Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 149297 |
| ensemblid | ENSG00000188859.7 |
| hgncid | 13495 |
| symbol | FAM78B |
| name | family with sequence similarity 78 member B |
| refseq_nuc | NM_001017961.5 |
| refseq_prot | NP_001017961.1 |
| ensembl_nuc | ENST00000354422.4 |
| ensembl_prot | ENSP00000346404.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 166069299 |
| end | 166167001 |
| strand | - |
| ver | v1.2 |
| region | chr1:166069299-166167001 |
| region5000 | chr1:166064299-166172001 |
| regionname0 | FAM78B_chr1_166069299_166167001 |
| regionname5000 | FAM78B_chr1_166064299_166172001 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 783 | 241 | 70 | 45 | 97 | 7 | 20 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGG others(778): Show |
chr1 | 166064299 | 166172001 | ||
| a0001c0002 | 0/0 | 783 | 77 | 12 | 23 | 33 | 1 | 8 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGG others(778): Show |
chr1 | 166064299 | 166172001 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2481 | 130 | 28 | 20 | 68 | 2 | 11 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0002 | 0/1 | 2481 | 61 | 9 | 18 | 24 | 2 | 7 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0003 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0004 | 0/0 | 2481 | 17 | 16 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0006 | 0/0 | 2481 | 8 | 0 | 4 | 0 | 3 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0007 | 0/0 | 2481 | 5 | 5 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0008 | 0/0 | 2481 | 3 | 3 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0009 | 0/0 | 2481 | 3 | 3 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0011 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0012 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0013 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0014 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0016 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0017 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0018 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0019 | 0/0 | 2481 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0020 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0021 | 0/0 | 2481 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0023 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0024 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0001t0025 | 0/0 | 2481 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0002t0001 | 0/0 | 2481 | 7 | 7 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0002t0003 | 0/0 | 2481 | 48 | 0 | 14 | 26 | 1 | 7 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0002t0005 | 0/0 | 2481 | 16 | 0 | 9 | 7 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0002t0010 | 0/0 | 2481 | 3 | 2 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0002t0011 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0002t0015 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| a0001c0002t0022 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | ATGGC others(2476): Show |
chr1 | 166064299 | 166172001 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0016g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0017g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0018g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0019g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0020g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0021g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0023g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0024g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0025g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0010g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0022g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0209 | EUR | GBR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0130 | EUR | GBR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0179 | EUR | FIN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0153 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00544 | hp1 | a0001 | c0002 | t0005 | g0296 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00597 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0150 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0195 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0199 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0112 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0072 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0200 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0196 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0201 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0202 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0119 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0276 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0064 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0011 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01243 | hp2 | a0001 | c0001 | t0025 | g0306 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0110 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0011 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0288 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01361 | hp2 | a0001 | c0002 | t0005 | g0001 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0087 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0074 | EUR | IBS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0289 | EUR | IBS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01934 | hp1 | a0001 | c0002 | t0005 | g0001 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01943 | hp2 | a0001 | c0002 | t0005 | g0298 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01952 | hp2 | a0001 | c0002 | t0005 | g0001 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01981 | hp1 | a0001 | c0002 | t0005 | g0297 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0164 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0075 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02055 | hp2 | a0001 | c0002 | t0015 | g0035 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0109 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0108 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02148 | hp1 | a0001 | c0002 | t0005 | g0294 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | CDX | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02258 | hp2 | a0001 | c0002 | t0011 | g0023 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02293 | hp1 | a0001 | c0002 | t0005 | g0295 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02300 | hp1 | a0001 | c0001 | t0019 | g0260 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0041 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02523 | hp1 | a0001 | c0002 | t0005 | g0299 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0068 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0204 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0291 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02970 | hp2 | a0001 | c0002 | t0010 | g0124 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0098 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0071 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03130 | hp1 | a0001 | c0001 | t0018 | g0057 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0292 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0038 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0261 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0208 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0039 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03834 | hp1 | a0001 | c0002 | t0010 | g0206 | SAS | BEB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | BEB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG04228 | hp2 | a0001 | c0001 | t0021 | g0207 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18522 | hp1 | a0001 | c0002 | t0010 | g0123 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | CHB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18942 | hp2 | a0001 | c0002 | t0005 | g0302 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0113 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18954 | hp1 | a0001 | c0001 | t0024 | g0305 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0226 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0114 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18963 | hp1 | a0001 | c0002 | t0005 | g0300 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18977 | hp1 | a0001 | c0002 | t0005 | g0301 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0111 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18987 | hp2 | a0001 | c0001 | t0016 | g0095 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0151 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19000 | hp1 | a0001 | c0001 | t0020 | g0157 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0283 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0284 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19007 | hp1 | a0001 | c0002 | t0005 | g0304 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0285 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0250 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0281 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19072 | hp2 | a0001 | c0001 | t0023 | g0293 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19074 | hp2 | a0001 | c0002 | t0005 | g0303 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0272 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0280 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19089 | hp2 | a0001 | c0002 | t0003 | g0152 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0213 | EUR | TSI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | GIH | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02559 | hp1 | a0001 | c0002 | t0022 | g0125 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | USA | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | USA | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0287 | REF | REF | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0056 | REF | REF | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:166070661 | C | G | 1 | a0001c0002 | 77 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
synonymous_variant | LOW | c.366G>C | p.Val122Val | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 1119/2481 | 366/786 | 122/261 | chr1 | 166070661 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:166069362 | A | G | 1 | a0001c0001t0023 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 879 | chr1 | 166069362 | ||||||
| chr1:166069558 | G | C | 1 | a0001c0001t0006 | 8 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*683C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 683 | chr1 | 166069558 | ||||||
| chr1:166069562 | G | A | 1 | a0001c0001t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 679 | chr1 | 166069562 | ||||||
| chr1:166069605 | T | C | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0005 others(2): Show |
69 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*636A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 636 | chr1 | 166069605 | ||||||
| chr1:166069623 | C | T | 1 | a0001c0001t0020 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*618G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 618 | chr1 | 166069623 | ||||||
| chr1:166069685 | T | C | 2 | a0001c0002t0010 a0001c0002t0015 |
4 | HG02055.hp2 HG02970.hp2 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*556A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 556 | chr1 | 166069685 | ||||||
| chr1:166069730 | A | G | 7 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(4): Show |
77 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*511T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 511 | chr1 | 166069730 | ||||||
| chr1:166069784 | C | T | 1 | a0001c0001t0019 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*457G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 457 | chr1 | 166069784 | ||||||
| chr1:166069961 | G | A | 1 | a0001c0001t0009 | 3 | HG02451.hp1 HG02922.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*280C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 280 | chr1 | 166069961 | ||||||
| chr1:166070011 | C | G | 4 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0017 others(1): Show |
20 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*230G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 230 | chr1 | 166070011 | ||||||
| chr1:166070045 | A | G | 1 | a0001c0001t0016 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*196T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 196 | chr1 | 166070045 | ||||||
| chr1:166070048 | G | C | 1 | a0001c0001t0021 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 193 | chr1 | 166070048 | ||||||
| chr1:166070064 | A | C | 1 | a0001c0001t0009 | 3 | HG02451.hp1 HG02922.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*177T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 177 | chr1 | 166070064 | ||||||
| chr1:166070194 | C | A | 1 | a0001c0002t0022 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*47G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 47 | chr1 | 166070194 | ||||||
| chr1:166166495 | G | A | 2 | a0001c0001t0023 a0001c0002t0005 |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-247C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 247 | chr1 | 166166495 | ||||||
| chr1:166166794 | G | T | 4 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(1): Show |
8 | HG01891.hp1 HG02055.hp2 HG02723.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-546C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 546 | chr1 | 166166794 | ||||||
| chr1:166166803 | G | A | 1 | a0001c0001t0024 | 1 | NA18954.hp1 | 5_prime_UTR_variant | MODIFIER | c.-555C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 555 | chr1 | 166166803 | ||||||
| chr1:166166854 | C | T | 3 | a0001c0001t0004 a0001c0001t0011 a0001c0002t0011 |
19 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-606G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 606 | chr1 | 166166854 | ||||||
| chr1:166166866 | G | C | 1 | a0001c0001t0025 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-618C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 618 | chr1 | 166166866 | ||||||
| chr1:166166880 | A | C | 1 | a0001c0001t0008 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-632T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 632 | chr1 | 166166880 | ||||||
| chr1:166166957 | A | G | 1 | a0001c0001t0012 | 1 | HG00597.hp1 | 5_prime_UTR_variant | MODIFIER | c.-709T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 709 | chr1 | 166166957 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:166070807 | G | T | 1 | a0001c0001t0002g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.264-44C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166070807 | |||||||
| chr1:166070825 | A | T | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-62T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166070825 | |||||||
| chr1:166070907 | G | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0076 a0001c0001t0002g0080 others(2): Show |
6 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-144C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166070907 | |||||||
| chr1:166071045 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(56): Show |
61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-282G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071045 | |||||||
| chr1:166071122 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.264-359C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071122 | |||||||
| chr1:166071318 | G | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-555C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071318 | |||||||
| chr1:166071411 | C | T | 25 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(22): Show |
26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-648G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071411 | |||||||
| chr1:166071415 | G | A | 1 | a0001c0002t0003g0281 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.264-652C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071415 | |||||||
| chr1:166071529 | G | A | 3 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 |
3 | HG01070.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.264-766C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071529 | |||||||
| chr1:166071556 | C | A | 1 | a0001c0001t0024g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.264-793G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071556 | |||||||
| chr1:166071557 | C | T | 1 | a0001c0002t0003g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.264-794G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071557 | |||||||
| chr1:166071579 | A | G | 2 | a0001c0001t0002g0073 a0001c0001t0002g0131 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.264-816T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071579 | |||||||
| chr1:166071880 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.264-1117A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071880 | |||||||
| chr1:166071932 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(83): Show |
89 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.264-1169C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071932 | |||||||
| chr1:166071936 | G | A | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-1173C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071936 | |||||||
| chr1:166072227 | A | G | 1 | a0001c0002t0003g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.264-1464T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072227 | |||||||
| chr1:166072231 | A | G | 29 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(26): Show |
31 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.264-1468T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072231 | |||||||
| chr1:166072310 | G | A | 27 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(24): Show |
29 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-1547C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072310 | |||||||
| chr1:166072316 | G | A | 8 | a0001c0001t0002g0058 a0001c0001t0002g0105 a0001c0001t0002g0170 others(5): Show |
9 | HG01081.hp1 HG01891.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-1553C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072316 | |||||||
| chr1:166072410 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.264-1647C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072410 | |||||||
| chr1:166072494 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
6 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-1731C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072494 | |||||||
| chr1:166072547 | G | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0266 |
2 | HG00597.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.264-1784C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072547 | |||||||
| chr1:166072550 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.264-1787G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072550 | |||||||
| chr1:166072580 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-1817A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072580 | |||||||
| chr1:166072825 | G | C | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-2062C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072825 | |||||||
| chr1:166072943 | G | C | 1 | a0001c0002t0022g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.264-2180C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072943 | |||||||
| chr1:166073110 | G | T | 25 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(22): Show |
26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-2347C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073110 | |||||||
| chr1:166073168 | T | A | 27 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(24): Show |
29 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-2405A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073168 | |||||||
| chr1:166073421 | C | T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(110): Show |
118 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.264-2658G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073421 | |||||||
| chr1:166073497 | CCTCT | C | 26 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(23): Show |
27 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.264-2738_264-2735d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073497 | |||||||
| chr1:166073518 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0235 |
2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.264-2755G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073518 | |||||||
| chr1:166073530 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-2767A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073530 | |||||||
| chr1:166073532 | CTCTCTTT | C | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(6): Show |
9 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-2776_264-2770d others(9): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073532 | |||||||
| chr1:166073536 | C | CT | 62 | a0001c0001t0003g0194 a0001c0002t0003g0010 a0001c0002t0003g0039 others(59): Show |
66 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.264-2774dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073536 | |||||||
| chr1:166073536 | C | T | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-2773G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073536 | |||||||
| chr1:166073536 | CTTTT | C | 25 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(22): Show |
26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-2777_264-2774d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073536 | |||||||
| chr1:166073537 | T | TC | 12 | a0001c0001t0002g0004 a0001c0001t0002g0076 a0001c0001t0002g0080 others(9): Show |
13 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-2775_264-2774i others(3): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073537 | |||||||
| chr1:166073538 | T | C | 15 | a0001c0001t0002g0048 a0001c0001t0002g0058 a0001c0001t0002g0073 others(12): Show |
16 | HG01081.hp1 HG01891.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-2775A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073538 | |||||||
| chr1:166073551 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0275 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.264-2788A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073551 | |||||||
| chr1:166073700 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.264-2937A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073700 | |||||||
| chr1:166073776 | G | A | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-3013C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073776 | |||||||
| chr1:166073973 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.264-3210G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073973 | |||||||
| chr1:166074155 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.264-3392G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074155 | |||||||
| chr1:166074221 | G | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-3458C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074221 | |||||||
| chr1:166074442 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.264-3679A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074442 | |||||||
| chr1:166074547 | A | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0077 others(19): Show |
23 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.264-3784T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074547 | |||||||
| chr1:166074616 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.264-3853T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074616 | |||||||
| chr1:166074702 | T | C | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-3939A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074702 | |||||||
| chr1:166074724 | C | T | 2 | a0001c0002t0001g0053 a0001c0002t0001g0212 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.264-3961G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074724 | |||||||
| chr1:166074818 | T | A | 1 | a0001c0001t0002g0128 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.264-4055A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074818 | |||||||
| chr1:166074820 | A | G | 60 | a0001c0002t0003g0010 a0001c0002t0003g0039 a0001c0002t0003g0064 others(57): Show |
64 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.264-4057T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074820 | |||||||
| chr1:166074853 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-4090A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074853 | |||||||
| chr1:166074867 | C | A | 25 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(22): Show |
26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-4104G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074867 | |||||||
| chr1:166075012 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.264-4249A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075012 | |||||||
| chr1:166075092 | C | G | 1 | a0001c0001t0024g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.264-4329G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075092 | |||||||
| chr1:166075158 | T | C | 28 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(25): Show |
30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-4395A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075158 | |||||||
| chr1:166075331 | T | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(58): Show |
63 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.264-4568A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075331 | |||||||
| chr1:166075423 | T | TTG | 3 | a0001c0001t0001g0244 a0001c0001t0001g0255 a0001c0001t0001g0286 |
3 | HG00423.hp1 HG00673.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.264-4662_264-4661d others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075423 | |||||||
| chr1:166075441 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-4678A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075441 | |||||||
| chr1:166075492 | C | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-4729G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075492 | |||||||
| chr1:166075494 | C | T | 67 | a0001c0002t0001g0053 a0001c0002t0001g0212 a0001c0002t0003g0010 others(64): Show |
71 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.264-4731G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075494 | |||||||
| chr1:166075564 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.264-4801A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075564 | |||||||
| chr1:166076010 | A | G | 145 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0042 others(142): Show |
150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.264-5247T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076010 | |||||||
| chr1:166076014 | C | CCACTCTT others(95): Show |
1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5252_264-5251i others(104): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076014 | |||||||
| chr1:166076028 | C | G | 25 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(22): Show |
26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-5265G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076028 | |||||||
| chr1:166076030 | G | A | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0042 others(66): Show |
71 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.264-5267C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076030 | |||||||
| chr1:166076166 | C | T | 1 | a0001c0002t0003g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.264-5403G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076166 | |||||||
| chr1:166076185 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5422T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076185 | |||||||
| chr1:166076187 | G | A | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
240 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.264-5424C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076187 | |||||||
| chr1:166076379 | G | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(56): Show |
61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-5616C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076379 | |||||||
| chr1:166076441 | T | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0168 |
3 | HG02040.hp1 NA18942.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.264-5678A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076441 | |||||||
| chr1:166076462 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.264-5699C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076462 | |||||||
| chr1:166076481 | C | A | 25 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(22): Show |
26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-5718G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076481 | |||||||
| chr1:166076519 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5756A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076519 | |||||||
| chr1:166076544 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-5781A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076544 | |||||||
| chr1:166076653 | A | G | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.264-5890T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076653 | |||||||
| chr1:166076656 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.264-5893A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076656 | |||||||
| chr1:166076666 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5903T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076666 | |||||||
| chr1:166076720 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5957T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076720 | |||||||
| chr1:166076723 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5960A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076723 | |||||||
| chr1:166076724 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5961C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076724 | |||||||
| chr1:166076745 | T | C | 3 | a0001c0001t0002g0058 a0001c0001t0002g0170 a0001c0001t0002g0172 |
3 | HG01081.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.264-5982A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076745 | |||||||
| chr1:166076758 | A | G | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-5995T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076758 | |||||||
| chr1:166076802 | C | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | NA18947.hp2 NA19063.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.264-6039G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076802 | |||||||
| chr1:166076948 | C | A | 67 | a0001c0002t0001g0053 a0001c0002t0001g0212 a0001c0002t0003g0010 others(64): Show |
71 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.264-6185G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076948 | |||||||
| chr1:166076956 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6193A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076956 | |||||||
| chr1:166077031 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.264-6268A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077031 | |||||||
| chr1:166077157 | A | T | 1 | a0001c0002t0001g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.264-6394T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077157 | |||||||
| chr1:166077173 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6410T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077173 | |||||||
| chr1:166077211 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6448A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077211 | |||||||
| chr1:166077273 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6510C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077273 | |||||||
| chr1:166077451 | A | C | 28 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(25): Show |
30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-6688T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077451 | |||||||
| chr1:166077558 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6795A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077558 | |||||||
| chr1:166077587 | A | AAATACAT others(29): Show |
1 | a0001c0001t0001g0266 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.264-6860_264-6825d others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077587 | |||||||
| chr1:166077587 | AAATACAT others(29): Show |
A | 1 | a0001c0001t0001g0279 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.264-6860_264-6825d others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077587 | |||||||
| chr1:166077629 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6866T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077629 | |||||||
| chr1:166077657 | TAATA | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(56): Show |
61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-6898_264-6895d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077657 | |||||||
| chr1:166077661 | A | ACATATAA others(23): Show |
25 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(22): Show |
26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-6899_264-6898i others(32): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077661 | |||||||
