||||
| chr13:114292465 | G | GTGTTCAT others(122): Show |
1 | a0001c0001t0001g0263 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.846+780_846+781ins others(129): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114292465 | ||||||
| chr13:114292513 | T | C | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+721T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292513 | |||||||
| chr13:114292530 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(97): Show |
120 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.846+738G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292530 | |||||||
| chr13:114292536 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0371 a0001c0001t0001g0373 |
4 | HG02818.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+744G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292536 | |||||||
| chr13:114292572 | C | T | 35 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(32): Show |
38 | HG01255.hp1 HG01433.hp1 HG02257.hp1 others(35): Show |
intron_variant | MODIFIER | c.846+780C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292572 | |||||||
| chr13:114292608 | T | TTCAAGGC others(36): Show |
1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.846+842_846+884dup others(43): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114292608 | ||||||
| chr13:114292616 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(33): Show |
40 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.846+824G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292616 | |||||||
| chr13:114292645 | T | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.846+853T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292645 | |||||||
| chr13:114292651 | C | CTCAAGGC others(165): Show |
8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+884_846+885ins others(172): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114292651 | ||||||
| chr13:114292658 | C | T | 2 | a0002c0002t0001g0132 a0002c0002t0001g0226 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.846+866C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292658 | |||||||
| chr13:114292785 | C | T | 1 | a0003c0003t0001g0199 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.846+993C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292785 | |||||||
| chr13:114292824 | C | T | 1 | a0002c0002t0001g0354 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.846+1032C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292824 | |||||||
| chr13:114292868 | TTCGAGAT others(1744): Show |
T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0067 |
2 | NA18957.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.846+1083_846+2833d others(2): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114292868 | ||||||
| chr13:114292871 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.846+1079G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292871 | |||||||
| chr13:114292933 | T | C | 115 | a0001c0001t0001g0015 a0001c0001t0001g0284 a0002c0002t0001g0011 others(112): Show |
136 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.846+1141T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292933 | |||||||
| chr13:114292954 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.846+1162C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114292954 | |||||||
| chr13:114293027 | G | A | 1 | a0002c0002t0001g0361 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.846+1235G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293027 | |||||||
| chr13:114293051 | G | A | 3 | a0002c0002t0001g0064 a0002c0002t0001g0132 a0002c0002t0001g0226 |
3 | HG02145.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.846+1259G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293051 | |||||||
| chr13:114293071 | C | CA | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
124 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.846+1303dupA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114293071 | ||||||
| chr13:114293071 | C | CAA | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(5): Show |
8 | HG00544.hp1 HG02071.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+1302_846+1303d others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114293071 | ||||||
| chr13:114293071 | CA | C | 65 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0033 others(62): Show |
72 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.846+1303delA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114293071 | ||||||
| chr13:114293071 | CAA | C | 5 | a0002c0002t0001g0012 a0002c0002t0001g0044 a0002c0002t0001g0358 others(2): Show |
6 | HG02630.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+1302_846+1303d others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114293071 | ||||||
| chr13:114293105 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(98): Show |
121 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.846+1313C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293105 | |||||||
| chr13:114293315 | C | T | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+1523C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293315 | |||||||
| chr13:114293329 | AG | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.846+1538delG | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293329 | |||||||
| chr13:114293338 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0372 a0001c0001t0001g0373 |
4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+1546C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293338 | |||||||
| chr13:114293341 | G | A | 2 | a0002c0002t0001g0046 a0002c0002t0001g0225 |
2 | HG00733.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.846+1549G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293341 | |||||||
| chr13:114293349 | A | C | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.846+1557A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293349 | |||||||
| chr13:114293383 | TA | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0185 a0001c0001t0001g0247 others(34): Show |
40 | HG01069.hp2 HG01070.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.846+1603delA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114293383 | ||||||
| chr13:114293455 | G | A | 36 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(33): Show |
39 | HG01255.hp1 HG01433.hp1 HG02257.hp1 others(36): Show |
intron_variant | MODIFIER | c.846+1663G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293455 | |||||||
| chr13:114293487 | G | T | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+1695G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293487 | |||||||
| chr13:114293490 | A | G | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+1698A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293490 | |||||||
| chr13:114293510 | G | C | 16 | a0002c0002t0001g0011 a0002c0002t0001g0016 a0002c0002t0001g0022 others(13): Show |
21 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.846+1718G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293510 | |||||||
| chr13:114293707 | T | A | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+1915T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293707 | |||||||
| chr13:114293726 | A | G | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+1934A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293726 | |||||||
| chr13:114293773 | G | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0298 a0001c0001t0001g0299 others(5): Show |
9 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.846+1981G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293773 | |||||||
| chr13:114293966 | A | G | 3 | a0002c0002t0001g0074 a0005c0006t0006g0218 a0005c0006t0006g0219 |
3 | HG02572.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.846+2174A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293966 | |||||||
| chr13:114293984 | A | G | 1 | a0002c0002t0001g0356 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.846+2192A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114293984 | |||||||
| chr13:114294198 | A | G | 1 | a0002c0002t0010g0355 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.846+2406A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294198 | |||||||
| chr13:114294254 | T | C | 35 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(32): Show |
38 | HG01255.hp1 HG01433.hp1 HG02257.hp1 others(35): Show |
intron_variant | MODIFIER | c.846+2462T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294254 | |||||||
| chr13:114294273 | T | TG | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
164 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.846+2491dupG | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114294273 | ||||||
| chr13:114294273 | T | TGG | 78 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(75): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.846+2490_846+2491d others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114294273 | ||||||
