Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51252 |
| ensemblid | ENSG00000168754.15 |
| hgncid | 28036 |
| symbol | FAM178B |
| name | family with sequence similarity 178 member B |
| refseq_nuc | NM_001122646.3 |
| refseq_prot | NP_001116118.2 |
| ensembl_nuc | ENST00000490605.3 |
| ensembl_prot | ENSP00000429896.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 96875885 |
| end | 96986580 |
| strand | - |
| ver | v1.2 |
| region | chr2:96875885-96986580 |
| region5000 | chr2:96870885-96991580 |
| regionname0 | FAM178B_chr2_96875885_96986580 |
| regionname5000 | FAM178B_chr2_96870885_96991580 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 679 | 115 | 52 | 14 | 40 | 1 | 8 | 31 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0002 | 1/1 | 679 | 85 | 11 | 20 | 35 | 0 | 17 | 21 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0003 | 0/0 | 679 | 13 | 10 | 1 | 2 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0004 | 0/0 | 679 | 12 | 3 | 7 | 0 | 1 | 1 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0005 | 0/0 | 679 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0006 | 0/0 | 679 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0007 | 0/0 | 679 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0008 | 0/0 | 679 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0009 | 0/0 | 679 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0010 | 0/0 | 679 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0011 | 0/0 | 679 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0012 | 0/0 | 679 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0013 | 0/0 | 679 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0014 | 0/0 | 679 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| a0015 | 0/0 | 679 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | MWPRL others(674): Show |
chr2 | 96870885 | 96991580 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2037 | 80 | 33 | 13 | 27 | 1 | 6 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0001c0003 | 0/0 | 2037 | 30 | 15 | 1 | 12 | 0 | 2 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0001c0012 | 0/0 | 2037 | 3 | 3 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0001c0017 | 0/0 | 2037 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0001c0019 | 0/0 | 2037 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0002c0002 | 0/1 | 2037 | 66 | 3 | 19 | 31 | 0 | 12 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0002c0008 | 0/0 | 2037 | 6 | 1 | 0 | 2 | 0 | 3 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0002c0009 | 1/0 | 2037 | 4 | 0 | 0 | 1 | 0 | 2 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0002c0010 | 0/0 | 2037 | 4 | 3 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0002c0015 | 0/0 | 2037 | 2 | 2 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0002c0023 | 0/0 | 2037 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0002c0024 | 0/0 | 2037 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0002c0027 | 0/0 | 2037 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0003c0005 | 0/0 | 2037 | 9 | 8 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0003c0011 | 0/0 | 2037 | 4 | 2 | 0 | 2 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0004c0004 | 0/0 | 2037 | 12 | 3 | 7 | 0 | 1 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0005c0006 | 0/0 | 2037 | 7 | 0 | 7 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0006c0007 | 0/0 | 2037 | 6 | 6 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0007c0014 | 0/0 | 2037 | 2 | 0 | 0 | 2 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0008c0013 | 0/0 | 2037 | 2 | 0 | 0 | 2 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0009c0016 | 0/0 | 2037 | 2 | 0 | 0 | 2 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0010c0018 | 0/0 | 2037 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0011c0021 | 0/0 | 2037 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0012c0026 | 0/0 | 2037 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0013c0025 | 0/0 | 2037 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0014c0020 | 0/0 | 2037 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 | ||
| a0015c0022 | 0/0 | 2037 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | ATGTG others(2032): Show |
chr2 | 96870885 | 96991580 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2698 | 79 | 33 | 12 | 27 | 1 | 6 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0001c0001t0004 | 0/0 | 2698 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0001c0003t0001 | 0/0 | 2698 | 29 | 15 | 1 | 11 | 0 | 2 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0001c0003t0008 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0001c0012t0001 | 0/0 | 2698 | 3 | 3 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0001c0017t0001 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0001c0019t0001 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0002t0001 | 0/1 | 2698 | 64 | 3 | 18 | 30 | 0 | 12 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0002t0006 | 0/0 | 2655 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2650): Show |
chr2 | 96870885 | 96991580 |
| a0002c0002t0007 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0008t0001 | 0/0 | 2698 | 6 | 1 | 0 | 2 | 0 | 3 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0009t0001 | 1/0 | 2698 | 4 | 0 | 0 | 1 | 0 | 2 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0010t0001 | 0/0 | 2698 | 4 | 3 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0015t0003 | 0/0 | 2698 | 2 | 2 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0023t0005 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0024t0001 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0002c0027t0001 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0003c0005t0001 | 0/0 | 2698 | 9 | 8 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0003c0011t0001 | 0/0 | 2698 | 4 | 2 | 0 | 2 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0004c0004t0001 | 0/0 | 2698 | 12 | 3 | 7 | 0 | 1 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0005c0006t0001 | 0/0 | 2698 | 7 | 0 | 7 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0006c0007t0002 | 0/0 | 2694 | 6 | 6 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2689): Show |
chr2 | 96870885 | 96991580 |
| a0007c0014t0001 | 0/0 | 2698 | 2 | 0 | 0 | 2 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0008c0013t0001 | 0/0 | 2698 | 2 | 0 | 0 | 2 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0009c0016t0001 | 0/0 | 2698 | 2 | 0 | 0 | 2 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0010c0018t0001 | 0/0 | 2698 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0011c0021t0001 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0012c0026t0001 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0013c0025t0001 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0014c0020t0001 | 0/0 | 2698 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| a0015c0022t0001 | 0/0 | 2698 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | GCACT others(2693): Show |
chr2 | 96870885 | 96991580 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0003t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0012t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0012t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0012t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0017t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0001c0019t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0002t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0008t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0008t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0008t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0008t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0008t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0009t0001g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0009t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0009t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0010t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0010t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0010t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0010t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0015t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0015t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0023t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0024t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0002c0027t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0011t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0011t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0011t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0003c0011t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0004c0004t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0005c0006t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0005c0006t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0005c0006t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0005c0006t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0005c0006t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0005c0006t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0005c0006t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0006c0007t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0006c0007t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0006c0007t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0006c0007t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0006c0007t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0006c0007t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0007c0014t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0007c0014t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0008c0013t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0008c0013t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0009c0016t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0009c0016t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0010c0018t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0011c0021t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0012c0026t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0013c0025t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0014c0020t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| a0015c0022t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00099 | hp2 | a0004 | c0004 | t0001 | g0123 | EUR | GBR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00597 | hp2 | a0001 | c0017 | t0001 | g0142 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00609 | hp1 | a0003 | c0011 | t0001 | g0236 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00642 | hp1 | a0005 | c0006 | t0001 | g0023 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00642 | hp2 | a0003 | c0005 | t0001 | g0240 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00741 | hp1 | a0005 | c0006 | t0001 | g0045 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01099 | hp1 | a0004 | c0004 | t0001 | g0125 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01175 | hp1 | a0004 | c0004 | t0001 | g0129 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01243 | hp1 | a0002 | c0010 | t0001 | g0144 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01257 | hp1 | a0004 | c0004 | t0001 | g0121 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01258 | hp1 | a0004 | c0004 | t0001 | g0124 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01261 | hp1 | a0004 | c0004 | t0001 | g0143 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01261 | hp2 | a0010 | c0018 | t0001 | g0010 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0201 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01891 | hp1 | a0011 | c0021 | t0001 | g0225 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0069 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01943 | hp1 | a0005 | c0006 | t0001 | g0048 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01943 | hp2 | a0002 | c0002 | t0006 | g0189 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01975 | hp1 | a0005 | c0006 | t0001 | g0021 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0043 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01993 | hp2 | a0005 | c0006 | t0001 | g0020 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02004 | hp1 | a0005 | c0006 | t0001 | g0022 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02027 | hp1 | a0007 | c0014 | t0001 | g0231 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02027 | hp2 | a0002 | c0008 | t0001 | g0234 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02040 | hp2 | a0003 | c0011 | t0001 | g0248 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0223 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02071 | hp2 | a0007 | c0014 | t0001 | g0228 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02083 | hp1 | a0002 | c0008 | t0001 | g0232 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02129 | hp1 | a0001 | c0003 | t0008 | g0249 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | KHV | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | CDX | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02165 | hp2 | a0012 | c0026 | t0001 | g0224 | EAS | CDX | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02258 | hp1 | a0003 | c0005 | t0001 | g0238 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02300 | hp1 | a0005 | c0006 | t0001 | g0063 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02572 | hp1 | a0002 | c0023 | t0005 | g0157 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02572 | hp2 | a0006 | c0007 | t0002 | g0087 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0211 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02622 | hp1 | a0004 | c0004 | t0001 | g0126 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02622 | hp2 | a0003 | c0011 | t0001 | g0247 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02630 | hp1 | a0003 | c0005 | t0001 | g0242 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02630 | hp2 | a0002 | c0010 | t0001 | g0007 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02647 | hp1 | a0013 | c0025 | t0001 | g0006 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0046 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02698 | hp1 | a0014 | c0020 | t0001 | g0235 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02717 | hp2 | a0001 | c0012 | t0001 | g0140 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02735 | hp1 | a0015 | c0022 | t0001 | g0178 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0100 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02922 | hp1 | a0002 | c0010 | t0001 | g0158 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02922 | hp2 | a0003 | c0005 | t0001 | g0237 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02965 | hp2 | a0001 | c0012 | t0001 | g0139 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03017 | hp2 | a0002 | c0009 | t0001 | g0161 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03041 | hp1 | a0006 | c0007 | t0002 | g0097 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03098 | hp2 | a0006 | c0007 | t0002 | g0041 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03130 | hp1 | a0003 | c0005 | t0001 | g0243 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03195 | hp1 | a0003 | c0005 | t0001 | g0245 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03209 | hp1 | a0006 | c0007 | t0002 | g0098 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0103 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03453 | hp2 | a0002 | c0024 | t0001 | g0222 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03486 | hp1 | a0003 | c0011 | t0001 | g0246 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03516 | hp1 | a0002 | c0015 | t0003 | g0004 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03579 | hp2 | a0001 | c0019 | t0001 | g0009 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | STU | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0198 | SAS | BEB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03834 | hp2 | a0002 | c0008 | t0001 | g0233 | SAS | BEB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | BEB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03927 | hp2 | a0004 | c0004 | t0001 | g0127 | SAS | BEB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG04115 | hp1 | a0002 | c0009 | t0001 | g0213 | SAS | STU | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG04115 | hp2 | a0002 | c0008 | t0001 | g0230 | SAS | STU | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0029 | SAS | BEB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0147 | SAS | BEB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0208 | SAS | STU | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG04204 | hp2 | a0002 | c0008 | t0001 | g0229 | SAS | STU | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | YRI | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0102 | AFR | YRI | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18747 | hp2 | a0002 | c0002 | t0007 | g0173 | EAS | CHB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | YRI | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18949 | hp1 | a0008 | c0013 | t0001 | g0092 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18965 | hp1 | a0009 | c0016 | t0001 | g0227 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18966 | hp2 | a0009 | c0016 | t0001 | g0226 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18987 | hp2 | a0002 | c0009 | t0001 | g0194 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19002 | hp2 | a0002 | c0027 | t0001 | g0200 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19030 | hp1 | a0003 | c0005 | t0001 | g0239 | AFR | LWK | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19030 | hp2 | a0002 | c0010 | t0001 | g0160 | AFR | LWK | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19043 | hp1 | a0006 | c0007 | t0002 | g0096 | AFR | LWK | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0156 | AFR | LWK | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19068 | hp2 | a0008 | c0013 | t0001 | g0090 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19080 | hp2 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19240 | hp1 | a0001 | c0012 | t0001 | g0141 | AFR | YRI | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA19240 | hp2 | a0002 | c0015 | t0003 | g0003 | AFR | YRI | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | GIH | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | GIH | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01123 | hp1 | a0004 | c0004 | t0001 | g0128 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02486 | hp1 | a0002 | c0008 | t0001 | g0159 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02559 | hp1 | a0006 | c0007 | t0002 | g0095 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG02559 | hp2 | a0004 | c0004 | t0001 | g0130 | AFR | ACB | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03471 | hp1 | a0003 | c0005 | t0001 | g0241 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG06807 | hp1 | a0003 | c0005 | t0001 | g0244 | AFR | USA | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | USA | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0101 | AFR | USA | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | USA | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA21309 | hp1 | a0004 | c0004 | t0001 | g0122 | AFR | LWK | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0084 | AFR | LWK | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0203 | REF | REF | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| homoSapiens | grch38p0 | a0002 | c0009 | t0001 | g0152 | REF | REF | FAM178B_chr2_96870885_96991580 | FAM178B | chr2 | 96870885 | 96991580 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96877964 | G | A | 1 | a0006 | 6 | HG02559.hp1 HG02572.hp2 HG03041.hp1 others(3): Show |
missense_variant | MODERATE | c.1933C>T | p.Arg645Cys | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/17 | 2200/2698 | 1933/2040 | 645/679 | chr2 | 96877964 | |||
| chr2:96902640 | G | C | 1 | a0014 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1630C>G | p.Leu544Val | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/17 | 1897/2698 | 1630/2040 | 544/679 | chr2 | 96902640 | |||
| chr2:96921195 | T | G | 1 | a0015 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1532A>C | p.Gln511Pro | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/17 | 1799/2698 | 1532/2040 | 511/679 | chr2 | 96921195 | |||
| chr2:96921551 | C | T | 1 | a0010 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1391G>A | p.Arg464His | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 11/17 | 1658/2698 | 1391/2040 | 464/679 | chr2 | 96921551 | |||
| chr2:96967530 | G | C | 1 | a0004 | 12 | HG00099.hp2 HG01099.hp1 HG01123.hp1 others(9): Show |
missense_variant | MODERATE | c.724C>G | p.Pro242Ala | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/17 | 991/2698 | 724/2040 | 242/679 | chr2 | 96967530 | |||
| chr2:96967604 | C | T | 1 | a0009 | 2 | NA18965.hp1 NA18966.hp2 |
missense_variant | MODERATE | c.650G>A | p.Arg217Gln | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/17 | 917/2698 | 650/2040 | 217/679 | chr2 | 96967604 | |||
| chr2:96971985 | G | T | 1 | a0011 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.480C>A | p.Asp160Glu | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 747/2698 | 480/2040 | 160/679 | chr2 | 96971985 | |||
| chr2:96972058 | C | A | 1 | a0012 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.407G>T | p.Gly136Val | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 674/2698 | 407/2040 | 136/679 | chr2 | 96972058 | |||
| chr2:96972122 | C | A | 1 | a0013 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.343G>T | p.Val115Leu | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 610/2698 | 343/2040 | 115/679 | chr2 | 96972122 | |||
| chr2:96972168 | T | C | 9 | a0001 a0003 a0004 others(6): Show |
158 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(155): Show |
missense_variant | MODERATE | c.297A>G | p.Ile99Met | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 564/2698 | 297/2040 | 99/679 | chr2 | 96972168 | |||
| chr2:96972249 | G | T | 1 | a0008 | 2 | NA18949.hp1 NA19068.hp2 |
missense_variant | MODERATE | c.216C>A | p.Asp72Glu | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 483/2698 | 216/2040 | 72/679 | chr2 | 96972249 | |||
| chr2:96972271 | C | G | 1 | a0007 | 2 | HG02027.hp1 HG02071.hp2 |
missense_variant | MODERATE | c.194G>C | p.Gly65Ala | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 461/2698 | 194/2040 | 65/679 | chr2 | 96972271 | |||
| chr2:96972301 | A | G | 7 | a0001 a0004 a0005 others(4): Show |
144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
missense_variant | MODERATE | c.164T>C | p.Val55Ala | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 431/2698 | 164/2040 | 55/679 | chr2 | 96972301 | |||
| chr2:96972574 | G | A | 1 | a0005 | 7 | HG00642.hp1 HG00741.hp1 HG01943.hp1 others(4): Show |
missense_variant | MODERATE | c.106C>T | p.Pro36Ser | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 2/17 | 373/2698 | 106/2040 | 36/679 | chr2 | 96972574 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96894022 | G | A | 9 | a0001c0003 a0001c0017 a0002c0002 others(6): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
synonymous_variant | LOW | c.1680C>T | p.Leu560Leu | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/17 | 1947/2698 | 1680/2040 | 560/679 | chr2 | 96894022 | |||
| chr2:96921625 | C | T | 1 | a0001c0019 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1317G>A | p.Pro439Pro | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 11/17 | 1584/2698 | 1317/2040 | 439/679 | chr2 | 96921625 | |||
| chr2:96921640 | A | G | 1 | a0010c0018 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1302T>C | p.Cys434Cys | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 11/17 | 1569/2698 | 1302/2040 | 434/679 | chr2 | 96921640 | |||
| chr2:96929226 | C | A | 1 | a0001c0012 | 3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.1173G>T | p.Gly391Gly | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/17 | 1440/2698 | 1173/2040 | 391/679 | chr2 | 96929226 | |||
| chr2:96947879 | T | C | 23 | a0001c0001 a0001c0003 a0001c0012 others(20): Show |
178 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(175): Show |
synonymous_variant | LOW | c.1017A>G | p.Thr339Thr | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/17 | 1284/2698 | 1017/2040 | 339/679 | chr2 | 96947879 | |||
| chr2:96951403 | T | C | 20 | a0001c0001 a0001c0003 a0001c0012 others(17): Show |
174 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(171): Show |
synonymous_variant | LOW | c.969A>G | p.Val323Val | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/17 | 1236/2698 | 969/2040 | 323/679 | chr2 | 96951403 | |||
| chr2:96972069 | C | T | 1 | a0002c0015 | 2 | HG03516.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.396G>A | p.Gln132Gln | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 663/2698 | 396/2040 | 132/679 | chr2 | 96972069 | |||
| chr2:96972186 | C | T | 1 | a0001c0017 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.279G>A | p.Ser93Ser | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/17 | 546/2698 | 279/2040 | 93/679 | chr2 | 96972186 | |||
| chr2:96972593 | G | A | 1 | a0002c0027 | 1 | NA19002.hp2 | synonymous_variant | LOW | c.87C>T | p.His29His | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 2/17 | 354/2698 | 87/2040 | 29/679 | chr2 | 96972593 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96875912 | A | G | 1 | a0002c0002t0007 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*364T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 17/17 | 364 | chr2 | 96875912 | ||||||
| chr2:96875947 | AGGAG | A | 1 | a0006c0007t0002 | 6 | HG02559.hp1 HG02572.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*325_*328delCTCC | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 17/17 | 325 | chr2 | 96875947 | ||||||
| chr2:96876079 | GGGGGTCG others(36): Show |
G | 1 | a0002c0002t0006 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*154_*196delTCTCCT others(37): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 17/17 | 154 | chr2 | 96876079 | ||||||
| chr2:96876099 | A | AGGCAGGC others(36): Show |
1 | a0002c0010t0001 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134_*176dupCCTGCC others(37): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 17/17 | 176 | chr2 | 96876099 | ||||||
| chr2:96876201 | C | T | 1 | a0002c0023t0005 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*75G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 17/17 | 75 | chr2 | 96876201 | ||||||
| chr2:96986353 | C | T | 1 | a0002c0015t0003 | 2 | HG03516.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-40G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/17 | 40 | chr2 | 96986353 | ||||||
| chr2:96986455 | C | T | 1 | a0001c0001t0004 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-142G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/17 | 142 | chr2 | 96986455 | ||||||
| chr2:96986504 | T | C | 1 | a0001c0003t0008 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-191A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/17 | 191 | chr2 | 96986504 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96876312 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02809.hp2 HG02895.hp2 |
splice_region_variant&intron_variant | LOW | c.2008-4G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96876312 | |||||||
| chr2:96876385 | C | T | 2 | a0001c0001t0001g0133 a0002c0002t0001g0204 |
2 | NA18956.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.2008-77G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96876385 | |||||||
| chr2:96876683 | T | C | 1 | a0001c0003t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2008-375A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96876683 | |||||||
| chr2:96876956 | T | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0088 others(5): Show |
8 | HG02572.hp1 HG02647.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2008-648A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96876956 | |||||||
| chr2:96877160 | C | T | 1 | a0014c0020t0001g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2007+730G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877160 | |||||||
| chr2:96877325 | G | A | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2007+565C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877325 | |||||||
| chr2:96877345 | T | G | 5 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG00438.hp1 HG00558.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.2007+545A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877345 | |||||||
| chr2:96877402 | A | AT | 19 | a0001c0001t0001g0077 a0001c0001t0001g0082 a0001c0001t0001g0089 others(16): Show |
19 | HG00741.hp1 HG01070.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.2007+487dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877402 | |||||||
| chr2:96877402 | AT | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0112 a0001c0001t0001g0119 others(2): Show |
5 | HG01257.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2007+487delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877402 | |||||||
| chr2:96877548 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2007+342C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877548 | |||||||
| chr2:96877563 | C | G | 3 | a0001c0003t0001g0069 a0001c0003t0001g0070 a0001c0003t0001g0073 |
3 | HG01891.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2007+327G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877563 | |||||||
| chr2:96877564 | G | A | 1 | a0003c0011t0001g0236 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2007+326C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877564 | |||||||
| chr2:96877628 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0089 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2007+262G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877628 | |||||||
| chr2:96877638 | G | A | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2007+252C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877638 | |||||||