| chr1:166077672 | A | G | 28 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(25): Show |
30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-6909T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077672 | |||||||
| chr1:166077688 | TA | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0019 others(10): Show |
14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.264-6926delT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077688 | |||||||
| chr1:166077696 | A | AATAAATA others(27): Show |
1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-6934_264-6933i others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077696 | |||||||
| chr1:166077699 | TAATA | T | 12 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
12 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-6940_264-6937d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077699 | |||||||
| chr1:166077701 | A | T | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-6938T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077701 | |||||||
| chr1:166077702 | T | A | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-6939A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077702 | |||||||
| chr1:166077703 | A | T | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-6940T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077703 | |||||||
| chr1:166077731 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6968T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077731 | |||||||
| chr1:166077733 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6970A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077733 | |||||||
| chr1:166077735 | TAATA | T | 28 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(25): Show |
30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-6976_264-6973d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077735 | |||||||
| chr1:166077740 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6977T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077740 | |||||||
| chr1:166077742 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6979A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077742 | |||||||
| chr1:166077744 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6981G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077744 | |||||||
| chr1:166077745 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6982T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077745 | |||||||
| chr1:166077746 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6983A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077746 | |||||||
| chr1:166077760 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6997A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077760 | |||||||
| chr1:166077819 | TATATAA | T | 6 | a0001c0002t0003g0098 a0001c0002t0003g0117 a0001c0002t0003g0250 others(3): Show |
6 | HG02055.hp2 HG02165.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-7062_264-7057d others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077819 | |||||||
| chr1:166077821 | TATAA | T | 62 | a0001c0001t0002g0210 a0001c0002t0001g0053 a0001c0002t0001g0212 others(59): Show |
66 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.264-7062_264-7059d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077821 | |||||||
| chr1:166077836 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.264-7073A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077836 | |||||||
| chr1:166077836 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-7073A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077836 | |||||||
| chr1:166077837 | TTATATAT others(118): Show |
T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(55): Show |
60 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.264-7199_264-7075d others(2): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077837 | |||||||
| chr1:166077837 | TTATATAT others(120): Show |
T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0192 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.264-7201_264-7075d others(2): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077837 | |||||||
| chr1:166077844 | TATAATAA others(122): Show |
T | 1 | a0001c0001t0020g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.264-7210_264-7082d others(2): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077844 | |||||||
| chr1:166077849 | TAATATAT others(117): Show |
T | 142 | a0001c0001t0001g0133 a0001c0001t0001g0217 a0001c0001t0002g0004 others(139): Show |
149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.264-7210_264-7087d others(2): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077849 | |||||||
| chr1:166077850 | AAT | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-7089_264-7088d others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077850 | |||||||
| chr1:166077853 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7090T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077853 | |||||||
| chr1:166077865 | TATATATA others(54): Show |
T | 6 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0060 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-7163_264-7103d others(63): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077865 | |||||||
| chr1:166077874 | TTATATAT others(6): Show |
T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(48): Show |
53 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.264-7124_264-7112d others(15): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077874 | |||||||
| chr1:166077874 | TTATATAT others(78): Show |
T | 2 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
2 | HG01515.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.264-7196_264-7112d others(87): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077874 | |||||||
| chr1:166077874 | TTATATAT others(92): Show |
T | 28 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
29 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-7210_264-7112d others(101): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077874 | |||||||
| chr1:166077875 | T | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0120 others(6): Show |
9 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-7112A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077875 | |||||||
| chr1:166077881 | TATAATAA others(7): Show |
T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7132_264-7119d others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077881 | |||||||
| chr1:166077887 | A | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0197 a0001c0001t0001g0238 others(4): Show |
7 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-7124T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077887 | |||||||
| chr1:166077888 | A | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0197 a0001c0001t0001g0238 others(4): Show |
7 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-7125T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077888 | |||||||
| chr1:166077889 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264-7126T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077889 | |||||||
| chr1:166077890 | T | TATATA | 7 | a0001c0001t0001g0079 a0001c0001t0001g0197 a0001c0001t0001g0238 others(4): Show |
7 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-7132_264-7128d others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077890 | |||||||
| chr1:166077908 | ATAATT | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(45): Show |
50 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.264-7150_264-7146d others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077908 | |||||||
| chr1:166077908 | ATAATTAT | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0218 a0001c0001t0001g0244 |
3 | NA18941.hp2 NA18990.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.264-7152_264-7146d others(9): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077908 | |||||||
| chr1:166077913 | T | A | 8 | a0001c0001t0001g0079 a0001c0001t0001g0197 a0001c0001t0001g0238 others(5): Show |
8 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-7150A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077913 | |||||||
| chr1:166077913 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264-7160_264-7151d others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077913 | |||||||
| chr1:166077921 | T | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(45): Show |
50 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.264-7158A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077921 | |||||||
| chr1:166077922 | A | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(45): Show |
50 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.264-7159T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077922 | |||||||
| chr1:166077923 | A | ATT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0197 a0001c0001t0001g0238 others(4): Show |
7 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-7161_264-7160i others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077923 | |||||||
| chr1:166077923 | A | ATTTATAT others(13): Show |
1 | a0001c0001t0001g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.264-7161_264-7160i others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077923 | |||||||
| chr1:166077923 | A | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(45): Show |
50 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.264-7160T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077923 | |||||||
| chr1:166077925 | A | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0218 a0001c0001t0001g0244 |
3 | NA18941.hp2 NA18990.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.264-7162T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077925 | |||||||
| chr1:166077926 | A | T | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(57): Show |
62 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.264-7163T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077926 | |||||||
| chr1:166077935 | T | TAATATAT others(31): Show |
1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.264-7210_264-7173d others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077935 | |||||||
| chr1:166077948 | TTATATAT others(7): Show |
T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0134 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.264-7199_264-7186d others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077948 | |||||||
| chr1:166077955 | TATAATTA others(8): Show |
T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7207_264-7193d others(17): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077955 | |||||||
| chr1:166077960 | TTATATAT others(6): Show |
T | 54 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(51): Show |
56 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.264-7210_264-7198d others(15): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077960 | |||||||
| chr1:166077961 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.264-7198A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077961 | |||||||
| chr1:166077961 | TATATATA others(6): Show |
T | 8 | a0001c0001t0001g0079 a0001c0001t0018g0057 a0001c0002t0001g0051 others(5): Show |
8 | HG00323.hp2 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-7211_264-7199d others(15): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077961 | |||||||
| chr1:166077970 | A | AATTTATA others(3): Show |
1 | a0001c0001t0001g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.264-7208_264-7207i others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077970 | |||||||
| chr1:166077972 | TA | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(61): Show |
66 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.264-7210delT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077972 | |||||||
| chr1:166077976 | T | G | 1 | a0001c0001t0002g0253 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.264-7213A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077976 | |||||||
| chr1:166077988 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7225T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077988 | |||||||
| chr1:166077989 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7226A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077989 | |||||||
| chr1:166077990 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7227T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077990 | |||||||
| chr1:166077996 | A | T | 74 | a0001c0001t0002g0170 a0001c0001t0002g0172 a0001c0001t0002g0210 others(71): Show |
78 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.264-7233T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077996 | |||||||
| chr1:166078009 | A | G | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-7246T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078009 | |||||||
| chr1:166078024 | A | T | 11 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(8): Show |
11 | HG02451.hp1 HG02615.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.264-7261T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078024 | |||||||
| chr1:166078096 | A | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(55): Show |
60 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.264-7333T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078096 | |||||||
| chr1:166078145 | C | T | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-7382G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078145 | |||||||
| chr1:166078147 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-7384A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078147 | |||||||
| chr1:166078167 | G | T | 3 | a0001c0002t0010g0123 a0001c0002t0010g0124 a0001c0002t0015g0035 |
3 | HG02055.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.264-7404C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078167 | |||||||
| chr1:166078272 | G | A | 28 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(25): Show |
30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-7509C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078272 | |||||||
| chr1:166078441 | A | G | 47 | a0001c0001t0001g0133 a0001c0001t0002g0009 a0001c0001t0002g0088 others(44): Show |
48 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.264-7678T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078441 | |||||||
| chr1:166078553 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-7790C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078553 | |||||||
| chr1:166078559 | C | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(56): Show |
61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-7796G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078559 | |||||||
| chr1:166078603 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7840C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078603 | |||||||
| chr1:166078604 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7841T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078604 | |||||||
| chr1:166078607 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7844G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078607 | |||||||
| chr1:166078797 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-8034C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078797 | |||||||
| chr1:166078816 | A | G | 159 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(156): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.264-8053T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078816 | |||||||
| chr1:166078927 | G | GT | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(59): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.264-8165dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078927 | |||||||
| chr1:166078927 | GT | G | 131 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(128): Show |
137 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.264-8165delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078927 | |||||||
| chr1:166078927 | GTT | G | 27 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(24): Show |
29 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-8166_264-8165d others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078927 | |||||||
| chr1:166078956 | G | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-8193C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078956 | |||||||
| chr1:166079044 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-8281C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079044 | |||||||
| chr1:166079086 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.264-8323G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079086 | |||||||
| chr1:166079140 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(56): Show |
61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-8377G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079140 | |||||||
| chr1:166079167 | C | T | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-8404G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079167 | |||||||
| chr1:166079351 | T | C | 28 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0058 others(25): Show |
30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-8588A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079351 | |||||||
| chr1:166079507 | G | A | 299 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.264-8744C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079507 | |||||||
| chr1:166079534 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0062 |
3 | HG00639.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.264-8771C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079534 | |||||||
| chr1:166079579 | T | G | 1 | a0001c0002t0001g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.264-8816A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079579 | |||||||
| chr1:166079742 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(56): Show |
61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-8979A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079742 | |||||||
| chr1:166079788 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.264-9025A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079788 | |||||||
| chr1:166079807 | C | T | 12 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0238 others(9): Show |
12 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-9044G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079807 | |||||||
| chr1:166079923 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-9160A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079923 | |||||||
| chr1:166080033 | T | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(109): Show |
117 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.264-9270A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080033 | |||||||
| chr1:166080089 | G | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(6): Show |
9 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-9326C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080089 | |||||||
| chr1:166080164 | T | C | 1 | a0001c0002t0005g0300 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.264-9401A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080164 | |||||||
| chr1:166080303 | T | C | 147 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
153 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.264-9540A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080303 | |||||||
| chr1:166080340 | CCCA | C | 45 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0271 others(42): Show |
46 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.264-9580_264-9578d others(5): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080340 | |||||||
| chr1:166080520 | C | T | 1 | a0001c0002t0022g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.264-9757G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080520 | |||||||
| chr1:166080585 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.264-9822C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080585 | |||||||
| chr1:166081140 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0270 |
2 | HG00621.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.264-10377G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081140 | |||||||
| chr1:166081149 | A | T | 1 | a0001c0002t0022g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.264-10386T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081149 | |||||||
| chr1:166081308 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0009g0291 a0001c0001t0009g0292 |
3 | HG02922.hp1 HG03130.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.264-10545C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081308 | |||||||
| chr1:166081314 | G | A | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-10551C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081314 | |||||||
| chr1:166081319 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-10556C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081319 | |||||||
| chr1:166081320 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-10557A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081320 | |||||||
| chr1:166081372 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.264-10609C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081372 | |||||||
| chr1:166081680 | G | A | 296 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(293): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.264-10917C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081680 | |||||||
| chr1:166081834 | A | G | 18 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(15): Show |
19 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.264-11071T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081834 | |||||||
| chr1:166082084 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-11321G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082084 | |||||||
| chr1:166082157 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-11394G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082157 | |||||||
| chr1:166082225 | C | G | 1 | a0001c0001t0021g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.264-11462G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082225 | |||||||
| chr1:166082264 | A | T | 1 | a0001c0001t0021g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.264-11501T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082264 | |||||||
| chr1:166082350 | G | T | 114 | a0001c0001t0001g0059 a0001c0001t0001g0079 a0001c0001t0001g0106 others(111): Show |
119 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.264-11587C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082350 | |||||||
| chr1:166082482 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.264-11719A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082482 | |||||||
| chr1:166082534 | G | C | 1 | a0001c0002t0003g0208 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.264-11771C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082534 | |||||||
| chr1:166082559 | A | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-11796T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082559 | |||||||
| chr1:166082842 | G | A | 3 | a0001c0001t0004g0016 a0001c0001t0009g0291 a0001c0001t0009g0292 |
3 | HG01243.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.264-12079C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082842 | |||||||
| chr1:166082865 | A | ACGAGTGT others(1): Show |
6 | a0001c0001t0001g0181 a0001c0001t0008g0013 a0001c0001t0008g0014 others(3): Show |
6 | HG00544.hp1 HG03516.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-12110_264-1210 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082865 | |||||||
| chr1:166083082 | G | T | 17 | a0001c0001t0004g0002 a0001c0001t0004g0018 a0001c0001t0004g0019 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-12319C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083082 | |||||||
| chr1:166083096 | G | T | 3 | a0001c0001t0009g0041 a0001c0001t0009g0291 a0001c0001t0009g0292 |
3 | HG02451.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.264-12333C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083096 | |||||||
| chr1:166083221 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0092 |
2 | HG01099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.264-12458C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083221 | |||||||
| chr1:166083289 | G | C | 66 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0106 others(63): Show |
67 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.264-12526C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083289 | |||||||
| chr1:166083433 | T | C | 1 | a0001c0001t0018g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.264-12670A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083433 | |||||||
| chr1:166083493 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.264-12730T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083493 | |||||||
| chr1:166083540 | G | T | 10 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(7): Show |
11 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.264-12777C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083540 | |||||||
| chr1:166083558 | G | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(80): Show |
85 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.264-12795C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083558 | |||||||
| chr1:166083642 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-12879G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083642 | |||||||
| chr1:166083799 | CT | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0135 others(5): Show |
8 | HG02109.hp2 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-13037delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083799 | |||||||
| chr1:166083799 | CTT | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
135 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.264-13038_264-1303 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083799 | |||||||
| chr1:166083799 | CTTT | C | 18 | a0001c0001t0001g0094 a0001c0001t0001g0138 a0001c0001t0001g0187 others(15): Show |
19 | HG01069.hp2 HG01070.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.264-13039_264-1303 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083799 | |||||||
| chr1:166083799 | CTTTT | C | 138 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(135): Show |
144 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.264-13040_264-1303 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083799 | |||||||
| chr1:166084119 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.264-13356G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084119 | |||||||
| chr1:166084205 | C | CCA | 53 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0121 others(50): Show |
56 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.264-13444_264-1344 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084205 | C | CCACA | 85 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0055 others(82): Show |
87 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.264-13446_264-1344 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084205 | C | CCACACA | 11 | a0001c0001t0001g0062 a0001c0001t0001g0096 a0001c0001t0001g0104 others(8): Show |
11 | HG00597.hp2 HG00639.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-13448_264-1344 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084205 | C | CCACACAC others(1): Show |
15 | a0001c0001t0001g0059 a0001c0001t0001g0078 a0001c0001t0001g0079 others(12): Show |
15 | HG00323.hp2 HG00597.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-13450_264-1344 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084205 | C | CCACACAC others(3): Show |
4 | a0001c0001t0025g0306 a0001c0002t0003g0107 a0001c0002t0003g0165 others(1): Show |
4 | HG01243.hp2 NA18949.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-13452_264-1344 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084205 | C | CCACACAC others(7): Show |
3 | a0001c0001t0002g0192 a0001c0001t0008g0013 a0001c0001t0008g0015 |
3 | HG02895.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-13456_264-1344 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084205 | C | CCACACAC others(11): Show |
1 | a0001c0001t0014g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.264-13460_264-1344 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084205 | C | CCACACAC others(17): Show |
1 | a0001c0001t0001g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.264-13466_264-1344 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084205 | CCA | C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0050 others(6): Show |
9 | HG01081.hp1 HG02155.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-13444_264-1344 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | |||||||
| chr1:166084224 | C | CACACACA others(15): Show |
3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0060 |
3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-13462_264-1346 others(26): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084224 | |||||||
| chr1:166084226 | C | CACACACA others(13): Show |
1 | a0001c0002t0011g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.264-13464_264-1346 others(24): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084226 | |||||||
| chr1:166084228 | C | CACACACA others(11): Show |
1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-13466_264-1346 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084228 | |||||||
| chr1:166084228 | C | CACAT | 3 | a0001c0002t0003g0111 a0001c0002t0003g0113 a0001c0002t0003g0151 |
3 | NA18952.hp2 NA18979.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.264-13466_264-1346 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084228 | |||||||
| chr1:166084231 | ACACACAC others(5): Show |
A | 2 | a0001c0001t0001g0271 a0001c0001t0002g0247 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.264-13480_264-1346 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084231 | |||||||
| chr1:166084235 | ACACTCTC others(3): Show |
A | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-13482_264-1347 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084235 | |||||||
| chr1:166084237 | A | ACACACAC others(19): Show |
1 | a0001c0001t0001g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(30): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(17): Show |
1 | a0001c0001t0001g0043 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.264-13475_264-1347 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(15): Show |
1 | a0001c0001t0001g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.264-13475_264-1347 others(26): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(13): Show |
1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.264-13475_264-1347 others(24): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(11): Show |
2 | a0001c0001t0008g0014 a0001c0002t0001g0212 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(9): Show |
1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(7): Show |
1 | a0001c0001t0002g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.264-13475_264-1347 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(5): Show |
1 | a0001c0001t0002g0171 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(1): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(3): Show |
7 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(3): Show |
3 | a0001c0001t0001g0077 a0001c0001t0001g0132 a0001c0001t0001g0282 |
3 | HG02129.hp1 HG04204.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0279 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(7): Show |
3 | a0001c0001t0001g0189 a0001c0001t0021g0207 a0001c0002t0005g0011 |
3 | HG01192.hp1 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(9): Show |
1 | a0001c0002t0003g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACAC others(11): Show |
3 | a0001c0002t0003g0196 a0001c0002t0003g0201 a0001c0002t0003g0202 |
3 | HG01081.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACT | 4 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0002t0003g0109 others(1): Show |
4 | HG02083.hp2 HG02735.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACTC others(1): Show |
3 | a0001c0002t0003g0039 a0001c0002t0003g0283 a0001c0002t0005g0001 |
3 | HG01952.hp2 HG03688.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACTC others(5): Show |
23 | a0001c0001t0001g0211 a0001c0001t0001g0286 a0001c0001t0002g0210 others(20): Show |
25 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACTC others(7): Show |
5 | a0001c0001t0002g0289 a0001c0002t0003g0276 a0001c0002t0005g0301 others(2): Show |
5 | HG01168.hp2 HG01515.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACACTC others(9): Show |
1 | a0001c0001t0002g0290 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACT | 8 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0097 others(5): Show |
8 | HG00558.hp2 HG02922.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | ACACTCTC others(7): Show |
1 | a0001c0002t0005g0299 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | A | T | 4 | a0001c0001t0001g0173 a0001c0002t0003g0111 a0001c0002t0003g0113 others(1): Show |
4 | HG03041.hp2 NA18952.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-13474T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | ACT | A | 9 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0220 others(6): Show |
9 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-13476_264-1347 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | ACTCT | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0219 a0001c0001t0013g0038 others(2): Show |