| chr13:114294281 | G | GC | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 others(1): Show |
4 | HG01109.hp1 HG02809.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2489_846+2490i others(3): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294281 | |||||||
| chr13:114294284 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.846+2492T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294284 | |||||||
| chr13:114294290 | A | G | 76 | a0001c0001t0001g0284 a0002c0002t0001g0011 a0002c0002t0001g0012 others(73): Show |
88 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.846+2498A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294290 | |||||||
| chr13:114294330 | A | G | 8 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+2538A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294330 | |||||||
| chr13:114294492 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.846+2700G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294492 | |||||||
| chr13:114294508 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.846+2716C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294508 | |||||||
| chr13:114294538 | C | T | 2 | a0001c0001t0005g0317 a0001c0001t0005g0318 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.846+2746C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294538 | |||||||
| chr13:114294551 | C | T | 1 | a0002c0002t0001g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.846+2759C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294551 | |||||||
| chr13:114294565 | A | G | 1 | a0001c0007t0001g0032 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.846+2773A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294565 | |||||||
| chr13:114294596 | C | T | 3 | a0001c0001t0004g0177 a0001c0001t0004g0178 a0001c0001t0004g0331 |
3 | HG02818.hp2 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.846+2804C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294596 | |||||||
| chr13:114294819 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.846+3027C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294819 | |||||||
| chr13:114294883 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.846+3091T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294883 | |||||||
| chr13:114294888 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.846+3096G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294888 | |||||||
| chr13:114294894 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.846+3102T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294894 | |||||||
| chr13:114294895 | T | G | 1 | a0001c0001t0001g0030 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.846+3103T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294895 | |||||||
| chr13:114294918 | C | T | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.846+3126C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294918 | |||||||
| chr13:114294919 | T | C | 2 | a0002c0002t0001g0369 a0002c0002t0001g0370 |
2 | HG02132.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.846+3127T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294919 | |||||||
| chr13:114294939 | T | C | 10 | a0001c0001t0001g0171 a0002c0002t0001g0014 a0002c0002t0001g0073 others(7): Show |
12 | HG00621.hp2 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.846+3147T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294939 | |||||||
| chr13:114294940 | A | G | 10 | a0001c0001t0001g0171 a0002c0002t0001g0014 a0002c0002t0001g0073 others(7): Show |
12 | HG00621.hp2 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.846+3148A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294940 | |||||||
| chr13:114294968 | T | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | NA18941.hp2 NA18977.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.846+3176T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114294968 | |||||||
| chr13:114295061 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
166 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.846+3269A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295061 | |||||||
| chr13:114295069 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0283 |
2 | HG01975.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.846+3277G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295069 | |||||||
| chr13:114295073 | C | T | 5 | a0002c0002t0001g0118 a0002c0002t0001g0125 a0002c0002t0001g0201 others(2): Show |
5 | NA18942.hp1 NA18962.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.846+3281C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295073 | |||||||
| chr13:114295077 | A | C | 1 | a0001c0001t0001g0296 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.846+3285A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295077 | |||||||
| chr13:114295090 | C | T | 1 | a0003c0003t0001g0129 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.846+3298C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295090 | |||||||
| chr13:114295091 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.846+3299G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295091 | |||||||
| chr13:114295104 | T | TC | 5 | a0001c0001t0001g0015 a0005c0006t0006g0218 a0005c0006t0006g0219 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+3314dupC | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295104 | ||||||
| chr13:114295107 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0043 others(13): Show |
21 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.846+3315G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295107 | |||||||
| chr13:114295107 | G | C | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.846+3315G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295107 | |||||||
| chr13:114295111 | C | CA | 61 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0148 others(58): Show |
73 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.846+3336dupA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295111 | ||||||
| chr13:114295111 | C | CAA | 10 | a0002c0002t0001g0012 a0002c0002t0001g0029 a0002c0002t0001g0135 others(7): Show |
13 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.846+3335_846+3336d others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295111 | ||||||
| chr13:114295111 | CA | C | 10 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0102 others(7): Show |
10 | HG01069.hp2 HG02735.hp1 HG03704.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+3336delA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295111 | ||||||
| chr13:114295122 | A | AAC | 7 | a0002c0002t0001g0027 a0002c0002t0001g0130 a0002c0002t0001g0131 others(4): Show |
8 | HG00738.hp1 HG01070.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.846+3331_846+3332i others(4): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295122 | ||||||
| chr13:114295124 | A | G | 1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.846+3332A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295124 | |||||||
| chr13:114295256 | C | A | 1 | a0002c0002t0001g0354 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.846+3464C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295256 | |||||||
| chr13:114295261 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0086 a0001c0001t0001g0167 others(1): Show |
6 | HG00621.hp2 HG02148.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.846+3469C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295261 | |||||||
| chr13:114295266 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.846+3474C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295266 | |||||||
| chr13:114295293 | C | T | 6 | a0002c0002t0001g0016 a0002c0002t0001g0027 a0002c0002t0001g0217 others(3): Show |
8 | HG00738.hp1 HG01070.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.846+3501C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295293 | |||||||
| chr13:114295301 | A | C | 1 | a0001c0001t0001g0039 | 2 | HG01496.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.846+3509A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295301 | |||||||
| chr13:114295302 | G | GCTGGCCT others(57): Show |
1 | a0001c0001t0001g0337 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.846+3516_847-3469d others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCCT others(153): Show |
1 | a0003c0003t0009g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.847-3446_847-3445i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCCT others(153): Show |
1 | a0001c0001t0001g0254 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCCT others(121): Show |
1 | a0003c0003t0001g0206 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.847-3501_847-3500i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCCT others(89): Show |
3 | a0004c0004t0003g0116 a0004c0004t0003g0188 a0004c0004t0003g0189 |