| chr2:96877641 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2007+249G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877641 | |||||||
| chr2:96877672 | G | C | 1 | a0002c0002t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2007+218C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877672 | |||||||
| chr2:96877675 | G | A | 1 | a0004c0004t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2007+215C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877675 | |||||||
| chr2:96877727 | G | C | 1 | a0001c0001t0001g0133 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2007+163C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 16/16 | chr2 | 96877727 | |||||||
| chr2:96878092 | C | T | 2 | a0006c0007t0002g0087 a0006c0007t0002g0098 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1855-50G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 15/16 | chr2 | 96878092 | |||||||
| chr2:96878199 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0018 others(166): Show |
170 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.1855-157A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 15/16 | chr2 | 96878199 | |||||||
| chr2:96878233 | C | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0131 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854+183G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 15/16 | chr2 | 96878233 | |||||||
| chr2:96878279 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0034 others(28): Show |
32 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1854+137C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 15/16 | chr2 | 96878279 | |||||||
| chr2:96878352 | G | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0018 others(149): Show |
153 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1854+64C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 15/16 | chr2 | 96878352 | |||||||
| chr2:96878352 | G | T | 4 | a0002c0002t0001g0168 a0002c0002t0001g0171 a0002c0002t0001g0172 others(1): Show |
4 | NA18982.hp1 NA18999.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1854+64C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 15/16 | chr2 | 96878352 | |||||||
| chr2:96878546 | T | C | 1 | a0001c0003t0001g0072 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1777-53A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96878546 | |||||||
| chr2:96878759 | T | TAGAAAAA others(335): Show |
1 | a0002c0002t0007g0173 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1777-267_1777-266i others(344): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96878759 | |||||||
| chr2:96878955 | C | T | 4 | a0006c0007t0002g0041 a0006c0007t0002g0095 a0006c0007t0002g0096 others(1): Show |
4 | HG02559.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-462G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96878955 | |||||||
| chr2:96878972 | C | T | 2 | a0001c0003t0001g0033 a0001c0003t0001g0053 |
2 | NA18995.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1777-479G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96878972 | |||||||
| chr2:96878986 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1777-493C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96878986 | |||||||
| chr2:96879261 | C | T | 2 | a0003c0011t0001g0246 a0003c0011t0001g0247 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1777-768G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96879261 | |||||||
| chr2:96879389 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1777-896C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96879389 | |||||||
| chr2:96879426 | G | A | 1 | a0001c0003t0001g0094 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1777-933C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96879426 | |||||||
| chr2:96879569 | C | T | 2 | a0001c0003t0001g0039 a0002c0002t0001g0209 |
2 | HG01106.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1777-1076G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96879569 | |||||||
| chr2:96879695 | G | C | 1 | a0001c0001t0004g0002 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1777-1202C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96879695 | |||||||
| chr2:96879750 | C | T | 1 | a0002c0002t0006g0189 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1777-1257G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96879750 | |||||||
| chr2:96879870 | C | CCTGCTGG others(7): Show |
1 | a0001c0003t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1777-1391_1777-137 others(18): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96879870 | |||||||
| chr2:96879904 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1777-1411G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96879904 | |||||||
| chr2:96880294 | G | A | 7 | a0001c0003t0001g0005 a0001c0003t0001g0029 a0001c0003t0001g0033 others(4): Show |
7 | HG00597.hp1 HG04184.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1777-1801C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96880294 | |||||||
| chr2:96880385 | G | A | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1777-1892C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96880385 | |||||||
| chr2:96880600 | A | AT | 58 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(55): Show |
59 | HG00423.hp2 HG00741.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.1777-2108dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96880600 | |||||||
| chr2:96880600 | A | ATT | 8 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1777-2109_1777-210 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96880600 | |||||||
| chr2:96880617 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1777-2124G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96880617 | |||||||
| chr2:96880735 | C | T | 1 | a0002c0002t0001g0177 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1777-2242G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96880735 | |||||||
| chr2:96880841 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1777-2348C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96880841 | |||||||
| chr2:96881270 | C | CA | 14 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0059 others(11): Show |
14 | HG00544.hp2 HG01123.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1777-2778dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96881270 | |||||||
| chr2:96881270 | CA | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(34): Show |
38 | HG00423.hp2 HG01070.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1777-2778delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96881270 | |||||||
| chr2:96881270 | CAA | C | 22 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0077 others(19): Show |
22 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1777-2779_1777-277 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96881270 | |||||||
| chr2:96881382 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1777-2889G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96881382 | |||||||
| chr2:96881383 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1777-2890C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96881383 | |||||||
| chr2:96881452 | C | T | 1 | a0002c0008t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1777-2959G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96881452 | |||||||
| chr2:96881663 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1777-3170G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96881663 | |||||||
| chr2:96881950 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1777-3457G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96881950 | |||||||
| chr2:96882032 | C | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0042 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1777-3539G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96882032 | |||||||
| chr2:96882132 | T | C | 2 | a0001c0003t0001g0039 a0002c0002t0001g0209 |
2 | HG01106.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1777-3639A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96882132 | |||||||
| chr2:96882230 | C | A | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1777-3737G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96882230 | |||||||
| chr2:96882300 | G | A | 3 | a0001c0003t0001g0069 a0001c0003t0001g0070 a0001c0003t0001g0073 |
3 | HG01891.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1777-3807C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96882300 | |||||||
| chr2:96882312 | G | A | 2 | a0001c0003t0001g0024 a0001c0003t0001g0025 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1777-3819C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96882312 | |||||||
| chr2:96882414 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1777-3921C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96882414 | |||||||
| chr2:96882654 | A | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(51): Show |
55 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.1777-4161T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96882654 | |||||||
| chr2:96883000 | G | A | 1 | a0002c0008t0001g0232 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1777-4507C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883000 | |||||||
| chr2:96883090 | G | A | 6 | a0002c0002t0001g0151 a0002c0002t0001g0169 a0002c0002t0001g0185 others(3): Show |
6 | HG01070.hp1 HG01257.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1777-4597C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883090 | |||||||
| chr2:96883440 | T | A | 4 | a0002c0008t0001g0229 a0002c0008t0001g0233 a0007c0014t0001g0228 others(1): Show |
4 | HG02027.hp1 HG02071.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-4947A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883440 | |||||||
| chr2:96883488 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1777-4995G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883488 | |||||||
| chr2:96883535 | G | A | 5 | a0002c0008t0001g0229 a0002c0008t0001g0233 a0002c0008t0001g0234 others(2): Show |
5 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1777-5042C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883535 | |||||||
| chr2:96883623 | G | C | 2 | a0003c0011t0001g0246 a0003c0011t0001g0247 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1777-5130C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883623 | |||||||
| chr2:96883623 | G | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-5130C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883623 | |||||||
| chr2:96883630 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1777-5137T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883630 | |||||||
| chr2:96883836 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1777-5343G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883836 | |||||||
| chr2:96883931 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(162): Show |
166 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.1777-5438T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883931 | |||||||
| chr2:96883948 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1777-5455G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883948 | |||||||
| chr2:96883992 | G | A | 2 | a0002c0002t0001g0206 a0002c0002t0001g0211 |
2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1777-5499C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96883992 | |||||||
| chr2:96884094 | C | CT | 5 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0131 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1777-5602dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96884094 | |||||||
| chr2:96884717 | G | A | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1777-6224C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96884717 | |||||||
| chr2:96884724 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1777-6231C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96884724 | |||||||
| chr2:96884853 | T | C | 6 | a0006c0007t0002g0041 a0006c0007t0002g0087 a0006c0007t0002g0095 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1777-6360A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96884853 | |||||||
| chr2:96884859 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(10): Show |
13 | HG01261.hp2 HG01358.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1777-6366T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96884859 | |||||||
| chr2:96885006 | G | A | 7 | a0005c0006t0001g0020 a0005c0006t0001g0021 a0005c0006t0001g0022 others(4): Show |
7 | HG00642.hp1 HG00741.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1777-6513C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885006 | |||||||
| chr2:96885099 | G | C | 4 | a0001c0003t0001g0084 a0001c0003t0001g0101 a0001c0003t0001g0102 others(1): Show |
4 | HG03225.hp2 NA18522.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1777-6606C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885099 | |||||||
| chr2:96885118 | T | C | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1777-6625A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885118 | |||||||
| chr2:96885420 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0131 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-6927G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885420 | |||||||
| chr2:96885508 | C | T | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1777-7015G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885508 | |||||||
| chr2:96885611 | C | G | 1 | a0002c0002t0001g0166 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1777-7118G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885611 | |||||||
| chr2:96885733 | G | A | 5 | a0002c0008t0001g0229 a0002c0008t0001g0233 a0002c0008t0001g0234 others(2): Show |
5 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1777-7240C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885733 | |||||||
| chr2:96885935 | C | A | 6 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(3): Show |
6 | HG00099.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1777-7442G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885935 | |||||||
| chr2:96885964 | C | T | 1 | a0001c0003t0001g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1777-7471G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96885964 | |||||||
| chr2:96886007 | C | CTT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(162): Show |
166 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.1777-7515_1777-751 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886007 | |||||||
| chr2:96886040 | T | C | 1 | a0001c0003t0001g0056 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1777-7547A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886040 | |||||||
| chr2:96886049 | G | A | 1 | a0001c0019t0001g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1777-7556C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886049 | |||||||
| chr2:96886145 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1777-7652C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886145 | |||||||
| chr2:96886365 | G | A | 1 | a0002c0002t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1776+7561C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886365 | |||||||
| chr2:96886483 | G | A | 6 | a0006c0007t0002g0041 a0006c0007t0002g0087 a0006c0007t0002g0095 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1776+7443C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886483 | |||||||
| chr2:96886641 | G | A | 7 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
7 | NA18941.hp1 NA18951.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1776+7285C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886641 | |||||||
| chr2:96886686 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1776+7240G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886686 | |||||||
| chr2:96886792 | C | G | 5 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1776+7134G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886792 | |||||||
| chr2:96886877 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(176): Show |
180 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.1776+7049T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886877 | |||||||
| chr2:96886890 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(157): Show |
161 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1776+7036C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886890 | |||||||
| chr2:96886907 | G | A | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1776+7019C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886907 | |||||||
| chr2:96886918 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1776+7008T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886918 | |||||||
| chr2:96886985 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1776+6941G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886985 | |||||||
| chr2:96886997 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0034 others(20): Show |
24 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1776+6929C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96886997 | |||||||
| chr2:96887175 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0034 others(54): Show |
58 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.1776+6751T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96887175 | |||||||
| chr2:96887215 | A | AAAC | 115 | a0001c0001t0001g0058 a0001c0001t0001g0138 a0001c0003t0001g0005 others(112): Show |
115 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1776+6708_1776+671 others(7): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96887215 | |||||||
| chr2:96887519 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1776+6407G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96887519 | |||||||
| chr2:96887531 | C | T | 1 | a0003c0011t0001g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1776+6395G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96887531 | |||||||
| chr2:96887563 | C | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0131 others(8): Show |
11 | HG00099.hp2 HG01175.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1776+6363G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96887563 | |||||||
| chr2:96887891 | C | T | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1776+6035G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96887891 | |||||||
| chr2:96888010 | G | A | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+5916C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888010 | |||||||
| chr2:96888172 | T | C | 6 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(3): Show |
6 | HG00099.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1776+5754A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888172 | |||||||
| chr2:96888343 | C | T | 3 | a0001c0003t0001g0014 a0001c0003t0001g0083 a0001c0003t0001g0100 |
3 | HG02896.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1776+5583G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888343 | |||||||
| chr2:96888483 | C | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1776+5443G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888483 | |||||||
| chr2:96888543 | C | T | 2 | a0003c0011t0001g0246 a0003c0011t0001g0247 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1776+5383G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888543 | |||||||
| chr2:96888601 | T | C | 1 | a0002c0010t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1776+5325A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888601 | |||||||
| chr2:96888617 | C | T | 1 | a0002c0002t0001g0182 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1776+5309G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888617 | |||||||
| chr2:96888667 | G | A | 1 | a0003c0011t0001g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1776+5259C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888667 | |||||||
| chr2:96888844 | G | A | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+5082C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888844 | |||||||
| chr2:96888878 | G | A | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+5048C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888878 | |||||||
| chr2:96888888 | C | T | 5 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1776+5038G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888888 | |||||||
| chr2:96888969 | G | A | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+4957C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888969 | |||||||
| chr2:96888977 | G | A | 1 | a0002c0002t0001g0146 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1776+4949C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888977 | |||||||
| chr2:96888999 | G | A | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1776+4927C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96888999 | |||||||
| chr2:96889022 | G | A | 1 | a0005c0006t0001g0021 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1776+4904C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889022 | |||||||
| chr2:96889045 | T | C | 1 | a0001c0012t0001g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1776+4881A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889045 | |||||||
| chr2:96889207 | G | C | 1 | a0002c0008t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1776+4719C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889207 | |||||||
| chr2:96889394 | G | A | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1776+4532C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889394 | |||||||
| chr2:96889505 | C | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1776+4421G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889505 | |||||||
| chr2:96889536 | G | A | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1776+4390C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889536 | |||||||
| chr2:96889584 | A | G | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+4342T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889584 | |||||||
| chr2:96889634 | T | C | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+4292A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889634 | |||||||
| chr2:96889677 | C | CAAAT | 33 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1776+4245_1776+424 others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889677 | |||||||
| chr2:96889677 | C | CAAATAAA others(1): Show |
8 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0085 others(5): Show |
8 | HG01123.hp1 HG01169.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1776+4241_1776+424 others(12): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889677 | |||||||
| chr2:96889677 | C | CAAATAAA others(5): Show |
3 | a0001c0001t0001g0105 a0001c0012t0001g0141 a0004c0004t0001g0143 |
3 | HG01261.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1776+4237_1776+424 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889677 | |||||||
| chr2:96889677 | C | T | 1 | a0001c0012t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1776+4249G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889677 | |||||||
| chr2:96889677 | CAAAT | C | 3 | a0001c0001t0001g0136 a0006c0007t0002g0041 a0013c0025t0001g0006 |
3 | HG02647.hp1 HG03098.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1776+4245_1776+424 others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889677 | |||||||
| chr2:96889709 | TAAATAAA others(3): Show |
T | 2 | a0003c0011t0001g0246 a0003c0011t0001g0247 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1776+4207_1776+421 others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889709 | |||||||
| chr2:96889711 | A | C | 2 | a0001c0003t0001g0049 a0001c0003t0001g0100 |
2 | HG02896.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1776+4215T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889711 | |||||||
| chr2:96889712 | ATAAATAA others(4): Show |
A | 2 | a0001c0003t0001g0049 a0001c0003t0001g0100 |
2 | HG02896.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1776+4203_1776+421 others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889712 | |||||||
| chr2:96889721 | T | C | 2 | a0003c0011t0001g0246 a0003c0011t0001g0247 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1776+4205A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889721 | |||||||
| chr2:96889722 | A | AAATAAAT others(6): Show |
2 | a0002c0002t0001g0177 a0002c0002t0001g0181 |
2 | HG02135.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1776+4203_1776+420 others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889722 | |||||||
| chr2:96889722 | A | AAATAAAT others(2): Show |
15 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 others(12): Show |
15 | HG01106.hp2 HG01192.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1776+4203_1776+420 others(13): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889722 | |||||||
| chr2:96889722 | A | AAATAC | 66 | a0001c0003t0001g0005 a0001c0003t0001g0029 a0001c0003t0001g0033 others(63): Show |
66 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1776+4203_1776+420 others(9): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889722 | |||||||
| chr2:96889722 | A | C | 2 | a0003c0011t0001g0246 a0003c0011t0001g0247 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1776+4204T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889722 | |||||||
| chr2:96889723 | C | A | 86 | a0001c0003t0001g0005 a0001c0003t0001g0024 a0001c0003t0001g0025 others(83): Show |
86 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1776+4203G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889723 | |||||||
| chr2:96889723 | C | CA | 20 | a0001c0003t0001g0014 a0001c0003t0001g0016 a0001c0003t0001g0046 others(17): Show |
20 | HG01891.hp2 HG02004.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1776+4202dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889723 | |||||||
| chr2:96889815 | T | C | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1776+4111A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889815 | |||||||
| chr2:96889841 | G | C | 1 | a0001c0003t0001g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1776+4085C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889841 | |||||||
| chr2:96889862 | G | A | 2 | a0001c0003t0001g0033 a0001c0003t0001g0053 |
2 | NA18995.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1776+4064C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889862 | |||||||
| chr2:96889954 | C | T | 1 | a0003c0011t0001g0236 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1776+3972G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889954 | |||||||
| chr2:96889976 | T | TA | 238 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.1776+3949dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96889976 | |||||||
| chr2:96890000 | G | A | 1 | a0003c0005t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1776+3926C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890000 | |||||||
| chr2:96890041 | C | A | 1 | a0002c0002t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1776+3885G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890041 | |||||||
| chr2:96890067 | T | C | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+3859A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890067 | |||||||
| chr2:96890183 | G | A | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+3743C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890183 | |||||||
| chr2:96890223 | C | T | 7 | a0003c0005t0001g0239 a0003c0005t0001g0240 a0003c0005t0001g0241 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1776+3703G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890223 | |||||||
| chr2:96890255 | G | A | 1 | a0001c0003t0001g0100 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1776+3671C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890255 | |||||||
| chr2:96890301 | T | G | 1 | a0004c0004t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1776+3625A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890301 | |||||||
| chr2:96890301 | TATAA | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0034 others(19): Show |
23 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1776+3621_1776+362 others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890301 | |||||||
| chr2:96890302 | A | C | 1 | a0004c0004t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1776+3624T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890302 | |||||||
| chr2:96890303 | T | A | 1 | a0004c0004t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1776+3623A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890303 | |||||||
| chr2:96890305 | A | T | 1 | a0004c0004t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1776+3621T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890305 | |||||||
| chr2:96890427 | G | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1776+3499C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890427 | |||||||
| chr2:96890535 | A | C | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+3391T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890535 | |||||||
| chr2:96890806 | C | T | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+3120G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890806 | |||||||
| chr2:96890843 | G | A | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1776+3083C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890843 | |||||||
| chr2:96890888 | C | A | 2 | a0006c0007t0002g0087 a0006c0007t0002g0098 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1776+3038G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96890888 | |||||||
| chr2:96891101 | AGCCAGGA others(6): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1776+2812_1776+282 others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891101 | |||||||
| chr2:96891131 | A | G | 7 | a0003c0005t0001g0239 a0003c0005t0001g0240 a0003c0005t0001g0241 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1776+2795T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891131 | |||||||
| chr2:96891217 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1776+2709G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891217 | |||||||