5 | HG00544.hp1 HG02886.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-13478_264-1347 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084237 | ACTCTCT | A | 3 | a0001c0001t0007g0003 a0001c0001t0007g0033 a0001c0001t0007g0037 |
4 | HG02723.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-13480_264-1347 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | |||||||
| chr1:166084239 | T | A | 96 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0089 others(93): Show |
98 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.264-13476A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084239 | |||||||
| chr1:166084241 | T | A | 79 | a0001c0001t0001g0059 a0001c0001t0001g0106 a0001c0001t0001g0156 others(76): Show |
80 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.264-13478A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084241 | |||||||
| chr1:166084243 | T | A | 68 | a0001c0001t0001g0059 a0001c0001t0001g0086 a0001c0001t0001g0106 others(65): Show |
69 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.264-13480A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084243 | |||||||
| chr1:166084245 | T | A | 9 | a0001c0001t0001g0086 a0001c0001t0002g0214 a0001c0001t0002g0215 others(6): Show |
10 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.264-13482A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084245 | |||||||
| chr1:166084247 | T | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.264-13484A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084247 | |||||||
| chr1:166084256 | CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-13503_264-1349 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084256 | |||||||
| chr1:166084266 | T | C | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-13503A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084266 | |||||||
| chr1:166084268 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-13505G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084268 | |||||||
| chr1:166084278 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-13515G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084278 | |||||||
| chr1:166084676 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-13913G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084676 | |||||||
| chr1:166084793 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.264-14030G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084793 | |||||||
| chr1:166084884 | G | A | 5 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(2): Show |
5 | HG02258.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-14121C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084884 | |||||||
| chr1:166084907 | A | G | 2 | a0001c0001t0023g0293 a0001c0002t0005g0296 |
2 | HG00544.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.264-14144T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084907 | |||||||
| chr1:166084938 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0002g0247 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.264-14175C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084938 | |||||||
| chr1:166084945 | C | A | 1 | a0001c0001t0002g0268 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.264-14182G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084945 | |||||||
| chr1:166084951 | G | T | 1 | a0001c0001t0002g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.264-14188C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084951 | |||||||
| chr1:166084978 | T | G | 70 | a0001c0001t0001g0059 a0001c0001t0001g0106 a0001c0001t0001g0193 others(67): Show |
71 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.264-14215A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084978 | |||||||
| chr1:166085230 | C | T | 2 | a0001c0002t0010g0123 a0001c0002t0010g0124 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.264-14467G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085230 | |||||||
| chr1:166085409 | A | C | 211 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.264-14646T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085409 | |||||||
| chr1:166085478 | A | C | 1 | a0001c0001t0004g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.264-14715T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085478 | |||||||
| chr1:166085531 | G | A | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.264-14768C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085531 | |||||||
| chr1:166085661 | A | C | 7 | a0001c0001t0002g0210 a0001c0002t0003g0196 a0001c0002t0003g0201 others(4): Show |
7 | HG00140.hp1 HG01081.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-14898T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085661 | |||||||
| chr1:166085857 | T | C | 1 | a0001c0002t0003g0202 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.264-15094A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085857 | |||||||
| chr1:166086073 | C | CT | 17 | a0001c0001t0001g0120 a0001c0001t0001g0132 a0001c0001t0001g0144 others(14): Show |
17 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-15311dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086073 | |||||||
| chr1:166086073 | CT | C | 6 | a0001c0001t0001g0086 a0001c0001t0001g0126 a0001c0001t0001g0134 others(3): Show |
6 | HG01515.hp2 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-15311delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086073 | |||||||
| chr1:166086082 | T | C | 1 | a0001c0001t0002g0268 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.264-15319A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086082 | |||||||
| chr1:166086096 | A | G | 2 | a0001c0001t0023g0293 a0001c0002t0005g0296 |
2 | HG00544.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.264-15333T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086096 | |||||||
| chr1:166086156 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.264-15393C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086156 | |||||||
| chr1:166086261 | C | T | 1 | a0001c0002t0003g0114 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.264-15498G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086261 | |||||||
| chr1:166086273 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.264-15510A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086273 | |||||||
| chr1:166086285 | C | T | 1 | a0001c0002t0003g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.264-15522G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086285 | |||||||
| chr1:166086336 | CAAAG | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0101 others(2): Show |
5 | HG01257.hp1 HG01943.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-15577_264-1557 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086336 | |||||||
| chr1:166086472 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.264-15709C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086472 | |||||||
| chr1:166086504 | G | T | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-15741C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086504 | |||||||
| chr1:166086771 | A | G | 1 | a0001c0001t0014g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.264-16008T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086771 | |||||||
| chr1:166086838 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0178 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.264-16075G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086838 | |||||||
| chr1:166086879 | G | A | 1 | a0001c0001t0013g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.264-16116C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086879 | |||||||
| chr1:166087063 | C | T | 1 | a0001c0001t0006g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.264-16300G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087063 | |||||||
| chr1:166087071 | AT | A | 13 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(10): Show |
16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-16309delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087071 | |||||||
| chr1:166087210 | C | T | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-16447G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087210 | |||||||
| chr1:166087342 | C | T | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-16579G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087342 | |||||||
| chr1:166087576 | G | GT | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-16814dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087576 | |||||||
| chr1:166087657 | T | C | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-16894A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087657 | |||||||
| chr1:166087917 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.264-17154A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087917 | |||||||
| chr1:166088128 | C | T | 1 | a0001c0001t0004g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.264-17365G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088128 | |||||||
| chr1:166088137 | G | T | 2 | a0001c0001t0001g0271 a0001c0001t0002g0247 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.264-17374C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088137 | |||||||
| chr1:166088261 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.264-17498G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088261 | |||||||
| chr1:166088327 | T | C | 32 | a0001c0001t0001g0189 a0001c0001t0001g0197 a0001c0001t0001g0198 others(29): Show |
33 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.264-17564A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088327 | |||||||
| chr1:166088633 | C | T | 73 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0193 others(70): Show |
74 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.264-17870G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088633 | |||||||
| chr1:166088680 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.264-17917G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088680 | |||||||
| chr1:166088779 | C | G | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-18016G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088779 | |||||||
| chr1:166088872 | A | T | 1 | a0001c0002t0003g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.264-18109T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088872 | |||||||
| chr1:166089175 | C | A | 1 | a0001c0001t0008g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.264-18412G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089175 | |||||||
| chr1:166089340 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0100 a0001c0002t0003g0064 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-18577G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089340 | |||||||
| chr1:166089412 | C | T | 1 | a0001c0001t0014g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.264-18649G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089412 | |||||||
| chr1:166089520 | G | C | 3 | a0001c0002t0003g0196 a0001c0002t0003g0201 a0001c0002t0003g0202 |
3 | HG01081.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.264-18757C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089520 | |||||||
| chr1:166089615 | AG | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-18853delC | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089615 | |||||||
| chr1:166089861 | G | A | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-19098C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089861 | |||||||
| chr1:166089917 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
6 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-19154C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089917 | |||||||
| chr1:166090275 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-19512C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166090275 | |||||||
| chr1:166090288 | A | AACAT | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-19529_264-1952 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166090288 | |||||||
| chr1:166090569 | CA | C | 11 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.264-19807delT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166090569 | |||||||
| chr1:166090788 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.264-20025G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166090788 | |||||||
| chr1:166091256 | G | C | 1 | a0001c0002t0003g0280 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.264-20493C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091256 | |||||||
| chr1:166091317 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264-20554A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091317 | |||||||
| chr1:166091392 | G | A | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.264-20629C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091392 | |||||||
| chr1:166091675 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-20912G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091675 | |||||||
| chr1:166091717 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-20954C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091717 | |||||||
| chr1:166091841 | A | G | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-21078T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091841 | |||||||
| chr1:166092032 | A | ATTT | 64 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0193 others(61): Show |
65 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.264-21272_264-2127 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092032 | |||||||
| chr1:166092032 | AT | A | 201 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.264-21270delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092032 | |||||||
| chr1:166092032 | ATT | A | 20 | a0001c0001t0002g0048 a0001c0001t0002g0192 a0001c0001t0006g0075 others(17): Show |
23 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.264-21271_264-2127 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092032 | |||||||
| chr1:166092218 | A | G | 4 | a0001c0001t0004g0016 a0001c0001t0009g0041 a0001c0001t0009g0291 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-21455T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092218 | |||||||
| chr1:166092757 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0161 |
2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.264-21994A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092757 | |||||||
| chr1:166092952 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.264-22189G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092952 | |||||||
| chr1:166092963 | C | T | 1 | a0001c0002t0001g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.264-22200G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092963 | |||||||
| chr1:166093025 | A | G | 18 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(15): Show |
19 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.264-22262T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093025 | |||||||
| chr1:166093060 | A | T | 297 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(294): Show |
309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.264-22297T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093060 | |||||||
| chr1:166093061 | A | T | 1 | a0001c0002t0003g0284 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.264-22298T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093061 | |||||||
| chr1:166093355 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0002g0128 |
2 | HG01175.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.264-22592T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093355 | |||||||
| chr1:166093588 | A | G | 4 | a0001c0001t0004g0016 a0001c0001t0009g0041 a0001c0001t0009g0291 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-22825T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093588 | |||||||
| chr1:166093598 | G | A | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-22835C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093598 | |||||||
| chr1:166093750 | CT | C | 12 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0102 others(9): Show |
12 | HG01168.hp2 HG01257.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-22988delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093750 | |||||||
| chr1:166093840 | T | C | 1 | a0001c0002t0003g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.264-23077A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093840 | |||||||
| chr1:166094003 | C | CTG | 25 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0197 others(22): Show |
26 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.264-23242_264-2324 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTG | 14 | a0001c0001t0001g0198 a0001c0001t0001g0203 a0001c0001t0001g0211 others(11): Show |
14 | HG00140.hp1 HG00741.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.264-23244_264-2324 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTG | 13 | a0001c0001t0001g0175 a0001c0001t0004g0002 a0001c0001t0004g0018 others(10): Show |
14 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.264-23246_264-2324 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(3): Show |
5 | a0001c0001t0002g0223 a0001c0001t0002g0257 a0001c0001t0002g0259 others(2): Show |
5 | HG02055.hp2 HG02083.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-23250_264-2324 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(5): Show |
5 | a0001c0001t0001g0190 a0001c0001t0001g0252 a0001c0001t0002g0048 others(2): Show |
5 | HG01255.hp2 HG02280.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-23252_264-2324 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(7): Show |
6 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0255 others(3): Show |
6 | HG00423.hp1 HG00673.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-23254_264-2324 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(9): Show |
6 | a0001c0001t0001g0188 a0001c0001t0001g0246 a0001c0001t0002g0230 others(3): Show |
6 | HG02257.hp1 HG03209.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-23256_264-2324 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(11): Show |
10 | a0001c0001t0001g0218 a0001c0001t0001g0241 a0001c0001t0001g0251 others(7): Show |
10 | HG01175.hp1 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-23258_264-2324 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(13): Show |
6 | a0001c0001t0001g0277 a0001c0001t0002g0009 a0001c0001t0002g0222 others(3): Show |
7 | HG00609.hp1 HG02040.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-23260_264-2324 others(24): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(15): Show |
13 | a0001c0001t0001g0059 a0001c0001t0001g0219 a0001c0001t0001g0242 others(10): Show |
13 | HG00597.hp2 HG00621.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-23262_264-2324 others(26): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(17): Show |
7 | a0001c0001t0001g0271 a0001c0001t0002g0220 a0001c0001t0002g0240 others(4): Show |
7 | HG01106.hp1 HG02451.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-23264_264-2324 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(19): Show |
10 | a0001c0001t0001g0084 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG00558.hp2 HG01071.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-23266_264-2324 others(30): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(21): Show |
4 | a0001c0001t0001g0238 a0001c0001t0002g0216 a0001c0001t0002g0228 others(1): Show |
4 | HG01069.hp1 HG01952.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-23268_264-2324 others(32): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(23): Show |
4 | a0001c0001t0001g0256 a0001c0001t0002g0213 a0001c0001t0002g0227 others(1): Show |
4 | HG01358.hp2 NA19083.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-23270_264-2324 others(34): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(25): Show |
1 | a0001c0001t0008g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.264-23272_264-2324 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | C | CTGTGTGT others(27): Show |
1 | a0001c0001t0002g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.264-23274_264-2324 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | CTG | C | 21 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0154 others(18): Show |
25 | HG00140.hp2 HG01070.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.264-23242_264-2324 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | CTGTGTGT others(3): Show |
C | 1 | a0001c0002t0005g0295 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.264-23250_264-2324 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094003 | CTGTGTGT others(9): Show |
C | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-23256_264-2324 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | |||||||
| chr1:166094035 | G | C | 124 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
129 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.264-23272C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094035 | |||||||
| chr1:166094035 | G | GTC | 13 | a0001c0001t0001g0079 a0001c0001t0001g0141 a0001c0001t0001g0145 others(10): Show |
13 | HG00323.hp2 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-23273_264-2327 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094035 | |||||||
| chr1:166094047 | G | GTGTGTGT others(10): Show |
1 | a0001c0001t0002g0269 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.264-23285_264-2328 others(21): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094047 | |||||||
| chr1:166094047 | G | GTGTGTGT others(14): Show |
1 | a0001c0001t0002g0263 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.264-23285_264-2328 others(25): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094047 | |||||||
| chr1:166094047 | G | GTGTGTGT others(18): Show |
1 | a0001c0001t0002g0215 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.264-23285_264-2328 others(29): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094047 | |||||||
| chr1:166094052 | T | A | 1 | a0001c0002t0003g0184 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.264-23289A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094052 | |||||||
| chr1:166094397 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0149 |
4 | HG00639.hp1 HG01261.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-23634G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094397 | |||||||
| chr1:166094417 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0016g0095 |
2 | NA18971.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.264-23654A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094417 | |||||||
| chr1:166094419 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.264-23656A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094419 | |||||||
| chr1:166094606 | G | T | 4 | a0001c0001t0004g0016 a0001c0001t0009g0041 a0001c0001t0009g0291 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-23843C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094606 | |||||||
| chr1:166094607 | A | G | 20 | a0001c0001t0002g0048 a0001c0001t0004g0002 a0001c0001t0004g0017 others(17): Show |
21 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.264-23844T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094607 | |||||||
| chr1:166094620 | G | C | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-23857C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094620 | |||||||
| chr1:166094750 | C | G | 6 | a0001c0001t0001g0279 a0001c0002t0003g0010 a0001c0002t0003g0280 others(3): Show |
7 | HG00438.hp2 NA18960.hp1 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-23987G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094750 | |||||||
| chr1:166094778 | C | T | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-24015G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094778 | |||||||
| chr1:166095016 | G | C | 17 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-24253C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095016 | |||||||
| chr1:166095199 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0134 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.264-24436G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095199 | |||||||
| chr1:166095252 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.264-24489C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095252 | |||||||
| chr1:166095765 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-25002C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095765 | |||||||
| chr1:166095824 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-25061G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095824 | |||||||
| chr1:166095830 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-25067C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095830 | |||||||
| chr1:166095908 | C | A | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-25145G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095908 | |||||||
| chr1:166096116 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.264-25353T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096116 | |||||||
| chr1:166096164 | C | T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0116 a0001c0001t0001g0147 others(1): Show |
4 | HG02071.hp2 NA18747.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-25401G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096164 | |||||||
| chr1:166096201 | T | A | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-25438A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096201 | |||||||
| chr1:166096330 | T | C | 3 | a0001c0001t0009g0041 a0001c0001t0009g0291 a0001c0001t0009g0292 |
3 | HG02451.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.264-25567A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096330 | |||||||
| chr1:166096448 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.264-25685G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096448 | |||||||
| chr1:166096493 | T | TTTG | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-25733_264-2573 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096493 | |||||||
| chr1:166096529 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.264-25766T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096529 | |||||||
| chr1:166096589 | A | G | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.264-25826T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096589 | |||||||
| chr1:166096677 | G | T | 17 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-25914C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096677 | |||||||
| chr1:166096685 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.264-25922G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096685 | |||||||
| chr1:166096852 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26089C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096852 | |||||||
| chr1:166096869 | C | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26106G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096869 | |||||||
| chr1:166096871 | G | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.264-26108C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096871 | |||||||
| chr1:166096929 | G | A | 4 | a0001c0001t0004g0016 a0001c0001t0009g0041 a0001c0001t0009g0291 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-26166C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096929 | |||||||
| chr1:166097138 | C | T | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-26375G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097138 | |||||||
| chr1:166097258 | T | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26495A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097258 | |||||||
| chr1:166097434 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26671G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097434 | |||||||
| chr1:166097444 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.264-26681C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097444 | |||||||
| chr1:166097557 | GACCA | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26798_264-2679 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097557 | |||||||
| chr1:166097579 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.264-26816G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097579 | |||||||
| chr1:166097580 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0155 others(1): Show |
5 | HG00423.hp2 NA18970.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-26817C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097580 | |||||||
| chr1:166098001 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0002g0171 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.264-27238G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098001 | |||||||
| chr1:166098091 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-27328C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098091 | |||||||
| chr1:166098255 | T | G | 2 | a0001c0001t0004g0030 a0001c0002t0011g0023 |
2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.264-27492A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098255 | |||||||
| chr1:166098338 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.264-27575G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098338 | |||||||
| chr1:166098341 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.264-27578G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098341 | |||||||
| chr1:166098383 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.264-27620C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098383 | |||||||
| chr1:166098569 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-27806A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098569 | |||||||
| chr1:166098621 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-27858G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098621 | |||||||
| chr1:166098769 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28006G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098769 | |||||||
| chr1:166098900 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-28137A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098900 | |||||||
| chr1:166098915 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28152C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098915 | |||||||
| chr1:166098916 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-28153T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098916 | |||||||
| chr1:166098959 | T | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.264-28196A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098959 | |||||||
| chr1:166098986 | C | T | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-28223G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098986 | |||||||
| chr1:166099054 | G | A | 1 | a0001c0001t0018g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.264-28291C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099054 | |||||||
| chr1:166099079 | G | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28316C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099079 | |||||||
| chr1:166099469 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28706C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099469 | |||||||
| chr1:166099476 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.264-28713G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099476 | |||||||
| chr1:166099499 | CAACT | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0049 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-28740_264-2873 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099499 | |||||||
| chr1:166099537 | A | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28774T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099537 | |||||||
| chr1:166099597 | G | A | 21 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0101 others(18): Show |
22 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.264-28834C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099597 | |||||||
| chr1:166099610 | A | G | 1 | a0001c0001t0025g0306 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.264-28847T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099610 | |||||||
| chr1:166099645 | A | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28882T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099645 | |||||||
| chr1:166099650 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.264-28887A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099650 | |||||||
| chr1:166099668 | AACAG | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-28909_264-2890 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099668 | |||||||
| chr1:166099787 | T | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-29024A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099787 | |||||||
| chr1:166099860 | C | T | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-29097G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099860 | |||||||
| chr1:166100156 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.264-29393A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100156 | |||||||
| chr1:166100262 | G | T | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.264-29499C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100262 | |||||||
| chr1:166100309 | C | T | 90 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(87): Show |