3 | HG01496.hp2 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.847-3510_847-3509i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(25): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0101 others(2): Show |
6 | HG02155.hp2 NA18943.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.846+3515_846+3516i others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(121): Show |
1 | a0001c0001t0007g0291 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.846+3515_846+3516i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(57): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0097 others(7): Show |
14 | HG02071.hp2 HG02300.hp1 HG04204.hp1 others(11): Show |
intron_variant | MODIFIER | c.846+3515_846+3516i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(185): Show |
1 | a0001c0001t0001g0094 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.846+3515_846+3516i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(57): Show |
1 | a0001c0001t0001g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.846+3515_846+3516i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(89): Show |
3 | a0001c0001t0001g0165 a0001c0001t0001g0304 a0001c0001t0012g0164 |
3 | HG02451.hp2 NA18948.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.846+3515_846+3516i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(281): Show |
1 | a0001c0001t0001g0159 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.846+3515_846+3516i others(290): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(153): Show |
2 | a0001c0001t0001g0160 a0001c0019t0001g0161 |
2 | NA18946.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.846+3515_846+3516i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(121): Show |
1 | a0001c0001t0001g0303 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.846+3515_846+3516i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | GCTGGCGT others(89): Show |
1 | a0001c0001t0001g0166 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.846+3515_846+3516i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | G | T | 1 | a0001c0001t0001g0039 | 2 | HG01496.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.846+3510G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295302 | |||||||
| chr13:114295302 | GCTGGCCT others(25): Show |
G | 1 | a0002c0002t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.847-3509_847-3478d others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295302 | GCTGGCCT others(57): Show |
G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0106 a0001c0001t0001g0149 others(2): Show |
7 | HG02027.hp1 HG02080.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.846+3516_847-3469d others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295302 | ||||||
| chr13:114295308 | C | CTGCTCCC others(121): Show |
1 | a0001c0001t0001g0263 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.847-3501_847-3500i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295308 | ||||||
| chr13:114295308 | C | CTGCTCCC others(185): Show |
1 | a0002c0002t0001g0198 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.847-3510_847-3509i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295308 | ||||||
| chr13:114295308 | C | CTGCTCCC others(25): Show |
3 | a0002c0002t0001g0234 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG02451.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.847-3510_847-3509i others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295308 | ||||||
| chr13:114295308 | C | CTGCTCCC others(89): Show |
1 | a0001c0001t0001g0051 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.847-3510_847-3509i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295308 | ||||||
| chr13:114295308 | C | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(73): Show |
91 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.846+3516C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295308 | |||||||
| chr13:114295308 | C | GTGCTCCC others(89): Show |
3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | NA19058.hp2 NA19070.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.846+3515_846+3516i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295308 | |||||||
| chr13:114295308 | CTGCTCCC others(57): Show |
C | 1 | a0002c0002t0001g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.847-3509_847-3446d others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295308 | ||||||
| chr13:114295308 | CTGCTCCC others(89): Show |
C | 2 | a0001c0001t0004g0331 a0002c0002t0001g0368 |
2 | HG03225.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.847-3509_847-3414d others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295308 | ||||||
| chr13:114295331 | A | AGCTCTGG others(121): Show |
1 | a0001c0001t0001g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.847-3478_847-3477i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(89): Show |
1 | a0001c0001t0001g0271 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.847-3478_847-3477i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(25): Show |
2 | a0002c0002t0001g0012 a0002c0002t0001g0233 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.847-3500_847-3469d others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(249): Show |
1 | a0001c0001t0001g0323 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(258): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(217): Show |
2 | a0001c0001t0001g0238 a0001c0001t0001g0240 |
2 | HG00323.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.847-3446_847-3445i others(226): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(217): Show |
1 | a0001c0001t0001g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.847-3446_847-3445i others(226): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(185): Show |
1 | a0008c0012t0001g0310 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.847-3446_847-3445i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(57): Show |
6 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0247 others(3): Show |
6 | HG00408.hp1 HG01069.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.847-3500_847-3437d others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(153): Show |
1 | a0002c0002t0001g0029 | 2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.847-3437_847-3436i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(89): Show |
1 | a0001c0001t0001g0054 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(89): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0249 a0001c0001t0001g0276 others(1): Show |
4 | HG02129.hp2 HG03654.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-3495_847-3400d others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(185): Show |
1 | a0001c0001t0001g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.847-3405_847-3404i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(25): Show |
1 | a0016c0014t0001g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.847-3501_847-3500i others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(185): Show |
1 | a0003c0003t0001g0072 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.847-3501_847-3500i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(57): Show |
1 | a0001c0001t0001g0264 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.847-3501_847-3500i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | AGCTCTGG others(185): Show |
1 | a0001c0001t0001g0287 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.847-3501_847-3500i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(93): Show |
111 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.847-3509A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295331 | |||||||
| chr13:114295331 | AGCTCTGG others(25): Show |
A | 1 | a0002c0002t0001g0014 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.847-3500_847-3469d others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295331 | AGCTCTGG others(57): Show |
A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.847-3500_847-3437d others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295331 | ||||||
| chr13:114295340 | C | CTGCTCCC others(121): Show |
1 | a0001c0001t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.847-3478_847-3477i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(89): Show |
1 | a0001c0001t0001g0371 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.847-3478_847-3477i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(57): Show |
1 | a0002c0002t0001g0232 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.847-3478_847-3477i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(25): Show |
1 | a0005c0006t0006g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.847-3478_847-3477i others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(57): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0372 |
2 | HG02886.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.847-3478_847-3477i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(89): Show |