| chr2:96891218 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1776+2708A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891218 | |||||||
| chr2:96891282 | T | C | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+2644A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891282 | |||||||
| chr2:96891524 | G | A | 105 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(102): Show |
105 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1776+2402C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891524 | |||||||
| chr2:96891556 | T | TG | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+2369_1776+237 others(5): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891556 | |||||||
| chr2:96891674 | C | T | 1 | a0009c0016t0001g0227 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1776+2252G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891674 | |||||||
| chr2:96891923 | G | T | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1776+2003C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96891923 | |||||||
| chr2:96892073 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1776+1853C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892073 | |||||||
| chr2:96892083 | C | G | 6 | a0006c0007t0002g0041 a0006c0007t0002g0087 a0006c0007t0002g0095 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1776+1843G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892083 | |||||||
| chr2:96892135 | C | T | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+1791G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892135 | |||||||
| chr2:96892229 | G | A | 4 | a0001c0003t0001g0084 a0001c0003t0001g0101 a0001c0003t0001g0102 others(1): Show |
4 | HG03225.hp2 NA18522.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1776+1697C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892229 | |||||||
| chr2:96892230 | C | A | 4 | a0001c0003t0001g0084 a0001c0003t0001g0101 a0001c0003t0001g0102 others(1): Show |
4 | HG03225.hp2 NA18522.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1776+1696G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892230 | |||||||
| chr2:96892313 | G | A | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1776+1613C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892313 | |||||||
| chr2:96892368 | A | C | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+1558T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892368 | |||||||
| chr2:96892413 | T | C | 105 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(102): Show |
105 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1776+1513A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892413 | |||||||
| chr2:96892623 | G | C | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1776+1303C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892623 | |||||||
| chr2:96892803 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1776+1123G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892803 | |||||||
| chr2:96892862 | C | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
7 | NA18941.hp1 NA18951.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1776+1064G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892862 | |||||||
| chr2:96892889 | C | T | 1 | a0001c0003t0001g0005 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1776+1037G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96892889 | |||||||
| chr2:96893013 | G | A | 1 | a0002c0002t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1776+913C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96893013 | |||||||
| chr2:96893189 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(168): Show |
172 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.1776+737A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96893189 | |||||||
| chr2:96893552 | C | T | 4 | a0001c0003t0001g0062 a0002c0002t0001g0146 a0002c0002t0001g0197 others(1): Show |
4 | HG00438.hp2 HG02040.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.1776+374G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96893552 | |||||||
| chr2:96893585 | C | A | 6 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(3): Show |
6 | HG00099.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1776+341G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96893585 | |||||||
| chr2:96893596 | A | T | 12 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0131 others(9): Show |
12 | HG00099.hp2 HG01175.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1776+330T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96893596 | |||||||
| chr2:96893734 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1776+192C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96893734 | |||||||
| chr2:96893895 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0037 |
2 | NA18979.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1776+31C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 14/16 | chr2 | 96893895 | |||||||
| chr2:96894247 | A | G | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1651-196T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894247 | |||||||
| chr2:96894347 | ACACCCAC others(5): Show |
A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1651-308_1651-297d others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894347 | |||||||
| chr2:96894400 | G | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(38): Show |
42 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1651-349C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894400 | |||||||
| chr2:96894427 | C | T | 7 | a0002c0002t0001g0145 a0002c0002t0001g0166 a0002c0002t0001g0175 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1651-376G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894427 | |||||||
| chr2:96894493 | T | C | 4 | a0001c0003t0001g0084 a0001c0003t0001g0101 a0001c0003t0001g0102 others(1): Show |
4 | HG03225.hp2 NA18522.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-442A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894493 | |||||||
| chr2:96894524 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1651-473G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894524 | |||||||
| chr2:96894526 | C | A | 8 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | NA18941.hp1 NA18951.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-475G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894526 | |||||||
| chr2:96894630 | A | C | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1651-579T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894630 | |||||||
| chr2:96894662 | C | A | 1 | a0003c0005t0001g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1651-611G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894662 | |||||||
| chr2:96894665 | C | T | 104 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(101): Show |
104 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1651-614G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894665 | |||||||
| chr2:96894713 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(200): Show |
204 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1651-662A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894713 | |||||||
| chr2:96894753 | C | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(19): Show |
23 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1651-702G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894753 | |||||||
| chr2:96894791 | TCACA | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0089 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-744_1651-741d others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894791 | |||||||
| chr2:96894876 | C | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1651-825G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894876 | |||||||
| chr2:96894892 | C | T | 111 | a0001c0003t0001g0005 a0001c0003t0001g0014 a0001c0003t0001g0016 others(108): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1651-841G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894892 | |||||||
| chr2:96894897 | CCTCACCC others(3): Show |
C | 1 | a0002c0002t0001g0017 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1651-856_1651-847d others(12): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894897 | |||||||
| chr2:96894924 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1651-873G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96894924 | |||||||
| chr2:96895064 | G | A | 6 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(3): Show |
6 | HG00099.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1651-1013C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895064 | |||||||
| chr2:96895097 | C | A | 1 | a0006c0007t0002g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1651-1046G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895097 | |||||||
| chr2:96895105 | T | G | 2 | a0001c0003t0001g0069 a0001c0003t0001g0073 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1651-1054A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895105 | |||||||
| chr2:96895176 | C | T | 103 | a0001c0003t0001g0014 a0001c0003t0001g0016 a0001c0003t0001g0024 others(100): Show |
103 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1651-1125G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895176 | |||||||
| chr2:96895207 | G | T | 1 | a0001c0003t0001g0072 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1651-1156C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895207 | |||||||
| chr2:96895346 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1651-1295C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895346 | |||||||
| chr2:96895703 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(161): Show |
165 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1651-1652T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895703 | |||||||
| chr2:96895814 | C | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | NA18941.hp1 NA18951.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-1763G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895814 | |||||||
| chr2:96895817 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1651-1766G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895817 | |||||||
| chr2:96895932 | C | T | 1 | a0002c0002t0001g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1651-1881G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895932 | |||||||
| chr2:96895933 | G | A | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1651-1882C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895933 | |||||||
| chr2:96895968 | G | C | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1651-1917C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895968 | |||||||
| chr2:96895973 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0080 |
2 | HG00544.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1651-1922C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895973 | |||||||
| chr2:96895996 | G | A | 2 | a0002c0010t0001g0007 a0004c0004t0001g0126 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1651-1945C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96895996 | |||||||
| chr2:96896026 | C | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1651-1975G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896026 | |||||||
| chr2:96896114 | T | C | 102 | a0001c0003t0001g0014 a0001c0003t0001g0016 a0001c0003t0001g0024 others(99): Show |
102 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1651-2063A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896114 | |||||||
| chr2:96896190 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(27): Show |
31 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1651-2139G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896190 | |||||||
| chr2:96896298 | C | T | 102 | a0001c0003t0001g0014 a0001c0003t0001g0016 a0001c0003t0001g0024 others(99): Show |
102 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1651-2247G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896298 | |||||||
| chr2:96896309 | T | G | 8 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | NA18941.hp1 NA18951.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-2258A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896309 | |||||||
| chr2:96896518 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1651-2467G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896518 | |||||||
| chr2:96896521 | G | A | 102 | a0001c0003t0001g0014 a0001c0003t0001g0016 a0001c0003t0001g0024 others(99): Show |
102 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1651-2470C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896521 | |||||||
| chr2:96896652 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1651-2601C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896652 | |||||||
| chr2:96896658 | C | G | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1651-2607G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896658 | |||||||
| chr2:96896814 | G | A | 102 | a0001c0003t0001g0014 a0001c0003t0001g0016 a0001c0003t0001g0024 others(99): Show |
102 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1651-2763C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896814 | |||||||
| chr2:96896865 | T | C | 1 | a0002c0002t0001g0017 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1651-2814A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896865 | |||||||
| chr2:96896985 | G | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0089 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-2934C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96896985 | |||||||
| chr2:96897039 | G | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0131 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-2988C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897039 | |||||||
| chr2:96897098 | C | G | 2 | a0002c0002t0001g0164 a0002c0002t0001g0179 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1651-3047G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897098 | |||||||
| chr2:96897206 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1651-3155G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897206 | |||||||
| chr2:96897271 | C | T | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1651-3220G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897271 | |||||||
| chr2:96897289 | CAT | C | 5 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0131 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-3240_1651-323 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897289 | |||||||
| chr2:96897294 | C | G | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1651-3243G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897294 | |||||||
| chr2:96897391 | C | T | 102 | a0001c0003t0001g0014 a0001c0003t0001g0016 a0001c0003t0001g0024 others(99): Show |
102 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1651-3340G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897391 | |||||||
| chr2:96897546 | G | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1651-3495C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897546 | |||||||
| chr2:96897556 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1651-3505C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897556 | |||||||
| chr2:96897653 | T | A | 1 | a0007c0014t0001g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1651-3602A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96897653 | |||||||
| chr2:96898008 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(156): Show |
160 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1651-3957A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96898008 | |||||||
| chr2:96898283 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1651-4232C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96898283 | |||||||
| chr2:96898290 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1651-4239C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96898290 | |||||||
| chr2:96898547 | G | A | 94 | a0001c0003t0001g0014 a0001c0003t0001g0016 a0001c0003t0001g0024 others(91): Show |
94 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1650+4073C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96898547 | |||||||
| chr2:96898642 | C | G | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650+3978G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96898642 | |||||||
| chr2:96898833 | G | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+3787C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96898833 | |||||||
| chr2:96898916 | C | T | 1 | a0006c0007t0002g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1650+3704G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96898916 | |||||||
| chr2:96898958 | T | C | 1 | a0006c0007t0002g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1650+3662A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96898958 | |||||||
| chr2:96899021 | G | C | 1 | a0002c0002t0001g0146 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1650+3599C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899021 | |||||||
| chr2:96899161 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(53): Show |
57 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.1650+3459T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899161 | |||||||
| chr2:96899362 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0001g0068 |
3 | HG01361.hp2 HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1650+3258G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899362 | |||||||
| chr2:96899482 | G | A | 3 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1650+3138C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899482 | |||||||
| chr2:96899520 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1650+3100A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899520 | |||||||
| chr2:96899810 | A | T | 1 | a0002c0008t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1650+2810T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899810 | |||||||
| chr2:96899834 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1650+2786G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899834 | |||||||
| chr2:96899851 | CT | C | 121 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0030 others(118): Show |
121 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1650+2768delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899851 | |||||||
| chr2:96899851 | CTT | C | 8 | a0001c0003t0001g0016 a0001c0003t0001g0025 a0001c0003t0001g0062 others(5): Show |
8 | HG01975.hp2 HG01993.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1650+2767_1650+276 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899851 | |||||||
| chr2:96899851 | CTTTTTTT others(2): Show |
C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1650+2760_1650+276 others(13): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899851 | |||||||
| chr2:96899851 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0110 others(4): Show |
7 | HG02145.hp1 HG02165.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1650+2759_1650+276 others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96899851 | |||||||
| chr2:96900009 | C | T | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1650+2611G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900009 | |||||||
| chr2:96900175 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1650+2445T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900175 | |||||||
| chr2:96900220 | C | T | 1 | a0002c0027t0001g0200 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1650+2400G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900220 | |||||||
| chr2:96900261 | G | C | 2 | a0009c0016t0001g0226 a0009c0016t0001g0227 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1650+2359C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900261 | |||||||
| chr2:96900314 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1650+2306G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900314 | |||||||
| chr2:96900373 | C | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1650+2247G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900373 | |||||||
| chr2:96900378 | C | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | NA18941.hp1 NA18951.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+2242G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900378 | |||||||
| chr2:96900411 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(51): Show |
55 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1650+2209C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900411 | |||||||
| chr2:96900565 | CA | C | 4 | a0001c0003t0001g0084 a0001c0003t0001g0101 a0001c0003t0001g0102 others(1): Show |
4 | HG03225.hp2 NA18522.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1650+2054delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900565 | |||||||
| chr2:96900764 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(51): Show |
55 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1650+1856C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900764 | |||||||
| chr2:96900826 | G | A | 5 | a0002c0002t0001g0206 a0002c0002t0001g0207 a0002c0002t0001g0208 others(2): Show |
5 | HG02602.hp2 HG02698.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1650+1794C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900826 | |||||||
| chr2:96900943 | C | G | 2 | a0002c0015t0003g0003 a0002c0015t0003g0004 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1650+1677G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96900943 | |||||||
| chr2:96901031 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(51): Show |
55 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1650+1589G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901031 | |||||||
| chr2:96901098 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1650+1522G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901098 | |||||||
| chr2:96901138 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1650+1482C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901138 | |||||||
| chr2:96901176 | CT | C | 50 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
50 | HG00558.hp1 HG00642.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1650+1443delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901176 | |||||||
| chr2:96901176 | CTT | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(51): Show |
55 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1650+1442_1650+144 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901176 | |||||||
| chr2:96901211 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(33): Show |
37 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1650+1409G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901211 | |||||||
| chr2:96901342 | TTTTG | T | 9 | a0001c0003t0008g0249 a0001c0017t0001g0142 a0002c0002t0001g0145 others(6): Show |
9 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1650+1274_1650+127 others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901342 | |||||||
| chr2:96901363 | G | A | 2 | a0002c0008t0001g0229 a0002c0008t0001g0233 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1650+1257C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901363 | |||||||
| chr2:96901485 | C | A | 1 | a0001c0003t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1650+1135G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901485 | |||||||
| chr2:96901652 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(102): Show |
106 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.1650+968G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901652 | |||||||
| chr2:96901891 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(102): Show |
106 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.1650+729A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901891 | |||||||
| chr2:96901962 | T | G | 1 | a0001c0012t0001g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1650+658A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901962 | |||||||
| chr2:96901979 | G | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | NA18941.hp1 NA18951.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+641C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96901979 | |||||||
| chr2:96902109 | A | ATTTTTTT others(1): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(24): Show |
28 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1650+503_1650+510d others(10): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96902109 | |||||||
| chr2:96902109 | A | ATTTTTTT others(2): Show |
9 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | HG02165.hp2 NA18941.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1650+502_1650+510d others(11): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96902109 | |||||||
| chr2:96902109 | AT | A | 60 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
60 | HG00642.hp2 HG01243.hp1 HG01261.hp2 others(57): Show |
intron_variant | MODIFIER | c.1650+510delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96902109 | |||||||
| chr2:96902169 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1650+451C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96902169 | |||||||
| chr2:96902207 | G | A | 1 | a0004c0004t0001g0043 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1650+413C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96902207 | |||||||
| chr2:96902334 | G | A | 7 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1650+286C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96902334 | |||||||
| chr2:96902339 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
34 | HG00642.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.1650+281G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 13/16 | chr2 | 96902339 | |||||||
| chr2:96902716 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(101): Show |
105 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.1563-9T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96902716 | |||||||
| chr2:96902989 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1563-282C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96902989 | |||||||
| chr2:96903034 | A | AT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(58): Show |
62 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.1563-328dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903034 | |||||||
| chr2:96903078 | C | T | 7 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563-371G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903078 | |||||||
| chr2:96903109 | G | A | 2 | a0002c0002t0001g0167 a0002c0008t0001g0230 |
2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1563-402C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903109 | |||||||
| chr2:96903182 | G | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1563-475C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903182 | |||||||
| chr2:96903232 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1563-525C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903232 | |||||||
| chr2:96903236 | T | C | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1563-529A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903236 | |||||||
| chr2:96903260 | C | T | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1563-553G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903260 | |||||||
| chr2:96903281 | C | T | 2 | a0002c0002t0001g0156 a0002c0024t0001g0222 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1563-574G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903281 | |||||||
| chr2:96903339 | G | C | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1563-632C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903339 | |||||||
| chr2:96903364 | C | T | 2 | a0002c0002t0001g0164 a0002c0002t0001g0179 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1563-657G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903364 | |||||||
| chr2:96903382 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(25): Show |
29 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1563-675G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903382 | |||||||
| chr2:96903463 | T | C | 7 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563-756A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903463 | |||||||
| chr2:96903525 | C | G | 1 | a0003c0011t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1563-818G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903525 | |||||||
| chr2:96903568 | G | A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-861C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903568 | |||||||
| chr2:96903927 | G | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
34 | HG00642.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.1563-1220C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903927 | |||||||
| chr2:96903992 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1563-1285G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903992 | |||||||
| chr2:96903998 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(14): Show |
18 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-1291C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96903998 | |||||||
| chr2:96904260 | C | T | 1 | a0001c0017t0001g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1563-1553G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904260 | |||||||
| chr2:96904263 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1563-1556C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904263 | |||||||
| chr2:96904344 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(51): Show |
55 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1563-1637T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904344 | |||||||
| chr2:96904522 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1563-1815G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904522 | |||||||
| chr2:96904541 | A | AT | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0035 others(16): Show |
19 | HG00597.hp2 HG00609.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1563-1835dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904541 | |||||||
| chr2:96904541 | AT | A | 60 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(57): Show |
60 | HG01261.hp2 HG01358.hp2 HG01496.hp1 others(57): Show |
intron_variant | MODIFIER | c.1563-1835delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904541 | |||||||