94 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.264-29546G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100309 | |||||||
| chr1:166100405 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.264-29642G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100405 | |||||||
| chr1:166100413 | T | C | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-29650A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100413 | |||||||
| chr1:166100443 | C | A | 3 | a0001c0001t0001g0238 a0001c0001t0001g0242 a0001c0001t0001g0256 |
3 | NA18987.hp1 NA18991.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.264-29680G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100443 | |||||||
| chr1:166100522 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-29759G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100522 | |||||||
| chr1:166100524 | G | A | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.264-29761C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100524 | |||||||
| chr1:166100547 | C | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-29784G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100547 | |||||||
| chr1:166100552 | G | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0149 |
4 | HG00639.hp1 HG01261.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-29789C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100552 | |||||||
| chr1:166100674 | C | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-29911G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100674 | |||||||
| chr1:166100718 | C | A | 1 | a0001c0002t0001g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.264-29955G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100718 | |||||||
| chr1:166100719 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.264-29956G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100719 | |||||||
| chr1:166101036 | A | G | 6 | a0001c0001t0001g0144 a0001c0002t0003g0111 a0001c0002t0003g0113 others(3): Show |
6 | HG00438.hp1 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-30273T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101036 | |||||||
| chr1:166101059 | G | A | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0060 |
3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-30296C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101059 | |||||||
| chr1:166101133 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-30370G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101133 | |||||||
| chr1:166101282 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.264-30519G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101282 | |||||||
| chr1:166101462 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.264-30699T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101462 | |||||||
| chr1:166101502 | G | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-30739C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101502 | |||||||
| chr1:166101527 | A | C | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-30764T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101527 | |||||||
| chr1:166101642 | A | T | 1 | a0001c0001t0002g0243 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.264-30879T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101642 | |||||||
| chr1:166101731 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.264-30968C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101731 | |||||||
| chr1:166101796 | TC | T | 6 | a0001c0002t0003g0107 a0001c0002t0003g0108 a0001c0002t0003g0109 others(3): Show |
6 | HG00642.hp2 HG00741.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-31034delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101796 | |||||||
| chr1:166101877 | C | T | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-31114G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101877 | |||||||
| chr1:166101880 | G | T | 1 | a0001c0001t0012g0012 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.264-31117C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101880 | |||||||
| chr1:166101906 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-31143C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101906 | |||||||
| chr1:166101931 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0134 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.264-31168T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101931 | |||||||
| chr1:166101993 | A | G | 1 | a0001c0002t0003g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.264-31230T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101993 | |||||||
| chr1:166102013 | G | A | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-31250C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102013 | |||||||
| chr1:166102032 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0155 a0001c0001t0002g0146 |
4 | NA18970.hp2 NA18977.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-31269T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102032 | |||||||
| chr1:166102273 | G | A | 2 | a0001c0001t0002g0223 a0001c0001t0002g0257 |
2 | HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.264-31510C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102273 | |||||||
| chr1:166102335 | C | A | 1 | a0001c0001t0002g0192 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.264-31572G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102335 | |||||||
| chr1:166102366 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-31603C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102366 | |||||||
| chr1:166102366 | G | T | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31603C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102366 | |||||||
| chr1:166102374 | A | T | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31611T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102374 | |||||||
| chr1:166102375 | A | G | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31612T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102375 | |||||||
| chr1:166102393 | A | G | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31630T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102393 | |||||||
| chr1:166102422 | A | T | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31659T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102422 | |||||||
| chr1:166102432 | G | A | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31669C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102432 | |||||||
| chr1:166102463 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-31700C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102463 | |||||||
| chr1:166102463 | G | T | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31700C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102463 | |||||||
| chr1:166102469 | T | C | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31706A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102469 | |||||||
| chr1:166102470 | C | A | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31707G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102470 | |||||||
| chr1:166102473 | T | C | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31710A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102473 | |||||||
| chr1:166102481 | A | C | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31718T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102481 | |||||||
| chr1:166102493 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-31730T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102493 | |||||||
| chr1:166102663 | C | A | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-31900G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102663 | |||||||
| chr1:166102673 | A | G | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-31910T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102673 | |||||||
| chr1:166102756 | A | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-31993T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102756 | |||||||
| chr1:166102757 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-31994G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102757 | |||||||
| chr1:166102799 | T | C | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-32036A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102799 | |||||||
| chr1:166102823 | T | C | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-32060A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102823 | |||||||
| chr1:166102852 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-32089C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102852 | |||||||
| chr1:166102853 | C | T | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-32090G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102853 | |||||||
| chr1:166102854 | A | G | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-32091T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102854 | |||||||
| chr1:166102918 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-32155G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102918 | |||||||
| chr1:166103118 | G | A | 2 | a0001c0001t0023g0293 a0001c0002t0005g0296 |
2 | HG00544.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.264-32355C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103118 | |||||||
| chr1:166103153 | C | A | 1 | a0001c0002t0003g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.264-32390G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103153 | |||||||
| chr1:166103171 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0002g0171 a0001c0002t0022g0125 |
3 | HG02280.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.264-32408T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103171 | |||||||
| chr1:166103256 | G | T | 2 | a0001c0001t0007g0037 a0001c0001t0014g0036 |
2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.264-32493C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103256 | |||||||
| chr1:166103350 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0002g0171 a0001c0002t0022g0125 |
3 | HG02280.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.264-32587C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103350 | |||||||
| chr1:166103450 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-32687G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103450 | |||||||
| chr1:166103481 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0129 a0001c0001t0025g0306 |
4 | HG00735.hp1 HG01192.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-32718C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103481 | |||||||
| chr1:166103656 | G | A | 2 | a0001c0001t0001g0175 a0001c0002t0001g0212 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.264-32893C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103656 | |||||||
| chr1:166103679 | G | A | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.264-32916C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103679 | |||||||
| chr1:166103719 | C | T | 67 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0193 others(64): Show |
68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.264-32956G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103719 | |||||||
| chr1:166103745 | T | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-32982A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103745 | |||||||
| chr1:166103772 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.264-33009G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103772 | |||||||
| chr1:166103772 | C | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33009G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103772 | |||||||
| chr1:166103789 | T | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33026A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103789 | |||||||
| chr1:166103922 | A | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33159T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103922 | |||||||
| chr1:166103970 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-33207G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103970 | |||||||
| chr1:166103972 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.264-33209C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103972 | |||||||
| chr1:166103989 | C | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-33226G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103989 | |||||||
| chr1:166104127 | G | C | 1 | a0001c0001t0002g0259 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.264-33364C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104127 | |||||||
| chr1:166104137 | T | C | 1 | a0001c0002t0003g0114 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.264-33374A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104137 | |||||||
| chr1:166104287 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-33524G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104287 | |||||||
| chr1:166104288 | T | G | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-33525A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104288 | |||||||
| chr1:166104319 | G | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33556C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104319 | |||||||
| chr1:166104322 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.264-33559G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104322 | |||||||
| chr1:166104379 | T | A | 92 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(89): Show |
96 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.264-33616A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104379 | |||||||
| chr1:166104498 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.264-33735A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104498 | |||||||
| chr1:166104575 | GC | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33813delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104575 | |||||||
| chr1:166104657 | G | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33894C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104657 | |||||||
| chr1:166104673 | C | A | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-33910G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104673 | |||||||
| chr1:166104733 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-33970A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104733 | |||||||
| chr1:166104735 | C | T | 10 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0101 others(7): Show |
11 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-33972G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104735 | |||||||
| chr1:166104792 | T | C | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0060 |
3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-34029A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104792 | |||||||
| chr1:166104897 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-34134C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104897 | |||||||
| chr1:166104910 | A | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-34147T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104910 | |||||||
| chr1:166105086 | C | G | 5 | a0001c0001t0001g0203 a0001c0001t0004g0016 a0001c0001t0009g0041 others(2): Show |
5 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-34323G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105086 | |||||||
| chr1:166105096 | C | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-34333G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105096 | |||||||
| chr1:166105101 | G | A | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-34338C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105101 | |||||||
| chr1:166105111 | T | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-34348A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105111 | |||||||
| chr1:166105282 | C | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-34519G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105282 | |||||||
| chr1:166105400 | C | T | 67 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0193 others(64): Show |
68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.264-34637G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105400 | |||||||
| chr1:166105405 | A | G | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-34642T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105405 | |||||||
| chr1:166105486 | A | G | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-34723T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105486 | |||||||
| chr1:166105499 | A | C | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-34736T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105499 | |||||||
| chr1:166105541 | C | T | 19 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.264-34778G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105541 | |||||||
| chr1:166105682 | T | C | 7 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0229 others(4): Show |
7 | HG00642.hp1 HG01257.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-34919A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105682 | |||||||
| chr1:166105751 | G | C | 1 | a0001c0002t0022g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.264-34988C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105751 | |||||||
| chr1:166105906 | C | T | 92 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(89): Show |
96 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.264-35143G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105906 | |||||||
| chr1:166105986 | C | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0001g0147 |
3 | HG02922.hp2 HG03195.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.264-35223G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105986 | |||||||
| chr1:166106054 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.264-35291A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106054 | |||||||
| chr1:166106101 | C | G | 4 | a0001c0001t0001g0115 a0001c0001t0001g0140 a0001c0001t0001g0145 others(1): Show |
4 | HG02155.hp2 HG02165.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-35338G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106101 | |||||||
| chr1:166106123 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0002g0247 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.264-35360C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106123 | |||||||
| chr1:166106148 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-35385A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106148 | |||||||
| chr1:166106155 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-35392C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106155 | |||||||
| chr1:166106194 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-35431G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106194 | |||||||
| chr1:166106203 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-35440A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106203 | |||||||
| chr1:166106349 | T | TA | 74 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(71): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.264-35587dupT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106349 | |||||||
| chr1:166106409 | A | G | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.264-35646T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106409 | |||||||
| chr1:166106446 | A | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.264-35683T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106446 | |||||||
| chr1:166106514 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-35751A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106514 | |||||||
| chr1:166106549 | A | G | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0060 |
3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-35786T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106549 | |||||||
| chr1:166106646 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-35883G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106646 | |||||||
| chr1:166106806 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-36043A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106806 | |||||||
| chr1:166106843 | G | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-36080C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106843 | |||||||
| chr1:166106858 | A | T | 1 | a0001c0001t0002g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.264-36095T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106858 | |||||||
| chr1:166107162 | G | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-36399C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107162 | |||||||
| chr1:166107330 | C | T | 11 | a0001c0001t0001g0252 a0001c0001t0002g0227 a0001c0001t0002g0228 others(8): Show |
11 | HG00642.hp1 HG01257.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-36567G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107330 | |||||||
| chr1:166107341 | T | C | 1 | a0001c0001t0006g0179 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.264-36578A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107341 | |||||||
| chr1:166107356 | A | G | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-36593T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107356 | |||||||
| chr1:166107595 | G | C | 1 | a0001c0001t0002g0192 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.264-36832C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107595 | |||||||
| chr1:166107631 | A | T | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-36868T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107631 | |||||||
| chr1:166107653 | T | C | 1 | a0001c0002t0005g0303 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.264-36890A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107653 | |||||||
| chr1:166107682 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(11): Show |
16 | HG00323.hp2 HG00558.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-36919T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107682 | |||||||
| chr1:166108015 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.264-37252G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108015 | |||||||
| chr1:166108316 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.264-37553C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108316 | |||||||
| chr1:166108334 | C | G | 4 | a0001c0001t0004g0016 a0001c0001t0009g0041 a0001c0001t0009g0291 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-37571G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108334 | |||||||
| chr1:166108351 | T | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-37588A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108351 | |||||||
| chr1:166108360 | A | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-37597T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108360 | |||||||
| chr1:166108383 | C | G | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG00597.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.264-37620G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108383 | |||||||
| chr1:166108674 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-37911G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108674 | |||||||
| chr1:166109044 | A | G | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-38281T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109044 | |||||||
| chr1:166109176 | A | G | 3 | a0001c0001t0004g0017 a0001c0001t0004g0031 a0001c0001t0004g0032 |
3 | HG02451.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.264-38413T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109176 | |||||||
| chr1:166109482 | T | C | 1 | a0001c0002t0003g0113 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.264-38719A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109482 | |||||||
| chr1:166109516 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0122 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.264-38753C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109516 | |||||||
| chr1:166109566 | G | A | 67 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0193 others(64): Show |
68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.264-38803C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109566 | |||||||
| chr1:166109655 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.264-38892T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109655 | |||||||
| chr1:166109806 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.264-39043C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109806 | |||||||
| chr1:166109806 | GTATATAT others(83): Show |
G | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-39133_264-3904 others(94): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109806 | |||||||
| chr1:166109812 | A | ATG | 3 | a0001c0001t0001g0189 a0001c0001t0002g0131 a0001c0001t0004g0002 |
3 | HG03453.hp2 HG04204.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264-39051_264-3905 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109812 | |||||||
| chr1:166109814 | G | GTA | 13 | a0001c0001t0001g0066 a0001c0001t0001g0079 a0001c0001t0001g0101 others(10): Show |
13 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-39053_264-3905 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | |||||||
| chr1:166109814 | G | GTATA | 5 | a0001c0001t0001g0136 a0001c0001t0021g0207 a0001c0002t0003g0195 others(2): Show |
5 | HG00738.hp1 HG02647.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-39055_264-3905 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | |||||||
| chr1:166109814 | GTATATAT others(29): Show |
G | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0060 |
3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-39087_264-3905 others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | |||||||
| chr1:166109814 | GTATATAT others(51): Show |
G | 3 | a0001c0001t0001g0042 a0001c0001t0002g0223 a0001c0001t0002g0257 |
3 | HG03492.hp1 HG03540.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.264-39109_264-3905 others(62): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | |||||||
| chr1:166109814 | GTATATAT others(81): Show |
G | 2 | a0001c0001t0002g0248 a0001c0002t0003g0261 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.264-39139_264-3905 others(92): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | |||||||
| chr1:166109816 | A | G | 29 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(26): Show |
30 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-39053T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109816 | |||||||
| chr1:166109816 | ATATATAT others(59): Show |
A | 1 | a0001c0001t0002g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.264-39119_264-3905 others(70): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109816 | |||||||
| chr1:166109818 | A | G | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-39055T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109818 | |||||||
| chr1:166109818 | ATATATAT others(43): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.264-39105_264-3905 others(54): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109818 | |||||||
| chr1:166109820 | ATATATAT others(35): Show |
A | 1 | a0001c0001t0001g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.264-39099_264-3905 others(46): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109820 | |||||||
| chr1:166109822 | ATATATAT others(11): Show |
A | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-39077_264-3906 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109822 | |||||||
| chr1:166109822 | ATATATAT others(37): Show |
A | 6 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0002g0009 others(3): Show |
6 | HG00609.hp1 HG01069.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-39103_264-3906 others(48): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109822 | |||||||
| chr1:166109824 | A | ATATATAT others(105): Show |
1 | a0001c0001t0001g0094 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.264-39062_264-3906 others(116): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109824 | |||||||
| chr1:166109824 | A | G | 62 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(59): Show |
62 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-39061T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109824 | |||||||
| chr1:166109826 | ATATATGT others(49): Show |
A | 2 | a0001c0001t0001g0047 a0001c0001t0002g0048 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.264-39119_264-3906 others(60): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109826 | |||||||
| chr1:166109828 | ATATG | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0097 a0001c0001t0007g0003 others(1): Show |
4 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39069_264-3906 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109828 | |||||||
| chr1:166109828 | ATATGTAT others(5): Show |
A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39077_264-3906 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109828 | |||||||
| chr1:166109828 | ATATGTAT others(33): Show |
A | 5 | a0001c0001t0001g0233 a0001c0001t0001g0252 a0001c0001t0001g0271 others(2): Show |
5 | HG01106.hp1 HG01255.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39105_264-3906 others(44): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109828 | |||||||
| chr1:166109828 | ATATGTAT others(47): Show |
A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0049 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39119_264-3906 others(58): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109828 | |||||||
| chr1:166109830 | ATG | A | 5 | a0001c0001t0001g0139 a0001c0001t0002g0103 a0001c0001t0006g0071 others(2): Show |
5 | HG00140.hp2 HG00738.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39069_264-3906 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109830 | |||||||
| chr1:166109830 | ATGTATAT others(31): Show |
A | 13 | a0001c0001t0001g0193 a0001c0001t0001g0241 a0001c0001t0001g0274 others(10): Show |
13 | HG00673.hp2 HG01257.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-39105_264-3906 others(42): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109830 | |||||||
| chr1:166109830 | ATGTATAT others(53): Show |
A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0265 a0001c0001t0001g0266 |
3 | HG00597.hp2 HG02615.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.264-39127_264-3906 others(64): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109830 | |||||||
| chr1:166109831 | T | C | 35 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0219 others(32): Show |
35 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.264-39068A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109831 | |||||||
| chr1:166109832 | G | A | 231 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
238 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.264-39069C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109832 | |||||||
| chr1:166109837 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.264-39074A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109837 | |||||||
| chr1:166109838 | A | ATATG | 13 | a0001c0001t0001g0197 a0001c0001t0001g0279 a0001c0001t0001g0286 others(10): Show |
13 | HG00140.hp1 HG00673.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-39076_264-3907 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109838 | |||||||
| chr1:166109840 | G | A | 226 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
234 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.264-39077C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109840 | |||||||
| chr1:166109841 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39078A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109841 | |||||||
| chr1:166109842 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0004g0002 |
2 | HG02074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264-39079T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109842 | |||||||
| chr1:166109843 | T | C | 4 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(1): Show |
4 | HG01433.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39080A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109843 | |||||||
| chr1:166109844 | A | G | 2 | a0001c0001t0001g0133 a0001c0002t0001g0061 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.264-39081T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109844 | |||||||
| chr1:166109846 | A | ATGTATG | 4 | a0001c0001t0004g0017 a0001c0001t0004g0022 a0001c0001t0004g0031 others(1): Show |
4 | HG02451.hp2 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39084_264-3908 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109846 | |||||||
| chr1:166109846 | A | G | 15 | a0001c0001t0004g0002 a0001c0001t0004g0018 a0001c0001t0004g0019 others(12): Show |
16 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-39083T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109846 | |||||||
| chr1:166109848 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0181 a0001c0002t0001g0061 |
3 | HG03209.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.264-39085T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109848 | |||||||
| chr1:166109850 | A | G | 26 | a0001c0001t0001g0133 a0001c0001t0001g0154 a0001c0001t0001g0187 others(23): Show |
27 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.264-39087T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109850 | |||||||
| chr1:166109852 | A | ATGTG | 18 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0004g0002 others(15): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-39090_264-3908 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109852 | |||||||