1 | a0001c0001t0001g0045 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.847-3478_847-3477i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(121): Show |
1 | a0001c0001t0001g0373 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.847-3478_847-3477i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(121): Show |
1 | a0001c0001t0001g0294 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.847-3469_847-3468i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(89): Show |
1 | a0002c0002t0001g0349 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.847-3469_847-3468i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(25): Show |
11 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0157 others(8): Show |
12 | HG00733.hp2 HG01243.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.847-3436_847-3405d others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(185): Show |
1 | a0002c0002t0001g0357 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(89): Show |
3 | a0001c0001t0001g0257 a0002c0002t0001g0215 a0002c0002t0001g0220 |
3 | HG00609.hp1 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-3437_847-3436i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(121): Show |
1 | a0002c0002t0001g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(57): Show |
6 | a0001c0001t0001g0148 a0001c0001t0001g0286 a0002c0002t0001g0223 others(3): Show |
6 | HG00639.hp2 HG01168.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.847-3468_847-3405d others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(217): Show |
1 | a0001c0007t0001g0032 | 2 | HG00140.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.847-3400_847-3399i others(226): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(89): Show |
1 | a0001c0001t0001g0251 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.847-3405_847-3404i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | CTGCTCCC others(121): Show |
3 | a0002c0002t0001g0064 a0002c0002t0001g0132 a0002c0002t0001g0226 |
3 | HG02145.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.847-3405_847-3404i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295340 | C | G | 18 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0163 others(15): Show |
20 | HG00408.hp2 HG00621.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.847-3500C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295340 | |||||||
| chr13:114295340 | C | GTGCTCCC others(89): Show |
1 | a0005c0006t0006g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.847-3501_847-3500i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295340 | |||||||
| chr13:114295340 | CTGCTCCC others(25): Show |
C | 36 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0058 others(33): Show |
39 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.847-3436_847-3405d others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295340 | ||||||
| chr13:114295363 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0298 a0001c0001t0007g0291 |
4 | HG00621.hp1 NA18967.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-3477G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295363 | |||||||
| chr13:114295363 | G | GGCTCTGG others(25): Show |
1 | a0002c0002t0001g0073 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.847-3469_847-3468i others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295363 | ||||||
| chr13:114295363 | G | GGCTCTGG others(57): Show |
1 | a0002c0002t0001g0356 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847-3469_847-3468i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295363 | ||||||
| chr13:114295363 | G | GGCTCTGG others(345): Show |
1 | a0003c0003t0001g0129 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.847-3469_847-3468i others(354): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295363 | ||||||
| chr13:114295363 | G | GGCTCTGG others(89): Show |
1 | a0001c0001t0013g0115 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.847-3446_847-3445i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295363 | ||||||
| chr13:114295363 | G | GGCTCTGG others(57): Show |
1 | a0001c0001t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295363 | ||||||
| chr13:114295363 | G | GGCTCTGG others(57): Show |
1 | a0001c0001t0001g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.847-3414_847-3413i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295363 | ||||||
| chr13:114295372 | G | C | 26 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0076 others(23): Show |
28 | HG00408.hp2 HG00621.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.847-3468G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295372 | |||||||
| chr13:114295372 | G | GTGCTCCC others(57): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0339 a0001c0001t0001g0340 |
3 | HG00642.hp2 HG01361.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.847-3455_847-3454i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(25): Show |
1 | a0003c0003t0001g0121 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(57): Show |
1 | a0002c0002t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(89): Show |
7 | a0002c0002t0001g0118 a0002c0002t0001g0125 a0003c0003t0001g0071 others(4): Show |
7 | NA18940.hp2 NA18942.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.847-3446_847-3445i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(121): Show |
10 | a0001c0001t0001g0031 a0002c0002t0001g0026 a0002c0002t0001g0119 others(7): Show |
12 | HG01081.hp2 HG03486.hp2 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.847-3446_847-3445i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(153): Show |
1 | a0003c0003t0001g0193 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(185): Show |
1 | a0003c0003t0001g0120 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(249): Show |
1 | a0007c0005t0001g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(258): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(409): Show |
1 | a0001c0001t0001g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.847-3446_847-3445i others(418): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(121): Show |
2 | a0001c0001t0001g0003 a0002c0002t0008g0362 |
2 | HG01257.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.847-3446_847-3445i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(121): Show |
1 | a0001c0001t0001g0031 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.847-3446_847-3445i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(249): Show |
1 | a0001c0001t0001g0335 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(258): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(185): Show |
2 | a0001c0001t0001g0314 a0009c0010t0001g0375 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.847-3446_847-3445i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(217): Show |
1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(226): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(89): Show |
1 | a0003c0003t0001g0010 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.847-3446_847-3445i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(25): Show |
15 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0001g0104 others(12): Show |
15 | HG00597.hp1 HG01175.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.847-3437_847-3436i others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(57): Show |
1 | a0001c0001t0001g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(89): Show |
1 | a0002c0002t0001g0228 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(57): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(12): Show |
24 | HG00642.hp1 HG00673.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.847-3437_847-3436i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(89): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0327 a0004c0004t0003g0190 |
3 | HG03471.hp1 NA19043.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.847-3437_847-3436i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(153): Show |
1 | a0002c0002t0001g0363 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(89): Show |
1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(121): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0088 |
2 | HG03453.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.847-3437_847-3436i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(153): Show |
1 | a0002c0002t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(57): Show |
2 | a0002c0002t0001g0130 a0002c0002t0001g0131 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.847-3414_847-3413i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(153): Show |
1 | a0001c0001t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.847-3414_847-3413i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(57): Show |
27 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0030 others(24): Show |
