Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54602 |
| ensemblid | ENSG00000102471.16 |
| hgncid | 18537 |
| symbol | NDFIP2 |
| name | Nedd4 family interacting protein 2 |
| refseq_nuc | NM_019080.3 |
| refseq_prot | NP_061953.2 |
| ensembl_nuc | ENST00000218652.12 |
| ensembl_prot | ENSP00000218652.7 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 79481155 |
| end | 79556077 |
| strand | + |
| ver | v1.2 |
| region | chr13:79481155-79556077 |
| region5000 | chr13:79476155-79561077 |
| regionname0 | NDFIP2_chr13_79481155_79556077 |
| regionname5000 | NDFIP2_chr13_79476155_79561077 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 336 | 248 | 63 | 41 | 100 | 13 | 29 | 82 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | MARRR others(331): Show |
chr13 | 79476155 | 79561077 |
| a0002 | 0/0 | 336 | 16 | 1 | 7 | 0 | 3 | 5 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | MARRR others(331): Show |
chr13 | 79476155 | 79561077 |
| a0003 | 0/0 | 336 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | MARRR others(331): Show |
chr13 | 79476155 | 79561077 |
| a0004 | 0/0 | 336 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | MARRR others(331): Show |
chr13 | 79476155 | 79561077 |
| a0005 | 0/0 | 336 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | MARRR others(331): Show |
chr13 | 79476155 | 79561077 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1008 | 247 | 63 | 41 | 99 | 13 | 29 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ATGGC others(1003): Show |
chr13 | 79476155 | 79561077 | ||
| a0001c0006 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ATGGC others(1003): Show |
chr13 | 79476155 | 79561077 | ||
| a0002c0002 | 0/0 | 1008 | 16 | 1 | 7 | 0 | 3 | 5 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ATGGC others(1003): Show |
chr13 | 79476155 | 79561077 | ||
| a0003c0003 | 0/0 | 1008 | 16 | 15 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ATGGC others(1003): Show |
chr13 | 79476155 | 79561077 | ||
| a0004c0004 | 0/0 | 1008 | 4 | 3 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ATGGC others(1003): Show |
chr13 | 79476155 | 79561077 | ||
| a0005c0005 | 0/0 | 1008 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ATGGC others(1003): Show |
chr13 | 79476155 | 79561077 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4624 | 99 | 22 | 23 | 37 | 6 | 10 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0002 | 0/0 | 4624 | 84 | 3 | 12 | 50 | 4 | 15 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0003 | 0/0 | 4624 | 21 | 18 | 1 | 1 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0004 | 0/1 | 4624 | 18 | 13 | 3 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0006 | 0/0 | 4626 | 8 | 0 | 0 | 5 | 0 | 3 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4621): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0008 | 0/0 | 4624 | 3 | 3 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0009 | 0/0 | 4624 | 2 | 1 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0011 | 0/0 | 4624 | 2 | 0 | 0 | 0 | 2 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0012 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0013 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0014 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0015 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0016 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4621): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0017 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0018 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0019 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0020 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0001t0021 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0001c0006t0006 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4621): Show |
chr13 | 79476155 | 79561077 |
| a0002c0002t0003 | 0/0 | 4624 | 16 | 1 | 7 | 0 | 3 | 5 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0003c0003t0005 | 0/0 | 4624 | 14 | 13 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0003c0003t0010 | 0/0 | 4624 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0004c0004t0007 | 0/0 | 4624 | 4 | 3 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| a0005c0005t0002 | 0/0 | 4624 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | ACTTT others(4619): Show |
chr13 | 79476155 | 79561077 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0001 | 0/0 | 8 | 0 | 1 | 4 | 0 | 3 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0004g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0006g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0011g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0012g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0013g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0014g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0016g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0017g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0018g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0019g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0020g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0001c0006t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0002c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0003c0003t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0004c0004t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0004c0004t0007g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0004c0004t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0004c0004t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0005c0005t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| a0005c0005t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00140 | hp1 | a0002 | c0002 | t0003 | g0223 | EUR | GBR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0222 | EUR | FIN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0220 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG00741 | hp2 | a0001 | c0001 | t0014 | g0002 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01069 | hp2 | a0002 | c0002 | t0003 | g0028 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01167 | hp2 | a0002 | c0002 | t0003 | g0218 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0229 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01175 | hp2 | a0002 | c0002 | t0003 | g0219 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0028 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0202 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01361 | hp2 | a0002 | c0002 | t0003 | g0217 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01515 | hp2 | a0001 | c0001 | t0011 | g0015 | EUR | IBS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01517 | hp1 | a0001 | c0001 | t0011 | g0015 | EUR | IBS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01952 | hp1 | a0004 | c0004 | t0007 | g0134 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG01981 | hp2 | a0003 | c0003 | t0005 | g0036 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02040 | hp2 | a0001 | c0006 | t0006 | g0091 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0197 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0090 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02145 | hp1 | a0004 | c0004 | t0007 | g0133 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CDX | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02451 | hp1 | a0003 | c0003 | t0005 | g0035 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02615 | hp2 | a0004 | c0004 | t0007 | g0137 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02622 | hp2 | a0003 | c0003 | t0005 | g0044 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02698 | hp1 | a0002 | c0002 | t0003 | g0213 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0097 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02723 | hp2 | a0003 | c0003 | t0005 | g0040 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02809 | hp1 | a0001 | c0001 | t0018 | g0129 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0140 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0225 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02895 | hp2 | a0003 | c0003 | t0005 | g0032 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02897 | hp2 | a0003 | c0003 | t0005 | g0033 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02965 | hp2 | a0003 | c0003 | t0010 | g0042 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03098 | hp2 | a0003 | c0003 | t0005 | g0034 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03130 | hp2 | a0003 | c0003 | t0005 | g0039 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03453 | hp1 | a0003 | c0003 | t0005 | g0041 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0027 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0027 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03540 | hp2 | a0003 | c0003 | t0005 | g0031 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0224 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0108 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0236 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03942 | hp2 | a0002 | c0002 | t0003 | g0234 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0014 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18522 | hp2 | a0003 | c0003 | t0010 | g0043 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18906 | hp2 | a0005 | c0005 | t0002 | g0205 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18945 | hp2 | a0001 | c0001 | t0021 | g0089 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18979 | hp2 | a0001 | c0001 | t0017 | g0110 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18986 | hp2 | a0001 | c0001 | t0013 | g0151 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18990 | hp1 | a0001 | c0001 | t0012 | g0163 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19002 | hp1 | a0001 | c0001 | t0016 | g0045 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19043 | hp1 | a0005 | c0005 | t0002 | g0204 | AFR | LWK | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19062 | hp1 | a0001 | c0001 | t0020 | g0008 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19078 | hp2 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA19240 | hp2 | a0003 | c0003 | t0005 | g0038 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA20129 | hp1 | a0003 | c0003 | t0005 | g0012 | AFR | ASW | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0195 | EUR | TSI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | TSI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA20805 | hp2 | a0002 | c0002 | t0003 | g0221 | EUR | TSI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02486 | hp1 | a0003 | c0003 | t0005 | g0012 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02559 | hp1 | a0004 | c0004 | t0007 | g0135 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| HG03471 | hp2 | a0001 | c0001 | t0019 | g0142 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | USA | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA20300 | hp2 | a0003 | c0003 | t0005 | g0037 | AFR | USA | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | LWK | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0144 | REF | REF | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0180 | REF | REF | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:79481220 | G | A | 1 | a0005 | 2 | NA18906.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.17G>A | p.Ser6Asn | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/8 | 66/4624 | 17/1011 | 6/336 | chr13 | 79481220 | |||
| chr13:79481302 | C | G | 1 | a0004 | 4 | HG01952.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
missense_variant | MODERATE | c.99C>G | p.Asn33Lys | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/8 | 148/4624 | 99/1011 | 33/336 | chr13 | 79481302 | |||
| chr13:79520858 | C | T | 1 | a0003 | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
missense_variant | MODERATE | c.370C>T | p.Pro124Ser | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/8 | 419/4624 | 370/1011 | 124/336 | chr13 | 79520858 | |||
| chr13:79520895 | C | T | 1 | a0002 | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
missense_variant | MODERATE | c.407C>T | p.Ala136Val | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/8 | 456/4624 | 407/1011 | 136/336 | chr13 | 79520895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:79533336 | C | T | 1 | a0001c0006 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.501C>T | p.Tyr167Tyr | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/8 | 550/4624 | 501/1011 | 167/336 | chr13 | 79533336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:79552633 | G | A | 6 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(3): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*120G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1513 | chr13 | 79552633 | ||||||
| chr13:79552645 | T | G | 3 | a0001c0001t0015 a0003c0003t0005 a0003c0003t0010 |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*132T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1525 | chr13 | 79552645 | ||||||
| chr13:79552673 | A | G | 3 | a0001c0001t0015 a0003c0003t0005 a0003c0003t0010 |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1553 | chr13 | 79552673 | ||||||
| chr13:79553040 | A | G | 1 | a0001c0001t0021 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1920 | chr13 | 79553040 | ||||||
| chr13:79553117 | A | C | 1 | a0001c0001t0008 | 3 | HG02723.hp1 HG02886.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*604A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1997 | chr13 | 79553117 | ||||||
| chr13:79553235 | C | T | 1 | a0001c0001t0020 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*722C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2115 | chr13 | 79553235 | ||||||
| chr13:79553244 | T | TAA | 3 | a0001c0001t0006 a0001c0001t0016 a0001c0006t0006 |
10 | HG02040.hp2 HG02074.hp1 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*733_*734dupAA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2128 | INFO_REALIGN_3_PRIME | chr13 | 79553244 | |||||
| chr13:79553323 | A | G | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*810A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2203 | chr13 | 79553323 | ||||||
| chr13:79553339 | T | C | 4 | a0001c0001t0003 a0001c0001t0009 a0002c0002t0003 others(1): Show |
43 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*826T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2219 | chr13 | 79553339 | ||||||
| chr13:79553500 | A | G | 5 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0018 others(2): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*987A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2380 | chr13 | 79553500 | ||||||
| chr13:79553586 | A | G | 1 | a0001c0001t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1073A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2466 | chr13 | 79553586 | ||||||
| chr13:79553614 | G | A | 1 | a0003c0003t0010 | 2 | HG02965.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1101G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2494 | chr13 | 79553614 | ||||||
| chr13:79554426 | G | A | 1 | a0001c0001t0016 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1913G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3306 | chr13 | 79554426 | ||||||
| chr13:79554549 | G | A | 2 | a0003c0003t0005 a0003c0003t0010 |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2036G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3429 | chr13 | 79554549 | ||||||
| chr13:79554857 | A | T | 1 | a0001c0001t0013 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2344A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3737 | chr13 | 79554857 | ||||||
| chr13:79554869 | A | G | 1 | a0001c0001t0011 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2356A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3749 | chr13 | 79554869 | ||||||
| chr13:79555110 | A | G | 1 | a0001c0001t0012 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2597A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3990 | chr13 | 79555110 | ||||||
| chr13:79555193 | T | C | 6 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(3): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2680T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 4073 | chr13 | 79555193 | ||||||
| chr13:79555391 | A | C | 1 | a0001c0001t0017 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2878A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 4271 | chr13 | 79555391 | ||||||