| chr2:96904541 | ATT | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(36): Show |
40 | HG00423.hp2 HG01070.hp2 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.1563-1836_1563-183 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904541 | |||||||
| chr2:96904640 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(34): Show |
38 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1563-1933A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904640 | |||||||
| chr2:96904909 | G | A | 2 | a0003c0011t0001g0246 a0003c0011t0001g0247 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1563-2202C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96904909 | |||||||
| chr2:96905022 | T | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(33): Show |
37 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1563-2315A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905022 | |||||||
| chr2:96905048 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1563-2341T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905048 | |||||||
| chr2:96905071 | G | A | 1 | a0015c0022t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1563-2364C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905071 | |||||||
| chr2:96905115 | G | A | 2 | a0006c0007t0002g0041 a0006c0007t0002g0097 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1563-2408C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905115 | |||||||
| chr2:96905174 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
34 | HG00642.hp2 HG01261.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.1563-2467G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905174 | |||||||
| chr2:96905527 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1563-2820T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905527 | |||||||
| chr2:96905556 | C | CA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(37): Show |
41 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1563-2850dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905556 | |||||||
| chr2:96905702 | C | T | 1 | a0002c0002t0001g0186 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1563-2995G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905702 | |||||||
| chr2:96905703 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1563-2996C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905703 | |||||||
| chr2:96905743 | C | A | 7 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563-3036G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905743 | |||||||
| chr2:96905812 | ATGTG | A | 40 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(37): Show |
40 | HG00642.hp2 HG01261.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.1563-3109_1563-310 others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905812 | |||||||
| chr2:96905814 | GTGTGTAT others(5): Show |
G | 3 | a0002c0008t0001g0229 a0002c0008t0001g0233 a0003c0011t0001g0236 |
3 | HG00609.hp1 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1563-3119_1563-310 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905814 | |||||||
| chr2:96905814 | GTGTGTAT others(7): Show |
G | 2 | a0007c0014t0001g0228 a0007c0014t0001g0231 |
2 | HG02027.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1563-3121_1563-310 others(18): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905814 | |||||||
| chr2:96905814 | GTGTGTAT others(11): Show |
G | 1 | a0002c0008t0001g0232 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1563-3125_1563-310 others(22): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905814 | |||||||
| chr2:96905816 | G | A | 2 | a0001c0003t0001g0223 a0002c0010t0001g0144 |
2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1563-3109C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905816 | |||||||
| chr2:96905816 | GTGTATAT others(5): Show |
G | 1 | a0002c0002t0001g0180 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1563-3121_1563-311 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905816 | |||||||
| chr2:96905816 | GTGTATAT others(7): Show |
G | 1 | a0002c0008t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1563-3123_1563-311 others(18): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905816 | |||||||
| chr2:96905818 | G | A | 96 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1563-3111C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905818 | |||||||
| chr2:96905818 | GTATA | G | 3 | a0001c0001t0001g0131 a0006c0007t0002g0096 a0006c0007t0002g0098 |
3 | HG02145.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1563-3115_1563-311 others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905818 | |||||||
| chr2:96905818 | GTATATA | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0108 a0011c0021t0001g0225 |
3 | HG01891.hp1 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1563-3117_1563-311 others(10): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905818 | |||||||
| chr2:96905818 | GTATATAT others(3): Show |
G | 2 | a0001c0001t0001g0051 a0001c0003t0001g0053 |
2 | HG00099.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1563-3121_1563-311 others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905818 | |||||||
| chr2:96905818 | GTATATAT others(9): Show |
G | 2 | a0001c0001t0001g0109 a0001c0003t0001g0118 |
2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1563-3127_1563-311 others(20): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905818 | |||||||
| chr2:96905820 | A | G | 18 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0060 others(15): Show |
18 | HG00544.hp1 HG01192.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-3113T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905820 | |||||||
| chr2:96905822 | A | G | 5 | a0001c0001t0001g0110 a0006c0007t0002g0041 a0006c0007t0002g0087 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1563-3115T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905822 | |||||||
| chr2:96905823 | T | C | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1563-3116A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905823 | |||||||
| chr2:96905824 | A | G | 3 | a0001c0001t0001g0131 a0006c0007t0002g0096 a0006c0007t0002g0098 |
3 | HG02145.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1563-3117T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905824 | |||||||
| chr2:96905826 | A | ATATATAC others(45): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1563-3120_1563-311 others(56): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905826 | |||||||
| chr2:96905826 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0108 a0006c0007t0002g0096 others(2): Show |
5 | HG01891.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1563-3119T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905826 | |||||||
| chr2:96905828 | A | ATATACGT others(43): Show |
1 | a0004c0004t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1563-3122_1563-312 others(54): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905828 | |||||||
| chr2:96905828 | A | ATATACGT others(45): Show |
2 | a0001c0001t0001g0067 a0004c0004t0001g0043 |
2 | HG01070.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1563-3122_1563-312 others(56): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905828 | |||||||
| chr2:96905828 | A | ATATACGT others(43): Show |
3 | a0001c0001t0001g0119 a0004c0004t0001g0125 a0004c0004t0001g0143 |
3 | HG01099.hp1 HG01261.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1563-3122_1563-312 others(54): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905828 | |||||||
| chr2:96905828 | ATATATAT others(4): Show |
A | 1 | a0002c0027t0001g0200 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1563-3132_1563-312 others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905828 | |||||||
| chr2:96905828 | ATATATAT others(32): Show |
A | 3 | a0002c0002t0001g0167 a0002c0002t0001g0176 a0002c0002t0001g0181 |
3 | HG02135.hp2 HG02165.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1563-3160_1563-312 others(43): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905828 | |||||||
| chr2:96905828 | ATATATAT others(33): Show |
A | 1 | a0002c0008t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1563-3161_1563-312 others(44): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905828 | |||||||
| chr2:96905830 | A | ATACGTAT others(43): Show |
1 | a0002c0009t0001g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1563-3124_1563-312 others(54): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905830 | |||||||
| chr2:96905830 | ATATATAT others(24): Show |
A | 1 | a0002c0002t0001g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1563-3154_1563-312 others(35): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905830 | |||||||
| chr2:96905830 | ATATATAT others(30): Show |
A | 1 | a0001c0003t0001g0069 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1563-3160_1563-312 others(41): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905830 | |||||||
| chr2:96905830 | ATATATAT others(31): Show |
A | 1 | a0002c0002t0001g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1563-3161_1563-312 others(42): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905830 | |||||||
| chr2:96905830 | ATATATAT others(32): Show |
A | 1 | a0002c0002t0001g0177 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1563-3162_1563-312 others(43): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905830 | |||||||
| chr2:96905832 | ATATATAT others(28): Show |
A | 1 | a0002c0009t0001g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1563-3160_1563-312 others(39): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905832 | |||||||
| chr2:96905832 | ATATATAT others(31): Show |
A | 1 | a0015c0022t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1563-3163_1563-312 others(42): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905832 | |||||||
| chr2:96905833 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(5): Show |
9 | HG00423.hp2 HG02602.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.1563-3126A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905833 | |||||||
| chr2:96905834 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(12): Show |
16 | HG00099.hp2 HG00423.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1563-3127T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905834 | |||||||
| chr2:96905834 | ATATATAT others(22): Show |
A | 1 | a0001c0003t0001g0039 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1563-3156_1563-312 others(33): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905834 | |||||||
| chr2:96905836 | A | ACG | 6 | a0001c0001t0001g0067 a0001c0001t0001g0119 a0004c0004t0001g0043 others(3): Show |
6 | HG01070.hp2 HG01099.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1563-3130_1563-312 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905836 | |||||||
| chr2:96905836 | A | G | 3 | a0001c0001t0001g0109 a0001c0003t0001g0118 a0012c0026t0001g0224 |
3 | HG02165.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1563-3129T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905836 | |||||||
| chr2:96905836 | ATATATAT others(20): Show |
A | 2 | a0002c0002t0001g0154 a0002c0002t0001g0163 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1563-3156_1563-313 others(31): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905836 | |||||||
| chr2:96905836 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1563-3158_1563-313 others(33): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905836 | |||||||
| chr2:96905838 | A | G | 2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1563-3131T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905838 | |||||||
| chr2:96905838 | ATATATAT others(20): Show |
A | 2 | a0002c0002t0001g0207 a0002c0002t0001g0208 |
2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1563-3158_1563-313 others(31): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905838 | |||||||
| chr2:96905840 | A | ATATATAT others(81): Show |
2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1563-3134_1563-313 others(92): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905840 | |||||||
| chr2:96905840 | A | G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0135 others(3): Show |
6 | NA18941.hp1 NA18951.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-3133T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905840 | |||||||
| chr2:96905840 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1563-3154_1563-313 others(25): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905840 | |||||||
| chr2:96905840 | ATATATAT others(17): Show |
A | 1 | a0002c0002t0001g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1563-3157_1563-313 others(28): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905840 | |||||||
| chr2:96905840 | ATATATAT others(18): Show |
A | 2 | a0002c0002t0001g0206 a0002c0002t0001g0211 |
2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1563-3158_1563-313 others(29): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905840 | |||||||
| chr2:96905842 | A | G | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1563-3135T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905842 | |||||||
| chr2:96905842 | ATATATAT others(18): Show |
A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0004c0004t0001g0126 |
3 | HG02622.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1563-3160_1563-313 others(29): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905842 | |||||||
| chr2:96905843 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(5): Show |
9 | HG00423.hp2 HG02602.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.1563-3136A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905843 | |||||||
| chr2:96905844 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(5): Show |
9 | HG00423.hp2 HG02602.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.1563-3137T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905844 | |||||||
| chr2:96905844 | ATATATAT others(12): Show |
A | 3 | a0001c0001t0001g0081 a0002c0002t0001g0204 a0002c0002t0007g0173 |
3 | NA18747.hp2 NA18995.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1563-3156_1563-313 others(23): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905844 | |||||||
| chr2:96905844 | ATATATAT others(13): Show |
A | 9 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0055 others(6): Show |
9 | HG02129.hp2 NA18965.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1563-3157_1563-313 others(24): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905844 | |||||||
| chr2:96905844 | ATATATAT others(16): Show |
A | 1 | a0003c0005t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1563-3160_1563-313 others(27): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905844 | |||||||
| chr2:96905844 | ATATATAT others(17): Show |
A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(7): Show |
10 | HG01261.hp2 HG01358.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1563-3161_1563-313 others(28): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905844 | |||||||
| chr2:96905844 | ATATATAT others(18): Show |
A | 5 | a0001c0001t0001g0013 a0001c0003t0001g0070 a0001c0012t0001g0139 others(2): Show |
5 | HG02717.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563-3162_1563-313 others(29): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905844 | |||||||
| chr2:96905844 | ATATATAT others(19): Show |
A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(3): Show |
6 | HG02109.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-3163_1563-313 others(30): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905844 | |||||||
| chr2:96905844 | ATATATAT others(20): Show |
A | 1 | a0001c0003t0001g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1563-3164_1563-313 others(31): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905844 | |||||||
| chr2:96905846 | ATATATAT others(8): Show |
A | 1 | a0002c0002t0001g0150 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1563-3154_1563-314 others(19): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(9): Show |
A | 1 | a0001c0003t0001g0025 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1563-3155_1563-314 others(20): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(10): Show |
A | 1 | a0001c0003t0001g0024 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1563-3156_1563-314 others(21): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG00438.hp1 HG00558.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1563-3159_1563-314 others(24): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(15): Show |
A | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1563-3161_1563-314 others(26): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(16): Show |
A | 3 | a0003c0005t0001g0239 a0003c0005t0001g0241 a0003c0005t0001g0245 |
3 | HG03195.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1563-3162_1563-314 others(27): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(17): Show |
A | 3 | a0001c0001t0001g0113 a0001c0003t0001g0102 a0003c0005t0001g0243 |
3 | HG01884.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1563-3163_1563-314 others(28): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(18): Show |
A | 2 | a0001c0001t0001g0116 a0001c0003t0001g0101 |
2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1563-3164_1563-314 others(29): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1563-3165_1563-314 others(30): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(20): Show |
A | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1563-3166_1563-314 others(31): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905846 | ATATATAT others(21): Show |
A | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1563-3167_1563-314 others(32): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905846 | |||||||
| chr2:96905847 | TATATATA others(4): Show |
T | 1 | a0002c0002t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1563-3151_1563-314 others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905847 | |||||||
| chr2:96905848 | ATATATAT others(6): Show |
A | 1 | a0002c0002t0001g0175 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1563-3154_1563-314 others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905848 | |||||||
| chr2:96905848 | ATATATAT others(9): Show |
A | 1 | a0001c0003t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1563-3157_1563-314 others(20): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905848 | |||||||
| chr2:96905848 | ATATATAT others(12): Show |
A | 1 | a0001c0003t0001g0075 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1563-3160_1563-314 others(23): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905848 | |||||||
| chr2:96905848 | ATATATAT others(14): Show |
A | 1 | a0003c0005t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1563-3162_1563-314 others(25): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905848 | |||||||
| chr2:96905848 | ATATATAT others(15): Show |
A | 1 | a0003c0005t0001g0240 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1563-3163_1563-314 others(26): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905848 | |||||||
| chr2:96905848 | ATATATAT others(18): Show |
A | 1 | a0001c0003t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1563-3166_1563-314 others(29): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905848 | |||||||
| chr2:96905850 | A | ATGTGTGT others(5): Show |
7 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563-3144_1563-314 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905850 | |||||||
| chr2:96905850 | ATATATAT others(6): Show |
A | 11 | a0001c0001t0001g0042 a0001c0017t0001g0142 a0002c0002t0001g0145 others(8): Show |
11 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1563-3156_1563-314 others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905850 | |||||||
| chr2:96905850 | ATATATAT others(7): Show |
A | 2 | a0002c0002t0001g0151 a0002c0002t0001g0166 |
2 | HG01257.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1563-3157_1563-314 others(18): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905850 | |||||||
| chr2:96905850 | ATATATAT others(8): Show |
A | 2 | a0002c0002t0001g0195 a0002c0002t0001g0202 |
2 | HG00423.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1563-3158_1563-314 others(19): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905850 | |||||||
| chr2:96905850 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1563-3163_1563-314 others(24): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905850 | |||||||
| chr2:96905850 | ATATATAT others(14): Show |
A | 1 | a0003c0005t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1563-3164_1563-314 others(25): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905850 | |||||||
| chr2:96905850 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1563-3165_1563-314 others(26): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905850 | |||||||
| chr2:96905852 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0082 a0001c0003t0001g0005 |
2 | HG00597.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1563-3155_1563-314 others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905852 | |||||||
| chr2:96905852 | ATATATAT others(4): Show |
A | 4 | a0002c0002t0001g0146 a0002c0002t0001g0170 a0002c0002t0001g0193 others(1): Show |
4 | HG00544.hp2 HG01361.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1563-3156_1563-314 others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905852 | |||||||
| chr2:96905852 | ATATATAT others(5): Show |
A | 3 | a0002c0002t0001g0168 a0002c0002t0001g0182 a0002c0002t0001g0185 |
3 | HG01981.hp2 NA18949.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1563-3157_1563-314 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905852 | |||||||
| chr2:96905852 | ATATATAT others(6): Show |
A | 4 | a0001c0003t0008g0249 a0002c0002t0001g0192 a0002c0002t0001g0201 others(1): Show |
4 | HG00609.hp2 HG01496.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1563-3158_1563-314 others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905852 | |||||||
| chr2:96905852 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1563-3163_1563-314 others(22): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905852 | |||||||
| chr2:96905852 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0066 others(1): Show |
4 | HG01258.hp2 HG01361.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1563-3165_1563-314 others(24): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905852 | |||||||
| chr2:96905854 | ATATATAT others(3): Show |
A | 2 | a0002c0002t0001g0017 a0002c0002t0001g0171 |
2 | HG01169.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1563-3157_1563-314 others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905854 | |||||||
| chr2:96905854 | ATATATAT others(4): Show |
A | 5 | a0001c0003t0001g0062 a0002c0002t0001g0165 a0002c0002t0001g0197 others(2): Show |
5 | HG00438.hp2 HG01106.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1563-3158_1563-314 others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905854 | |||||||
| chr2:96905854 | ATATATAT others(5): Show |
A | 1 | a0003c0011t0001g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1563-3159_1563-314 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905854 | |||||||
| chr2:96905854 | ATATATAT others(6): Show |
A | 1 | a0002c0002t0001g0148 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1563-3160_1563-314 others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905854 | |||||||
| chr2:96905854 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1563-3166_1563-314 others(23): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905854 | |||||||
| chr2:96905855 | TATATA | T | 3 | a0006c0007t0002g0041 a0006c0007t0002g0095 a0006c0007t0002g0097 |
3 | HG02559.hp1 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1563-3153_1563-314 others(9): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905855 | |||||||
| chr2:96905856 | A | ATATGTAT others(19): Show |
1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1563-3150_1563-314 others(30): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905856 | |||||||
| chr2:96905856 | A | G | 9 | a0001c0001t0001g0067 a0001c0001t0001g0085 a0001c0001t0001g0086 others(6): Show |
9 | HG01070.hp2 HG01099.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1563-3149T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905856 | |||||||
| chr2:96905856 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1563-3149T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905856 | |||||||
| chr2:96905856 | ATATATTT others(3): Show |
A | 1 | a0001c0003t0001g0094 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1563-3159_1563-315 others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905856 | |||||||
| chr2:96905858 | A | G | 9 | a0001c0001t0001g0067 a0001c0001t0001g0085 a0001c0001t0001g0086 others(6): Show |
9 | HG01070.hp2 HG01099.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1563-3151T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905858 | |||||||
| chr2:96905858 | A | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0006c0007t0002g0087 |
3 | HG01884.hp1 HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1563-3151T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905858 | |||||||
| chr2:96905858 | ATATTTTT others(3): Show |
A | 1 | a0002c0002t0001g0169 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1563-3161_1563-315 others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905858 | |||||||
| chr2:96905858 | ATATTTTT others(4): Show |
A | 2 | a0002c0002t0001g0147 a0002c0002t0001g0199 |
2 | HG03927.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1563-3162_1563-315 others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905858 | |||||||
| chr2:96905858 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1563-3163_1563-315 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905858 | |||||||
| chr2:96905858 | ATATTTTT others(8): Show |
A | 1 | a0002c0002t0001g0219 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1563-3166_1563-315 others(19): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905858 | |||||||
| chr2:96905860 | A | T | 15 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0108 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1563-3153T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905860 | |||||||
| chr2:96905860 | AT | A | 7 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563-3154delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905860 | |||||||
| chr2:96905860 | ATTTTTTT | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0064 others(2): Show |
5 | HG01169.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1563-3160_1563-315 others(11): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905860 | |||||||
| chr2:96905860 | ATTTTTTT others(5): Show |
A | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1563-3165_1563-315 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905860 | |||||||
| chr2:96905861 | T | TA | 5 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | NA18956.hp2 NA18962.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563-3155_1563-315 others(5): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905861 | |||||||
| chr2:96905861 | T | TGTATATA others(46): Show |
1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1563-3155_1563-315 others(57): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905861 | |||||||
| chr2:96905861 | T | TGTATATA others(48): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(4): Show |
8 | HG00423.hp2 HG02602.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.1563-3155_1563-315 others(59): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905861 | |||||||
| chr2:96905862 | T | A | 15 | a0001c0001t0001g0067 a0001c0001t0001g0085 a0001c0001t0001g0086 others(12): Show |
15 | HG01070.hp2 HG01099.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1563-3155A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905862 | |||||||
| chr2:96905863 | T | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(13): Show |
17 | HG00099.hp2 HG00423.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1563-3156A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905863 | |||||||
| chr2:96905864 | T | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
10 | HG01070.hp2 HG01099.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1563-3157A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905864 | |||||||
| chr2:96905865 | T | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(15): Show |
19 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1563-3158A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905865 | |||||||
| chr2:96905866 | T | A | 12 | a0001c0001t0001g0067 a0001c0001t0001g0085 a0001c0001t0001g0086 others(9): Show |
12 | HG01070.hp2 HG01099.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1563-3159A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905866 | |||||||
| chr2:96905867 | T | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(14): Show |
18 | HG00099.hp2 HG00423.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-3160A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905867 | |||||||
| chr2:96905868 | T | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
10 | HG01070.hp2 HG01099.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1563-3161A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905868 | |||||||
| chr2:96905869 | T | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0120 |
2 | HG03710.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1563-3162A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905869 | |||||||
| chr2:96905870 | T | A | 2 | a0001c0003t0001g0014 a0001c0003t0001g0083 |
2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1563-3163A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96905870 | |||||||
| chr2:96906136 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(52): Show |
56 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.1563-3429T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906136 | |||||||
| chr2:96906175 | C | T | 19 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(16): Show |