33 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.847-3463_847-3400d others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(89): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0260 |
3 | HG00558.hp2 HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.847-3400_847-3399i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(121): Show |
1 | a0004c0004t0003g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.847-3400_847-3399i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(153): Show |
1 | a0002c0002t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.847-3400_847-3399i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(185): Show |
1 | a0001c0001t0001g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.847-3400_847-3399i others(194): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(89): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0315 a0001c0001t0001g0333 others(2): Show |
6 | HG00099.hp2 HG00323.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.847-3405_847-3404i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295372 | G | GTGCTCCC others(121): Show |
1 | a0002c0002t0001g0361 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.847-3405_847-3404i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295372 | ||||||
| chr13:114295386 | G | A | 1 | a0002c0002t0001g0349 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.847-3454G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295386 | |||||||
| chr13:114295395 | G | A | 21 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0067 others(18): Show |
25 | HG00733.hp1 HG01081.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.847-3445G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295395 | |||||||
| chr13:114295395 | G | GGCTCTGG others(121): Show |
2 | a0002c0002t0001g0122 a0003c0003t0001g0124 |
2 | NA18968.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.847-3437_847-3436i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295395 | ||||||
| chr13:114295395 | G | GGCTCTGG others(121): Show |
1 | a0001c0001t0001g0306 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.847-3437_847-3436i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295395 | ||||||
| chr13:114295395 | G | GGCTCTGG others(217): Show |
1 | a0003c0003t0001g0199 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.847-3437_847-3436i others(226): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295395 | ||||||
| chr13:114295404 | G | C | 123 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
142 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.847-3436G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295404 | |||||||
| chr13:114295404 | G | GTGCTCCC others(153): Show |
1 | a0002c0002t0001g0137 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.847-3414_847-3413i others(162): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(25): Show |
9 | a0001c0001t0001g0048 a0001c0001t0001g0258 a0001c0001t0001g0284 others(6): Show |
11 | HG02071.hp2 HG02132.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.847-3431_847-3400d others(34): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(121): Show |
1 | a0003c0003t0001g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.847-3400_847-3399i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(57): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0169 a0001c0001t0001g0297 others(1): Show |
4 | HG02135.hp1 HG02738.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.847-3400_847-3399i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(121): Show |
3 | a0001c0001t0001g0050 a0001c0001t0001g0293 a0001c0001t0001g0295 |
3 | HG01168.hp2 HG01169.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.847-3400_847-3399i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(89): Show |
2 | a0001c0001t0001g0141 a0001c0001t0001g0336 |
2 | HG01346.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.847-3400_847-3399i others(98): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(121): Show |
1 | a0001c0001t0001g0332 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.847-3400_847-3399i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(57): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0282 |
3 | HG02056.hp2 NA18950.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.847-3405_847-3404i others(66): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(121): Show |
4 | a0001c0001t0001g0307 a0004c0004t0002g0006 a0004c0004t0002g0377 others(1): Show |
7 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.847-3405_847-3404i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295404 | G | GTGCTCCC others(121): Show |
1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.847-3405_847-3404i others(130): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295404 | ||||||
| chr13:114295427 | G | A | 1 | a0003c0003t0001g0121 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.847-3413G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295427 | |||||||
| chr13:114295427 | G | GGCTCTGG others(249): Show |
1 | a0001c0001t0001g0242 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.847-3400_847-3399i others(258): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114295427 | ||||||
| chr13:114295456 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0373 |
3 | HG02818.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.847-3384C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295456 | |||||||
| chr13:114295470 | A | C | 2 | a0004c0004t0002g0006 a0004c0004t0002g0378 |
5 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.847-3370A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295470 | |||||||
| chr13:114295483 | G | A | 4 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0002c0002t0001g0046 others(1): Show |
4 | HG00733.hp2 HG03471.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-3357G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295483 | |||||||
| chr13:114295582 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.847-3258G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295582 | |||||||
| chr13:114295780 | T | G | 1 | a0001c0001t0001g0294 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.847-3060T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295780 | |||||||
| chr13:114295800 | G | A | 85 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
100 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.847-3040G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295800 | |||||||
| chr13:114295901 | G | C | 26 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(23): Show |
29 | HG02698.hp1 HG02698.hp2 HG04199.hp1 others(26): Show |
intron_variant | MODIFIER | c.847-2939G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295901 | |||||||
| chr13:114295999 | C | T | 1 | a0002c0002t0001g0044 | 2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.847-2841C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114295999 | |||||||
| chr13:114296030 | C | T | 2 | a0004c0004t0002g0006 a0004c0004t0002g0377 |
5 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.847-2810C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296030 | |||||||
| chr13:114296031 | G | A | 1 | a0002c0002t0001g0369 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.847-2809G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296031 | |||||||
| chr13:114296064 | A | G | 8 | a0001c0001t0001g0299 a0001c0001t0001g0301 a0001c0001t0001g0302 others(5): Show |
10 | HG00741.hp1 HG01123.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.847-2776A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296064 | |||||||
| chr13:114296122 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA18980.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.847-2718C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296122 | |||||||
| chr13:114296244 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0003c0003t0001g0129 |
3 | HG01255.hp1 NA18957.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.847-2596A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296244 | |||||||
| chr13:114296252 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0039 others(106): Show |
131 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.847-2588G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296252 | |||||||
| chr13:114296261 | T | C | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.847-2579T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296261 | |||||||
| chr13:114296291 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0067 |
2 | NA18957.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.847-2549A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296291 | |||||||
| chr13:114296331 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.847-2509G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296331 | |||||||