| chr13:79555476 | A | G | 1 | a0001c0001t0019 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2963A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 4356 | chr13 | 79555476 | ||||||
| chr13:79555615 | G | A | 1 | a0001c0001t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3102G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 4495 | chr13 | 79555615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:79481564 | C | T | 1 | a0001c0001t0006g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.321+40C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481564 | |||||||
| chr13:79481629 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.321+105T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481629 | |||||||
| chr13:79481673 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.321+149C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481673 | |||||||
| chr13:79481706 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.321+182G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481706 | |||||||
| chr13:79481772 | G | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+248G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481772 | |||||||
| chr13:79482165 | C | T | 8 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0034 others(5): Show |
9 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+641C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482165 | |||||||
| chr13:79482169 | C | CT | 14 | a0001c0001t0002g0001 a0001c0001t0002g0021 a0001c0001t0002g0025 others(11): Show |
18 | HG00741.hp1 HG01243.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.321+671dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | ||||||
| chr13:79482169 | C | T | 1 | a0001c0001t0003g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.321+645C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482169 | |||||||
| chr13:79482169 | CT | C | 88 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(85): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.321+671delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | ||||||
| chr13:79482169 | CTT | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0126 others(12): Show |
17 | HG00280.hp2 HG01891.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.321+670_321+671del others(2): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | ||||||
| chr13:79482169 | CTTTT | C | 8 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0034 others(5): Show |
9 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+668_321+671del others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | ||||||
| chr13:79482169 | CTTTTTTT | C | 12 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0217 others(9): Show |
14 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.321+665_321+671del others(7): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | ||||||
| chr13:79482169 | CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0003g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.321+661_321+671del others(11): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | ||||||
| chr13:79482172 | T | TC | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG00735.hp1 HG01192.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+648_321+649ins others(1): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482172 | |||||||
| chr13:79482173 | T | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(11): Show |
16 | HG00738.hp2 HG01074.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+649T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482173 | |||||||
| chr13:79482174 | T | C | 77 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(74): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.321+650T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482174 | |||||||
| chr13:79482175 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0126 |
5 | HG00280.hp2 HG03017.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+651T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482175 | |||||||
| chr13:79482176 | T | C | 3 | a0001c0001t0004g0003 a0001c0001t0004g0127 a0001c0001t0004g0128 |
6 | HG02486.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+652T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482176 | |||||||
| chr13:79482177 | T | C | 6 | a0001c0001t0004g0020 a0001c0001t0004g0130 a0001c0001t0004g0131 others(3): Show |
7 | HG01243.hp2 HG02145.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.321+653T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482177 | |||||||
| chr13:79482178 | T | C | 10 | a0001c0001t0004g0136 a0001c0001t0004g0141 a0001c0001t0004g0143 others(7): Show |
10 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.321+654T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482178 | |||||||
| chr13:79482309 | A | G | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+785A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482309 | |||||||
| chr13:79482366 | T | C | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+842T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482366 | |||||||
| chr13:79482451 | C | G | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(20): Show |
30 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.321+927C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482451 | |||||||
| chr13:79482497 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.321+973A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482497 | |||||||
| chr13:79482630 | AG | A | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.321+1108delG | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482630 | ||||||
| chr13:79482772 | C | T | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.321+1248C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482772 | |||||||
| chr13:79482831 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.321+1307A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482831 | |||||||
| chr13:79483178 | A | G | 1 | a0001c0001t0002g0203 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.321+1654A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483178 | |||||||
| chr13:79483546 | A | C | 32 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(29): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+2022A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483546 | |||||||
| chr13:79483696 | C | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(20): Show |
30 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.321+2172C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483696 | |||||||
| chr13:79483704 | G | T | 35 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(32): Show |
42 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.321+2180G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483704 | |||||||
| chr13:79483744 | A | C | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+2220A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483744 | |||||||
| chr13:79483820 | A | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+2296A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483820 | |||||||
| chr13:79483859 | T | C | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.321+2335T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483859 | |||||||
| chr13:79483947 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+2423C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483947 | |||||||
| chr13:79484101 | C | T | 1 | a0002c0002t0003g0234 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.321+2577C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484101 | |||||||
| chr13:79484173 | A | G | 35 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(32): Show |
42 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.321+2649A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484173 | |||||||
| chr13:79484187 | T | C | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.321+2663T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484187 | |||||||
| chr13:79484339 | T | C | 13 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(10): Show |
14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.321+2815T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484339 | |||||||
| chr13:79484372 | C | T | 4 | a0001c0001t0003g0006 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
7 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+2848C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484372 | |||||||
| chr13:79484654 | A | T | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+3130A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484654 | |||||||
| chr13:79484797 | G | T | 1 | a0001c0001t0009g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.321+3273G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484797 | |||||||
| chr13:79484945 | C | T | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+3421C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484945 | |||||||
| chr13:79484963 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0062 |
3 | HG02630.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.321+3439G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484963 | |||||||
| chr13:79485076 | C | T | 1 | a0001c0001t0002g0026 | 2 | NA18990.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.321+3552C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485076 | |||||||
| chr13:79485420 | T | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+3896T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485420 | |||||||
| chr13:79485461 | G | C | 1 | a0001c0001t0002g0147 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.321+3937G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485461 | |||||||
| chr13:79485488 | A | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+3964A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485488 | |||||||
| chr13:79485716 | T | A | 1 | a0001c0001t0002g0148 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.321+4192T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485716 | |||||||
| chr13:79485743 | C | T | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.321+4219C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485743 | |||||||
| chr13:79485976 | A | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+4452A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485976 | |||||||
| chr13:79486111 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+4587C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486111 | |||||||
| chr13:79486334 | G | A | 1 | a0004c0004t0007g0134 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.321+4810G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486334 | |||||||
| chr13:79486341 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.321+4817A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486341 | |||||||
| chr13:79486391 | A | G | 1 | a0001c0001t0003g0230 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.321+4867A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486391 | |||||||
| chr13:79486552 | A | G | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.321+5028A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486552 | |||||||
| chr13:79486572 | G | A | 12 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(9): Show |
15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+5048G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486572 | |||||||
| chr13:79486579 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.321+5055T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486579 | |||||||
| chr13:79486669 | G | A | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+5145G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486669 | |||||||
| chr13:79486727 | G | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+5203G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486727 | |||||||
| chr13:79486728 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.321+5204T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486728 | |||||||
| chr13:79486741 | T | C | 1 | a0003c0003t0010g0042 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.321+5217T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486741 | |||||||
| chr13:79486767 | A | G | 1 | a0002c0002t0003g0229 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.321+5243A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486767 | |||||||
| chr13:79486856 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.321+5332G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486856 | |||||||
| chr13:79486939 | T | C | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.321+5415T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486939 | |||||||
| chr13:79487028 | T | A | 1 | a0002c0002t0003g0027 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.321+5504T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487028 | |||||||
| chr13:79487044 | A | G | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG03017.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.321+5520A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487044 | |||||||
| chr13:79487233 | T | G | 1 | a0001c0001t0002g0150 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.321+5709T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487233 | |||||||
| chr13:79487322 | A | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+5798A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487322 | |||||||
| chr13:79487352 | C | T | 3 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | NA18969.hp2 NA19006.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.321+5828C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487352 | |||||||
| chr13:79487372 | A | C | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+5848A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487372 | |||||||
| chr13:79487440 | G | A | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+5916G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487440 | |||||||
| chr13:79487453 | G | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+5929G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487453 | |||||||
| chr13:79487487 | C | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02698.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.321+5963C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487487 | |||||||
| chr13:79487594 | T | C | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.321+6070T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487594 | |||||||
| chr13:79487702 | C | T | 3 | a0001c0001t0002g0196 a0001c0001t0009g0197 a0001c0001t0009g0202 |
3 | HG01243.hp1 HG02055.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.321+6178C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487702 | |||||||
| chr13:79487785 | G | C | 1 | a0004c0004t0007g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.321+6261G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487785 | |||||||
| chr13:79487882 | T | C | 28 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0021 others(25): Show |
36 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.321+6358T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487882 | |||||||
| chr13:79488140 | G | GA | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.321+6622dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79488140 | ||||||
| chr13:79488210 | A | G | 1 | a0003c0003t0005g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.321+6686A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488210 | |||||||
| chr13:79488364 | G | A | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+6840G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488364 | |||||||
| chr13:79488465 | G | C | 7 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(4): Show |
7 | HG00735.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+6941G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488465 | |||||||
| chr13:79488631 | T | A | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+7107T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488631 | |||||||
| chr13:79488941 | T | G | 2 | a0001c0001t0002g0152 a0001c0001t0013g0151 |
2 | NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.321+7417T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488941 | |||||||
| chr13:79489344 | C | T | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.321+7820C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489344 | |||||||