19 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1563-3468G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906175 | |||||||
| chr2:96906204 | C | CTT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(29): Show |
33 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.1563-3499_1563-349 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906204 | |||||||
| chr2:96906262 | C | T | 10 | a0001c0003t0008g0249 a0001c0017t0001g0142 a0002c0002t0001g0145 others(7): Show |
10 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1563-3555G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906262 | |||||||
| chr2:96906398 | A | T | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1563-3691T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906398 | |||||||
| chr2:96906485 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(34): Show |
38 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1563-3778G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906485 | |||||||
| chr2:96906492 | G | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(34): Show |
38 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1563-3785C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906492 | |||||||
| chr2:96906508 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1563-3801G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906508 | |||||||
| chr2:96906533 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(34): Show |
38 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1563-3826A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906533 | |||||||
| chr2:96906586 | C | T | 1 | a0005c0006t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1563-3879G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906586 | |||||||
| chr2:96906676 | C | T | 1 | a0001c0003t0001g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1563-3969G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906676 | |||||||
| chr2:96906733 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(34): Show |
38 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1563-4026G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906733 | |||||||
| chr2:96906738 | G | A | 1 | a0002c0002t0001g0204 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1563-4031C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906738 | |||||||
| chr2:96906755 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1563-4048G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906755 | |||||||
| chr2:96906763 | A | G | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-4056T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906763 | |||||||
| chr2:96906766 | G | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(17): Show |
21 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1563-4059C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906766 | |||||||
| chr2:96906811 | G | A | 2 | a0001c0001t0001g0112 a0002c0024t0001g0222 |
2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1563-4104C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906811 | |||||||
| chr2:96906814 | A | AAC | 37 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(34): Show |
38 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1563-4109_1563-410 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906814 | |||||||
| chr2:96906917 | C | A | 5 | a0001c0003t0001g0069 a0001c0003t0001g0070 a0001c0003t0001g0073 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563-4210G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906917 | |||||||
| chr2:96906935 | C | T | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1563-4228G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906935 | |||||||
| chr2:96906949 | G | A | 8 | a0002c0002t0001g0145 a0002c0002t0001g0151 a0002c0002t0001g0166 others(5): Show |
8 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1563-4242C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906949 | |||||||
| chr2:96906967 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1563-4260G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96906967 | |||||||
| chr2:96907035 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(35): Show |
39 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1563-4328C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907035 | |||||||
| chr2:96907061 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(72): Show |
76 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1563-4354A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907061 | |||||||
| chr2:96907261 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1563-4554C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907261 | |||||||
| chr2:96907325 | C | T | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-4618G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907325 | |||||||
| chr2:96907427 | G | C | 7 | a0001c0003t0001g0084 a0001c0003t0001g0101 a0001c0003t0001g0102 others(4): Show |
7 | HG00609.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1563-4720C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907427 | |||||||
| chr2:96907528 | G | A | 9 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 others(6): Show |
9 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1563-4821C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907528 | |||||||
| chr2:96907608 | G | A | 5 | a0001c0003t0001g0084 a0001c0003t0001g0101 a0001c0003t0001g0102 others(2): Show |
5 | HG03225.hp2 NA18522.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563-4901C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907608 | |||||||
| chr2:96907680 | G | A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-4973C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907680 | |||||||
| chr2:96907689 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(103): Show |
107 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1563-4982G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907689 | |||||||
| chr2:96907779 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1563-5072A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96907779 | |||||||
| chr2:96908005 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(14): Show |
18 | HG00423.hp2 HG01070.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-5298C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908005 | |||||||
| chr2:96908107 | A | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(60): Show |
64 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1563-5400T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908107 | |||||||
| chr2:96908213 | C | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(25): Show |
29 | HG00423.hp2 HG00609.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1563-5506G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908213 | |||||||
| chr2:96908238 | G | A | 1 | a0014c0020t0001g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1563-5531C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908238 | |||||||
| chr2:96908253 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1563-5546G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908253 | |||||||
| chr2:96908286 | C | T | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1563-5579G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908286 | |||||||
| chr2:96908711 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1563-6004C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908711 | |||||||
| chr2:96908782 | A | C | 18 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-6075T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908782 | |||||||
| chr2:96908784 | TCATACCA | T | 18 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-6084_1563-607 others(11): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908784 | |||||||
| chr2:96908842 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1563-6135C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908842 | |||||||
| chr2:96908855 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(26): Show |
30 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1563-6148G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96908855 | |||||||
| chr2:96909106 | G | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-6399C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909106 | |||||||
| chr2:96909142 | C | CA | 9 | a0001c0001t0001g0054 a0001c0003t0001g0062 a0002c0002t0001g0145 others(6): Show |
9 | HG00741.hp1 HG01243.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1563-6436dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909142 | |||||||
| chr2:96909142 | CAAAAAAA others(8): Show |
C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(26): Show |
30 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1563-6450_1563-643 others(19): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909142 | |||||||
| chr2:96909148 | A | G | 7 | a0003c0005t0001g0239 a0003c0005t0001g0240 a0003c0005t0001g0241 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563-6441T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909148 | |||||||
| chr2:96909247 | A | G | 7 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563-6540T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909247 | |||||||
| chr2:96909282 | T | C | 12 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1563-6575A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909282 | |||||||
| chr2:96909327 | C | T | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-6620G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909327 | |||||||
| chr2:96909437 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1563-6730G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909437 | |||||||
| chr2:96909554 | C | G | 1 | a0002c0002t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1563-6847G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909554 | |||||||
| chr2:96909928 | C | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(14): Show |
17 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1563-7221G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96909928 | |||||||
| chr2:96910284 | C | T | 3 | a0002c0008t0001g0159 a0002c0010t0001g0158 a0002c0010t0001g0160 |
3 | HG02486.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1563-7577G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910284 | |||||||
| chr2:96910531 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | HG01261.hp2 HG01358.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1563-7824C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910531 | |||||||
| chr2:96910563 | A | T | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-7856T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910563 | |||||||
| chr2:96910623 | CG | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | HG01261.hp2 HG01358.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1563-7917delC | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910623 | |||||||
| chr2:96910786 | C | T | 18 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563-8079G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910786 | |||||||
| chr2:96910797 | A | AT | 10 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0076 others(7): Show |
10 | HG01175.hp2 HG02165.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.1563-8091dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910797 | |||||||
| chr2:96910797 | AT | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0042 others(22): Show |
25 | HG01884.hp1 HG01891.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.1563-8091delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910797 | |||||||
| chr2:96910797 | ATTTTTT | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-8096_1563-809 others(10): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910797 | |||||||
| chr2:96910892 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1563-8185A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910892 | |||||||
| chr2:96910902 | G | T | 11 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0153 others(8): Show |
11 | HG00423.hp1 HG00609.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.1563-8195C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910902 | |||||||
| chr2:96910922 | A | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(28): Show |
32 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1563-8215T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96910922 | |||||||
| chr2:96911084 | T | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-8377A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911084 | |||||||
| chr2:96911117 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.1563-8410T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911117 | |||||||
| chr2:96911345 | C | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(27): Show |
31 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1563-8638G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911345 | |||||||
| chr2:96911450 | G | A | 1 | a0007c0014t0001g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1563-8743C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911450 | |||||||
| chr2:96911479 | G | A | 3 | a0001c0003t0001g0069 a0001c0003t0001g0070 a0001c0003t0001g0073 |
3 | HG01891.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1563-8772C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911479 | |||||||
| chr2:96911504 | T | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(27): Show |
31 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1563-8797A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911504 | |||||||
| chr2:96911606 | C | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(45): Show |
49 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.1563-8899G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911606 | |||||||
| chr2:96911618 | G | A | 1 | a0001c0003t0001g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1563-8911C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911618 | |||||||
| chr2:96911677 | G | A | 1 | a0005c0006t0001g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1563-8970C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911677 | |||||||
| chr2:96911758 | T | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(27): Show |
31 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1563-9051A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911758 | |||||||
| chr2:96911924 | A | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.1563-9217T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911924 | |||||||
| chr2:96911998 | G | A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0088 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1562+9167C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96911998 | |||||||
| chr2:96912352 | C | T | 1 | a0001c0003t0001g0016 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1562+8813G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912352 | |||||||
| chr2:96912413 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(100): Show |
104 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.1562+8752T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912413 | |||||||
| chr2:96912453 | G | T | 37 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(34): Show |
37 | HG00609.hp1 HG00642.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1562+8712C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912453 | |||||||
| chr2:96912510 | GGGAA | G | 6 | a0002c0002t0001g0149 a0002c0002t0001g0153 a0002c0002t0001g0183 others(3): Show |
6 | HG00609.hp2 NA18945.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1562+8651_1562+865 others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912510 | |||||||
| chr2:96912592 | C | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(53): Show |
57 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.1562+8573G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912592 | |||||||
| chr2:96912656 | C | T | 7 | a0004c0004t0001g0121 a0004c0004t0001g0122 a0004c0004t0001g0123 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1562+8509G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912656 | |||||||
| chr2:96912703 | G | A | 1 | a0004c0004t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1562+8462C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912703 | |||||||
| chr2:96912823 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1562+8342G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912823 | |||||||
| chr2:96912824 | T | G | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1562+8341A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912824 | |||||||
| chr2:96912942 | T | C | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1562+8223A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96912942 | |||||||
| chr2:96913045 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1562+8120G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96913045 | |||||||
| chr2:96913527 | C | T | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+7638G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96913527 | |||||||
| chr2:96913533 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(50): Show |
54 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1562+7632A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96913533 | |||||||
| chr2:96913545 | C | T | 1 | a0002c0002t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1562+7620G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96913545 | |||||||
| chr2:96913715 | G | A | 9 | a0001c0003t0008g0249 a0001c0017t0001g0142 a0002c0002t0001g0145 others(6): Show |
9 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1562+7450C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96913715 | |||||||
| chr2:96913770 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(106): Show |
110 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1562+7395A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96913770 | |||||||
| chr2:96914390 | C | T | 7 | a0001c0003t0001g0100 a0006c0007t0002g0041 a0006c0007t0002g0087 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1562+6775G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96914390 | |||||||
| chr2:96914432 | G | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+6733C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96914432 | |||||||
| chr2:96914479 | A | G | 1 | a0003c0005t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1562+6686T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96914479 | |||||||
| chr2:96914545 | T | C | 1 | a0001c0003t0001g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1562+6620A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96914545 | |||||||
| chr2:96914591 | T | C | 1 | a0003c0005t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1562+6574A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96914591 | |||||||
| chr2:96914695 | G | A | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1562+6470C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96914695 | |||||||
| chr2:96914993 | A | G | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1562+6172T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96914993 | |||||||
| chr2:96915021 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1562+6144C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915021 | |||||||
| chr2:96915028 | T | C | 13 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0010t0001g0158 others(10): Show |
13 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1562+6137A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915028 | |||||||
| chr2:96915112 | A | AT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(37): Show |
41 | HG00423.hp2 HG01099.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.1562+6052dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915112 | |||||||
| chr2:96915112 | A | T | 1 | a0006c0007t0002g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1562+6053T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915112 | |||||||
| chr2:96915286 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0068 |
2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1562+5879A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915286 | |||||||
| chr2:96915730 | C | T | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1562+5435G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915730 | |||||||
| chr2:96915814 | A | G | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1562+5351T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915814 | |||||||
| chr2:96915901 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1562+5264G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915901 | |||||||
| chr2:96915907 | C | T | 1 | a0002c0002t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1562+5258G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915907 | |||||||
| chr2:96915963 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1562+5202G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915963 | |||||||
| chr2:96915984 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1562+5181G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96915984 | |||||||
| chr2:96916338 | C | T | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1562+4827G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96916338 | |||||||
| chr2:96916498 | A | T | 1 | a0001c0001t0001g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1562+4667T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96916498 | |||||||
| chr2:96916602 | T | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1562+4563A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96916602 | |||||||
| chr2:96916614 | G | A | 6 | a0002c0002t0001g0151 a0002c0002t0001g0169 a0002c0002t0001g0185 others(3): Show |
6 | HG01070.hp1 HG01257.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1562+4551C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96916614 | |||||||
| chr2:96917367 | G | A | 4 | a0001c0003t0001g0069 a0001c0003t0001g0070 a0001c0003t0001g0073 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1562+3798C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96917367 | |||||||
| chr2:96917462 | T | A | 1 | a0002c0002t0001g0202 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1562+3703A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96917462 | |||||||
| chr2:96917504 | T | C | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+3661A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96917504 | |||||||
| chr2:96917832 | G | C | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1562+3333C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96917832 | |||||||
| chr2:96917946 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(10): Show |
14 | HG00423.hp2 HG02602.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1562+3219G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96917946 | |||||||
| chr2:96917947 | C | G | 28 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(25): Show |
28 | HG00642.hp2 HG01261.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1562+3218G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96917947 | |||||||
| chr2:96917967 | T | C | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1562+3198A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96917967 | |||||||
| chr2:96918148 | T | C | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1562+3017A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918148 | |||||||
| chr2:96918153 | T | TA | 6 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0010t0001g0158 others(3): Show |
6 | HG02055.hp1 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1562+3011dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918153 | |||||||
| chr2:96918208 | C | T | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+2957G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918208 | |||||||
| chr2:96918224 | A | G | 3 | a0002c0015t0003g0003 a0002c0015t0003g0004 a0002c0024t0001g0222 |
3 | HG03453.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1562+2941T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918224 | |||||||
| chr2:96918447 | C | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+2718G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918447 | |||||||
| chr2:96918521 | A | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(29): Show |
33 | HG00423.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1562+2644T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918521 | |||||||
| chr2:96918537 | T | G | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0133 others(7): Show |
10 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.1562+2628A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918537 | |||||||
| chr2:96918646 | C | CCCAAAGC others(5): Show |
6 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0010t0001g0158 others(3): Show |
6 | HG02055.hp1 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1562+2518_1562+251 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918646 | |||||||
| chr2:96918855 | C | T | 3 | a0001c0003t0001g0223 a0002c0010t0001g0158 a0002c0010t0001g0160 |
3 | HG02055.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1562+2310G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918855 | |||||||
| chr2:96918893 | C | T | 1 | a0001c0003t0001g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1562+2272G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96918893 | |||||||
| chr2:96919132 | C | T | 6 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0010t0001g0158 others(3): Show |
6 | HG02055.hp1 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1562+2033G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96919132 | |||||||
| chr2:96919948 | G | A | 1 | a0002c0002t0001g0148 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1562+1217C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96919948 | |||||||
| chr2:96920149 | G | A | 1 | a0002c0002t0001g0148 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1562+1016C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920149 | |||||||
| chr2:96920173 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(28): Show |
32 | HG00423.hp2 HG01884.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1562+992C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920173 | |||||||
| chr2:96920199 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(34): Show |
38 | HG00423.hp2 HG01884.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.1562+966G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920199 | |||||||
| chr2:96920328 | G | A | 2 | a0004c0004t0001g0121 a0004c0004t0001g0124 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1562+837C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920328 | |||||||
| chr2:96920417 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1562+748G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920417 | |||||||
| chr2:96920484 | C | T | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1562+681G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920484 | |||||||
| chr2:96920521 | A | T | 1 | a0001c0003t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1562+644T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920521 | |||||||
| chr2:96920555 | G | A | 1 | a0003c0011t0001g0236 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1562+610C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920555 | |||||||
| chr2:96920571 | G | A | 9 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1562+594C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920571 | |||||||
| chr2:96920780 | T | TAGGCAGA others(16): Show |
1 | a0001c0003t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1562+362_1562+384d others(25): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920780 | |||||||
| chr2:96920831 | G | A | 9 | a0001c0001t0001g0079 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1562+334C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | 96920831 | |||||||
| chr2:96921312 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1465-50A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 11/16 | chr2 | 96921312 | |||||||
| chr2:96921325 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1465-63G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 11/16 | chr2 | 96921325 | |||||||
| chr2:96921469 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1464+9C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 11/16 | chr2 | 96921469 | |||||||
| chr2:96921766 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1288-112G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96921766 | |||||||
| chr2:96921926 | G | T | 1 | a0002c0002t0001g0181 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1288-272C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96921926 | |||||||
| chr2:96922040 | C | A | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1288-386G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922040 | |||||||
| chr2:96922127 | C | T | 7 | a0003c0005t0001g0239 a0003c0005t0001g0240 a0003c0005t0001g0241 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1288-473G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922127 | |||||||
| chr2:96922143 | A | G | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288-489T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922143 | |||||||
| chr2:96922162 | G | A | 8 | a0001c0003t0001g0016 a0001c0003t0001g0094 a0001c0003t0001g0223 others(5): Show |
8 | HG02055.hp1 HG02165.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1288-508C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922162 | |||||||
| chr2:96922359 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1288-705G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922359 | |||||||
| chr2:96922498 | C | T | 6 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0010t0001g0158 others(3): Show |
6 | HG02055.hp1 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1288-844G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922498 | |||||||
| chr2:96922862 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1287+628G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922862 | |||||||