| chr13:114296339 | G | A | 31 | a0002c0002t0001g0118 a0002c0002t0001g0125 a0002c0002t0001g0197 others(28): Show |
33 | HG00733.hp1 HG01255.hp1 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.847-2501G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296339 | |||||||
| chr13:114296358 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.847-2482G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296358 | |||||||
| chr13:114296622 | G | A | 1 | a0002c0002t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.847-2218G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296622 | |||||||
| chr13:114296644 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0067 |
2 | NA18957.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.847-2196G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296644 | |||||||
| chr13:114296677 | T | G | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.847-2163T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296677 | |||||||
| chr13:114296687 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0261 |
3 | HG00642.hp1 HG01175.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.847-2153C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296687 | |||||||
| chr13:114296713 | G | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG00735.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.847-2127G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296713 | |||||||
| chr13:114296730 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.847-2110G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296730 | |||||||
| chr13:114296759 | G | C | 1 | a0001c0001t0001g0311 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.847-2081G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296759 | |||||||
| chr13:114296760 | A | G | 46 | a0001c0001t0001g0015 a0002c0002t0001g0026 a0002c0002t0001g0118 others(43): Show |
53 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.847-2080A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296760 | |||||||
| chr13:114296794 | T | C | 2 | a0001c0001t0004g0177 a0001c0001t0004g0178 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.847-2046T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296794 | |||||||
| chr13:114296800 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0170 |
2 | NA18964.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.847-2040C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296800 | |||||||
| chr13:114296801 | G | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG00735.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.847-2039G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296801 | |||||||
| chr13:114296805 | G | A | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.847-2035G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114296805 | |||||||
| chr13:114297031 | T | C | 46 | a0001c0001t0001g0015 a0002c0002t0001g0026 a0002c0002t0001g0118 others(43): Show |
53 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.847-1809T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297031 | |||||||
| chr13:114297040 | C | T | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.847-1800C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297040 | |||||||
| chr13:114297041 | G | A | 1 | a0001c0001t0004g0331 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.847-1799G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297041 | |||||||
| chr13:114297054 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.847-1786C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297054 | |||||||
| chr13:114297104 | C | T | 3 | a0002c0002t0001g0216 a0002c0002t0001g0351 a0002c0002t0001g0352 |
3 | HG02486.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.847-1736C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297104 | |||||||
| chr13:114297148 | T | A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.847-1692T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297148 | |||||||
| chr13:114297221 | C | CA | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.847-1619_847-1618i others(3): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297221 | |||||||
| chr13:114297221 | CG | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0043 others(45): Show |
56 | HG00642.hp2 HG00733.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.847-1618delG | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297221 | |||||||
| chr13:114297222 | G | GT | 27 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0047 others(24): Show |
29 | HG00408.hp2 HG00741.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.847-1604dupT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114297222 | ||||||
| chr13:114297222 | G | T | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.847-1618G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297222 | |||||||
| chr13:114297222 | GT | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0153 others(3): Show |
8 | HG03486.hp2 NA18945.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.847-1604delT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114297222 | ||||||
| chr13:114297223 | T | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0043 others(45): Show |
56 | HG00642.hp2 HG00733.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.847-1617T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297223 | |||||||
| chr13:114297267 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.847-1573T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297267 | |||||||
| chr13:114297432 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.847-1408T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297432 | |||||||
| chr13:114297437 | A | T | 1 | a0004c0004t0003g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.847-1403A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297437 | |||||||
| chr13:114297453 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.847-1387T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297453 | |||||||
| chr13:114297632 | C | A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.847-1208C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297632 | |||||||
| chr13:114297723 | A | G | 46 | a0001c0001t0001g0015 a0002c0002t0001g0026 a0002c0002t0001g0118 others(43): Show |
53 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.847-1117A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297723 | |||||||
| chr13:114297821 | G | A | 1 | a0002c0002t0001g0367 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.847-1019G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297821 | |||||||
| chr13:114297834 | A | T | 30 | a0002c0002t0001g0012 a0002c0002t0001g0013 a0002c0002t0001g0028 others(27): Show |
35 | HG00408.hp1 HG00423.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.847-1006A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297834 | |||||||
| chr13:114297837 | C | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(8): Show |
15 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.847-1003C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297837 | |||||||
| chr13:114297839 | A | G | 35 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(32): Show |
38 | HG00733.hp1 HG01255.hp1 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.847-1001A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297839 | |||||||
| chr13:114297877 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.847-963A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297877 | |||||||
| chr13:114297879 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.847-961G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297879 | |||||||
| chr13:114297961 | C | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
278 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.847-879C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114297961 | |||||||
| chr13:114298018 | A | G | 1 | a0001c0001t0004g0331 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.847-822A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298018 | |||||||
| chr13:114298075 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.847-765A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298075 | |||||||
| chr13:114298185 | G | A | 1 | a0005c0006t0006g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.847-655G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298185 | |||||||
| chr13:114298217 | C | T | 1 | a0002c0002t0001g0232 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.847-623C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298217 | |||||||
| chr13:114298373 | C | CA | 6 | a0001c0001t0001g0237 a0001c0001t0001g0280 a0001c0001t0001g0308 others(3): Show |
7 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.847-450dupA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114298373 | ||||||