| chr13:79489412 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(9): Show |
15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+7888A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489412 | |||||||
| chr13:79489641 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.321+8117C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489641 | |||||||
| chr13:79489780 | G | T | 12 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(9): Show |
15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+8256G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489780 | |||||||
| chr13:79489962 | A | G | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+8438A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489962 | |||||||
| chr13:79489967 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.321+8443C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489967 | |||||||
| chr13:79490000 | G | A | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.321+8476G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490000 | |||||||
| chr13:79490018 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.321+8494A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490018 | |||||||
| chr13:79490269 | A | G | 1 | a0001c0001t0017g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.321+8745A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490269 | |||||||
| chr13:79490289 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+8765C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490289 | |||||||
| chr13:79490322 | A | G | 3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.321+8798A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490322 | |||||||
| chr13:79490472 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.321+8948T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490472 | |||||||
| chr13:79490645 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9121T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490645 | |||||||
| chr13:79490646 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9122G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490646 | |||||||
| chr13:79490647 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9123G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490647 | |||||||
| chr13:79490649 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9125T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490649 | |||||||
| chr13:79490651 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9127T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490651 | |||||||
| chr13:79490756 | T | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0170 |
3 | NA18982.hp2 NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.321+9232T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490756 | |||||||
| chr13:79490895 | A | C | 2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG00544.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.321+9371A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490895 | |||||||
| chr13:79491422 | GTC | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+9908_321+9909d others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79491422 | ||||||
| chr13:79491514 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+9990C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79491514 | |||||||
| chr13:79491643 | G | A | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.321+10119G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79491643 | |||||||
| chr13:79492033 | G | C | 3 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 |
3 | HG00741.hp1 HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.321+10509G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492033 | |||||||
| chr13:79492171 | T | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+10647T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492171 | |||||||
| chr13:79492184 | A | T | 1 | a0002c0002t0003g0234 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.321+10660A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492184 | |||||||
| chr13:79492213 | C | T | 12 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(9): Show |
15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+10689C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492213 | |||||||
| chr13:79492244 | AGT | A | 2 | a0002c0002t0003g0027 a0002c0002t0003g0213 |
3 | HG02698.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.321+10722_321+1072 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79492244 | ||||||
| chr13:79492252 | C | CT | 6 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0109 others(3): Show |
6 | HG00735.hp1 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+10745dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79492252 | ||||||
| chr13:79492252 | CT | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+10745delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79492252 | ||||||
| chr13:79492323 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.321+10799C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492323 | |||||||
| chr13:79492435 | G | A | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+10911G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492435 | |||||||
| chr13:79492487 | T | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+10963T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492487 | |||||||
| chr13:79492531 | A | G | 32 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(29): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+11007A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492531 | |||||||
| chr13:79492566 | T | C | 1 | a0001c0001t0004g0130 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.321+11042T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492566 | |||||||
| chr13:79492641 | T | C | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.321+11117T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492641 | |||||||
| chr13:79492867 | A | G | 1 | a0001c0001t0002g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.321+11343A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492867 | |||||||
| chr13:79492868 | T | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+11344T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492868 | |||||||
| chr13:79493105 | G | T | 1 | a0001c0001t0002g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.321+11581G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493105 | |||||||
| chr13:79493209 | T | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0170 |
3 | NA18982.hp2 NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.321+11685T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493209 | |||||||
| chr13:79493242 | G | A | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+11718G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493242 | |||||||
| chr13:79493251 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+11727A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493251 | |||||||
| chr13:79493467 | A | G | 1 | a0001c0001t0006g0108 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.321+11943A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493467 | |||||||
| chr13:79493596 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.321+12072C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493596 | |||||||
| chr13:79493708 | A | G | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+12184A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493708 | |||||||
| chr13:79493853 | A | T | 1 | a0001c0001t0002g0192 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.321+12329A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493853 | |||||||
| chr13:79493871 | T | C | 12 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(9): Show |
15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+12347T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493871 | |||||||
| chr13:79493941 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+12417C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493941 | |||||||
| chr13:79494433 | T | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+12909T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494433 | |||||||
| chr13:79494531 | G | A | 1 | a0001c0001t0003g0227 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.321+13007G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494531 | |||||||
| chr13:79494666 | T | C | 1 | a0001c0001t0003g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.321+13142T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494666 | |||||||
| chr13:79494730 | A | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0166 |
2 | NA18962.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.321+13206A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494730 | |||||||
| chr13:79494922 | A | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+13398A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494922 | |||||||
| chr13:79494947 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.321+13423A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494947 | |||||||
| chr13:79495453 | T | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+13929T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495453 | |||||||
| chr13:79495454 | T | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+13930T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495454 | |||||||
| chr13:79495546 | G | T | 32 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(29): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+14022G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495546 | |||||||
| chr13:79495832 | A | G | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+14308A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495832 | |||||||
| chr13:79495852 | CT | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 |
4 | HG02630.hp2 HG02922.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+14331delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79495852 | ||||||
| chr13:79495943 | A | C | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+14419A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495943 | |||||||
| chr13:79496097 | C | A | 1 | a0001c0001t0002g0156 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.321+14573C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496097 | |||||||
| chr13:79496144 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.321+14620T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496144 | |||||||
| chr13:79496152 | G | T | 14 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+14628G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496152 | |||||||
| chr13:79496307 | A | G | 1 | a0001c0001t0003g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.321+14783A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496307 | |||||||
| chr13:79496672 | T | TA | 94 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(91): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.321+15156dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79496672 | ||||||
| chr13:79496860 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.321+15336C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496860 | |||||||
| chr13:79496925 | T | G | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+15401T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496925 | |||||||
| chr13:79496939 | G | A | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+15415G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496939 | |||||||
| chr13:79496952 | A | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+15428A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496952 | |||||||
| chr13:79497159 | A | G | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+15635A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497159 | |||||||
| chr13:79497199 | T | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+15675T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497199 | |||||||
| chr13:79497316 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0011g0015 |
4 | HG00733.hp2 HG00738.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+15792G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497316 | |||||||
| chr13:79497414 | C | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+15890C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497414 | |||||||
| chr13:79497484 | T | C | 35 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(32): Show |
42 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.321+15960T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497484 | |||||||
| chr13:79497660 | G | GT | 26 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0025 others(23): Show |
31 | HG00099.hp2 HG01243.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.321+16153dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497660 | ||||||
| chr13:79497660 | GT | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0062 others(11): Show |
15 | HG02080.hp1 HG02622.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.321+16153delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497660 | ||||||
| chr13:79497677 | T | C | 18 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
21 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.321+16153T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497677 | |||||||
| chr13:79497677 | T | TC | 13 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(10): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+16154dupC | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497677 | ||||||
| chr13:79497708 | T | C | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+16184T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497708 | |||||||
| chr13:79497790 | TGG | T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(48): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.321+16271_321+1627 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497790 | ||||||
| chr13:79497790 | TGGGG | T | 15 | a0001c0001t0001g0104 a0001c0001t0004g0003 a0001c0001t0004g0011 others(12): Show |
21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.321+16269_321+1627 others(8): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497790 | ||||||
| chr13:79497791 | G | GGT | 22 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0095 others(19): Show |
25 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.321+16268_321+1626 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | ||||||
| chr13:79497791 | G | GGTGT | 6 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(3): Show |
8 | HG01258.hp1 HG01943.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.321+16268_321+1626 others(8): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | ||||||
| chr13:79497791 | G | GGTGTGT | 16 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0052 others(13): Show |
18 | HG00544.hp1 HG00735.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.321+16268_321+1626 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | ||||||
| chr13:79497791 | GGGGGGT | G | 6 | a0001c0001t0001g0070 a0003c0003t0005g0031 a0003c0003t0005g0032 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+16269_321+1627 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | ||||||
| chr13:79497791 | GGGGGGTG others(1): Show |
G | 10 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 others(7): Show |
11 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.321+16269_321+1627 others(12): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | ||||||
| chr13:79497791 | GGGGGGTG others(7): Show |
G | 2 | a0004c0004t0007g0135 a0004c0004t0007g0137 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.321+16269_321+1628 others(18): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | ||||||
| chr13:79497793 | G | T | 83 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(80): Show |
96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.321+16269G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497793 | |||||||
| chr13:79497795 | G | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.321+16271G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497795 | |||||||
| chr13:79497797 | T | G | 4 | a0001c0001t0002g0171 a0001c0001t0002g0196 a0001c0001t0009g0197 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+16273T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497797 | |||||||