| chr1:166109852 | A | G | 11 | a0001c0001t0001g0096 a0001c0001t0001g0181 a0001c0001t0001g0190 others(8): Show |
11 | HG01167.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-39089T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109852 | |||||||
| chr1:166109854 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0147 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.264-39092_264-3909 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | |||||||
| chr1:166109854 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0161 |
2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.264-39092_264-3909 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | |||||||
| chr1:166109854 | A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0115 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.264-39092_264-3909 others(50): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | |||||||
| chr1:166109854 | A | ATG | 10 | a0001c0001t0001g0085 a0001c0001t0001g0099 a0001c0001t0001g0100 others(7): Show |
10 | HG00609.hp2 HG00741.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.264-39092_264-3909 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | |||||||
| chr1:166109854 | A | ATGTATG | 5 | a0001c0001t0001g0086 a0001c0001t0001g0137 a0001c0001t0002g0073 others(2): Show |
5 | HG01358.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39092_264-3909 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | |||||||
| chr1:166109854 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0069 a0001c0001t0001g0078 others(13): Show |
16 | HG00544.hp2 HG01074.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.264-39091T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | |||||||
| chr1:166109854 | ATATATAT others(21): Show |
A | 5 | a0001c0001t0001g0242 a0001c0001t0001g0244 a0001c0001t0001g0273 others(2): Show |
5 | NA18941.hp2 NA18954.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-39119_264-3909 others(32): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | |||||||
| chr1:166109854 | ATATATAT others(29): Show |
A | 10 | a0001c0001t0001g0238 a0001c0001t0001g0251 a0001c0001t0001g0256 others(7): Show |
10 | HG00621.hp2 HG01952.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.264-39127_264-3909 others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | |||||||
| chr1:166109856 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0162 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.264-39094_264-3909 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109856 | A | ATATATAT others(3): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0155 others(4): Show |
7 | HG00423.hp2 HG02155.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109856 | A | ATATGTAT others(3): Show |
9 | a0001c0001t0001g0070 a0001c0001t0001g0120 a0001c0001t0002g0172 others(6): Show |
9 | HG00558.hp1 HG00735.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109856 | A | ATATGTG | 20 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0145 others(17): Show |
20 | HG00597.hp1 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109856 | A | ATGTATGT others(1): Show |
10 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0065 others(7): Show |
10 | HG00735.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109856 | A | ATGTG | 17 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0040 others(14): Show |
18 | HG00639.hp1 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109856 | A | G | 29 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0001g0086 others(26): Show |
29 | HG00544.hp2 HG00609.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-39093T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109856 | ATATATGT others(19): Show |
A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0255 a0001c0001t0002g0263 others(1): Show |
4 | HG00423.hp1 HG00642.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39119_264-3909 others(30): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109856 | ATATATGT others(27): Show |
A | 8 | a0001c0001t0001g0219 a0001c0001t0002g0222 a0001c0001t0002g0237 others(5): Show |
8 | HG01175.hp1 HG02055.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-39127_264-3909 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | |||||||
| chr1:166109858 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0004g0016 others(1): Show |
4 | HG01070.hp2 HG01243.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39095T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109858 | |||||||
| chr1:166109858 | ATATGTAT others(25): Show |
A | 3 | a0001c0001t0001g0084 a0001c0002t0003g0165 a0001c0002t0003g0225 |
3 | HG00558.hp2 NA18949.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.264-39127_264-3909 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109858 | |||||||
| chr1:166109860 | A | G | 4 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0002g0171 others(1): Show |
4 | HG01243.hp1 HG02280.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39097T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109860 | |||||||
| chr1:166109860 | ATGTATGT others(15): Show |
A | 1 | a0001c0001t0002g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.264-39119_264-3909 others(26): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109860 | |||||||
| chr1:166109860 | ATGTATGT others(23): Show |
A | 4 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0230 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39127_264-3909 others(34): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109860 | |||||||
| chr1:166109862 | G | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
137 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.264-39099C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109862 | |||||||
| chr1:166109862 | G | GTGTATAT others(1): Show |
4 | a0001c0001t0001g0083 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG01433.hp2 NA18971.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39100_264-3909 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109862 | |||||||
| chr1:166109864 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0104 |
2 | HG01346.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.264-39101T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109864 | |||||||
| chr1:166109866 | G | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
108 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.264-39103C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109866 | |||||||
| chr1:166109866 | G | GTGTATAT others(5): Show |
11 | a0001c0001t0001g0007 a0001c0001t0001g0217 a0001c0001t0002g0080 others(8): Show |
11 | HG00323.hp1 HG00438.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-39115_264-3910 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109866 | |||||||
| chr1:166109868 | G | A | 34 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0094 others(31): Show |
35 | HG01192.hp2 HG01243.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.264-39105C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109868 | |||||||
| chr1:166109869 | T | C | 13 | a0001c0001t0001g0193 a0001c0001t0001g0241 a0001c0001t0001g0274 others(10): Show |
13 | HG00673.hp2 HG01257.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-39106A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109869 | |||||||
| chr1:166109870 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0006 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.264-39108_264-3910 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109870 | |||||||
| chr1:166109870 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0145 a0001c0001t0001g0159 |
3 | HG02165.hp1 NA18942.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.264-39107T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109870 | |||||||
| chr1:166109871 | T | C | 5 | a0001c0001t0001g0233 a0001c0001t0001g0252 a0001c0001t0001g0271 others(2): Show |
5 | HG01106.hp1 HG01255.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39108A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109871 | |||||||
| chr1:166109873 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.264-39110A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109873 | |||||||
| chr1:166109874 | A | ATATATGT others(13): Show |
3 | a0001c0001t0003g0194 a0001c0001t0006g0071 a0001c0001t0006g0130 |
3 | HG00140.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.264-39112_264-3911 others(24): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109874 | |||||||
| chr1:166109874 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0004g0016 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.264-39111T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109874 | |||||||
| chr1:166109875 | T | C | 6 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0002g0009 others(3): Show |
6 | HG00609.hp1 HG01069.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-39112A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109875 | |||||||
| chr1:166109876 | A | ATATG | 14 | a0001c0001t0001g0055 a0001c0001t0001g0066 a0001c0001t0001g0067 others(11): Show |
15 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-39114_264-3911 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109876 | |||||||
| chr1:166109876 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0104 a0001c0001t0004g0016 |
3 | HG01243.hp1 HG01346.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.264-39113T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109876 | |||||||
| chr1:166109878 | A | ATGTATAT others(17): Show |
2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG00323.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.264-39116_264-3911 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109878 | |||||||
| chr1:166109878 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.264-39115T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109878 | |||||||
| chr1:166109880 | ATG | A | 6 | a0001c0001t0001g0232 a0001c0001t0002g0009 a0001c0001t0002g0258 others(3): Show |
6 | HG00609.hp1 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-39119_264-3911 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109880 | |||||||
| chr1:166109881 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.264-39118A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109881 | |||||||
| chr1:166109882 | G | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0066 others(40): Show |
44 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.264-39119C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(25): Show |
1 | a0001c0002t0003g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(17): Show |
1 | a0001c0002t0003g0276 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.264-39120_264-3911 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(19): Show |
1 | a0001c0001t0021g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.264-39120_264-3911 others(30): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(23): Show |
3 | a0001c0001t0001g0286 a0001c0002t0003g0010 a0001c0002t0003g0039 |
3 | HG00438.hp2 HG00673.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(34): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(25): Show |
5 | a0001c0001t0001g0203 a0001c0002t0003g0010 a0001c0002t0003g0204 others(2): Show |
5 | HG02735.hp1 NA19003.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-39120_264-3911 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(27): Show |
4 | a0001c0002t0003g0200 a0001c0002t0003g0284 a0001c0002t0003g0285 others(1): Show |
4 | HG01074.hp1 HG02523.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39120_264-3911 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(29): Show |
2 | a0001c0001t0001g0282 a0001c0002t0003g0280 |
2 | HG02129.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(31): Show |
1 | a0001c0001t0001g0279 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(42): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(27): Show |
2 | a0001c0001t0002g0210 a0001c0002t0003g0209 |
2 | HG00140.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(29): Show |
3 | a0001c0001t0001g0197 a0001c0002t0003g0205 a0001c0002t0010g0206 |
3 | HG03239.hp1 HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(31): Show |
2 | a0001c0002t0003g0196 a0001c0002t0003g0202 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(42): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(33): Show |
1 | a0001c0002t0003g0201 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(44): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(25): Show |
1 | a0001c0002t0003g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(21): Show |
1 | a0001c0002t0003g0208 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.264-39120_264-3911 others(32): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0275 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(34): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTATATAT others(25): Show |
1 | a0001c0001t0001g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | G | GTGTATAT others(1): Show |
8 | a0001c0001t0001g0189 a0001c0001t0002g0169 a0001c0001t0007g0003 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-39120_264-3911 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109882 | GTATATAT others(9): Show |
G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39135_264-3912 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | |||||||
| chr1:166109885 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0049 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39122A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109885 | |||||||
| chr1:166109886 | A | ATATG | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(5): Show |
8 | HG01243.hp2 HG01358.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-39127_264-3912 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109886 | |||||||
| chr1:166109886 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.264-39123T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109886 | |||||||
| chr1:166109887 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0002g0048 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.264-39124A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109887 | |||||||
| chr1:166109889 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0002g0223 a0001c0001t0002g0257 |
3 | HG03492.hp1 HG03540.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.264-39126A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109889 | |||||||
| chr1:166109890 | G | A | 84 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.264-39127C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109890 | G | GTA | 18 | a0001c0001t0001g0065 a0001c0001t0001g0116 a0001c0001t0001g0122 others(15): Show |
18 | HG00544.hp2 HG00621.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-39129_264-3912 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109890 | G | GTATA | 5 | a0001c0001t0001g0070 a0001c0001t0001g0158 a0001c0001t0006g0072 others(2): Show |
5 | HG00323.hp1 HG00609.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-39131_264-3912 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109890 | G | GTATATA | 3 | a0001c0001t0002g0148 a0001c0001t0006g0075 a0001c0001t0006g0127 |
3 | HG00735.hp2 HG02004.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.264-39133_264-3912 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109890 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.264-39137_264-3912 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109890 | G | GTATGTA | 4 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0129 others(1): Show |
4 | HG00558.hp1 HG00735.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39128_264-3912 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109890 | GTA | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(51): Show |
55 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.264-39129_264-3912 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109890 | GTATA | G | 27 | a0001c0001t0001g0046 a0001c0001t0001g0187 a0001c0001t0001g0188 others(24): Show |
28 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.264-39131_264-3912 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109890 | GTATATA | G | 3 | a0001c0001t0002g0058 a0001c0001t0007g0003 a0001c0001t0018g0057 |
3 | HG01081.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.264-39133_264-3912 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | |||||||
| chr1:166109891 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0265 a0001c0001t0001g0266 |
3 | HG00597.hp2 HG02615.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.264-39128A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109891 | |||||||
| chr1:166109892 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0140 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.264-39130_264-3912 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109892 | |||||||
| chr1:166109892 | A | ATATATG | 14 | a0001c0001t0001g0055 a0001c0001t0001g0066 a0001c0001t0001g0067 others(11): Show |
15 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-39130_264-3912 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109892 | |||||||
| chr1:166109892 | A | ATATGTAT others(5): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0159 |
2 | NA18942.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.264-39130_264-3912 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109892 | |||||||
| chr1:166109892 | A | G | 2 | a0001c0001t0002g0073 a0001c0001t0002g0131 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.264-39129T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109892 | |||||||
| chr1:166109894 | A | ATATG | 4 | a0001c0001t0001g0104 a0001c0001t0001g0175 a0001c0001t0002g0090 others(1): Show |
4 | HG01346.hp1 HG01346.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39132_264-3913 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109894 | |||||||
| chr1:166109894 | A | G | 3 | a0001c0001t0004g0016 a0001c0001t0004g0030 a0001c0002t0011g0023 |
3 | HG01243.hp1 HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.264-39131T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109894 | |||||||
| chr1:166109896 | A | ATG | 7 | a0001c0001t0001g0189 a0001c0001t0007g0003 a0001c0001t0007g0033 others(4): Show |
7 | HG01891.hp1 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-39134_264-3913 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109896 | |||||||
| chr1:166109896 | A | G | 17 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-39133T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109896 | |||||||
| chr1:166109897 | T | C | 2 | a0001c0001t0001g0282 a0001c0001t0002g0224 |
2 | HG02129.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.264-39134A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109897 | |||||||
| chr1:166109898 | A | G | 20 | a0001c0001t0001g0097 a0001c0001t0001g0175 a0001c0001t0004g0028 others(17): Show |
23 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.264-39135T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109898 | |||||||
| chr1:166109902 | A | G | 6 | a0001c0001t0001g0181 a0001c0002t0001g0051 a0001c0002t0001g0052 others(3): Show |
6 | HG01433.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-39139T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109902 | |||||||
| chr1:166109904 | A | G | 5 | a0001c0001t0001g0167 a0001c0002t0003g0064 a0001c0002t0003g0119 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39141T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109904 | |||||||
| chr1:166109910 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.264-39147T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109910 | |||||||
| chr1:166109912 | A | G | 1 | a0001c0002t0003g0184 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.264-39149T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109912 | |||||||
| chr1:166109919 | T | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0163 |
2 | NA19063.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.264-39156A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109919 | |||||||
| chr1:166110124 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39361A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110124 | |||||||
| chr1:166110142 | A | T | 1 | a0001c0001t0002g0258 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.264-39379T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110142 | |||||||
| chr1:166110268 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.264-39505T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110268 | |||||||
| chr1:166110294 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39531C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110294 | |||||||
| chr1:166110303 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-39540G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110303 | |||||||
| chr1:166110424 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.264-39661C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110424 | |||||||
| chr1:166110869 | A | G | 4 | a0001c0001t0004g0016 a0001c0001t0009g0041 a0001c0001t0009g0291 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-40106T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110869 | |||||||
| chr1:166110921 | C | T | 3 | a0001c0002t0003g0196 a0001c0002t0003g0201 a0001c0002t0003g0202 |
3 | HG01081.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.264-40158G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110921 | |||||||
| chr1:166110937 | T | C | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-40174A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110937 | |||||||
| chr1:166111188 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.264-40425A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111188 | |||||||
| chr1:166111225 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-40462G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111225 | |||||||
| chr1:166111468 | A | G | 6 | a0001c0001t0007g0003 a0001c0001t0007g0033 a0001c0001t0007g0034 others(3): Show |
7 | HG01891.hp1 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-40705T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111468 | |||||||
| chr1:166111475 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.264-40712A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111475 | |||||||
| chr1:166111502 | C | T | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-40739G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111502 | |||||||
| chr1:166111503 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-40740C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111503 | |||||||
| chr1:166111598 | G | A | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-40835C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111598 | |||||||
| chr1:166111674 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.264-40911A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111674 | |||||||
| chr1:166111709 | T | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-40946A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111709 | |||||||
| chr1:166112096 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-41333G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112096 | |||||||
| chr1:166112137 | A | G | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-41374T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112137 | |||||||
| chr1:166112332 | T | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-41569A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112332 | |||||||
| chr1:166112491 | G | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-41728C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112491 | |||||||
| chr1:166112505 | C | A | 1 | a0001c0001t0002g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.264-41742G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112505 | |||||||
| chr1:166112588 | C | T | 1 | a0001c0002t0005g0299 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.264-41825G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112588 | |||||||
| chr1:166112610 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-41847G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112610 | |||||||
| chr1:166112617 | A | C | 3 | a0001c0001t0001g0086 a0001c0001t0002g0170 a0001c0001t0002g0172 |
3 | HG02258.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.264-41854T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112617 | |||||||
| chr1:166112696 | A | G | 6 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0229 others(3): Show |
6 | HG00642.hp1 HG01257.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-41933T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112696 | |||||||
| chr1:166112825 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.264-42062A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112825 | |||||||
| chr1:166112876 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-42113C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112876 | |||||||
| chr1:166112913 | G | A | 1 | a0001c0002t0003g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.264-42150C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112913 | |||||||
| chr1:166113115 | C | T | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-42352G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113115 | |||||||
| chr1:166113170 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-42407G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113170 | |||||||
| chr1:166113443 | C | T | 17 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-42680G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113443 | |||||||
| chr1:166113582 | T | C | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-42819A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113582 | |||||||
| chr1:166113658 | C | G | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-42895G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113658 | |||||||
| chr1:166113720 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-42957C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113720 | |||||||
| chr1:166113921 | A | G | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-43158T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113921 | |||||||
| chr1:166113995 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-43232C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113995 | |||||||
| chr1:166114090 | C | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-43327G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114090 | |||||||
| chr1:166114251 | T | G | 160 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
166 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.264-43488A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114251 | |||||||
| chr1:166114274 | A | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-43511T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114274 | |||||||
| chr1:166114348 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.264-43585A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114348 | |||||||
| chr1:166114539 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.264-43776T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114539 | |||||||
| chr1:166114541 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.264-43778C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114541 | |||||||
| chr1:166114735 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-43972G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114735 | |||||||
| chr1:166114790 | A | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(1): Show |
4 | HG02615.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-44027T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114790 | |||||||
| chr1:166114800 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0002g0058 a0001c0001t0018g0057 |
3 | HG01081.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.264-44037C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114800 | |||||||
| chr1:166114862 | A | C | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-44099T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114862 | |||||||
| chr1:166115059 | A | G | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.264-44296T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115059 | |||||||
| chr1:166115334 | G | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44571C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115334 | |||||||
| chr1:166115342 | G | C | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44579C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115342 | |||||||
| chr1:166115343 | G | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44580C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115343 | |||||||
| chr1:166115347 | G | A | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44584C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115347 | |||||||
| chr1:166115351 | G | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44588C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115351 | |||||||
| chr1:166115353 | A | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44590T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115353 | |||||||
| chr1:166115354 | T | C | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44591A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115354 | |||||||
| chr1:166115355 | G | C | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44592C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115355 | |||||||
| chr1:166115356 | G | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44593C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115356 | |||||||
| chr1:166115358 | T | TCCCCTCC others(7): Show |
1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44596_264-4459 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115358 | |||||||
| chr1:166115359 | A | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44596T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115359 | |||||||
| chr1:166115362 | T | A | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44599A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115362 | |||||||
| chr1:166115363 | G | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44600C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115363 | |||||||
| chr1:166115365 | A | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44602T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115365 | |||||||
| chr1:166115366 | G | A | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44603C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115366 | |||||||
| chr1:166115369 | A | T | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44606T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115369 | |||||||
| chr1:166115471 | G | A | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-44708C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115471 | |||||||
| chr1:166115580 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-44817A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115580 | |||||||
| chr1:166115633 | G | A | 1 | a0001c0001t0006g0179 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.264-44870C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115633 | |||||||
| chr1:166115700 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.264-44937C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115700 | |||||||
| chr1:166115710 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.264-44947G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115710 | |||||||
| chr1:166115736 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.264-44973G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115736 | |||||||
| chr1:166115873 | G | C | 1 | a0001c0001t0002g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.264-45110C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115873 | |||||||
| chr1:166115896 | T | C | 67 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0193 others(64): Show |
68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.264-45133A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115896 | |||||||
| chr1:166115915 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.264-45152C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115915 | |||||||
| chr1:166115953 | T | C | 19 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.264-45190A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115953 | |||||||
| chr1:166116021 | T | C | 31 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(28): Show |
32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.264-45258A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116021 | |||||||
| chr1:166116185 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0161 |
2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.264-45422C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116185 | |||||||
| chr1:166116227 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-45464A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116227 | |||||||
| chr1:166116236 | T | C | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-45473A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116236 | |||||||
| chr1:166116390 | A | G | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.264-45627T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116390 | |||||||