| chr2:96922915 | C | T | 1 | a0002c0002t0001g0204 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1287+575G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922915 | |||||||
| chr2:96922999 | C | T | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287+491G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96922999 | |||||||
| chr2:96923091 | C | T | 2 | a0003c0011t0001g0246 a0003c0011t0001g0247 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1287+399G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96923091 | |||||||
| chr2:96923276 | A | G | 12 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0008t0001g0229 others(9): Show |
12 | HG02027.hp1 HG02027.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287+214T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96923276 | |||||||
| chr2:96923287 | T | A | 1 | a0001c0003t0001g0075 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1287+203A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96923287 | |||||||
| chr2:96923302 | T | C | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287+188A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96923302 | |||||||
| chr2:96923323 | G | A | 1 | a0001c0019t0001g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1287+167C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96923323 | |||||||
| chr2:96923329 | G | A | 1 | a0001c0003t0001g0049 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1287+161C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96923329 | |||||||
| chr2:96923472 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1287+18C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96923472 | |||||||
| chr2:96923477 | C | T | 2 | a0002c0002t0001g0164 a0002c0002t0001g0179 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1287+13G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 10/16 | chr2 | 96923477 | |||||||
| chr2:96923607 | C | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194-24G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96923607 | |||||||
| chr2:96923610 | T | C | 3 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1194-27A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96923610 | |||||||
| chr2:96923805 | G | A | 3 | a0002c0015t0003g0003 a0002c0015t0003g0004 a0002c0024t0001g0222 |
3 | HG03453.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1194-222C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96923805 | |||||||
| chr2:96923825 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0052 |
2 | HG01123.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1194-242G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96923825 | |||||||
| chr2:96923840 | T | C | 6 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0010t0001g0158 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1194-257A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96923840 | |||||||
| chr2:96923857 | G | A | 1 | a0009c0016t0001g0227 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1194-274C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96923857 | |||||||
| chr2:96924007 | C | A | 1 | a0002c0002t0001g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1194-424G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96924007 | |||||||
| chr2:96924416 | C | A | 1 | a0001c0003t0001g0029 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1194-833G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96924416 | |||||||
| chr2:96924426 | C | T | 1 | a0002c0027t0001g0200 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1194-843G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96924426 | |||||||
| chr2:96924615 | C | T | 12 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0008t0001g0229 others(9): Show |
12 | HG02027.hp1 HG02027.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1194-1032G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96924615 | |||||||
| chr2:96924757 | A | C | 1 | a0002c0002t0006g0189 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1194-1174T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96924757 | |||||||
| chr2:96924780 | G | C | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1194-1197C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96924780 | |||||||
| chr2:96924975 | A | G | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194-1392T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96924975 | |||||||
| chr2:96925042 | G | T | 3 | a0002c0015t0003g0003 a0002c0015t0003g0004 a0002c0024t0001g0222 |
3 | HG03453.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1194-1459C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925042 | |||||||
| chr2:96925075 | C | T | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1194-1492G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925075 | |||||||
| chr2:96925113 | G | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194-1530C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925113 | |||||||
| chr2:96925142 | G | A | 3 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0010t0001g0160 |
3 | HG02055.hp1 HG02486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1194-1559C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925142 | |||||||
| chr2:96925151 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(28): Show |
32 | HG00423.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.1194-1568C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925151 | |||||||
| chr2:96925339 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1194-1756T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925339 | |||||||
| chr2:96925379 | T | C | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1194-1796A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925379 | |||||||
| chr2:96925394 | A | G | 15 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0008t0001g0229 others(12): Show |
15 | HG02027.hp1 HG02027.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1194-1811T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925394 | |||||||
| chr2:96925783 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1194-2200G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925783 | |||||||
| chr2:96925921 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | HG01261.hp2 HG01358.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1194-2338A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925921 | |||||||
| chr2:96925933 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(28): Show |
32 | HG00423.hp2 HG01884.hp1 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.1194-2350A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925933 | |||||||
| chr2:96925952 | A | T | 2 | a0001c0003t0001g0033 a0001c0003t0001g0053 |
2 | NA18995.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1194-2369T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925952 | |||||||
| chr2:96925978 | CT | C | 6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-2396delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96925978 | |||||||
| chr2:96926167 | G | A | 4 | a0001c0001t0001g0105 a0001c0012t0001g0139 a0001c0012t0001g0140 others(1): Show |
4 | HG02717.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194-2584C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926167 | |||||||
| chr2:96926260 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(42): Show |
46 | HG00423.hp2 HG01884.hp1 HG02027.hp1 others(43): Show |
intron_variant | MODIFIER | c.1194-2677A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926260 | |||||||
| chr2:96926302 | C | CA | 12 | a0001c0003t0001g0223 a0002c0008t0001g0159 a0002c0008t0001g0229 others(9): Show |
12 | HG02027.hp1 HG02027.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1194-2720dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926302 | |||||||
| chr2:96926386 | C | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(27): Show |
31 | HG00423.hp2 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1194-2803G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926386 | |||||||
| chr2:96926416 | G | T | 3 | a0002c0015t0003g0003 a0002c0015t0003g0004 a0002c0024t0001g0222 |
3 | HG03453.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1193+2790C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926416 | |||||||
| chr2:96926516 | T | C | 1 | a0005c0006t0001g0045 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1193+2690A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926516 | |||||||
| chr2:96926619 | C | T | 1 | a0003c0005t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1193+2587G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926619 | |||||||
| chr2:96926641 | CTCA | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(27): Show |
31 | HG00423.hp2 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1193+2562_1193+256 others(7): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926641 | |||||||
| chr2:96926709 | C | A | 1 | a0004c0004t0001g0130 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1193+2497G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926709 | |||||||
| chr2:96926784 | G | A | 4 | a0001c0001t0001g0105 a0001c0012t0001g0139 a0001c0012t0001g0140 others(1): Show |
4 | HG02717.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1193+2422C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926784 | |||||||
| chr2:96926966 | T | C | 3 | a0002c0015t0003g0003 a0002c0015t0003g0004 a0002c0024t0001g0222 |
3 | HG03453.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1193+2240A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96926966 | |||||||
| chr2:96927043 | C | A | 2 | a0002c0002t0001g0164 a0002c0002t0001g0179 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1193+2163G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927043 | |||||||
| chr2:96927258 | T | A | 19 | a0001c0003t0001g0084 a0001c0003t0001g0101 a0001c0003t0001g0102 others(16): Show |
19 | HG00609.hp1 HG02027.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1193+1948A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927258 | |||||||
| chr2:96927258 | T | C | 13 | a0001c0001t0001g0038 a0001c0001t0001g0067 a0004c0004t0001g0043 others(10): Show |
13 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1193+1948A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927258 | |||||||
| chr2:96927389 | T | G | 1 | a0001c0003t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1193+1817A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927389 | |||||||
| chr2:96927476 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(10): Show |
14 | HG00423.hp2 HG02602.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1193+1730G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927476 | |||||||
| chr2:96927700 | G | A | 1 | a0002c0002t0001g0190 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1193+1506C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927700 | |||||||
| chr2:96927701 | C | A | 3 | a0002c0015t0003g0003 a0002c0015t0003g0004 a0002c0024t0001g0222 |
3 | HG03453.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1193+1505G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927701 | |||||||
| chr2:96927877 | C | T | 13 | a0001c0001t0001g0067 a0001c0012t0001g0141 a0004c0004t0001g0043 others(10): Show |
13 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1193+1329G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927877 | |||||||
| chr2:96927912 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1193+1294G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96927912 | |||||||
| chr2:96928154 | G | A | 1 | a0002c0002t0001g0155 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1193+1052C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928154 | |||||||
| chr2:96928156 | C | T | 2 | a0001c0003t0001g0069 a0001c0003t0001g0073 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1193+1050G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928156 | |||||||
| chr2:96928231 | T | C | 4 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(1): Show |
4 | HG02027.hp2 HG02083.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193+975A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928231 | |||||||
| chr2:96928451 | A | G | 5 | a0001c0001t0001g0105 a0002c0015t0003g0003 a0002c0015t0003g0004 others(2): Show |
5 | HG02630.hp1 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193+755T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928451 | |||||||
| chr2:96928452 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1193+754A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928452 | |||||||
| chr2:96928486 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1193+720G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928486 | |||||||
| chr2:96928505 | A | AAACTGAG others(9): Show |
1 | a0001c0001t0001g0055 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1193+685_1193+700d others(18): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928505 | |||||||
| chr2:96928566 | C | T | 4 | a0001c0001t0001g0067 a0004c0004t0001g0043 a0004c0004t0001g0125 others(1): Show |
4 | HG01070.hp2 HG01099.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1193+640G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928566 | |||||||
| chr2:96928567 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1193+639C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928567 | |||||||
| chr2:96928579 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0112 others(7): Show |
10 | HG02027.hp1 HG02071.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1193+627G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928579 | |||||||
| chr2:96928629 | A | T | 34 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0057 others(31): Show |
34 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1193+577T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928629 | |||||||
| chr2:96928783 | G | A | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1193+423C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928783 | |||||||
| chr2:96928937 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1193+269G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928937 | |||||||
| chr2:96928974 | AC | A | 71 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0042 others(68): Show |
71 | HG00544.hp2 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1193+231delG | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928974 | |||||||
| chr2:96928979 | C | T | 3 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0233 |
3 | HG03834.hp2 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1193+227G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928979 | |||||||
| chr2:96928981 | C | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1193+225G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96928981 | |||||||
| chr2:96929012 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1193+194C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96929012 | |||||||
| chr2:96929012 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1193+194C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96929012 | |||||||
| chr2:96929019 | G | A | 6 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1193+187C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96929019 | |||||||
| chr2:96929069 | G | A | 2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1193+137C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 9/16 | chr2 | 96929069 | |||||||
| chr2:96929372 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.1079-52A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96929372 | |||||||
| chr2:96929572 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1079-252T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96929572 | |||||||
| chr2:96929593 | C | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(26): Show |
30 | HG00423.hp2 HG00639.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1079-273G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96929593 | |||||||
| chr2:96929666 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0038 others(3): Show |
6 | HG01123.hp2 HG01169.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079-346G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96929666 | |||||||
| chr2:96929699 | G | A | 1 | a0002c0002t0001g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1079-379C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96929699 | |||||||
| chr2:96929740 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1079-420G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96929740 | |||||||
| chr2:96929891 | C | A | 62 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(59): Show |
62 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1079-571G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96929891 | |||||||
| chr2:96929935 | C | T | 1 | a0001c0003t0001g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1079-615G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96929935 | |||||||
| chr2:96930033 | C | T | 1 | a0014c0020t0001g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1079-713G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930033 | |||||||
| chr2:96930044 | C | T | 9 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0133 others(6): Show |
9 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1079-724G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930044 | |||||||
| chr2:96930194 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079-874G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930194 | |||||||
| chr2:96930210 | C | CA | 24 | a0001c0001t0001g0028 a0001c0001t0001g0109 a0001c0003t0001g0100 others(21): Show |
24 | HG01106.hp2 HG01175.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1079-891dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | C | CAA | 16 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0108 others(13): Show |
16 | HG00642.hp2 HG01099.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1079-892_1079-891d others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | C | CAAA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01358.hp2 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-893_1079-891d others(5): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | C | CAAAA | 6 | a0001c0001t0001g0019 a0001c0001t0001g0104 a0001c0001t0001g0115 others(3): Show |
6 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1079-894_1079-891d others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1079-900_1079-891d others(12): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | C | CAAAAAAA others(4): Show |
1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079-901_1079-891d others(13): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CA | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0042 others(46): Show |
50 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1079-891delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAA | C | 11 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
11 | HG01975.hp2 HG02809.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1079-892_1079-891d others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAA | C | 8 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 others(5): Show |
8 | HG00642.hp1 HG01975.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079-893_1079-891d others(5): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAAA | C | 13 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0044 others(10): Show |
13 | HG00597.hp1 HG01123.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1079-894_1079-891d others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAAAA | C | 33 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0034 others(30): Show |
33 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1079-895_1079-891d others(7): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0218 |
2 | NA18956.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1079-900_1079-891d others(12): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAAAAAA others(4): Show |
C | 8 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0134 others(5): Show |
8 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.1079-901_1079-891d others(13): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0136 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1079-902_1079-891d others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAAAAAA others(6): Show |
C | 8 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(5): Show |
8 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079-903_1079-891d others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAAAAAA others(8): Show |
C | 2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1079-905_1079-891d others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930210 | CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0055 a0002c0002t0001g0168 |
2 | NA19074.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1079-908_1079-891d others(20): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930210 | |||||||
| chr2:96930243 | A | AAAAAAAA others(14): Show |
3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1079-924_1079-923i others(23): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930243 | |||||||
| chr2:96930254 | G | A | 75 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(72): Show |
75 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1079-934C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930254 | |||||||
| chr2:96930279 | T | C | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079-959A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930279 | |||||||
| chr2:96930416 | T | C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(22): Show |
25 | HG01261.hp2 HG01358.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1079-1096A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930416 | |||||||
| chr2:96930425 | C | T | 10 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0058 others(7): Show |
10 | HG00438.hp1 HG00558.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-1105G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930425 | |||||||
| chr2:96930427 | G | A | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1079-1107C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930427 | |||||||
| chr2:96930481 | T | C | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079-1161A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930481 | |||||||
| chr2:96930497 | G | T | 60 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(57): Show |
60 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1079-1177C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930497 | |||||||
| chr2:96930834 | C | T | 3 | a0001c0003t0001g0069 a0001c0003t0001g0070 a0001c0003t0001g0073 |
3 | HG01891.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1079-1514G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930834 | |||||||
| chr2:96930898 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0037 others(4): Show |
8 | HG00423.hp2 HG02602.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079-1578A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96930898 | |||||||
| chr2:96931198 | C | T | 1 | a0002c0002t0001g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1079-1878G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931198 | |||||||
| chr2:96931470 | A | G | 2 | a0002c0015t0003g0003 a0002c0015t0003g0004 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1079-2150T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931470 | |||||||
| chr2:96931516 | A | T | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1079-2196T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931516 | |||||||
| chr2:96931569 | C | T | 1 | a0002c0002t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1079-2249G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931569 | |||||||
| chr2:96931634 | C | T | 1 | a0002c0009t0001g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1079-2314G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931634 | |||||||
| chr2:96931635 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079-2315C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931635 | |||||||
| chr2:96931732 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1079-2412C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931732 | |||||||
| chr2:96931840 | A | G | 56 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(53): Show |
56 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1079-2520T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931840 | |||||||
| chr2:96931856 | G | GT | 5 | a0001c0001t0001g0035 a0001c0001t0001g0220 a0001c0003t0001g0029 others(2): Show |
5 | HG01192.hp1 HG01981.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-2537dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931856 | |||||||
| chr2:96931856 | GT | G | 5 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0233 others(2): Show |
5 | HG02027.hp1 HG02071.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-2537delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931856 | |||||||
| chr2:96931870 | T | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1079-2550A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96931870 | |||||||
| chr2:96932241 | C | A | 1 | a0002c0002t0001g0212 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1079-2921G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932241 | |||||||
| chr2:96932264 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(110): Show |
114 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.1079-2944A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932264 | |||||||
| chr2:96932312 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(22): Show |
25 | HG01261.hp2 HG01358.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1079-2992G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932312 | |||||||
| chr2:96932393 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1079-3073C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932393 | |||||||
| chr2:96932508 | G | A | 2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1079-3188C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932508 | |||||||
| chr2:96932566 | C | T | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1079-3246G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932566 | |||||||
| chr2:96932935 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(58): Show |
62 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1079-3615C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932935 | |||||||
| chr2:96932941 | C | CA | 83 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
83 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1079-3622dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932941 | |||||||
| chr2:96932941 | C | CAA | 17 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0110 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1079-3623_1079-362 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932941 | |||||||
| chr2:96932982 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0074 others(2): Show |
5 | HG01099.hp2 HG01106.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-3662G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96932982 | |||||||
| chr2:96933162 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(110): Show |
114 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.1079-3842T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933162 | |||||||
| chr2:96933203 | A | G | 1 | a0001c0003t0001g0029 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1079-3883T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933203 | |||||||
| chr2:96933484 | C | T | 2 | a0001c0012t0001g0139 a0001c0012t0001g0141 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1079-4164G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933484 | |||||||
| chr2:96933529 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(27): Show |
31 | HG00423.hp2 HG00639.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1079-4209G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933529 | |||||||
| chr2:96933536 | T | C | 2 | a0003c0011t0001g0236 a0003c0011t0001g0248 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1079-4216A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933536 | |||||||
| chr2:96933667 | C | T | 2 | a0002c0008t0001g0159 a0002c0010t0001g0144 |
2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1079-4347G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933667 | |||||||
| chr2:96933864 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1079-4544A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933864 | |||||||
| chr2:96933881 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
116 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1079-4561A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933881 | |||||||
| chr2:96933912 | G | A | 1 | a0002c0002t0001g0180 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1079-4592C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96933912 | |||||||
| chr2:96934149 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0047 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1079-4829A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96934149 | |||||||
| chr2:96934308 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1079-4988G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96934308 | |||||||
| chr2:96934341 | G | A | 12 | a0004c0004t0001g0043 a0004c0004t0001g0121 a0004c0004t0001g0122 others(9): Show |
12 | HG00099.hp2 HG01099.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.1079-5021C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96934341 | |||||||
| chr2:96934525 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1079-5205T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96934525 | |||||||
| chr2:96934628 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1079-5308C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96934628 | |||||||
| chr2:96934790 | C | T | 1 | a0003c0011t0001g0236 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1079-5470G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96934790 | |||||||
| chr2:96934889 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