| chr13:114298373 | CA | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0083 a0001c0001t0001g0184 others(47): Show |
57 | HG00733.hp1 HG00735.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.847-450delA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 114298373 | ||||||
| chr13:114298401 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
289 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.847-439A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298401 | |||||||
| chr13:114298467 | G | A | 34 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(31): Show |
37 | HG00733.hp1 HG01255.hp1 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.847-373G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298467 | |||||||
| chr13:114298468 | A | G | 34 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(31): Show |
37 | HG00733.hp1 HG01255.hp1 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.847-372A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298468 | |||||||
| chr13:114298488 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0371 a0001c0001t0001g0372 others(1): Show |
5 | HG02818.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.847-352C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298488 | |||||||
| chr13:114298501 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0014c0015t0001g0274 |
3 | NA18951.hp2 NA19057.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.847-339C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298501 | |||||||
| chr13:114298518 | C | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG00735.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.847-322C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298518 | |||||||
| chr13:114298568 | G | A | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.847-272G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298568 | |||||||
| chr13:114298676 | A | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0162 a0001c0001t0007g0291 |
3 | NA18943.hp1 NA18950.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.847-164A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 7/9 | chr13 | 114298676 | |||||||
| chr13:114299007 | G | A | 67 | a0001c0001t0001g0149 a0001c0001t0001g0174 a0001c0001t0001g0302 others(64): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
splice_region_variant&intron_variant | LOW | c.1007+7G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299007 | |||||||
| chr13:114299064 | G | A | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1007+64G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299064 | |||||||
| chr13:114299067 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(263): Show |
321 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.1007+67T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299067 | |||||||
| chr13:114299128 | G | A | 1 | a0009c0010t0001g0375 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1007+128G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299128 | |||||||
| chr13:114299175 | C | T | 7 | a0002c0002t0001g0012 a0002c0002t0001g0135 a0002c0002t0001g0136 others(4): Show |
9 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1007+175C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299175 | |||||||
| chr13:114299207 | G | A | 30 | a0002c0002t0001g0118 a0002c0002t0001g0125 a0002c0002t0001g0201 others(27): Show |
32 | HG00733.hp1 HG01255.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.1007+207G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299207 | |||||||
| chr13:114299210 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0021 others(108): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1007+210A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299210 | |||||||
| chr13:114299233 | G | T | 2 | a0001c0001t0001g0371 a0001c0001t0001g0372 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1007+233G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299233 | |||||||
| chr13:114299271 | C | T | 1 | a0006c0008t0001g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1007+271C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299271 | |||||||
| chr13:114299587 | T | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.1007+587T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299587 | |||||||
| chr13:114299657 | G | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1007+657G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299657 | |||||||
| chr13:114299731 | A | AGGGCCCC others(26): Show |
1 | a0002c0002t0001g0046 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1007+735_1007+767d others(35): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 114299731 | ||||||
| chr13:114299773 | T | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0255 |
2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1007+773T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299773 | |||||||
| chr13:114299902 | A | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0070 |
2 | HG00438.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1007+902A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114299902 | |||||||
| chr13:114300092 | G | A | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1007+1092G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300092 | |||||||
| chr13:114300163 | G | A | 1 | a0009c0010t0001g0375 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1007+1163G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300163 | |||||||
| chr13:114300494 | A | G | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-1237A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300494 | |||||||
| chr13:114300529 | T | C | 157 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0039 others(154): Show |
184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1008-1202T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300529 | |||||||
| chr13:114300541 | G | GT | 103 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0100 others(100): Show |
122 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1008-1180dupT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 114300541 | ||||||
| chr13:114300541 | GT | G | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-1180delT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 114300541 | ||||||
| chr13:114300593 | G | A | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-1138G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300593 | |||||||
| chr13:114300695 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1008-1036A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300695 | |||||||
| chr13:114300781 | T | C | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-950T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300781 | |||||||
| chr13:114300826 | G | A | 74 | a0001c0001t0001g0039 a0001c0001t0001g0299 a0001c0001t0001g0301 others(71): Show |
89 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1008-905G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300826 | |||||||
| chr13:114300870 | T | A | 1 | a0002c0002t0001g0225 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008-861T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300870 | |||||||
| chr13:114300889 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0333 |
2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.1008-842G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300889 | |||||||
| chr13:114300961 | C | T | 1 | a0012c0017t0011g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1008-770C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114300961 | |||||||
| chr13:114300973 | G | GCTAATTT others(309): Show |
10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-741_1008-740i others(318): Show |
UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 114300973 | ||||||
| chr13:114301040 | G | A | 7 | a0004c0004t0003g0116 a0004c0004t0003g0187 a0004c0004t0003g0188 others(4): Show |
7 | HG01496.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-691G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301040 | |||||||
| chr13:114301189 | C | T | 74 | a0001c0001t0001g0039 a0001c0001t0001g0299 a0001c0001t0001g0301 others(71): Show |
89 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1008-542C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301189 | |||||||
| chr13:114301213 | G | A | 1 | a0001c0001t0001g0338 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1008-518G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301213 | |||||||
| chr13:114301224 | G | C | 1 | a0002c0002t0001g0014 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1008-507G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301224 | |||||||
| chr13:114301238 | T | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0043 others(56): Show |
70 | HG00642.hp2 HG00733.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.1008-493T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301238 | |||||||