| chr1:166116430 | T | G | 1 | a0001c0002t0001g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.264-45667A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116430 | |||||||
| chr1:166116504 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-45741C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116504 | |||||||
| chr1:166116565 | C | T | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-45802G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116565 | |||||||
| chr1:166116915 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-46152G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116915 | |||||||
| chr1:166116934 | G | A | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.264-46171C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116934 | |||||||
| chr1:166117734 | T | C | 1 | a0001c0002t0003g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.264-46971A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166117734 | |||||||
| chr1:166117753 | T | G | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.264-46990A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166117753 | |||||||
| chr1:166117861 | C | G | 4 | a0001c0001t0001g0063 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-47098G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166117861 | |||||||
| chr1:166117964 | G | A | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-47201C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166117964 | |||||||
| chr1:166118143 | C | T | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0060 |
3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-47380G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118143 | |||||||
| chr1:166118341 | T | C | 192 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.264-47578A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118341 | |||||||
| chr1:166118365 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.264-47602A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118365 | |||||||
| chr1:166118384 | T | C | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.263+47602A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118384 | |||||||
| chr1:166118456 | T | C | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+47530A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118456 | |||||||
| chr1:166118533 | A | G | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+47453T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118533 | |||||||
| chr1:166118617 | A | G | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.263+47369T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118617 | |||||||
| chr1:166118673 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+47313A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118673 | |||||||
| chr1:166118717 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.263+47269G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118717 | |||||||
| chr1:166118748 | A | G | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+47238T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118748 | |||||||
| chr1:166118910 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+47076G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118910 | |||||||
| chr1:166118910 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.263+47076G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118910 | |||||||
| chr1:166118985 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+47001C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118985 | |||||||
| chr1:166119130 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.263+46856C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119130 | |||||||
| chr1:166119167 | C | T | 1 | a0001c0001t0004g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.263+46819G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119167 | |||||||
| chr1:166119168 | A | G | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.263+46818T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119168 | |||||||
| chr1:166119190 | A | G | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+46796T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119190 | |||||||
| chr1:166119616 | G | A | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+46370C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119616 | |||||||
| chr1:166119774 | C | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.263+46212G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119774 | |||||||
| chr1:166119886 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+46100C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119886 | |||||||
| chr1:166120083 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.263+45903A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120083 | |||||||
| chr1:166120416 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.263+45570C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120416 | |||||||
| chr1:166120486 | T | C | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.263+45500A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120486 | |||||||
| chr1:166120491 | T | C | 67 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0193 others(64): Show |
68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.263+45495A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120491 | |||||||
| chr1:166120569 | C | T | 1 | a0001c0001t0009g0291 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.263+45417G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120569 | |||||||
| chr1:166120586 | G | C | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.263+45400C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120586 | |||||||
| chr1:166120645 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0185 |
3 | HG00544.hp2 HG00621.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.263+45341G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120645 | |||||||
| chr1:166120738 | G | A | 89 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(86): Show |
93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.263+45248C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120738 | |||||||
| chr1:166120748 | AAGAGCAG others(3): Show |
A | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(72): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.263+45228_263+4523 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120748 | |||||||
| chr1:166120898 | C | A | 3 | a0001c0001t0004g0016 a0001c0001t0009g0291 a0001c0001t0009g0292 |
3 | HG01243.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+45088G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120898 | |||||||
| chr1:166120902 | C | T | 292 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(289): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.263+45084G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120902 | |||||||
| chr1:166121284 | T | C | 2 | a0001c0001t0001g0175 a0001c0002t0001g0212 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.263+44702A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121284 | |||||||
| chr1:166121318 | T | C | 1 | a0001c0002t0003g0208 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.263+44668A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121318 | |||||||
| chr1:166121329 | C | T | 20 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(17): Show |
21 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.263+44657G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121329 | |||||||
| chr1:166121332 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.263+44654C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121332 | |||||||
| chr1:166121532 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.263+44454A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121532 | |||||||
| chr1:166121589 | C | A | 6 | a0001c0001t0001g0144 a0001c0002t0003g0111 a0001c0002t0003g0113 others(3): Show |
6 | HG00438.hp1 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+44397G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121589 | |||||||
| chr1:166121749 | G | A | 3 | a0001c0001t0004g0016 a0001c0001t0009g0291 a0001c0001t0009g0292 |
3 | HG01243.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+44237C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121749 | |||||||
| chr1:166121758 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+44228A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121758 | |||||||
| chr1:166121806 | C | T | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+44180G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121806 | |||||||
| chr1:166121807 | G | A | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+44179C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121807 | |||||||
| chr1:166121966 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+44020G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121966 | |||||||
| chr1:166121997 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+43989A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121997 | |||||||
| chr1:166122033 | C | G | 1 | a0001c0001t0006g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.263+43953G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122033 | |||||||
| chr1:166122312 | A | G | 292 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(289): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.263+43674T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122312 | |||||||
| chr1:166122529 | C | T | 292 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(289): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.263+43457G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122529 | |||||||
| chr1:166122759 | G | A | 5 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0024 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+43227C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122759 | |||||||
| chr1:166122967 | C | T | 3 | a0001c0002t0003g0112 a0001c0002t0003g0150 a0001c0002t0003g0164 |
3 | HG00642.hp2 HG00741.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.263+43019G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122967 | |||||||
| chr1:166123080 | C | T | 11 | a0001c0001t0001g0059 a0001c0001t0001g0233 a0001c0001t0001g0235 others(8): Show |
11 | HG00597.hp2 HG01106.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.263+42906G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123080 | |||||||
| chr1:166123188 | C | T | 20 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(17): Show |
21 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.263+42798G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123188 | |||||||
| chr1:166123233 | C | G | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+42753G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123233 | |||||||
| chr1:166123233 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.263+42753G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123233 | |||||||
| chr1:166123338 | C | T | 1 | a0001c0002t0005g0297 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.263+42648G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123338 | |||||||
| chr1:166123436 | G | A | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+42550C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123436 | |||||||
| chr1:166123467 | C | A | 22 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0017 others(19): Show |
23 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.263+42519G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123467 | |||||||
| chr1:166123504 | T | G | 1 | a0001c0001t0002g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.263+42482A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123504 | |||||||
| chr1:166123516 | A | G | 1 | a0001c0001t0007g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263+42470T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123516 | |||||||
| chr1:166123802 | G | A | 191 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.263+42184C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123802 | |||||||
| chr1:166123836 | C | G | 74 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(71): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.263+42150G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123836 | |||||||
| chr1:166124042 | A | C | 74 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(71): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.263+41944T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124042 | |||||||
| chr1:166124080 | C | T | 1 | a0001c0001t0024g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.263+41906G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124080 | |||||||
| chr1:166124131 | C | A | 4 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(1): Show |
4 | HG02451.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+41855G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124131 | |||||||
| chr1:166124181 | C | G | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+41805G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124181 | |||||||
| chr1:166124347 | T | C | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.263+41639A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124347 | |||||||
| chr1:166124392 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+41594C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124392 | |||||||
| chr1:166124488 | G | C | 1 | a0001c0001t0019g0260 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.263+41498C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124488 | |||||||
| chr1:166124693 | C | T | 1 | a0001c0001t0019g0260 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.263+41293G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124693 | |||||||
| chr1:166124828 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0140 |
2 | NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.263+41158A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124828 | |||||||
| chr1:166124943 | AC | A | 5 | a0001c0001t0001g0104 a0001c0001t0002g0004 a0001c0001t0002g0076 others(2): Show |
6 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.263+41042delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124943 | |||||||
| chr1:166125076 | C | T | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.263+40910G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125076 | |||||||
| chr1:166125230 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+40756G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125230 | |||||||
| chr1:166125267 | T | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0275 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.263+40719A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125267 | |||||||
| chr1:166125268 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0275 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.263+40718T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125268 | |||||||
| chr1:166125326 | T | C | 204 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.263+40660A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125326 | |||||||
| chr1:166125362 | A | G | 204 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.263+40624T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125362 | |||||||
| chr1:166125645 | T | C | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+40341A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125645 | |||||||
| chr1:166125700 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.263+40286G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125700 | |||||||
| chr1:166125755 | C | T | 204 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.263+40231G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125755 | |||||||
| chr1:166125832 | A | AT | 33 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0122 others(30): Show |
34 | HG01169.hp2 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.263+40153dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125832 | |||||||
| chr1:166125832 | A | ATT | 163 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.263+40152_263+4015 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125832 | |||||||
| chr1:166125832 | A | ATTT | 13 | a0001c0001t0001g0102 a0001c0001t0001g0126 a0001c0001t0001g0134 others(10): Show |
13 | HG00438.hp1 HG01993.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.263+40151_263+4015 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125832 | |||||||
| chr1:166125858 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0178 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+40128G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125858 | |||||||
| chr1:166125893 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.263+40093C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125893 | |||||||
| chr1:166125994 | G | A | 7 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0074 others(4): Show |
7 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+39992C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125994 | |||||||
| chr1:166126381 | T | C | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.263+39605A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126381 | |||||||
| chr1:166126427 | T | C | 13 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.263+39559A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126427 | |||||||
| chr1:166126542 | T | A | 2 | a0001c0001t0002g0237 a0001c0001t0002g0245 |
2 | NA19011.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.263+39444A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126542 | |||||||
| chr1:166126728 | G | A | 71 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(68): Show |
72 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.263+39258C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126728 | |||||||
| chr1:166126834 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.263+39152C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126834 | |||||||
| chr1:166126983 | A | G | 2 | a0001c0001t0002g0170 a0001c0001t0002g0172 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.263+39003T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126983 | |||||||
| chr1:166127005 | C | T | 278 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(275): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.263+38981G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127005 | |||||||
| chr1:166127045 | G | C | 1 | a0001c0002t0003g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.263+38941C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127045 | |||||||
| chr1:166127111 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.263+38875T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127111 | |||||||
| chr1:166127155 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+38831C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127155 | |||||||
| chr1:166127181 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+38805A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127181 | |||||||
| chr1:166127302 | T | G | 2 | a0001c0001t0001g0166 a0001c0002t0003g0098 |
2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.263+38684A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127302 | |||||||
| chr1:166127328 | C | T | 73 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(70): Show |
74 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.263+38658G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127328 | |||||||
| chr1:166127379 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.263+38607A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127379 | |||||||
| chr1:166127392 | T | A | 1 | a0001c0001t0002g0192 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+38594A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127392 | |||||||
| chr1:166127589 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.263+38397T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127589 | |||||||
| chr1:166127625 | T | C | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.263+38361A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127625 | |||||||
| chr1:166127762 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.263+38224C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127762 | |||||||
| chr1:166127783 | C | T | 1 | a0001c0001t0024g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.263+38203G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127783 | |||||||
| chr1:166128207 | T | TA | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+37778_263+3777 others(5): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128207 | |||||||
| chr1:166128214 | T | C | 15 | a0001c0001t0023g0293 a0001c0002t0001g0212 a0001c0002t0003g0110 others(12): Show |
18 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+37772A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128214 | |||||||
| chr1:166128214 | T | TATTC | 282 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.263+37768_263+3777 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128214 | |||||||
| chr1:166128427 | C | G | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+37559G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128427 | |||||||
| chr1:166128521 | C | T | 72 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(69): Show |
73 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.263+37465G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128521 | |||||||
| chr1:166128577 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.263+37409A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128577 | |||||||
| chr1:166128688 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0178 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+37298G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128688 | |||||||
| chr1:166128716 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.263+37270A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128716 | |||||||
| chr1:166128847 | G | A | 3 | a0001c0001t0004g0016 a0001c0001t0009g0291 a0001c0001t0009g0292 |
3 | HG01243.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+37139C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128847 | |||||||
| chr1:166128942 | A | G | 6 | a0001c0002t0003g0107 a0001c0002t0003g0108 a0001c0002t0003g0109 others(3): Show |
6 | HG00642.hp2 HG00741.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+37044T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128942 | |||||||
| chr1:166129158 | G | A | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+36828C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129158 | |||||||
| chr1:166129328 | T | C | 13 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.263+36658A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129328 | |||||||
| chr1:166129438 | A | G | 207 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.263+36548T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129438 | |||||||
| chr1:166129530 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0122 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.263+36456A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129530 | |||||||
| chr1:166129551 | C | A | 14 | a0001c0001t0023g0293 a0001c0002t0003g0110 a0001c0002t0005g0001 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+36435G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129551 | |||||||
| chr1:166129724 | T | G | 194 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.263+36262A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129724 | |||||||
| chr1:166129973 | A | G | 3 | a0001c0001t0001g0166 a0001c0002t0003g0098 a0001c0002t0003g0117 |
3 | HG02015.hp1 HG02165.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.263+36013T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129973 | |||||||
| chr1:166129980 | T | C | 31 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(28): Show |
32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+36006A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129980 | |||||||
| chr1:166130057 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.263+35929T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130057 | |||||||
| chr1:166130079 | G | C | 207 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.263+35907C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130079 | |||||||
| chr1:166130188 | TC | T | 13 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.263+35797delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130188 | |||||||
| chr1:166130353 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.263+35633T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130353 | |||||||
| chr1:166130684 | T | C | 74 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(71): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.263+35302A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130684 | |||||||
| chr1:166130684 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+35302A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130684 | |||||||
| chr1:166130753 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0055 others(18): Show |
22 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.263+35233T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130753 | |||||||
| chr1:166130981 | C | CT | 39 | a0001c0001t0001g0044 a0001c0001t0001g0055 a0001c0001t0001g0065 others(36): Show |
40 | HG00738.hp1 HG01175.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.263+35004dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130981 | |||||||
| chr1:166130981 | CT | C | 13 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0001g0096 others(10): Show |
13 | HG01069.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.263+35004delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130981 | |||||||
| chr1:166130981 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+34992_263+3500 others(17): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130981 | |||||||
| chr1:166131011 | A | G | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.263+34975T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131011 | |||||||
| chr1:166131014 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.263+34972C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131014 | |||||||
| chr1:166131166 | A | G | 1 | a0001c0002t0003g0281 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.263+34820T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131166 | |||||||
| chr1:166131193 | T | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0178 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+34793A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131193 | |||||||
| chr1:166131239 | G | A | 4 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(1): Show |
4 | HG02451.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+34747C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131239 | |||||||
| chr1:166131487 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+34499C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131487 | |||||||
| chr1:166131707 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.263+34279C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131707 | |||||||
| chr1:166132156 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+33830A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166132156 | |||||||
| chr1:166132296 | C | CCTAA | 83 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0040 others(80): Show |
85 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.263+33686_263+3368 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166132296 | |||||||
| chr1:166132365 | G | A | 63 | a0001c0001t0001g0193 a0001c0001t0001g0218 a0001c0001t0001g0219 others(60): Show |
64 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.263+33621C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166132365 | |||||||
| chr1:166132779 | C | A | 1 | a0001c0001t0017g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.263+33207G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166132779 | |||||||
| chr1:166133123 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.263+32863A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133123 | |||||||
| chr1:166133190 | C | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG00597.hp1 NA18947.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+32796G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133190 | |||||||
| chr1:166133529 | CTG | C | 71 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(68): Show |
72 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.263+32455_263+3245 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133529 | |||||||
| chr1:166133601 | T | TA | 29 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0135 others(26): Show |
33 | HG00544.hp1 HG01070.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.263+32384dupT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133601 | |||||||
| chr1:166133601 | T | TAA | 196 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.263+32383_263+3238 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133601 | |||||||
| chr1:166133664 | A | C | 1 | a0001c0001t0002g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.263+32322T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133664 | |||||||
| chr1:166133762 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0002g0058 a0001c0001t0018g0057 |
3 | HG01081.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.263+32224A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133762 | |||||||
| chr1:166134022 | C | G | 1 | a0001c0001t0002g0290 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.263+31964G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134022 | |||||||
| chr1:166134040 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.263+31946G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134040 | |||||||
| chr1:166134273 | G | T | 13 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(10): Show |
16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+31713C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134273 | |||||||
| chr1:166134435 | T | C | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.263+31551A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134435 | |||||||
| chr1:166134454 | C | T | 1 | a0001c0001t0006g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.263+31532G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134454 | |||||||
| chr1:166134458 | A | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0122 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.263+31528T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134458 | |||||||
| chr1:166134516 | G | GTAATAA | 12 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(9): Show |
15 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.263+31464_263+3146 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134516 | |||||||
| chr1:166134519 | A | G | 2 | a0001c0001t0002g0239 a0001c0001t0002g0269 |
2 | HG03927.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.263+31467T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134519 | |||||||
| chr1:166134540 | A | ATAG | 3 | a0001c0001t0001g0079 a0001c0001t0001g0132 a0001c0001t0001g0180 |
3 | HG00323.hp2 HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.263+31445_263+3144 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134540 | |||||||
| chr1:166134540 | A | G | 190 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.263+31446T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134540 | |||||||
| chr1:166134733 | C | T | 1 | a0001c0001t0018g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263+31253G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134733 | |||||||
| chr1:166135183 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.263+30803T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135183 | |||||||
| chr1:166135186 | C | T | 13 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(10): Show |
16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+30800G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135186 | |||||||
| chr1:166135200 | C | T | 76 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(73): Show |
78 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.263+30786G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135200 | |||||||
| chr1:166135428 | T | C | 31 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(28): Show |
32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+30558A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135428 | |||||||
| chr1:166135489 | C | A | 1 | a0001c0001t0002g0192 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+30497G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135489 | |||||||
| chr1:166135531 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.263+30455C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135531 | |||||||
| chr1:166135625 | T | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+30361A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135625 | |||||||
| chr1:166136060 | A | G | 31 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(28): Show |
32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+29926T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136060 | |||||||
| chr1:166136077 | C | A | 2 | a0001c0001t0001g0175 a0001c0002t0001g0212 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.263+29909G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136077 | |||||||