116 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1079-5569C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96934889 | |||||||
| chr2:96935058 | C | T | 2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1079-5738G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935058 | |||||||
| chr2:96935059 | G | A | 5 | a0002c0002t0001g0145 a0002c0002t0001g0186 a0002c0002t0001g0188 others(2): Show |
5 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-5739C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935059 | |||||||
| chr2:96935090 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
116 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1079-5770A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935090 | |||||||
| chr2:96935179 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
116 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1079-5859G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935179 | |||||||
| chr2:96935211 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1079-5891C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935211 | |||||||
| chr2:96935287 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
116 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1079-5967T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935287 | |||||||
| chr2:96935369 | C | T | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(45): Show |
48 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1079-6049G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935369 | |||||||
| chr2:96935382 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(44): Show |
48 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1079-6062G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935382 | |||||||
| chr2:96935422 | C | T | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079-6102G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935422 | |||||||
| chr2:96935534 | A | G | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1079-6214T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935534 | |||||||
| chr2:96935569 | A | G | 9 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(6): Show |
9 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1079-6249T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935569 | |||||||
| chr2:96935605 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
12 | HG00423.hp2 HG00639.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1079-6285T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935605 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
7 | a0003c0005t0001g0239 a0003c0005t0001g0240 a0003c0005t0001g0241 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
1 | a0001c0001t0001g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1321): Show |
2 | a0001c0001t0001g0120 a0006c0007t0002g0041 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1332): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
19 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(16): Show |
20 | HG00423.hp2 HG00639.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1321): Show |
4 | a0001c0001t0001g0037 a0006c0007t0002g0098 a0008c0013t0001g0090 others(1): Show |
4 | HG03209.hp1 NA18949.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1332): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1319): Show |
1 | a0001c0003t0001g0094 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1330): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1319): Show |
1 | a0001c0003t0001g0100 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1330): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
2 | a0003c0011t0001g0236 a0003c0011t0001g0248 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1321): Show |
1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1332): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1322): Show |
1 | a0001c0001t0001g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1333): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
3 | a0001c0001t0001g0089 a0002c0010t0001g0158 a0002c0010t0001g0160 |
3 | HG02922.hp1 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1321): Show |
20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(17): Show |
20 | HG01261.hp2 HG01358.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1332): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1322): Show |
5 | a0001c0001t0001g0116 a0001c0003t0001g0118 a0001c0003t0001g0223 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1333): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1323): Show |
1 | a0001c0001t0001g0117 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1334): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
3 | a0002c0015t0003g0003 a0002c0015t0003g0004 a0002c0023t0005g0157 |
3 | HG02572.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
32 | a0001c0001t0001g0019 a0001c0001t0001g0078 a0001c0001t0001g0079 others(29): Show |
32 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1321): Show |
1 | a0004c0004t0001g0129 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1332): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
6 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 others(3): Show |
6 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1321): Show |
1 | a0002c0008t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1332): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1318): Show |
1 | a0009c0016t0001g0226 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1329): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1319): Show |
1 | a0009c0016t0001g0227 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1330): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935711 | G | GCAACCTC others(1320): Show |
1 | a0001c0001t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1079-6392_1079-639 others(1331): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935711 | |||||||
| chr2:96935763 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
116 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1079-6443C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935763 | |||||||
| chr2:96935801 | T | G | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079-6481A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935801 | |||||||
| chr2:96935956 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1079-6636G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935956 | |||||||
| chr2:96935965 | A | G | 1 | a0002c0002t0001g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1079-6645T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96935965 | |||||||
| chr2:96936114 | T | G | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079-6794A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936114 | |||||||
| chr2:96936179 | ATTC | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0111 |
2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1079-6862_1079-686 others(7): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936179 | |||||||
| chr2:96936240 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1079-6920A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936240 | |||||||
| chr2:96936294 | C | T | 1 | a0003c0005t0001g0241 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1079-6974G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936294 | |||||||
| chr2:96936295 | G | A | 1 | a0002c0002t0006g0189 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1079-6975C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936295 | |||||||
| chr2:96936342 | C | G | 1 | a0002c0002t0001g0146 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1079-7022G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936342 | |||||||
| chr2:96936350 | C | T | 4 | a0004c0004t0001g0043 a0004c0004t0001g0125 a0004c0004t0001g0127 others(1): Show |
4 | HG01099.hp1 HG01261.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-7030G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936350 | |||||||
| chr2:96936359 | G | A | 61 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(58): Show |
61 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1079-7039C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936359 | |||||||
| chr2:96936363 | G | A | 2 | a0007c0014t0001g0228 a0007c0014t0001g0231 |
2 | HG02027.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1079-7043C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936363 | |||||||
| chr2:96936368 | AG | A | 65 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(62): Show |
65 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1079-7049delC | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936368 | |||||||
| chr2:96936375 | G | C | 65 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(62): Show |
65 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1079-7055C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936375 | |||||||
| chr2:96936409 | G | C | 9 | a0001c0001t0001g0131 a0001c0012t0001g0139 a0001c0012t0001g0140 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1079-7089C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936409 | |||||||
| chr2:96936423 | G | T | 56 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(53): Show |
56 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1079-7103C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936423 | |||||||
| chr2:96936430 | C | T | 56 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(53): Show |
56 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1079-7110G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936430 | |||||||
| chr2:96936468 | T | TG | 12 | a0004c0004t0001g0043 a0004c0004t0001g0121 a0004c0004t0001g0122 others(9): Show |
12 | HG00099.hp2 HG01099.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.1079-7149dupC | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936468 | |||||||
| chr2:96936471 | A | T | 1 | a0002c0002t0001g0146 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1079-7151T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936471 | |||||||
| chr2:96936490 | A | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0060 others(2): Show |
5 | HG00544.hp1 HG01123.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-7170T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936490 | |||||||
| chr2:96936498 | G | GT | 65 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0078 others(62): Show |
65 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1079-7179dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936498 | |||||||
| chr2:96936498 | G | GTT | 24 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(21): Show |
24 | HG01099.hp1 HG01261.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.1079-7180_1079-717 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936498 | |||||||
| chr2:96936498 | GTTT | G | 6 | a0001c0003t0001g0100 a0006c0007t0002g0087 a0006c0007t0002g0095 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1079-7181_1079-717 others(7): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936498 | |||||||
| chr2:96936515 | GT | G | 86 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.1079-7196delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936515 | |||||||
| chr2:96936548 | C | A | 63 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(60): Show |
63 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1079-7228G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936548 | |||||||
| chr2:96936571 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1079-7251T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936571 | |||||||
| chr2:96936813 | C | G | 3 | a0001c0003t0001g0069 a0001c0003t0001g0070 a0001c0003t0001g0073 |
3 | HG01891.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1079-7493G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936813 | |||||||
| chr2:96936846 | G | C | 1 | a0005c0006t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1079-7526C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96936846 | |||||||
| chr2:96937019 | C | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
75 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.1079-7699G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96937019 | |||||||
| chr2:96937052 | TTTG | T | 4 | a0001c0001t0001g0099 a0001c0003t0001g0101 a0001c0003t0001g0102 others(1): Show |
4 | HG03139.hp1 HG03225.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079-7735_1079-773 others(7): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96937052 | |||||||
| chr2:96937120 | C | CCTGAGCT others(34): Show |
75 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
75 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.1079-7841_1079-780 others(45): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96937120 | |||||||
| chr2:96937383 | G | T | 5 | a0002c0008t0001g0159 a0002c0010t0001g0144 a0002c0010t0001g0158 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-8063C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96937383 | |||||||
| chr2:96937898 | C | T | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079-8578G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96937898 | |||||||
| chr2:96937927 | C | T | 7 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0010t0001g0144 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1079-8607G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96937927 | |||||||
| chr2:96937981 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(19): Show |
22 | HG01261.hp2 HG01358.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1079-8661G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96937981 | |||||||
| chr2:96938653 | G | A | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1078+9165C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96938653 | |||||||
| chr2:96938718 | C | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
75 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.1078+9100G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96938718 | |||||||
| chr2:96938781 | A | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(62): Show |
65 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.1078+9037T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96938781 | |||||||
| chr2:96938931 | T | C | 1 | a0001c0003t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+8887A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96938931 | |||||||
| chr2:96939130 | G | A | 1 | a0002c0002t0001g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1078+8688C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939130 | |||||||
| chr2:96939131 | A | G | 1 | a0002c0002t0001g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1078+8687T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939131 | |||||||
| chr2:96939158 | A | G | 75 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
75 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.1078+8660T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939158 | |||||||
| chr2:96939160 | G | C | 1 | a0002c0002t0001g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1078+8658C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939160 | |||||||
| chr2:96939369 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0060 |
2 | HG00544.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1078+8449C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939369 | |||||||
| chr2:96939427 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1078+8391G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939427 | |||||||
| chr2:96939428 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1078+8390C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939428 | |||||||
| chr2:96939453 | G | A | 3 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0177 |
3 | HG02135.hp1 HG02148.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1078+8365C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939453 | |||||||
| chr2:96939474 | C | A | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1078+8344G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939474 | |||||||
| chr2:96939538 | G | A | 1 | a0004c0004t0001g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1078+8280C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939538 | |||||||
| chr2:96939860 | C | G | 35 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0078 others(32): Show |
35 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1078+7958G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939860 | |||||||
| chr2:96939898 | T | G | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1078+7920A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939898 | |||||||
| chr2:96939990 | C | T | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1078+7828G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96939990 | |||||||
| chr2:96940011 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(109): Show |
113 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.1078+7807T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96940011 | |||||||
| chr2:96940146 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1078+7672C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96940146 | |||||||
| chr2:96940547 | C | G | 2 | a0002c0002t0001g0165 a0002c0002t0001g0198 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1078+7271G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96940547 | |||||||
| chr2:96940575 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0080 others(1): Show |
4 | HG00544.hp1 NA18956.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+7243C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96940575 | |||||||
| chr2:96940613 | C | T | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1078+7205G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96940613 | |||||||
| chr2:96940917 | C | A | 2 | a0003c0011t0001g0236 a0003c0011t0001g0248 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1078+6901G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96940917 | |||||||
| chr2:96940917 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1078+6901G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96940917 | |||||||
| chr2:96941073 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(15): Show |
19 | HG00423.hp2 HG02602.hp1 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.1078+6745A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941073 | |||||||
| chr2:96941143 | T | A | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1078+6675A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941143 | |||||||
| chr2:96941246 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1078+6572A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941246 | |||||||
| chr2:96941334 | A | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.1078+6484T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941334 | |||||||
| chr2:96941418 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1078+6400C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941418 | |||||||
| chr2:96941747 | G | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0065 others(3): Show |
6 | HG00099.hp1 HG01099.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078+6071C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941747 | |||||||
| chr2:96941807 | G | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(55): Show |
58 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.1078+6011C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941807 | |||||||
| chr2:96941918 | T | A | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.1078+5900A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941918 | |||||||
| chr2:96941931 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(34): Show |
38 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1078+5887T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96941931 | |||||||
| chr2:96942057 | C | T | 1 | a0004c0004t0001g0130 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1078+5761G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942057 | |||||||
| chr2:96942269 | G | T | 1 | a0002c0002t0001g0175 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1078+5549C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942269 | |||||||
| chr2:96942348 | G | A | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.1078+5470C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942348 | |||||||
| chr2:96942350 | G | A | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+5468C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942350 | |||||||
| chr2:96942376 | G | A | 1 | a0002c0002t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1078+5442C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942376 | |||||||
| chr2:96942387 | C | A | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.1078+5431G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942387 | |||||||
| chr2:96942402 | A | G | 1 | a0002c0002t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1078+5416T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942402 | |||||||
| chr2:96942432 | G | A | 9 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(6): Show |
9 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+5386C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942432 | |||||||
| chr2:96942585 | C | T | 1 | a0002c0002t0001g0177 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1078+5233G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96942585 | |||||||
| chr2:96943036 | A | G | 9 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(6): Show |
9 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+4782T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96943036 | |||||||
| chr2:96943100 | G | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(174): Show |
178 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1078+4718C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96943100 | |||||||
| chr2:96943341 | C | T | 2 | a0009c0016t0001g0226 a0009c0016t0001g0227 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1078+4477G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96943341 | |||||||
| chr2:96943505 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1078+4313C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96943505 | |||||||
| chr2:96943760 | GC | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.1078+4057delG | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96943760 | |||||||
| chr2:96943775 | C | T | 1 | a0002c0010t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1078+4043G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96943775 | |||||||
| chr2:96943963 | C | G | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1078+3855G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96943963 | |||||||
| chr2:96943969 | G | A | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1078+3849C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96943969 | |||||||
| chr2:96944241 | C | CA | 14 | a0001c0001t0001g0044 a0001c0001t0001g0081 a0001c0003t0001g0075 others(11): Show |
14 | HG00642.hp2 HG01358.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1078+3576dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944241 | |||||||
| chr2:96944241 | CA | C | 32 | a0001c0001t0001g0032 a0001c0001t0001g0042 a0001c0001t0001g0064 others(29): Show |
32 | HG01258.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.1078+3576delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944241 | |||||||
| chr2:96944241 | CAA | C | 48 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
48 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.1078+3575_1078+357 others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944241 | |||||||
| chr2:96944241 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1078+3565_1078+357 others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944241 | |||||||
| chr2:96944340 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1078+3478G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944340 | |||||||
| chr2:96944386 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1078+3432G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944386 | |||||||
| chr2:96944538 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(19): Show |
22 | HG01261.hp2 HG01358.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1078+3280A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944538 | |||||||
| chr2:96944547 | C | T | 1 | a0009c0016t0001g0226 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1078+3271G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944547 | |||||||
| chr2:96944782 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1078+3036A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944782 | |||||||
| chr2:96944897 | T | C | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1078+2921A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96944897 | |||||||
| chr2:96945037 | A | T | 1 | a0002c0002t0001g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1078+2781T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945037 | |||||||
| chr2:96945274 | C | A | 6 | a0002c0002t0001g0206 a0002c0002t0001g0207 a0002c0002t0001g0208 others(3): Show |
6 | HG01106.hp2 HG02602.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078+2544G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945274 | |||||||
| chr2:96945284 | CACACTAG others(11): Show |
C | 6 | a0002c0002t0001g0206 a0002c0002t0001g0207 a0002c0002t0001g0208 others(3): Show |
6 | HG01106.hp2 HG02602.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078+2516_1078+253 others(22): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945284 | |||||||
| chr2:96945303 | A | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1078+2515T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945303 | |||||||
| chr2:96945379 | C | CT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1078+2438dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945379 | |||||||
| chr2:96945440 | G | A | 9 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(6): Show |
9 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+2378C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945440 | |||||||
| chr2:96945520 | AGCGGCTT others(38): Show |
A | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1078+2253_1078+229 others(49): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945520 | |||||||
| chr2:96945601 | A | G | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1078+2217T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945601 | |||||||
| chr2:96945659 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1078+2159A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945659 | |||||||
| chr2:96945815 | C | CT | 4 | a0005c0006t0001g0020 a0005c0006t0001g0021 a0005c0006t0001g0022 others(1): Show |
4 | HG00642.hp1 HG01975.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+2002dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96945815 | |||||||
| chr2:96946102 | C | T | 1 | a0006c0007t0002g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1078+1716G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96946102 | |||||||
| chr2:96946119 | G | A | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1078+1699C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96946119 | |||||||
| chr2:96946227 | T | A | 1 | a0002c0002t0001g0155 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1078+1591A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96946227 | |||||||
| chr2:96946457 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1078+1361C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96946457 | |||||||
| chr2:96946462 | C | A | 1 | a0001c0003t0001g0062 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1078+1356G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96946462 | |||||||
| chr2:96946463 | A | G | 1 | a0001c0003t0001g0062 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1078+1355T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96946463 | |||||||
| chr2:96946477 | G | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1078+1341C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96946477 | |||||||
| chr2:96947038 | G | C | 7 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0010t0001g0144 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078+780C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96947038 | |||||||
| chr2:96947109 | C | T | 2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1078+709G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96947109 | |||||||
| chr2:96947489 | T | C | 2 | a0003c0011t0001g0236 a0003c0011t0001g0248 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1078+329A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96947489 | |||||||
| chr2:96947630 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1078+188C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96947630 | |||||||
| chr2:96947782 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1078+36T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | 96947782 | |||||||
| chr2:96947915 | A | C | 3 | a0003c0005t0001g0240 a0003c0005t0001g0243 a0003c0005t0001g0245 |
3 | HG00642.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.994-13T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96947915 | |||||||
| chr2:96947920 | AC | A | 18 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0008t0001g0229 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.994-19delG | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96947920 | |||||||
| chr2:96947927 | C | A | 7 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0010t0001g0144 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-25G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96947927 | |||||||
| chr2:96948011 | C | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(155): Show |
159 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.994-109G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948011 | |||||||
| chr2:96948219 | C | T | 65 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(62): Show |
65 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.994-317G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948219 | |||||||