| chr13:79497904 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.321+16380C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497904 | |||||||
| chr13:79498029 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.321+16505G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498029 | |||||||
| chr13:79498244 | A | C | 1 | a0001c0001t0003g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.321+16720A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498244 | |||||||
| chr13:79498256 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.321+16732G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498256 | |||||||
| chr13:79498262 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.321+16738A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498262 | |||||||
| chr13:79498275 | G | A | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+16751G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498275 | |||||||
| chr13:79498325 | T | G | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | NA19062.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.321+16801T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498325 | |||||||
| chr13:79498336 | A | G | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+16812A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498336 | |||||||
| chr13:79498519 | A | C | 1 | a0003c0003t0005g0039 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.321+16995A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498519 | |||||||
| chr13:79498595 | A | C | 1 | a0001c0001t0002g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.321+17071A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498595 | |||||||
| chr13:79498851 | G | GA | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+17333dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79498851 | ||||||
| chr13:79499091 | A | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+17567A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79499091 | |||||||
| chr13:79499192 | A | G | 32 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(29): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+17668A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79499192 | |||||||
| chr13:79499382 | A | G | 6 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+17858A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79499382 | |||||||
| chr13:79499499 | CAG | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+17977_321+1797 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79499499 | ||||||
| chr13:79499668 | A | G | 3 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | NA18969.hp2 NA19006.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.321+18144A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79499668 | |||||||
| chr13:79499670 | CTG | C | 5 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0034 others(2): Show |
6 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+18149_321+1815 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79499670 | ||||||
| chr13:79500093 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.321+18569A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500093 | |||||||
| chr13:79500166 | C | CA | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0088 others(10): Show |
14 | HG02630.hp1 HG03017.hp1 HG04199.hp2 others(11): Show |
intron_variant | MODIFIER | c.321+18659dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79500166 | ||||||
| chr13:79500166 | CA | C | 21 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0053 others(18): Show |
22 | HG00738.hp2 HG01192.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.321+18659delA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79500166 | ||||||
| chr13:79500447 | T | G | 2 | a0001c0001t0003g0215 a0001c0001t0003g0226 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.321+18923T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500447 | |||||||
| chr13:79500634 | G | A | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+19110G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500634 | |||||||
| chr13:79500640 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.321+19116C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500640 | |||||||
| chr13:79500646 | T | C | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.321+19122T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500646 | |||||||
| chr13:79500815 | T | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.321+19291T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500815 | |||||||
| chr13:79500849 | C | G | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+19325C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500849 | |||||||
| chr13:79500988 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+19464A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500988 | |||||||
| chr13:79501175 | G | A | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-19635G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501175 | |||||||
| chr13:79501406 | G | C | 3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-19404G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501406 | |||||||
| chr13:79501426 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-19384C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501426 | |||||||
| chr13:79501470 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.322-19340G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501470 | |||||||
| chr13:79501633 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.322-19177C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501633 | |||||||
| chr13:79501901 | A | G | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-18909A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501901 | |||||||
| chr13:79502250 | A | T | 1 | a0001c0001t0001g0083 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.322-18560A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502250 | |||||||
| chr13:79502296 | A | G | 101 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.322-18514A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502296 | |||||||
| chr13:79502424 | G | A | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.322-18386G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502424 | |||||||
| chr13:79502463 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.322-18347C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502463 | |||||||
| chr13:79502654 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.322-18156A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502654 | |||||||
| chr13:79502721 | G | A | 3 | a0003c0003t0005g0032 a0003c0003t0005g0033 a0003c0003t0005g0041 |
3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.322-18089G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502721 | |||||||
| chr13:79502757 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.322-18053A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502757 | |||||||
| chr13:79502781 | A | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-18029A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502781 | |||||||
| chr13:79502890 | GT | G | 25 | a0001c0001t0002g0022 a0001c0001t0002g0170 a0001c0001t0004g0003 others(22): Show |
32 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.322-17908delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79502890 | ||||||
| chr13:79503282 | C | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-17528C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503282 | |||||||
| chr13:79503314 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-17496C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503314 | |||||||
| chr13:79503412 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.322-17398G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503412 | |||||||
| chr13:79503434 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.322-17376A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503434 | |||||||
| chr13:79503515 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.322-17295G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503515 | |||||||
| chr13:79503759 | T | C | 1 | a0003c0003t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.322-17051T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503759 | |||||||
| chr13:79503788 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.322-17022T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503788 | |||||||
| chr13:79503952 | G | A | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | NA19062.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.322-16858G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503952 | |||||||
| chr13:79503990 | C | T | 1 | a0001c0001t0012g0163 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.322-16820C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503990 | |||||||
| chr13:79504091 | A | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-16719A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504091 | |||||||
| chr13:79504106 | A | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-16704A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504106 | |||||||
| chr13:79504114 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA19054.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.322-16696A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504114 | |||||||
| chr13:79504136 | T | C | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-16674T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504136 | |||||||
| chr13:79504316 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0235 |
2 | NA18995.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.322-16494G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504316 | |||||||
| chr13:79504340 | T | A | 1 | a0001c0001t0002g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.322-16470T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504340 | |||||||
| chr13:79504633 | AT | A | 155 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.322-16164delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79504633 | ||||||
| chr13:79504647 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(20): Show |
30 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.322-16163G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504647 | |||||||
| chr13:79504739 | T | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-16071T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504739 | |||||||
| chr13:79505019 | G | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-15791G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505019 | |||||||
| chr13:79505220 | G | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-15590G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505220 | |||||||
| chr13:79505257 | A | G | 32 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(29): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.322-15553A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505257 | |||||||
| chr13:79505400 | CAG | C | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-15409_322-1540 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505400 | |||||||
| chr13:79505472 | A | C | 3 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0122 |
3 | NA18987.hp1 NA19072.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.322-15338A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505472 | |||||||
| chr13:79505579 | A | AT | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-15231_322-1523 others(5): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505579 | |||||||
| chr13:79505601 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.322-15209C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505601 | |||||||
| chr13:79505752 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.322-15058A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505752 | |||||||
| chr13:79505819 | T | C | 1 | a0002c0002t0003g0234 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.322-14991T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505819 | |||||||
| chr13:79505836 | G | T | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-14974G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505836 | |||||||
| chr13:79505874 | G | T | 3 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 |
3 | HG00741.hp1 HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.322-14936G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505874 | |||||||
| chr13:79505960 | A | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-14850A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505960 | |||||||
| chr13:79505966 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.322-14844G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505966 | |||||||
| chr13:79505972 | G | A | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-14838G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505972 | |||||||
| chr13:79506472 | G | A | 3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-14338G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79506472 | |||||||
| chr13:79506663 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.322-14147A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79506663 | |||||||
| chr13:79507179 | A | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-13631A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507179 | |||||||
| chr13:79507249 | G | T | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.322-13561G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507249 | |||||||
| chr13:79507257 | TTCTGATT others(309): Show |
T | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.322-13537_322-1322 others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79507257 | ||||||
| chr13:79507267 | G | GT | 11 | a0001c0001t0002g0001 a0001c0001t0002g0023 a0001c0001t0002g0153 others(8): Show |
11 | HG00741.hp1 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.322-13519dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79507267 | ||||||
| chr13:79507626 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(9): Show |
15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.322-13184A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507626 | |||||||
| chr13:79507780 | G | A | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-13030G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507780 | |||||||
| chr13:79507845 | G | T | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-12965G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507845 | |||||||
| chr13:79507882 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA19054.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.322-12928A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507882 | |||||||
| chr13:79508379 | G | A | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-12431G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508379 | |||||||
| chr13:79508513 | T | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0060 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.322-12297T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508513 | |||||||
| chr13:79508550 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.322-12260A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508550 | |||||||
| chr13:79508619 | G | A | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-12191G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508619 | |||||||
| chr13:79508646 | C | T | 4 | a0001c0001t0004g0020 a0001c0001t0004g0130 a0001c0001t0004g0131 others(1): Show |
5 | HG01243.hp2 HG03540.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-12164C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508646 | |||||||
| chr13:79508675 | A | T | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-12135A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508675 | |||||||
| chr13:79509005 | T | C | 3 | a0001c0001t0003g0207 a0001c0001t0003g0208 a0001c0001t0003g0230 |
3 | HG01884.hp2 HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.322-11805T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509005 | |||||||
| chr13:79509034 | A | AT | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-11767dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509034 | ||||||
| chr13:79509064 | G | A | 14 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-11746G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509064 | |||||||