| chr1:166136151 | T | C | 13 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(10): Show |
16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+29835A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136151 | |||||||
| chr1:166136221 | T | C | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+29765A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136221 | |||||||
| chr1:166136244 | A | C | 29 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(26): Show |
32 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+29742T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136244 | |||||||
| chr1:166136363 | G | T | 1 | a0001c0002t0010g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.263+29623C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136363 | |||||||
| chr1:166136373 | G | C | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.263+29613C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136373 | |||||||
| chr1:166136376 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+29610C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136376 | |||||||
| chr1:166136387 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.263+29599C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136387 | |||||||
| chr1:166136419 | A | G | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.263+29567T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136419 | |||||||
| chr1:166136465 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.263+29521G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136465 | |||||||
| chr1:166136491 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+29495A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136491 | |||||||
| chr1:166136652 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.263+29334T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136652 | |||||||
| chr1:166136678 | C | T | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.263+29308G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136678 | |||||||
| chr1:166136729 | T | G | 1 | a0001c0001t0017g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.263+29257A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136729 | |||||||
| chr1:166136898 | T | C | 2 | a0001c0002t0003g0064 a0001c0002t0003g0119 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.263+29088A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136898 | |||||||
| chr1:166136934 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0002g0172 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.263+29052C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136934 | |||||||
| chr1:166137002 | A | T | 1 | a0001c0002t0003g0276 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.263+28984T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137002 | |||||||
| chr1:166137059 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+28927A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137059 | |||||||
| chr1:166137302 | T | C | 2 | a0001c0002t0001g0061 a0001c0002t0001g0178 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+28684A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137302 | |||||||
| chr1:166137500 | C | CT | 6 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0004g0018 others(3): Show |
6 | HG00597.hp2 HG02257.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+28485dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137500 | |||||||
| chr1:166137500 | CT | C | 191 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.263+28485delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137500 | |||||||
| chr1:166137654 | G | A | 6 | a0001c0001t0001g0279 a0001c0002t0003g0010 a0001c0002t0003g0280 others(3): Show |
7 | HG00438.hp2 NA18960.hp1 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.263+28332C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137654 | |||||||
| chr1:166137923 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.263+28063C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137923 | |||||||
| chr1:166138027 | A | G | 13 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(10): Show |
16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+27959T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138027 | |||||||
| chr1:166138054 | C | G | 4 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(1): Show |
4 | HG02451.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+27932G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138054 | |||||||
| chr1:166138130 | G | C | 16 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(13): Show |
16 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.263+27856C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138130 | |||||||
| chr1:166138133 | G | A | 1 | a0001c0002t0003g0186 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.263+27853C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138133 | |||||||
| chr1:166138333 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.263+27653G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138333 | |||||||
| chr1:166138388 | C | A | 63 | a0001c0001t0001g0193 a0001c0001t0001g0218 a0001c0001t0001g0219 others(60): Show |
64 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.263+27598G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138388 | |||||||
| chr1:166138474 | C | A | 1 | a0001c0001t0002g0259 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.263+27512G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138474 | |||||||
| chr1:166138544 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.263+27442A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138544 | |||||||
| chr1:166138546 | A | G | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.263+27440T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138546 | |||||||
| chr1:166138741 | T | C | 63 | a0001c0001t0001g0193 a0001c0001t0001g0218 a0001c0001t0001g0219 others(60): Show |
64 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.263+27245A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138741 | |||||||
| chr1:166138850 | G | A | 30 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(27): Show |
31 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+27136C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138850 | |||||||
| chr1:166138875 | G | T | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+27111C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138875 | |||||||
| chr1:166138905 | T | C | 5 | a0001c0001t0001g0104 a0001c0001t0002g0004 a0001c0001t0002g0076 others(2): Show |
6 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.263+27081A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138905 | |||||||
| chr1:166138974 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+27012A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138974 | |||||||
| chr1:166139077 | A | G | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+26909T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139077 | |||||||
| chr1:166139099 | A | T | 4 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+26887T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139099 | |||||||
| chr1:166139288 | C | A | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.263+26698G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139288 | |||||||
| chr1:166139428 | A | T | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+26558T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139428 | |||||||
| chr1:166139489 | T | C | 1 | a0001c0002t0003g0164 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.263+26497A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139489 | |||||||
| chr1:166139629 | C | G | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.263+26357G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139629 | |||||||
| chr1:166139650 | T | C | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.263+26336A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139650 | |||||||
| chr1:166139878 | C | G | 1 | a0001c0001t0001g0279 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.263+26108G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139878 | |||||||
| chr1:166139889 | T | G | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.263+26097A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139889 | |||||||
| chr1:166139920 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.263+26066G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139920 | |||||||
| chr1:166139937 | C | G | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+26049G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139937 | |||||||
| chr1:166140139 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0002g0009 |
3 | HG00609.hp1 HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.263+25847C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140139 | |||||||
| chr1:166140158 | C | T | 4 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(1): Show |
4 | HG02451.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+25828G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140158 | |||||||
| chr1:166140396 | T | G | 1 | a0001c0001t0004g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.263+25590A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140396 | |||||||
| chr1:166140471 | C | T | 2 | a0001c0001t0002g0248 a0001c0002t0003g0261 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.263+25515G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140471 | |||||||
| chr1:166140474 | T | C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+25512A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140474 | |||||||
| chr1:166140631 | G | A | 3 | a0001c0001t0004g0017 a0001c0001t0004g0031 a0001c0001t0004g0032 |
3 | HG02451.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.263+25355C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140631 | |||||||
| chr1:166140647 | T | C | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+25339A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140647 | |||||||
| chr1:166140726 | C | T | 267 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
278 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.263+25260G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140726 | |||||||
| chr1:166140756 | G | T | 251 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.263+25230C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140756 | |||||||
| chr1:166140944 | T | C | 223 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(220): Show |
230 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.263+25042A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140944 | |||||||
| chr1:166141258 | T | C | 14 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(11): Show |
15 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.263+24728A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141258 | |||||||
| chr1:166141285 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.263+24701T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141285 | |||||||
| chr1:166141349 | T | C | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+24637A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141349 | |||||||
| chr1:166141370 | C | T | 1 | a0001c0001t0024g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.263+24616G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141370 | |||||||
| chr1:166141456 | T | C | 223 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(220): Show |
230 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.263+24530A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141456 | |||||||
| chr1:166141675 | T | C | 9 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(6): Show |
9 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.263+24311A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141675 | |||||||
| chr1:166141685 | T | C | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
142 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.263+24301A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141685 | |||||||
| chr1:166141784 | A | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+24202T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141784 | |||||||
| chr1:166141845 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+24141A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141845 | |||||||
| chr1:166142049 | C | A | 1 | a0001c0002t0003g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263+23937G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142049 | |||||||
| chr1:166142209 | G | A | 1 | a0001c0001t0004g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.263+23777C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142209 | |||||||
| chr1:166142212 | T | C | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+23774A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142212 | |||||||
| chr1:166142320 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.263+23666G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142320 | |||||||
| chr1:166142346 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.263+23640G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142346 | |||||||
| chr1:166142394 | G | A | 3 | a0001c0001t0017g0068 a0001c0002t0010g0123 a0001c0002t0010g0124 |
3 | HG02572.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.263+23592C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142394 | |||||||
| chr1:166142527 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.263+23459C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142527 | |||||||
| chr1:166142595 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.263+23391C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142595 | |||||||
| chr1:166142668 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.263+23318G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142668 | |||||||
| chr1:166142679 | C | A | 1 | a0001c0002t0003g0186 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.263+23307G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142679 | |||||||
| chr1:166142888 | A | G | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+23098T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142888 | |||||||
| chr1:166142985 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.263+23001T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142985 | |||||||
| chr1:166143166 | A | T | 1 | a0001c0002t0022g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.263+22820T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143166 | |||||||
| chr1:166143219 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(1): Show |
4 | HG02615.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+22767A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143219 | |||||||
| chr1:166143280 | G | A | 1 | a0001c0002t0003g0208 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.263+22706C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143280 | |||||||
| chr1:166143347 | G | A | 1 | a0001c0001t0019g0260 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.263+22639C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143347 | |||||||
| chr1:166143369 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0134 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.263+22617A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143369 | |||||||
| chr1:166143506 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0002g0131 |
2 | HG03453.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.263+22480G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143506 | |||||||
| chr1:166143509 | G | A | 3 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 |
3 | HG01070.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.263+22477C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143509 | |||||||
| chr1:166143593 | T | C | 1 | a0001c0001t0018g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263+22393A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143593 | |||||||
| chr1:166143662 | T | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.263+22324A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143662 | |||||||
| chr1:166143668 | T | C | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.263+22318A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143668 | |||||||
| chr1:166143712 | C | G | 1 | a0001c0001t0002g0231 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.263+22274G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143712 | |||||||
| chr1:166143719 | G | T | 1 | a0001c0001t0002g0231 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.263+22267C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143719 | |||||||
| chr1:166143829 | T | C | 31 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(28): Show |
32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+22157A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143829 | |||||||
| chr1:166144118 | G | A | 260 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.263+21868C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144118 | |||||||
| chr1:166144168 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.263+21818A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144168 | |||||||
| chr1:166144314 | GC | G | 13 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(10): Show |
16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+21671delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144314 | |||||||
| chr1:166144618 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+21368C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144618 | |||||||
| chr1:166144621 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.263+21365G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144621 | |||||||
| chr1:166144724 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.263+21262G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144724 | |||||||
| chr1:166144791 | AAAG | A | 3 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 |
3 | HG01070.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.263+21192_263+2119 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144791 | |||||||
| chr1:166144944 | T | C | 1 | a0001c0002t0003g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263+21042A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144944 | |||||||
| chr1:166145107 | T | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0077 others(1): Show |
5 | HG00558.hp1 NA18949.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.263+20879A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145107 | |||||||
| chr1:166145196 | A | G | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+20790T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145196 | |||||||
| chr1:166145375 | C | T | 246 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
256 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.263+20611G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145375 | |||||||
| chr1:166145402 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+20584C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145402 | |||||||
| chr1:166145603 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.263+20383T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145603 | |||||||
| chr1:166145723 | C | T | 30 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(27): Show |
31 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+20263G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145723 | |||||||
| chr1:166145777 | T | G | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+20209A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145777 | |||||||
| chr1:166145785 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0002g0058 a0001c0001t0018g0057 |
3 | HG01081.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.263+20201A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145785 | |||||||
| chr1:166145980 | T | C | 2 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+20006A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145980 | |||||||
| chr1:166146152 | T | C | 17 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+19834A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146152 | |||||||
| chr1:166146224 | T | A | 17 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+19762A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146224 | |||||||
| chr1:166146259 | A | G | 3 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0178 |
3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+19727T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146259 | |||||||
| chr1:166146281 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+19705G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146281 | |||||||
| chr1:166146324 | T | C | 30 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(27): Show |
31 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+19662A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146324 | |||||||
| chr1:166146531 | C | G | 1 | a0001c0001t0002g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.263+19455G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146531 | |||||||
| chr1:166146623 | A | G | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.263+19363T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146623 | |||||||
| chr1:166146749 | T | A | 98 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0193 others(95): Show |
100 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.263+19237A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146749 | |||||||
| chr1:166146803 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+19183A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146803 | |||||||
| chr1:166147035 | G | C | 1 | a0001c0001t0002g0268 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.263+18951C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147035 | |||||||
| chr1:166147036 | G | T | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+18950C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147036 | |||||||
| chr1:166147060 | T | A | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+18926A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147060 | |||||||
| chr1:166147250 | T | C | 1 | a0001c0002t0022g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.263+18736A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147250 | |||||||
| chr1:166147396 | G | C | 2 | a0001c0001t0001g0070 a0001c0001t0002g0128 |
2 | HG01175.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.263+18590C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147396 | |||||||
| chr1:166147412 | T | TG | 8 | a0001c0001t0001g0059 a0001c0001t0001g0233 a0001c0001t0001g0265 others(5): Show |
8 | HG00597.hp2 HG01255.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.263+18573dupC | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147412 | |||||||
| chr1:166147637 | A | AT | 13 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(10): Show |
13 | HG00544.hp1 HG02523.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+18348dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147637 | |||||||
| chr1:166147637 | A | ATT | 9 | a0001c0001t0001g0181 a0001c0002t0005g0001 a0001c0002t0005g0011 others(6): Show |
12 | HG01192.hp1 HG01261.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.263+18347_263+1834 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147637 | |||||||
| chr1:166147693 | G | A | 98 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0193 others(95): Show |
100 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.263+18293C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147693 | |||||||
| chr1:166147743 | C | T | 257 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
265 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.263+18243G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147743 | |||||||
| chr1:166147937 | A | G | 1 | a0001c0001t0004g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.263+18049T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147937 | |||||||
| chr1:166147954 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0002g0058 a0001c0001t0018g0057 |
3 | HG01081.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.263+18032A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147954 | |||||||
| chr1:166148080 | G | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.263+17906C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148080 | |||||||
| chr1:166148081 | T | C | 1 | a0001c0001t0018g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263+17905A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148081 | |||||||
| chr1:166148270 | T | C | 2 | a0001c0002t0003g0284 a0001c0002t0003g0285 |
2 | NA19006.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.263+17716A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148270 | |||||||
| chr1:166148299 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG00323.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.263+17687C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148299 | |||||||
| chr1:166148332 | G | C | 1 | a0001c0002t0003g0261 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.263+17654C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148332 | |||||||
| chr1:166148344 | T | C | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.263+17642A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148344 | |||||||
| chr1:166148377 | T | C | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+17609A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148377 | |||||||
| chr1:166148546 | C | T | 2 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+17440G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148546 | |||||||
| chr1:166148631 | C | T | 89 | a0001c0001t0001g0040 a0001c0001t0001g0193 a0001c0001t0001g0197 others(86): Show |
91 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.263+17355G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148631 | |||||||
| chr1:166148644 | T | C | 7 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0229 others(4): Show |
7 | HG00642.hp1 HG01257.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+17342A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148644 | |||||||
| chr1:166148673 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(6): Show |
9 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.263+17313G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148673 | |||||||
| chr1:166148786 | C | T | 6 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.263+17200G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148786 | |||||||
| chr1:166148824 | C | G | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.263+17162G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148824 | |||||||
| chr1:166148875 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.263+17111T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148875 | |||||||
| chr1:166149011 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.263+16975T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149011 | |||||||
| chr1:166149153 | T | C | 3 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0178 |
3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+16833A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149153 | |||||||
| chr1:166149245 | TAAAC | T | 139 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(136): Show |
144 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.263+16737_263+1674 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149245 | |||||||
| chr1:166149245 | TAAACAAA others(1): Show |
T | 6 | a0001c0001t0007g0003 a0001c0001t0007g0033 a0001c0001t0008g0013 others(3): Show |
7 | HG00544.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+16733_263+1674 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149245 | |||||||
| chr1:166149245 | TAAACAAA others(5): Show |
T | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.263+16729_263+1674 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149245 | |||||||
| chr1:166149262 | AAACAAAC others(4): Show |
A | 1 | a0001c0002t0003g0165 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.263+16713_263+1672 others(15): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149262 | |||||||
| chr1:166149316 | T | C | 301 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.263+16670A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149316 | |||||||
| chr1:166149410 | A | G | 112 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0187 others(109): Show |
115 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.263+16576T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149410 | |||||||
| chr1:166149646 | T | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0055 others(74): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.263+16340A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149646 | |||||||
| chr1:166149659 | C | T | 97 | a0001c0001t0001g0040 a0001c0001t0001g0193 a0001c0001t0001g0197 others(94): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.263+16327G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149659 | |||||||
| chr1:166150010 | T | C | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+15976A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150010 | |||||||
| chr1:166150014 | G | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+15972C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150014 | |||||||
| chr1:166150045 | C | G | 258 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.263+15941G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150045 | |||||||
| chr1:166150107 | G | A | 1 | a0001c0002t0003g0209 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.263+15879C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150107 | |||||||
| chr1:166150107 | G | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0055 others(74): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.263+15879C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150107 | |||||||
| chr1:166150137 | T | G | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+15849A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150137 | |||||||
| chr1:166150177 | G | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0055 others(74): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.263+15809C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150177 | |||||||
| chr1:166150201 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.263+15785C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150201 | |||||||
| chr1:166150202 | A | AC | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.263+15783dupG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150202 | |||||||
| chr1:166150202 | A | C | 1 | a0001c0001t0001g0238 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.263+15784T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150202 | |||||||
| chr1:166150222 | G | C | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+15764C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150222 | |||||||
| chr1:166150717 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+15269C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150717 | |||||||
| chr1:166150794 | T | C | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+15192A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150794 | |||||||
| chr1:166150884 | A | C | 1 | a0001c0001t0002g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.263+15102T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150884 | |||||||
| chr1:166151090 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+14896C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151090 | |||||||
| chr1:166151228 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0122 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.263+14758G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151228 | |||||||
| chr1:166151274 | G | T | 3 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0178 |
3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+14712C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151274 | |||||||
| chr1:166151284 | T | C | 1 | a0001c0002t0005g0303 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.263+14702A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151284 | |||||||
| chr1:166151390 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+14596A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151390 | |||||||
| chr1:166151414 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.263+14572C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151414 | |||||||
| chr1:166151477 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.263+14509G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151477 | |||||||
| chr1:166151738 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263+14248C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151738 | |||||||
| chr1:166151857 | A | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.263+14129T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151857 | |||||||
| chr1:166151934 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.263+14052C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151934 | |||||||
| chr1:166151959 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.263+14027G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151959 | |||||||
| chr1:166151981 | C | G | 1 | a0001c0001t0006g0127 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.263+14005G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151981 | |||||||