| chr13:114301258 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
98 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1008-473G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301258 | |||||||
| chr13:114301307 | C | A | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-424C>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301307 | |||||||
| chr13:114301356 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1008-375G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301356 | |||||||
| chr13:114301379 | T | C | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-352T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301379 | |||||||
| chr13:114301388 | A | G | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-343A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301388 | |||||||
| chr13:114301394 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01192.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1008-337C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301394 | |||||||
| chr13:114301411 | T | C | 41 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 others(38): Show |
44 | HG00733.hp1 HG01109.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.1008-320T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301411 | |||||||
| chr13:114301418 | C | G | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008-313C>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301418 | |||||||
| chr13:114301419 | C | T | 1 | a0002c0002t0001g0354 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1008-312C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301419 | |||||||
| chr13:114301455 | T | TC | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008-274dupC | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 114301455 | ||||||
| chr13:114301464 | GA | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
103 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1008-252delA | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 114301464 | ||||||
| chr13:114301558 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0081 a0001c0001t0001g0087 others(2): Show |
7 | NA18959.hp2 NA18960.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-173T>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301558 | |||||||
| chr13:114301618 | C | T | 36 | a0001c0001t0001g0284 a0002c0002t0001g0026 a0002c0002t0001g0118 others(33): Show |
39 | HG00733.hp1 HG01255.hp1 HG01433.hp1 others(36): Show |
intron_variant | MODIFIER | c.1008-113C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301618 | |||||||
| chr13:114301688 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1008-43C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 8/9 | chr13 | 114301688 | |||||||
| chr13:114302125 | C | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0237 others(9): Show |
16 | HG00642.hp2 HG01361.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+100C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302125 | |||||||
| chr13:114302160 | C | T | 1 | a0002c0002t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1302+135C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302160 | |||||||
| chr13:114302265 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1302+240G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302265 | |||||||
| chr13:114302354 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1302+329C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302354 | |||||||
| chr13:114302475 | C | CT | 11 | a0001c0001t0001g0096 a0004c0004t0002g0006 a0004c0004t0002g0377 others(8): Show |
14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1302+460dupT | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 114302475 | ||||||
| chr13:114302590 | G | C | 12 | a0002c0002t0001g0064 a0002c0002t0001g0073 a0002c0002t0001g0132 others(9): Show |
12 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.1302+565G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302590 | |||||||
| chr13:114302759 | T | G | 1 | a0002c0002t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1302+734T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302759 | |||||||
| chr13:114302874 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1302+849G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302874 | |||||||
| chr13:114302962 | C | T | 1 | a0004c0004t0003g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1302+937C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302962 | |||||||
| chr13:114302972 | C | T | 10 | a0001c0001t0001g0024 a0001c0001t0001g0105 a0001c0001t0001g0142 others(7): Show |
11 | HG01123.hp2 HG01975.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1302+947C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114302972 | |||||||
| chr13:114303194 | C | T | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+1169C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303194 | |||||||
| chr13:114303317 | T | G | 1 | a0002c0002t0001g0232 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1302+1292T>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303317 | |||||||
| chr13:114303335 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1302+1310G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303335 | |||||||
| chr13:114303411 | C | T | 1 | a0002c0002t0001g0198 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1303-1378C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303411 | |||||||
| chr13:114303412 | C | T | 1 | a0001c0001t0001g0373 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1303-1377C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303412 | |||||||
| chr13:114303543 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1303-1246T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303543 | |||||||
| chr13:114303623 | G | T | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1303-1166G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303623 | |||||||
| chr13:114303643 | G | A | 35 | a0002c0002t0001g0026 a0002c0002t0001g0118 a0002c0002t0001g0119 others(32): Show |
38 | HG00733.hp1 HG01255.hp1 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.1303-1146G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303643 | |||||||
| chr13:114303750 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1303-1039C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303750 | |||||||
| chr13:114303845 | G | T | 1 | a0003c0003t0001g0121 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1303-944G>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303845 | |||||||
| chr13:114303892 | A | C | 1 | a0002c0002t0001g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1303-897A>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303892 | |||||||
| chr13:114303898 | A | G | 2 | a0001c0001t0004g0177 a0001c0001t0004g0178 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1303-891A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303898 | |||||||
| chr13:114303984 | C | T | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1303-805C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303984 | |||||||
| chr13:114303987 | G | A | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1303-802G>A | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114303987 | |||||||
| chr13:114304198 | A | T | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1303-591A>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114304198 | |||||||
| chr13:114304215 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(9): Show |
12 | HG00597.hp2 HG00673.hp1 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.1303-574C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114304215 | |||||||
| chr13:114304226 | C | T | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1303-563C>T | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114304226 | |||||||
| chr13:114304232 | T | C | 3 | a0001c0001t0004g0177 a0001c0001t0004g0178 a0012c0017t0011g0334 |
3 | HG02280.hp1 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1303-557T>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114304232 | |||||||
| chr13:114304324 | A | G | 47 | a0001c0001t0001g0015 a0001c0001t0001g0284 a0002c0002t0001g0026 others(44): Show |
54 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1303-465A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114304324 | |||||||
| chr13:114304477 | G | C | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | NA18959.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1303-312G>C | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114304477 | |||||||
| chr13:114304677 | A | G | 10 | a0004c0004t0002g0006 a0004c0004t0002g0377 a0004c0004t0002g0378 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1303-112A>G | UPF3A | ENSG00000169062.15 | transcript | ENST00000375299.8 | protein_coding | 9/9 | chr13 | 114304677 |