| chr13:79509152 | G | A | 1 | a0002c0002t0003g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.322-11658G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509152 | |||||||
| chr13:79509179 | G | A | 12 | a0001c0001t0001g0094 a0001c0001t0006g0014 a0001c0001t0006g0090 others(9): Show |
13 | HG02040.hp2 HG02074.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.322-11631G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509179 | |||||||
| chr13:79509366 | A | G | 13 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(10): Show |
14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.322-11444A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509366 | |||||||
| chr13:79509418 | G | A | 1 | a0002c0002t0003g0218 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.322-11392G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509418 | |||||||
| chr13:79509503 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0060 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.322-11307T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509503 | |||||||
| chr13:79509661 | A | G | 2 | a0001c0001t0004g0011 a0001c0001t0004g0136 |
4 | HG01069.hp1 HG01071.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-11149A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509661 | |||||||
| chr13:79509686 | T | TAGAGAG | 31 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(28): Show |
36 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.322-11123_322-1112 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509686 | ||||||
| chr13:79509688 | T | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(30): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.322-11122T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509688 | |||||||
| chr13:79509688 | T | TAGAGAG | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(58): Show |
69 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.322-11121_322-1112 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509688 | ||||||
| chr13:79509688 | T | TAGAGAGA others(1): Show |
11 | a0001c0001t0003g0006 a0001c0001t0003g0207 a0001c0001t0003g0208 others(8): Show |
15 | HG00735.hp2 HG01069.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.322-11121_322-1112 others(12): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509688 | ||||||
| chr13:79509690 | T | G | 113 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.322-11120T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509690 | |||||||
| chr13:79509690 | T | TAG | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-11104_322-1110 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | ||||||
| chr13:79509690 | T | TAGAGAG | 6 | a0001c0001t0001g0061 a0001c0001t0001g0101 a0001c0001t0001g0102 others(3): Show |
6 | HG01978.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-11108_322-1110 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | ||||||
| chr13:79509690 | T | TAGAGAGA others(1): Show |
11 | a0001c0001t0003g0211 a0001c0001t0003g0232 a0002c0002t0003g0027 others(8): Show |
12 | HG00733.hp1 HG01167.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-11110_322-1110 others(12): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | ||||||
| chr13:79509690 | T | TAGAGAGA others(3): Show |
1 | a0001c0001t0001g0103 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.322-11112_322-1110 others(14): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | ||||||
| chr13:79509690 | T | TATAG | 9 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(6): Show |
10 | HG01981.hp2 HG02486.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.322-11119_322-1111 others(8): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | ||||||
| chr13:79509690 | T | TATAGAGA others(1): Show |
6 | a0001c0001t0003g0206 a0002c0002t0003g0217 a0002c0002t0003g0222 others(3): Show |
6 | HG00140.hp1 HG00280.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-11119_322-1111 others(12): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | ||||||
| chr13:79509692 | G | T | 21 | a0001c0001t0002g0002 a0001c0001t0002g0025 a0001c0001t0002g0172 others(18): Show |
25 | HG00741.hp2 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.322-11118G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509692 | |||||||
| chr13:79509694 | G | T | 6 | a0001c0001t0002g0025 a0001c0001t0002g0172 a0001c0001t0002g0173 others(3): Show |
7 | HG02615.hp1 HG02615.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.322-11116G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509694 | |||||||
| chr13:79509837 | C | A | 1 | a0001c0001t0002g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.322-10973C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509837 | |||||||
| chr13:79509933 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.322-10877T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509933 | |||||||
| chr13:79510004 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.322-10806T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510004 | |||||||
| chr13:79510042 | A | C | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.322-10768A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510042 | |||||||
| chr13:79510134 | C | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-10676C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510134 | |||||||
| chr13:79510215 | G | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.322-10595G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510215 | |||||||
| chr13:79510246 | A | G | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-10564A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510246 | |||||||
| chr13:79510265 | C | A | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.322-10545C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510265 | |||||||
| chr13:79510382 | G | GT | 21 | a0001c0001t0001g0080 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
24 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.322-10415dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79510382 | ||||||
| chr13:79510998 | C | CA | 37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(34): Show |
42 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.322-9794dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79510998 | ||||||
| chr13:79510998 | C | CAA | 64 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(61): Show |
73 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.322-9795_322-9794d others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79510998 | ||||||
| chr13:79511171 | T | C | 15 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0071 others(12): Show |
15 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.322-9639T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511171 | |||||||
| chr13:79511562 | A | G | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-9248A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511562 | |||||||
| chr13:79511712 | A | T | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-9098A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511712 | |||||||
| chr13:79511829 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.322-8981G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511829 | |||||||
| chr13:79511936 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.322-8874C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511936 | |||||||
| chr13:79512023 | G | T | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.322-8787G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79512023 | |||||||
| chr13:79512316 | A | G | 3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-8494A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79512316 | |||||||
| chr13:79512376 | T | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-8434T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79512376 | |||||||
| chr13:79512459 | A | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0079 others(1): Show |
4 | HG01109.hp1 HG01496.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-8351A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79512459 | |||||||
| chr13:79513047 | C | T | 1 | a0001c0001t0003g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.322-7763C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513047 | |||||||
| chr13:79513141 | T | A | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-7669T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513141 | |||||||
| chr13:79513281 | A | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0060 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.322-7529A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513281 | |||||||
| chr13:79513512 | T | C | 6 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-7298T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513512 | |||||||
| chr13:79513686 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.322-7124C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513686 | |||||||
| chr13:79513688 | T | C | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-7122T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513688 | |||||||
| chr13:79513715 | CT | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(36): Show |
48 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.322-7083delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79513715 | ||||||
| chr13:79513802 | T | A | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-7008T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513802 | |||||||
| chr13:79513849 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.322-6961A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513849 | |||||||
| chr13:79513930 | C | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-6880C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513930 | |||||||
| chr13:79513972 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
4 | NA18944.hp2 NA18969.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-6838G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513972 | |||||||
| chr13:79514186 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-6624C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514186 | |||||||
| chr13:79514469 | A | T | 1 | a0001c0001t0002g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.322-6341A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514469 | |||||||
| chr13:79514504 | A | ATC | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.322-6306_322-6305i others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514504 | |||||||
| chr13:79514505 | A | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.322-6305A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514505 | |||||||
| chr13:79514548 | A | G | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.322-6262A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514548 | |||||||
| chr13:79514550 | A | T | 1 | a0002c0002t0003g0225 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.322-6260A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514550 | |||||||
| chr13:79514593 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0017g0110 |
2 | NA18943.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.322-6217C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514593 | |||||||
| chr13:79514677 | T | C | 1 | a0001c0001t0013g0151 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.322-6133T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514677 | |||||||
| chr13:79514787 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.322-6023G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514787 | |||||||
| chr13:79514942 | G | A | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-5868G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514942 | |||||||
| chr13:79514964 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.322-5846T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514964 | |||||||
| chr13:79515003 | G | C | 8 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0034 others(5): Show |
9 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.322-5807G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515003 | |||||||
| chr13:79515135 | A | C | 1 | a0003c0003t0010g0042 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.322-5675A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515135 | |||||||
| chr13:79515208 | A | AATCTTAT others(14): Show |
17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.322-5601_322-5600i others(23): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79515208 | ||||||
| chr13:79515211 | G | A | 17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.322-5599G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515211 | |||||||
| chr13:79515213 | T | A | 17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.322-5597T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515213 | |||||||
| chr13:79515214 | T | A | 17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.322-5596T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515214 | |||||||
| chr13:79515813 | T | C | 6 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0003g0209 others(3): Show |
6 | HG00735.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-4997T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515813 | |||||||
| chr13:79515858 | G | GT | 89 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.322-4942dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79515858 | ||||||
| chr13:79515858 | GT | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-4942delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79515858 | ||||||
| chr13:79515868 | T | TC | 12 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0071 others(9): Show |
12 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-4938dupC | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79515868 | ||||||
| chr13:79515902 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.322-4908A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515902 | |||||||
| chr13:79515910 | C | T | 1 | a0001c0001t0003g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.322-4900C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515910 | |||||||
| chr13:79515941 | G | C | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-4869G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515941 | |||||||
| chr13:79515979 | C | T | 28 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0021 others(25): Show |
36 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.322-4831C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515979 | |||||||
| chr13:79516024 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(20): Show |
30 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.322-4786G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516024 | |||||||
| chr13:79516028 | T | C | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-4782T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516028 | |||||||
| chr13:79516244 | T | TTTTTG | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-4546_322-4542d others(7): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79516244 | ||||||
| chr13:79516311 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.322-4499C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516311 | |||||||
| chr13:79516452 | G | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
7 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-4358G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516452 | |||||||
| chr13:79516480 | C | T | 14 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-4330C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516480 | |||||||
| chr13:79516593 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.322-4217T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516593 | |||||||
| chr13:79516622 | T | A | 1 | a0001c0001t0002g0172 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.322-4188T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516622 | |||||||
| chr13:79516730 | A | G | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.322-4080A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516730 | |||||||
| chr13:79516748 | T | C | 1 | a0003c0003t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.322-4062T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516748 | |||||||
| chr13:79516767 | T | A | 1 | a0001c0001t0002g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.322-4043T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516767 | |||||||