| chr1:166151993 | G | C | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.263+13993C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151993 | |||||||
| chr1:166152081 | G | C | 255 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
263 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.263+13905C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152081 | |||||||
| chr1:166152166 | T | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0054 others(9): Show |
14 | HG00323.hp2 HG00558.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.263+13820A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152166 | |||||||
| chr1:166152340 | G | A | 3 | a0001c0001t0001g0166 a0001c0002t0003g0098 a0001c0002t0003g0117 |
3 | HG02015.hp1 HG02165.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.263+13646C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152340 | |||||||
| chr1:166152358 | G | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+13628C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152358 | |||||||
| chr1:166152377 | G | T | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+13609C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152377 | |||||||
| chr1:166152522 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.263+13464T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152522 | |||||||
| chr1:166152529 | C | T | 97 | a0001c0001t0001g0040 a0001c0001t0001g0193 a0001c0001t0001g0197 others(94): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.263+13457G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152529 | |||||||
| chr1:166152577 | G | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+13409C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152577 | |||||||
| chr1:166152596 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0134 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.263+13390G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152596 | |||||||
| chr1:166152654 | G | GGATT | 10 | a0001c0001t0001g0045 a0001c0001t0001g0133 a0001c0001t0004g0002 others(7): Show |
11 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.263+13328_263+1333 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152654 | |||||||
| chr1:166152654 | G | GGATTGAT others(5): Show |
1 | a0001c0001t0002g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263+13331_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152654 | |||||||
| chr1:166152655 | G | GATTGATT others(5): Show |
3 | a0001c0001t0001g0047 a0001c0001t0004g0022 a0001c0002t0011g0023 |
3 | HG02258.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.263+13330_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152655 | G | GATTGATT others(1): Show |
5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0049 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.263+13330_263+1333 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152655 | G | GATTGATT others(5): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.263+13330_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152655 | G | GATTT | 37 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0066 others(34): Show |
38 | HG00544.hp1 HG01069.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.263+13327_263+1333 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152655 | G | GATTTATT others(1): Show |
3 | a0001c0001t0001g0138 a0001c0001t0004g0020 a0001c0001t0004g0021 |
3 | HG02965.hp2 HG03098.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.263+13323_263+1333 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152655 | G | GATTTATT others(5): Show |
1 | a0001c0001t0004g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.263+13319_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152655 | GATTT | G | 24 | a0001c0001t0001g0054 a0001c0001t0001g0134 a0001c0001t0001g0187 others(21): Show |
25 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.263+13327_263+1333 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152655 | GATTTATT others(5): Show |
G | 8 | a0001c0001t0001g0232 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG00597.hp1 HG00621.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.263+13319_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152655 | GATTTATT others(17): Show |
G | 1 | a0001c0001t0008g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.263+13307_263+1333 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | |||||||
| chr1:166152659 | T | G | 12 | a0001c0001t0001g0059 a0001c0001t0001g0099 a0001c0001t0001g0133 others(9): Show |
12 | HG00597.hp2 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.263+13327A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152659 | |||||||
| chr1:166152663 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.263+13323A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152663 | |||||||
| chr1:166152665 | T | G | 1 | a0001c0001t0002g0269 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.263+13321A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152665 | |||||||
| chr1:166152695 | T | G | 1 | a0001c0001t0001g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.263+13291A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152695 | |||||||
| chr1:166152695 | T | TATTGATT others(1): Show |
3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02109.hp2 HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.263+13290_263+1329 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152695 | |||||||
| chr1:166152731 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+13255C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152731 | |||||||
| chr1:166152732 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+13254G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152732 | |||||||
| chr1:166153010 | A | G | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+12976T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153010 | |||||||
| chr1:166153142 | G | C | 2 | a0001c0001t0002g0058 a0001c0001t0018g0057 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.263+12844C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153142 | |||||||
| chr1:166153179 | T | C | 6 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(3): Show |
6 | HG02970.hp1 HG03195.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+12807A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153179 | |||||||
| chr1:166153385 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.263+12601G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153385 | |||||||
| chr1:166153386 | C | T | 3 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0178 |
3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+12600G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153386 | |||||||
| chr1:166153395 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+12591A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153395 | |||||||
| chr1:166153539 | G | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0055 others(74): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.263+12447C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153539 | |||||||
| chr1:166153559 | T | G | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+12427A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153559 | |||||||
| chr1:166153565 | T | C | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+12421A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153565 | |||||||
| chr1:166153703 | C | T | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+12283G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153703 | |||||||
| chr1:166153777 | G | C | 22 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(19): Show |
25 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.263+12209C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153777 | |||||||
| chr1:166153877 | G | C | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+12109C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153877 | |||||||
| chr1:166153887 | T | C | 3 | a0001c0001t0004g0017 a0001c0001t0004g0031 a0001c0001t0004g0032 |
3 | HG02451.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.263+12099A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153887 | |||||||
| chr1:166154295 | G | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+11691C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154295 | |||||||
| chr1:166154351 | C | T | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+11635G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154351 | |||||||
| chr1:166154500 | G | C | 1 | a0001c0001t0002g0234 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.263+11486C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154500 | |||||||
| chr1:166154589 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.263+11397T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154589 | |||||||
| chr1:166154605 | C | T | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+11381G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154605 | |||||||
| chr1:166154871 | C | T | 1 | a0001c0001t0006g0288 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.263+11115G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154871 | |||||||
| chr1:166154873 | C | T | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+11113G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154873 | |||||||
| chr1:166154897 | A | G | 302 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(299): Show |
314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.263+11089T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154897 | |||||||
| chr1:166154908 | T | C | 1 | a0001c0002t0003g0272 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.263+11078A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154908 | |||||||
| chr1:166155030 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.263+10956G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155030 | |||||||
| chr1:166155037 | G | A | 6 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(3): Show |
6 | HG02970.hp1 HG03195.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+10949C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155037 | |||||||
| chr1:166155119 | A | G | 20 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(17): Show |
23 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+10867T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155119 | |||||||
| chr1:166155190 | A | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+10796T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155190 | |||||||
| chr1:166155217 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.263+10769G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155217 | |||||||
| chr1:166155323 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.263+10663G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155323 | |||||||
| chr1:166155362 | G | A | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.263+10624C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155362 | |||||||
| chr1:166155448 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.263+10538G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155448 | |||||||
| chr1:166155499 | C | T | 20 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(17): Show |
23 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+10487G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155499 | |||||||
| chr1:166155549 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.263+10437A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155549 | |||||||
| chr1:166155687 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+10299G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155687 | |||||||
| chr1:166155765 | A | G | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+10221T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155765 | |||||||
| chr1:166155926 | T | C | 3 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0178 |
3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+10060A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155926 | |||||||
| chr1:166156002 | G | A | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.263+9984C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156002 | |||||||
| chr1:166156014 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.263+9972T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156014 | |||||||
| chr1:166156155 | C | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+9831G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156155 | |||||||
| chr1:166156186 | T | C | 111 | a0001c0001t0001g0040 a0001c0001t0001g0187 a0001c0001t0001g0188 others(108): Show |
114 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.263+9800A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156186 | |||||||
| chr1:166156222 | C | T | 1 | a0001c0001t0012g0012 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.263+9764G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156222 | |||||||
| chr1:166156273 | G | A | 2 | a0001c0001t0001g0286 a0001c0002t0003g0281 |
2 | HG00673.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.263+9713C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156273 | |||||||
| chr1:166156356 | T | G | 20 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(17): Show |
23 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+9630A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156356 | |||||||
| chr1:166156365 | G | C | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+9621C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156365 | |||||||
| chr1:166156370 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0002g0171 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.263+9616C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156370 | |||||||
| chr1:166156446 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+9540A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156446 | |||||||
| chr1:166156560 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.263+9426A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156560 | |||||||
| chr1:166156561 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.263+9425T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156561 | |||||||
| chr1:166156608 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+9378C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156608 | |||||||
| chr1:166156745 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+9241A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156745 | |||||||
| chr1:166156749 | A | C | 2 | a0001c0002t0003g0064 a0001c0002t0003g0119 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.263+9237T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156749 | |||||||
| chr1:166156793 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0175 a0001c0002t0001g0212 |
3 | HG02818.hp1 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.263+9193A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156793 | |||||||
| chr1:166156882 | A | G | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.263+9104T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156882 | |||||||
| chr1:166156982 | AGAG | A | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+9001_263+9003d others(5): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156982 | |||||||
| chr1:166157027 | GGGC | G | 45 | a0001c0001t0001g0062 a0001c0001t0001g0100 a0001c0001t0001g0101 others(42): Show |
45 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.263+8956_263+8958d others(5): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157027 | |||||||
| chr1:166157030 | C | T | 2 | a0001c0001t0008g0013 a0001c0001t0008g0014 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.263+8956G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157030 | |||||||
| chr1:166157030 | CGGCGGA | C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0133 others(21): Show |
26 | HG00423.hp1 HG01891.hp1 HG02723.hp2 others(23): Show |
intron_variant | MODIFIER | c.263+8950_263+8955d others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157030 | |||||||
| chr1:166157031 | GGC | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0055 others(23): Show |
27 | HG00544.hp1 HG00544.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.263+8953_263+8954d others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157031 | |||||||
| chr1:166157031 | GGCGGA | G | 75 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(72): Show |
78 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.263+8950_263+8954d others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157031 | |||||||
| chr1:166157032 | GC | G | 6 | a0001c0001t0001g0138 a0001c0001t0001g0149 a0001c0002t0005g0001 others(3): Show |
8 | HG01192.hp1 HG01261.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+8953delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157032 | |||||||
| chr1:166157032 | GCGGA | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(88): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.263+8950_263+8953d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157032 | |||||||
| chr1:166157033 | C | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0002t0005g0001 |
3 | HG01361.hp2 NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.263+8953G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157033 | |||||||
| chr1:166157035 | G | C | 1 | a0001c0002t0005g0001 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.263+8951C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157035 | |||||||
| chr1:166157035 | GA | G | 10 | a0001c0001t0004g0002 a0001c0001t0004g0016 a0001c0001t0004g0019 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+8950delT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157035 | |||||||
| chr1:166157036 | A | C | 4 | a0001c0002t0005g0001 a0001c0002t0005g0011 a0001c0002t0005g0294 others(1): Show |
6 | HG01192.hp1 HG01261.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+8950T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157036 | |||||||
| chr1:166157036 | A | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0055 others(75): Show |
79 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.263+8950T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157036 | |||||||
| chr1:166157036 | A | T | 1 | a0001c0001t0008g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.263+8950T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157036 | |||||||
| chr1:166157037 | G | C | 4 | a0001c0002t0005g0296 a0001c0002t0005g0297 a0001c0002t0005g0298 others(1): Show |
4 | HG00544.hp1 HG01943.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+8949C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157037 | |||||||
| chr1:166157038 | G | C | 6 | a0001c0001t0023g0293 a0001c0002t0005g0300 a0001c0002t0005g0301 others(3): Show |
6 | NA18942.hp2 NA18963.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+8948C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157038 | |||||||
| chr1:166157042 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+8944C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157042 | |||||||
| chr1:166157099 | T | G | 1 | a0001c0001t0001g0273 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.263+8887A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157099 | |||||||
| chr1:166157186 | C | G | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+8800G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157186 | |||||||
| chr1:166157295 | C | G | 3 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 |
3 | HG01070.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.263+8691G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157295 | |||||||
| chr1:166157335 | G | C | 20 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(17): Show |
23 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+8651C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157335 | |||||||
| chr1:166157545 | G | T | 1 | a0001c0001t0004g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.263+8441C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157545 | |||||||
| chr1:166157710 | C | T | 3 | a0001c0001t0004g0017 a0001c0001t0004g0031 a0001c0001t0004g0032 |
3 | HG02451.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.263+8276G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157710 | |||||||
| chr1:166157730 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.263+8256A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157730 | |||||||
| chr1:166157760 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.263+8226A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157760 | |||||||
| chr1:166157891 | G | A | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+8095C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157891 | |||||||
| chr1:166158132 | C | G | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+7854G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158132 | |||||||
| chr1:166158217 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.263+7769G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158217 | |||||||
| chr1:166158262 | C | T | 3 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0178 |
3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+7724G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158262 | |||||||
| chr1:166158550 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0002g0170 a0001c0001t0002g0171 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+7436C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158550 | |||||||
| chr1:166158607 | C | T | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+7379G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158607 | |||||||
| chr1:166158691 | C | T | 1 | a0001c0001t0023g0293 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.263+7295G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158691 | |||||||
| chr1:166158792 | C | T | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.263+7194G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158792 | |||||||
| chr1:166158823 | C | G | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.263+7163G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158823 | |||||||
| chr1:166159118 | C | G | 279 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(276): Show |
290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.263+6868G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159118 | |||||||
| chr1:166159141 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.263+6845A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159141 | |||||||
| chr1:166159152 | T | C | 259 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(256): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.263+6834A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159152 | |||||||
| chr1:166159169 | A | G | 17 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+6817T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159169 | |||||||
| chr1:166159339 | C | T | 1 | a0001c0001t0009g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+6647G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159339 | |||||||
| chr1:166159385 | C | T | 30 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0203 others(27): Show |
31 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+6601G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159385 | |||||||
| chr1:166159410 | C | T | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+6576G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159410 | |||||||
| chr1:166159723 | A | T | 131 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0187 others(128): Show |
137 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.263+6263T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159723 | |||||||
| chr1:166159752 | C | G | 3 | a0001c0001t0007g0003 a0001c0001t0007g0033 a0001c0001t0007g0034 |
4 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+6234G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159752 | |||||||
| chr1:166159847 | T | C | 1 | a0001c0002t0003g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.263+6139A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159847 | |||||||
| chr1:166159915 | G | A | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+6071C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159915 | |||||||
| chr1:166159959 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.263+6027G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159959 | |||||||
| chr1:166160169 | C | A | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.263+5817G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160169 | |||||||
| chr1:166160263 | T | C | 17 | a0001c0001t0004g0002 a0001c0001t0004g0017 a0001c0001t0004g0018 others(14): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+5723A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160263 | |||||||
| chr1:166160429 | G | A | 1 | a0001c0001t0012g0012 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.263+5557C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160429 | |||||||
| chr1:166160719 | G | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.263+5267C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160719 | |||||||
| chr1:166160756 | T | C | 7 | a0001c0001t0007g0003 a0001c0001t0007g0033 a0001c0001t0007g0034 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+5230A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160756 | |||||||
| chr1:166160900 | G | A | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+5086C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160900 | |||||||
| chr1:166160981 | G | A | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.263+5005C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160981 | |||||||
| chr1:166161156 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+4830A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161156 | |||||||
| chr1:166161157 | CT | C | 15 | a0001c0001t0001g0275 a0001c0001t0023g0293 a0001c0002t0005g0001 others(12): Show |
18 | HG00544.hp1 HG01169.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+4828delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161157 | |||||||
| chr1:166161233 | A | G | 32 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(29): Show |
36 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.263+4753T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161233 | |||||||
| chr1:166161891 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.263+4095C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161891 | |||||||
| chr1:166161904 | C | T | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+4082G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161904 | |||||||
| chr1:166162010 | C | T | 1 | a0001c0001t0004g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.263+3976G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162010 | |||||||
| chr1:166162174 | C | T | 98 | a0001c0001t0001g0040 a0001c0001t0001g0193 a0001c0001t0001g0197 others(95): Show |
100 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.263+3812G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162174 | |||||||
| chr1:166162208 | G | A | 302 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(299): Show |
314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.263+3778C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162208 | |||||||
| chr1:166162248 | G | C | 2 | a0001c0001t0004g0031 a0001c0001t0004g0032 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.263+3738C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162248 | |||||||
| chr1:166162436 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.263+3550C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162436 | |||||||
| chr1:166162442 | G | A | 1 | a0001c0002t0003g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263+3544C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162442 | |||||||
| chr1:166162855 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.263+3131G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162855 | |||||||
| chr1:166162956 | G | C | 1 | a0001c0002t0001g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.263+3030C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162956 | |||||||
| chr1:166162979 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.263+3007G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162979 | |||||||
| chr1:166163082 | T | A | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+2904A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163082 | |||||||
| chr1:166163126 | G | A | 1 | a0001c0002t0003g0276 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.263+2860C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163126 | |||||||
| chr1:166163131 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+2855A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163131 | |||||||
| chr1:166163170 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.263+2816G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163170 | |||||||
| chr1:166163289 | G | A | 1 | a0001c0001t0006g0179 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.263+2697C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163289 | |||||||
| chr1:166163340 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.263+2646A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163340 | |||||||
| chr1:166163397 | A | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+2589T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163397 | |||||||
| chr1:166163583 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.263+2403G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163583 | |||||||
| chr1:166163591 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.263+2395A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163591 | |||||||
| chr1:166163617 | A | T | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0053 |
3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+2369T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163617 | |||||||
| chr1:166163805 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+2181C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163805 | |||||||
| chr1:166163869 | A | T | 14 | a0001c0001t0023g0293 a0001c0002t0005g0001 a0001c0002t0005g0011 others(11): Show |
17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+2117T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163869 | |||||||
| chr1:166164107 | T | C | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0185 others(2): Show |
5 | HG00544.hp2 HG00621.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+1879A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164107 | |||||||
| chr1:166164247 | C | T | 32 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(29): Show |
36 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.263+1739G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164247 | |||||||
| chr1:166164573 | A | T | 32 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(29): Show |
36 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.263+1413T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164573 | |||||||
| chr1:166164576 | G | C | 32 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(29): Show |
36 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.263+1410C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164576 | |||||||
| chr1:166164613 | C | T | 108 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(105): Show |
110 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.263+1373G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164613 | |||||||
| chr1:166164737 | G | C | 1 | a0001c0001t0002g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.263+1249C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164737 | |||||||
| chr1:166164792 | T | C | 9 | a0001c0001t0001g0279 a0001c0001t0001g0282 a0001c0001t0001g0286 others(6): Show |
10 | HG00438.hp2 HG00673.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.263+1194A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164792 | |||||||
| chr1:166164917 | G | A | 2 | a0001c0001t0009g0291 a0001c0001t0009g0292 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+1069C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164917 | |||||||
| chr1:166164941 | T | C | 18 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(15): Show |
19 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.263+1045A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164941 | |||||||
| chr1:166165156 | T | C | 98 | a0001c0001t0001g0040 a0001c0001t0001g0193 a0001c0001t0001g0197 others(95): Show |
100 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.263+830A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165156 | |||||||
| chr1:166165220 | G | C | 3 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0006g0288 |
3 | HG01358.hp1 HG01515.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.263+766C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165220 | |||||||
| chr1:166165327 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.263+659G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165327 | |||||||
| chr1:166165405 | G | C | 5 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 others(2): Show |
5 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+581C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165405 | |||||||
| chr1:166165855 | A | G | 1 | a0001c0002t0003g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263+131T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165855 |