| chr13:79517288 | G | A | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-3522G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517288 | |||||||
| chr13:79517404 | A | G | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.322-3406A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517404 | |||||||
| chr13:79517408 | T | C | 56 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(53): Show |
62 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.322-3402T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517408 | |||||||
| chr13:79517408 | T | TTACTCTC others(16): Show |
3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-3400_322-3399i others(25): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79517408 | ||||||
| chr13:79517411 | T | C | 3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-3399T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517411 | |||||||
| chr13:79517646 | A | G | 101 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.322-3164A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517646 | |||||||
| chr13:79517724 | T | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.322-3086T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517724 | |||||||
| chr13:79517883 | G | C | 17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.322-2927G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517883 | |||||||
| chr13:79518032 | A | AC | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.322-2778_322-2777i others(3): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518032 | |||||||
| chr13:79518120 | G | A | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.322-2690G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518120 | |||||||
| chr13:79518148 | C | T | 3 | a0003c0003t0005g0032 a0003c0003t0005g0033 a0003c0003t0005g0041 |
3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.322-2662C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518148 | |||||||
| chr13:79518149 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.322-2661G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518149 | |||||||
| chr13:79518787 | A | C | 6 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2023A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518787 | |||||||
| chr13:79519353 | A | G | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.322-1457A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519353 | |||||||
| chr13:79519370 | A | G | 1 | a0001c0001t0001g0018 | 2 | NA18944.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.322-1440A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519370 | |||||||
| chr13:79519543 | T | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-1267T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519543 | |||||||
| chr13:79519656 | G | A | 13 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(10): Show |
14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.322-1154G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519656 | |||||||
| chr13:79519690 | T | G | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.322-1120T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519690 | |||||||
| chr13:79519756 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.322-1054A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519756 | |||||||
| chr13:79519764 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(9): Show |
15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.322-1046A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519764 | |||||||
| chr13:79519998 | AC | A | 14 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-810delC | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79519998 | ||||||
| chr13:79520108 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.322-702A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79520108 | |||||||
| chr13:79520359 | G | T | 1 | a0001c0001t0006g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.322-451G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79520359 | |||||||
| chr13:79520711 | G | C | 12 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-99G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79520711 | |||||||
| chr13:79521008 | C | CT | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+45dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 79521008 | ||||||
| chr13:79521008 | C | CTT | 19 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(16): Show |
25 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.487+44_487+45dupTT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 79521008 | ||||||
| chr13:79521022 | A | T | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+47A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521022 | |||||||
| chr13:79521313 | C | T | 2 | a0001c0001t0004g0020 a0001c0001t0004g0132 |
3 | HG01243.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.487+338C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521313 | |||||||
| chr13:79521406 | C | T | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.487+431C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521406 | |||||||
| chr13:79521791 | A | G | 32 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(29): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.487+816A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521791 | |||||||
| chr13:79521821 | T | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0170 a0001c0001t0002g0199 |
4 | NA18982.hp2 NA19060.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+846T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521821 | |||||||
| chr13:79521822 | G | T | 1 | a0002c0002t0003g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.487+847G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521822 | |||||||
| chr13:79521823 | C | CT | 26 | a0001c0001t0001g0053 a0001c0001t0002g0002 a0001c0001t0002g0159 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.487+865dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 79521823 | ||||||
| chr13:79521823 | C | T | 1 | a0002c0002t0003g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.487+848C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521823 | |||||||
| chr13:79521976 | G | C | 167 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.487+1001G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521976 | |||||||
| chr13:79522166 | A | G | 2 | a0004c0004t0007g0133 a0004c0004t0007g0134 |
2 | HG01952.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.487+1191A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522166 | |||||||
| chr13:79522262 | A | C | 1 | a0001c0001t0003g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.487+1287A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522262 | |||||||
| chr13:79522810 | G | A | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+1835G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522810 | |||||||
| chr13:79522862 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+1887G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522862 | |||||||
| chr13:79522880 | A | G | 1 | a0001c0001t0006g0092 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.487+1905A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522880 | |||||||
| chr13:79523021 | A | G | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+2046A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523021 | |||||||
| chr13:79523132 | C | T | 35 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(32): Show |
42 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.487+2157C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523132 | |||||||
| chr13:79523136 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+2161A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523136 | |||||||
| chr13:79523159 | A | G | 6 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+2184A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523159 | |||||||
| chr13:79523262 | C | T | 1 | a0005c0005t0002g0205 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.487+2287C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523262 | |||||||
| chr13:79523282 | G | T | 14 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+2307G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523282 | |||||||
| chr13:79523485 | G | T | 1 | a0001c0001t0002g0147 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.487+2510G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523485 | |||||||
| chr13:79523567 | C | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+2592C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523567 | |||||||
| chr13:79523574 | T | G | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.487+2599T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523574 | |||||||
| chr13:79523580 | C | G | 71 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(68): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.487+2605C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523580 | |||||||
| chr13:79523701 | T | A | 4 | a0004c0004t0007g0133 a0004c0004t0007g0134 a0004c0004t0007g0135 others(1): Show |
4 | HG01952.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+2726T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523701 | |||||||
| chr13:79523726 | G | A | 14 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+2751G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523726 | |||||||
| chr13:79523833 | G | T | 1 | a0001c0001t0003g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.487+2858G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523833 | |||||||
| chr13:79523869 | C | G | 3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.487+2894C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523869 | |||||||
| chr13:79523903 | T | G | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+2928T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523903 | |||||||
| chr13:79524039 | T | G | 17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.487+3064T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524039 | |||||||
| chr13:79524047 | T | C | 1 | a0001c0001t0002g0160 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.487+3072T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524047 | |||||||
| chr13:79524057 | G | A | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+3082G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524057 | |||||||
| chr13:79524108 | C | A | 14 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+3133C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524108 | |||||||
| chr13:79524133 | C | G | 1 | a0001c0006t0006g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.487+3158C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524133 | |||||||
| chr13:79524188 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0122 |
3 | NA18987.hp1 NA19072.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.487+3213G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524188 | |||||||
| chr13:79524526 | A | C | 3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.487+3551A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524526 | |||||||
| chr13:79524854 | C | A | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.487+3879C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524854 | |||||||
| chr13:79524983 | G | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(64): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.487+4008G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524983 | |||||||
| chr13:79525217 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.487+4242C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525217 | |||||||
| chr13:79525338 | G | A | 136 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(133): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.487+4363G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525338 | |||||||
| chr13:79525396 | T | G | 1 | a0002c0002t0003g0222 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.487+4421T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525396 | |||||||
| chr13:79525542 | A | G | 15 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0071 others(12): Show |
15 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.487+4567A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525542 | |||||||
| chr13:79525771 | T | C | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.487+4796T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525771 | |||||||
| chr13:79525833 | C | A | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.487+4858C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525833 | |||||||
| chr13:79525958 | G | A | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+4983G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525958 | |||||||
| chr13:79526092 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+5117A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526092 | |||||||
| chr13:79526186 | G | T | 10 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0156 others(7): Show |
14 | HG00408.hp2 HG02071.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.487+5211G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526186 | |||||||
| chr13:79526677 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.487+5702G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526677 | |||||||
| chr13:79526723 | A | C | 1 | a0001c0001t0002g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.487+5748A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526723 | |||||||
| chr13:79526977 | T | A | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+6002T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526977 | |||||||
| chr13:79527250 | A | G | 1 | a0001c0001t0013g0151 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.488-6073A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527250 | |||||||
| chr13:79527274 | A | G | 5 | a0001c0001t0002g0026 a0001c0001t0002g0150 a0001c0001t0002g0166 others(2): Show |
6 | HG00544.hp2 HG02074.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-6049A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527274 | |||||||
| chr13:79527372 | T | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.488-5951T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527372 | |||||||
| chr13:79527399 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.488-5924A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527399 | |||||||
| chr13:79527549 | T | C | 3 | a0003c0003t0005g0032 a0003c0003t0005g0033 a0003c0003t0005g0041 |
3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.488-5774T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527549 | |||||||
| chr13:79527584 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.488-5739C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527584 | |||||||
| chr13:79527868 | C | T | 1 | a0001c0001t0017g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.488-5455C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527868 | |||||||
| chr13:79527985 | T | C | 234 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(231): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.488-5338T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527985 | |||||||
| chr13:79528011 | T | C | 234 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(231): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.488-5312T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79528011 | |||||||
| chr13:79528199 | G | A | 3 | a0001c0001t0006g0090 a0001c0001t0006g0106 a0001c0001t0016g0045 |
3 | HG02129.hp2 NA19002.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.488-5124G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79528199 | |||||||
| chr13:79528925 | A | G | 1 | a0003c0003t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.488-4398A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79528925 | |||||||
| chr13:79529094 | C | T | 136 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(133): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.488-4229C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529094 | |||||||
| chr13:79529143 | T | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(134): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.488-4180T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529143 | |||||||
| chr13:79529211 | T | C | 7 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(4): Show |
7 | HG00735.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-4112T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529211 | |||||||
| chr13:79529318 | A | G | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.488-4005A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529318 | |||||||
| chr13:79529551 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.488-3772G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529551 | |||||||
| chr13:79529950 | A | G | 7 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(4): Show |
7 | HG00735.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-3373A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529950 | |||||||
| chr13:79529988 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.488-3335G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529988 | |||||||
| chr13:79530170 | A | G | 13 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(10): Show |
14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.488-3153A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530170 | |||||||
| chr13:79530279 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.488-3044A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530279 | |||||||
| chr13:79530464 | A | G | 14 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(11): Show |
15 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.488-2859A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530464 | |||||||
| chr13:79530633 | G | C | 1 | a0001c0001t0002g0167 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.488-2690G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530633 | |||||||
| chr13:79530807 | T | C | 7 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(4): Show |
7 | HG00735.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-2516T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530807 | |||||||
| chr13:79530872 | C | T | 13 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0213 others(10): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.488-2451C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530872 | |||||||
| chr13:79530930 | C | G | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.488-2393C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530930 | |||||||
| chr13:79530992 | G | T | 1 | a0001c0001t0003g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488-2331G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530992 | |||||||
| chr13:79531050 | T | A | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.488-2273T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79531050 | |||||||
| chr13:79531583 | C | T | 1 | a0002c0002t0003g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.488-1740C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79531583 | |||||||
| chr13:79531934 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.488-1389C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79531934 | |||||||
| chr13:79532036 | C | T | 1 | a0001c0001t0004g0011 | 3 | HG01069.hp1 HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.488-1287C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532036 | |||||||
| chr13:79532038 | A | G | 17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.488-1285A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532038 | |||||||
| chr13:79532110 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.488-1213G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532110 | |||||||
| chr13:79532241 | T | C | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.488-1082T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532241 | |||||||
| chr13:79532465 | C | A | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.488-858C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532465 | |||||||
| chr13:79532802 | T | C | 1 | a0001c0001t0011g0015 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.488-521T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532802 | |||||||
| chr13:79533153 | G | A | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.488-170G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79533153 | |||||||
| chr13:79533197 | A | G | 34 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(31): Show |
39 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.488-126A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79533197 | |||||||
| chr13:79533202 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.488-121A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79533202 | |||||||
| chr13:79533510 | T | G | 6 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+54T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79533510 | |||||||
| chr13:79533776 | A | G | 2 | a0004c0004t0007g0133 a0004c0004t0007g0134 |
2 | HG01952.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.621+320A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79533776 | |||||||
| chr13:79533776 | ATGT | A | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+322_621+324del others(3): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79533776 | ||||||
| chr13:79533780 | T | A | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+324T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79533780 | |||||||
| chr13:79533838 | G | A | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+382G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79533838 | |||||||
| chr13:79534326 | G | A | 3 | a0003c0003t0005g0032 a0003c0003t0005g0033 a0003c0003t0005g0041 |
3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.621+870G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79534326 | |||||||
| chr13:79534350 | G | GT | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(115): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.621+917dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79534350 | ||||||
| chr13:79534350 | G | GTT | 31 | a0001c0001t0001g0019 a0001c0001t0001g0059 a0001c0001t0001g0072 others(28): Show |
33 | HG00408.hp1 HG01175.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.621+916_621+917dup others(2): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79534350 | ||||||
| chr13:79534490 | T | C | 36 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(33): Show |
43 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.621+1034T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79534490 | |||||||
| chr13:79534607 | T | A | 3 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0019g0142 |
3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.621+1151T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79534607 | |||||||
| chr13:79535011 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.621+1555A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535011 | |||||||
| chr13:79535015 | C | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0166 |
2 | NA18962.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.621+1559C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535015 | |||||||
| chr13:79535077 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.621+1621A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535077 | |||||||
| chr13:79535303 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.621+1847C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535303 | |||||||
| chr13:79535388 | A | G | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+1932A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535388 | |||||||
| chr13:79535602 | A | C | 1 | a0001c0001t0002g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.621+2146A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535602 | |||||||
| chr13:79535732 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(62): Show |
87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.621+2276A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535732 | |||||||
| chr13:79535742 | A | G | 1 | a0002c0002t0003g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.621+2286A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535742 | |||||||
| chr13:79535786 | C | CA | 36 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(33): Show |
43 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.621+2338dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79535786 | ||||||
| chr13:79535906 | A | G | 1 | a0001c0001t0002g0025 | 2 | NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.621+2450A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535906 | |||||||
| chr13:79535923 | T | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0185 a0001c0001t0002g0193 others(1): Show |
7 | HG00741.hp2 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+2467T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535923 | |||||||
| chr13:79536012 | A | G | 1 | a0001c0001t0009g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.621+2556A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536012 | |||||||
| chr13:79536029 | TATAG | T | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.621+2578_621+2581d others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79536029 | ||||||
| chr13:79536082 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2626A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536082 | |||||||
| chr13:79536158 | T | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.621+2702T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536158 | |||||||
| chr13:79536191 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.621+2735A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536191 | |||||||
| chr13:79536239 | A | C | 1 | a0001c0001t0002g0185 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.621+2783A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536239 | |||||||
| chr13:79536454 | A | G | 3 | a0001c0001t0004g0003 a0001c0001t0004g0127 a0001c0001t0004g0128 |
6 | HG02486.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+2998A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536454 | |||||||
| chr13:79536569 | A | G | 12 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(9): Show |
13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.621+3113A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536569 | |||||||
| chr13:79536588 | A | G | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.622-3094A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536588 | |||||||
| chr13:79536637 | A | C | 3 | a0003c0003t0005g0032 a0003c0003t0005g0033 a0003c0003t0005g0041 |
3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.622-3045A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536637 | |||||||
| chr13:79536980 | A | G | 1 | a0001c0001t0021g0089 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.622-2702A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536980 | |||||||
| chr13:79537027 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0126 |
4 | HG00280.hp2 HG03017.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-2655G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537027 | |||||||
| chr13:79537049 | A | AT | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(63): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.622-2620dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79537049 | ||||||
| chr13:79537049 | AT | A | 6 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.622-2620delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79537049 | ||||||
| chr13:79537100 | T | G | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.622-2582T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537100 | |||||||
| chr13:79537114 | T | G | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.622-2568T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537114 | |||||||
| chr13:79537231 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.622-2451T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537231 | |||||||
| chr13:79537317 | G | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0155 |
2 | HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.622-2365G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537317 | |||||||
| chr13:79537980 | T | TA | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(63): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.622-1701dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79537980 | ||||||
| chr13:79538001 | G | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(134): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.622-1681G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538001 | |||||||
| chr13:79538191 | C | A | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.622-1491C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538191 | |||||||
| chr13:79538240 | G | A | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622-1442G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538240 | |||||||
| chr13:79538261 | A | G | 3 | a0001c0001t0008g0138 a0001c0001t0008g0139 a0001c0001t0008g0140 |
3 | HG02723.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.622-1421A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538261 | |||||||
| chr13:79538552 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.622-1130G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538552 | |||||||
| chr13:79538622 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.622-1060G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538622 | |||||||
| chr13:79538673 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.622-1009C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538673 | |||||||
| chr13:79538686 | G | C | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.622-996G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538686 | |||||||
| chr13:79538800 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.622-882C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538800 | |||||||
| chr13:79538804 | A | G | 1 | a0001c0006t0006g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.622-878A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538804 | |||||||
| chr13:79538876 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.622-806C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538876 | |||||||
| chr13:79538979 | T | C | 1 | a0002c0002t0003g0234 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.622-703T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538979 | |||||||
| chr13:79538997 | C | G | 1 | a0001c0001t0002g0186 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.622-685C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538997 | |||||||
| chr13:79539067 | CAT | C | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(64): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.622-614_622-613del others(2): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79539067 | |||||||
| chr13:79539243 | T | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.622-439T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79539243 | |||||||
| chr13:79539517 | G | C | 136 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(133): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.622-165G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79539517 | |||||||
| chr13:79540265 | A | G | 5 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0034 others(2): Show |
6 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.715+490A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540265 | |||||||
| chr13:79540346 | T | G | 14 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(11): Show |
20 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.715+571T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540346 | |||||||
| chr13:79540503 | T | C | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.715+728T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540503 | |||||||
| chr13:79540621 | A | G | 1 | a0001c0001t0002g0023 | 2 | NA18945.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.715+846A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540621 | |||||||
| chr13:79540633 | T | C | 1 | a0001c0001t0002g0023 | 2 | NA18945.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.715+858T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540633 | |||||||
| chr13:79541197 | A | G | 11 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0071 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.715+1422A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541197 | |||||||
| chr13:79541254 | G | A | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.715+1479G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541254 | |||||||
| chr13:79541330 | T | C | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.715+1555T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541330 | |||||||
| chr13:79541333 | A | G | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.715+1558A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541333 | |||||||
| chr13:79541479 | A | G | 2 | a0003c0003t0005g0032 a0003c0003t0005g0033 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.715+1704A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541479 | |||||||
| chr13:79541980 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(9): Show |
15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.716-1578A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541980 | |||||||
| chr13:79542022 | C | T | 2 | a0001c0001t0004g0141 a0001c0001t0004g0143 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.716-1536C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542022 | |||||||
| chr13:79542487 | G | T | 1 | a0001c0001t0002g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.716-1071G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542487 | |||||||
| chr13:79542505 | G | GTTTT | 13 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(10): Show |
14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.716-1050_716-1047d others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 79542505 | ||||||
| chr13:79542510 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-1048T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542510 | |||||||
| chr13:79542512 | G | T | 15 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.716-1046G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542512 | |||||||
| chr13:79542556 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.716-1002T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542556 | |||||||
| chr13:79542624 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0185 a0001c0001t0002g0193 others(1): Show |
7 | HG00741.hp2 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.716-934A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542624 | |||||||
| chr13:79542666 | T | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.716-892T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542666 | |||||||
| chr13:79542764 | C | T | 1 | a0003c0003t0005g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.716-794C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542764 | |||||||
| chr13:79542844 | C | G | 151 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0071 others(148): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.716-714C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542844 | |||||||
| chr13:79542883 | CT | C | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.716-664delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 79542883 | ||||||
| chr13:79542991 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.716-567C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542991 | |||||||
| chr13:79543171 | C | T | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.716-387C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79543171 | |||||||
| chr13:79543296 | A | T | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.716-262A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79543296 | |||||||
| chr13:79543916 | T | C | 14 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(11): Show |
15 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+234T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79543916 | |||||||
| chr13:79543946 | CTTTA | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(21): Show |
31 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.840+269_840+272del others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 79543946 | ||||||
| chr13:79543965 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.840+283G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79543965 | |||||||
| chr13:79544161 | A | T | 8 | a0001c0001t0004g0003 a0001c0001t0004g0020 a0001c0001t0004g0127 others(5): Show |
12 | HG01243.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.840+479A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544161 | |||||||
| chr13:79544390 | AG | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0156 a0001c0001t0002g0203 |
4 | NA18941.hp2 NA18944.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+709delG | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544390 | |||||||
| chr13:79544428 | G | A | 2 | a0001c0001t0006g0106 a0001c0001t0016g0045 |
2 | NA19002.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.840+746G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544428 | |||||||
| chr13:79544492 | G | GT | 17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.840+824dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 79544492 | ||||||
| chr13:79544492 | GT | G | 19 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0107 others(16): Show |
20 | HG01256.hp1 HG01981.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.840+824delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 79544492 | ||||||
| chr13:79544516 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.840+834A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544516 | |||||||
| chr13:79544691 | A | G | 1 | a0001c0001t0006g0108 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.840+1009A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544691 | |||||||
| chr13:79544692 | T | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.840+1010T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544692 | |||||||
| chr13:79544737 | T | C | 1 | a0001c0001t0008g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.840+1055T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544737 | |||||||
| chr13:79544797 | T | C | 14 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(11): Show |
15 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+1115T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544797 | |||||||
| chr13:79545000 | A | T | 14 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(11): Show |
15 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+1318A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545000 | |||||||
| chr13:79545089 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.840+1407A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545089 | |||||||
| chr13:79545124 | T | A | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.840+1442T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545124 | |||||||
| chr13:79545180 | C | T | 32 | a0001c0001t0003g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 others(29): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.840+1498C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545180 | |||||||
| chr13:79545181 | A | G | 1 | a0001c0001t0004g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.840+1499A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545181 | |||||||
| chr13:79545287 | T | C | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.840+1605T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545287 | |||||||
| chr13:79545604 | A | G | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.840+1922A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545604 | |||||||
| chr13:79545610 | G | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.840+1928G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545610 | |||||||
| chr13:79545631 | C | T | 16 | a0001c0001t0015g0097 a0003c0003t0005g0012 a0003c0003t0005g0031 others(13): Show |
17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.840+1949C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545631 | |||||||
| chr13:79545676 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0118 others(2): Show |
7 | HG01258.hp1 HG01346.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.840+1994A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545676 | |||||||
| chr13:79545759 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.840+2077C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545759 | |||||||
| chr13:79545797 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.840+2115T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545797 | |||||||
| chr13:79545938 | G | A | 2 | a0002c0002t0003g0027 a0002c0002t0003g0213 |
3 | HG02698.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.840+2256G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545938 | |||||||
| chr13:79546020 | G | A | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.841-2308G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546020 | |||||||
| chr13:79546072 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.841-2256A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546072 | |||||||
| chr13:79546128 | T | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(17): Show |
26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.841-2200T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546128 | |||||||
| chr13:79546145 | G | A | 17 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(14): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.841-2183G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546145 | |||||||
| chr13:79546223 | TA | T | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(64): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.841-2103delA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 79546223 | ||||||
| chr13:79546248 | G | C | 1 | a0003c0003t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.841-2080G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546248 | |||||||
| chr13:79546272 | C | T | 6 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-2056C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546272 | |||||||
| chr13:79546541 | T | C | 1 | a0003c0003t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.841-1787T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546541 | |||||||
| chr13:79547000 | T | G | 234 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(231): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.841-1328T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547000 | |||||||
| chr13:79547049 | A | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-1279A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547049 | |||||||
| chr13:79547096 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.841-1232A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547096 | |||||||
| chr13:79547227 | A | C | 28 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0021 others(25): Show |
36 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.841-1101A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547227 | |||||||
| chr13:79547281 | C | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-1047C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547281 | |||||||
| chr13:79547339 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.841-989A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547339 | |||||||
| chr13:79547415 | G | A | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.841-913G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547415 | |||||||
| chr13:79547610 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.841-718C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547610 | |||||||
| chr13:79547614 | G | C | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.841-714G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547614 | |||||||
| chr13:79547675 | A | G | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.841-653A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547675 | |||||||
| chr13:79547839 | A | T | 1 | a0001c0001t0006g0108 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.841-489A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547839 | |||||||
| chr13:79547847 | T | C | 1 | a0002c0002t0003g0229 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.841-481T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547847 | |||||||
| chr13:79548152 | C | G | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.841-176C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79548152 | |||||||
| chr13:79548214 | C | T | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-114C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79548214 | |||||||
| chr13:79548300 | G | A | 1 | a0001c0001t0012g0163 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.841-28G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79548300 | |||||||
| chr13:79548894 | G | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
7 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.907+500G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79548894 | |||||||
| chr13:79549009 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.907+615A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549009 | |||||||
| chr13:79549038 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0117 |
3 | NA18979.hp1 NA18986.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.907+644A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549038 | |||||||
| chr13:79549299 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.907+905T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549299 | |||||||
| chr13:79549382 | T | G | 2 | a0001c0001t0003g0207 a0001c0001t0003g0208 |
2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.907+988T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549382 | |||||||
| chr13:79549528 | A | C | 1 | a0001c0001t0003g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.907+1134A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549528 | |||||||
| chr13:79549849 | A | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(134): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.908-1168A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549849 | |||||||
| chr13:79549961 | C | T | 16 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0020 others(13): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.908-1056C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549961 | |||||||
| chr13:79550205 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.908-812C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550205 | |||||||
| chr13:79550241 | T | G | 1 | a0003c0003t0005g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.908-776T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550241 | |||||||
| chr13:79550572 | T | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(134): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.908-445T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550572 | |||||||
| chr13:79550582 | T | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(134): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.908-435T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550582 | |||||||
| chr13:79550906 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.908-111A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550906 | |||||||
| chr13:79551551 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.*2+429C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551551 | |||||||
| chr13:79551603 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.*2+481A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551603 | |||||||
| chr13:79551768 | T | C | 2 | a0005c0005t0002g0204 a0005c0005t0002g0205 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*2+646T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551768 | |||||||
| chr13:79551801 | C | T | 2 | a0003c0003t0010g0042 a0003c0003t0010g0043 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.*2+679C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551801 | |||||||
| chr13:79551850 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.*3-666A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551850 | |||||||
| chr13:79551979 | C | G | 1 | a0001c0001t0003g0227 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.*3-537C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551979 | |||||||
| chr13:79552026 | A | G | 1 | a0001c0001t0003g0227 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.*3-490A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79552026 | |||||||
| chr13:79552213 | C | G | 15 | a0003c0003t0005g0012 a0003c0003t0005g0031 a0003c0003t0005g0032 others(12): Show |
16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.*3-303C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79552213 | |||||||
| chr13:79552355 | A | G | 1 | a0001c0001t0019g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.*3-161A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79552355 |