| chr2:96948237 | C | G | 18 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0008t0001g0229 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.994-335G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948237 | |||||||
| chr2:96948325 | C | T | 18 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0008t0001g0229 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.994-423G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948325 | |||||||
| chr2:96948357 | A | G | 1 | a0003c0005t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.994-455T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948357 | |||||||
| chr2:96948470 | C | T | 2 | a0009c0016t0001g0226 a0009c0016t0001g0227 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.994-568G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948470 | |||||||
| chr2:96948664 | G | T | 1 | a0002c0002t0001g0172 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.994-762C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948664 | |||||||
| chr2:96948768 | G | A | 1 | a0004c0004t0001g0126 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.994-866C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948768 | |||||||
| chr2:96948822 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(53): Show |
57 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.994-920A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96948822 | |||||||
| chr2:96949101 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.994-1199C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949101 | |||||||
| chr2:96949157 | C | T | 7 | a0001c0003t0001g0005 a0001c0003t0001g0029 a0001c0003t0001g0033 others(4): Show |
7 | HG00597.hp1 HG02129.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-1255G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949157 | |||||||
| chr2:96949199 | C | T | 59 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(56): Show |
59 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.994-1297G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949199 | |||||||
| chr2:96949271 | C | A | 17 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0008t0001g0229 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.994-1369G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949271 | |||||||
| chr2:96949381 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0052 |
2 | HG01123.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.994-1479G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949381 | |||||||
| chr2:96949429 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.994-1527T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949429 | |||||||
| chr2:96949548 | T | C | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.994-1646A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949548 | |||||||
| chr2:96949647 | T | A | 4 | a0001c0001t0001g0077 a0001c0003t0001g0024 a0001c0003t0001g0025 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+1732A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949647 | |||||||
| chr2:96949653 | C | A | 7 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0010t0001g0144 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+1726G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949653 | |||||||
| chr2:96949686 | C | A | 59 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(56): Show |
59 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.993+1693G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949686 | |||||||
| chr2:96949785 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.993+1594C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949785 | |||||||
| chr2:96949830 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.993+1549C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96949830 | |||||||
| chr2:96950041 | G | T | 6 | a0002c0002t0001g0151 a0002c0002t0001g0169 a0002c0002t0001g0185 others(3): Show |
6 | HG01070.hp1 HG01257.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+1338C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96950041 | |||||||
| chr2:96950256 | C | T | 32 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0042 others(29): Show |
32 | HG00099.hp2 HG01099.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.993+1123G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96950256 | |||||||
| chr2:96950436 | G | A | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.993+943C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96950436 | |||||||
| chr2:96950462 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.993+917C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96950462 | |||||||
| chr2:96950663 | G | T | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.993+716C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96950663 | |||||||
| chr2:96950966 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.993+413A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96950966 | |||||||
| chr2:96951108 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.993+271T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96951108 | |||||||
| chr2:96951244 | C | T | 1 | a0003c0011t0001g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.993+135G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96951244 | |||||||
| chr2:96951266 | C | G | 1 | a0011c0021t0001g0225 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.993+113G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 7/16 | chr2 | 96951266 | |||||||
| chr2:96951490 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(176): Show |
splice_region_variant&intron_variant | LOW | c.888-6T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96951490 | |||||||
| chr2:96951703 | G | A | 3 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0177 |
3 | HG02135.hp1 HG02148.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.888-219C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96951703 | |||||||
| chr2:96951851 | T | C | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.888-367A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96951851 | |||||||
| chr2:96951864 | T | C | 3 | a0001c0001t0004g0002 a0001c0019t0001g0009 a0010c0018t0001g0010 |
3 | HG01261.hp2 HG01358.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.888-380A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96951864 | |||||||
| chr2:96951945 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(35): Show |
39 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.888-461G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96951945 | |||||||
| chr2:96952187 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.888-703T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96952187 | |||||||
| chr2:96952400 | C | A | 1 | a0001c0019t0001g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.888-916G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96952400 | |||||||
| chr2:96952417 | C | T | 3 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0214 |
3 | NA18982.hp1 NA18999.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.888-933G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96952417 | |||||||
| chr2:96952429 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.888-945A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96952429 | |||||||
| chr2:96952778 | C | T | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.888-1294G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96952778 | |||||||
| chr2:96952835 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.888-1351G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96952835 | |||||||
| chr2:96952846 | T | G | 7 | a0002c0002t0001g0145 a0002c0002t0001g0166 a0002c0002t0001g0186 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.888-1362A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96952846 | |||||||
| chr2:96952935 | T | C | 3 | a0001c0003t0001g0069 a0001c0003t0001g0070 a0001c0003t0001g0073 |
3 | HG01891.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.888-1451A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96952935 | |||||||
| chr2:96953216 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.888-1732C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96953216 | |||||||
| chr2:96953410 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.888-1926C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96953410 | |||||||
| chr2:96953412 | C | T | 1 | a0005c0006t0001g0048 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.888-1928G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96953412 | |||||||
| chr2:96953588 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.888-2104C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96953588 | |||||||
| chr2:96953945 | G | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.888-2461C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96953945 | |||||||
| chr2:96954014 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.888-2530A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954014 | |||||||
| chr2:96954073 | T | C | 1 | a0008c0013t0001g0092 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.888-2589A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954073 | |||||||
| chr2:96954098 | C | A | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.888-2614G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954098 | |||||||
| chr2:96954176 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.888-2692A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954176 | |||||||
| chr2:96954336 | C | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.888-2852G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954336 | |||||||
| chr2:96954464 | C | T | 1 | a0002c0008t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.888-2980G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954464 | |||||||
| chr2:96954558 | A | AG | 38 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(35): Show |
39 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.888-3075dupC | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954558 | |||||||
| chr2:96954636 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.888-3152A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954636 | |||||||
| chr2:96954885 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0091 others(3): Show |
7 | HG00423.hp2 HG02602.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.888-3401T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96954885 | |||||||
| chr2:96955130 | C | T | 1 | a0009c0016t0001g0226 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.888-3646G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955130 | |||||||
| chr2:96955148 | C | T | 2 | a0009c0016t0001g0226 a0009c0016t0001g0227 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.888-3664G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955148 | |||||||
| chr2:96955195 | G | A | 7 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0010t0001g0144 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.888-3711C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955195 | |||||||
| chr2:96955209 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.888-3725A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955209 | |||||||
| chr2:96955224 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.888-3740A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955224 | |||||||
| chr2:96955226 | C | T | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.888-3742G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955226 | |||||||
| chr2:96955238 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.888-3754G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955238 | |||||||
| chr2:96955239 | G | A | 1 | a0002c0002t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.888-3755C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955239 | |||||||
| chr2:96955384 | G | A | 59 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(56): Show |
59 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.888-3900C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955384 | |||||||
| chr2:96955487 | G | A | 1 | a0003c0005t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.888-4003C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955487 | |||||||
| chr2:96955537 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.888-4053C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955537 | |||||||
| chr2:96955552 | C | T | 1 | a0009c0016t0001g0227 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.888-4068G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955552 | |||||||
| chr2:96955624 | G | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(7): Show |
10 | HG01261.hp2 HG01358.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.888-4140C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955624 | |||||||
| chr2:96955910 | G | C | 52 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
52 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.887+4378C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96955910 | |||||||
| chr2:96956026 | C | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+4262G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96956026 | |||||||
| chr2:96956061 | C | G | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.887+4227G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96956061 | |||||||
| chr2:96956261 | T | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(174): Show |
178 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.887+4027A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96956261 | |||||||
| chr2:96956316 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0081 |
3 | NA18979.hp1 NA19000.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.887+3972C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96956316 | |||||||
| chr2:96956386 | G | A | 2 | a0002c0015t0003g0003 a0002c0015t0003g0004 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.887+3902C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96956386 | |||||||
| chr2:96956671 | G | C | 118 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.887+3617C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96956671 | |||||||
| chr2:96956926 | C | T | 1 | a0002c0002t0001g0170 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.887+3362G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96956926 | |||||||
| chr2:96957023 | AT | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+3264delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96957023 | |||||||
| chr2:96957035 | C | A | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.887+3253G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96957035 | |||||||
| chr2:96957183 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+3105G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96957183 | |||||||
| chr2:96957273 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+3015C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96957273 | |||||||
| chr2:96957372 | A | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+2916T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96957372 | |||||||
| chr2:96957575 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(74): Show |
78 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.887+2713A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96957575 | |||||||
| chr2:96957676 | G | A | 55 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
55 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.887+2612C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96957676 | |||||||
| chr2:96958067 | CT | C | 162 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(159): Show |
162 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.887+2220delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958067 | |||||||
| chr2:96958303 | C | T | 1 | a0002c0002t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.887+1985G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958303 | |||||||
| chr2:96958322 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.887+1966C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958322 | |||||||
| chr2:96958324 | C | G | 2 | a0009c0016t0001g0226 a0009c0016t0001g0227 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.887+1964G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958324 | |||||||
| chr2:96958350 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.887+1938C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958350 | |||||||
| chr2:96958360 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+1928T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958360 | |||||||
| chr2:96958527 | A | G | 3 | a0002c0008t0001g0159 a0002c0010t0001g0144 a0013c0025t0001g0006 |
3 | HG01243.hp1 HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.887+1761T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958527 | |||||||
| chr2:96958567 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+1721C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958567 | |||||||
| chr2:96958697 | T | TA | 5 | a0002c0002t0001g0154 a0002c0002t0001g0199 a0002c0002t0001g0208 others(2): Show |
5 | HG01106.hp2 HG02055.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+1590dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | T | TAA | 6 | a0002c0002t0001g0174 a0002c0002t0001g0190 a0002c0002t0001g0197 others(3): Show |
6 | HG02040.hp1 HG04115.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.887+1589_887+1590d others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TA | T | 21 | a0002c0002t0001g0151 a0002c0002t0001g0162 a0002c0002t0001g0166 others(18): Show |
21 | HG00639.hp2 HG00741.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.887+1590delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAA | T | 9 | a0001c0001t0001g0131 a0002c0002t0001g0017 a0002c0002t0001g0156 others(6): Show |
9 | HG01070.hp1 HG01169.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.887+1589_887+1590d others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAAAAAAA others(3): Show |
T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0034 others(8): Show |
11 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.887+1581_887+1590d others(12): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAAAAAAA others(4): Show |
T | 39 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0036 others(36): Show |
39 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.887+1580_887+1590d others(13): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAAAAAAA others(5): Show |
T | 48 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0077 others(45): Show |
48 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.887+1579_887+1590d others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAAAAAAA others(6): Show |
T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
52 | HG00099.hp2 HG00423.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.887+1578_887+1590d others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAAAAAAA others(7): Show |
T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0107 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+1577_887+1590d others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAAAAAAA others(9): Show |
T | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.887+1575_887+1590d others(18): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAAAAAAA others(16): Show |
T | 8 | a0002c0002t0001g0175 a0002c0008t0001g0229 a0002c0008t0001g0230 others(5): Show |
8 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.887+1568_887+1590d others(25): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958697 | TAAAAAAA others(20): Show |
T | 2 | a0002c0002t0001g0204 a0002c0002t0001g0219 |
2 | HG01192.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.887+1564_887+1590d others(29): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958697 | |||||||
| chr2:96958745 | A | T | 1 | a0002c0002t0001g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.887+1543T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958745 | |||||||
| chr2:96958755 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+1533A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958755 | |||||||
| chr2:96958787 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+1501T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958787 | |||||||
| chr2:96958955 | C | T | 11 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(8): Show |
11 | HG00642.hp2 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.887+1333G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96958955 | |||||||
| chr2:96959060 | A | T | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.887+1228T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959060 | |||||||
| chr2:96959072 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.887+1216C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959072 | |||||||
| chr2:96959186 | G | A | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+1102C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959186 | |||||||
| chr2:96959199 | G | GA | 22 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0066 others(19): Show |
22 | HG00609.hp2 HG00642.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.887+1088dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | G | GAA | 9 | a0001c0003t0001g0069 a0001c0012t0001g0139 a0001c0012t0001g0140 others(6): Show |
9 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.887+1087_887+1088d others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | G | GAAAAAAA others(5): Show |
1 | a0003c0011t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.887+1077_887+1088d others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | G | GAAAAAAA others(6): Show |
3 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0011t0001g0236 |
3 | HG00609.hp1 HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.887+1076_887+1088d others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | G | GGA | 3 | a0002c0008t0001g0229 a0002c0008t0001g0232 a0002c0008t0001g0233 |
3 | HG02083.hp1 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.887+1088_887+1089i others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | G | GGAA | 3 | a0002c0008t0001g0230 a0002c0008t0001g0234 a0007c0014t0001g0231 |
3 | HG02027.hp1 HG02027.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.887+1088_887+1089i others(5): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | G | GGAAAAAA others(6): Show |
1 | a0003c0011t0001g0247 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.887+1088_887+1089i others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | G | GGAAAAAA others(8): Show |
1 | a0003c0011t0001g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.887+1088_887+1089i others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | GA | G | 11 | a0001c0001t0001g0038 a0001c0001t0001g0055 a0001c0001t0001g0074 others(8): Show |
11 | HG01169.hp1 HG01975.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.887+1088delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | GAAAA | G | 7 | a0003c0005t0001g0239 a0003c0005t0001g0240 a0003c0005t0001g0241 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.887+1085_887+1088d others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959199 | GAAAAAAA others(6): Show |
G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(74): Show |
78 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.887+1076_887+1088d others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959199 | |||||||
| chr2:96959362 | G | T | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.887+926C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959362 | |||||||
| chr2:96959398 | T | C | 1 | a0006c0007t0002g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.887+890A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959398 | |||||||
| chr2:96959401 | C | T | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.887+887G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959401 | |||||||
| chr2:96959511 | T | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0081 |
3 | NA18979.hp1 NA19000.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.887+777A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959511 | |||||||
| chr2:96959779 | G | A | 7 | a0002c0002t0001g0145 a0002c0002t0001g0166 a0002c0002t0001g0186 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+509C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959779 | |||||||
| chr2:96959862 | C | T | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.887+426G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959862 | |||||||
| chr2:96959953 | C | T | 1 | a0003c0005t0001g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.887+335G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | 96959953 | |||||||
| chr2:96960579 | G | A | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.735-139C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96960579 | |||||||
| chr2:96960602 | C | T | 1 | a0002c0002t0001g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.735-162G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96960602 | |||||||
| chr2:96960615 | G | A | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.735-175C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96960615 | |||||||
| chr2:96960748 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.735-308G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96960748 | |||||||
| chr2:96960874 | C | T | 1 | a0004c0004t0001g0126 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.735-434G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96960874 | |||||||
| chr2:96960913 | G | A | 3 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.735-473C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96960913 | |||||||
| chr2:96961063 | C | T | 1 | a0001c0003t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.735-623G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961063 | |||||||
| chr2:96961097 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.735-657C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961097 | |||||||
| chr2:96961189 | A | G | 1 | a0002c0002t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.735-749T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961189 | |||||||
| chr2:96961312 | G | GGGGT | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0108 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-873_735-872ins others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961312 | G | GGT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(123): Show |
127 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.735-874_735-873dup others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961312 | G | GGTGT | 19 | a0001c0001t0001g0034 a0001c0003t0001g0084 a0002c0002t0001g0155 others(16): Show |
19 | HG01099.hp1 HG01123.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.735-876_735-873dup others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961312 | G | GGTGTGT | 8 | a0003c0011t0001g0248 a0004c0004t0001g0121 a0004c0004t0001g0122 others(5): Show |
8 | HG00099.hp2 HG01175.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.735-878_735-873dup others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961312 | G | GGTGTGTG others(1): Show |
10 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(7): Show |
10 | HG01261.hp2 HG01358.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.735-880_735-873dup others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961312 | G | GGTGTGTG others(5): Show |
1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.735-884_735-873dup others(12): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961312 | GGT | G | 3 | a0002c0002t0001g0149 a0002c0002t0001g0153 a0002c0002t0001g0192 |
3 | HG00609.hp2 NA19064.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.735-874_735-873del others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961312 | GGTGT | G | 5 | a0002c0002t0001g0148 a0002c0002t0001g0190 a0002c0002t0001g0206 others(2): Show |
5 | HG02602.hp2 HG03688.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-876_735-873del others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961312 | GGTGTGTG others(5): Show |
G | 1 | a0002c0002t0001g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.735-884_735-873del others(12): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961312 | |||||||
| chr2:96961334 | T | TGC | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0133 others(7): Show |
10 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.735-895_735-894ins others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961334 | |||||||
| chr2:96961371 | G | A | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.735-931C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961371 | |||||||
| chr2:96961406 | C | T | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-966G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961406 | |||||||
| chr2:96961520 | C | T | 1 | a0002c0002t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.735-1080G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961520 | |||||||
| chr2:96961523 | C | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.735-1083G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961523 | |||||||
| chr2:96961666 | G | A | 1 | a0001c0012t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.735-1226C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961666 | |||||||
| chr2:96961682 | G | A | 2 | a0002c0015t0003g0003 a0002c0015t0003g0004 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.735-1242C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961682 | |||||||
| chr2:96961922 | A | G | 2 | a0002c0002t0001g0198 a0002c0002t0001g0199 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.735-1482T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961922 | |||||||
| chr2:96961964 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735-1524G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96961964 | |||||||
| chr2:96962044 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.735-1604C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962044 | |||||||
| chr2:96962131 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.735-1691C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962131 | |||||||
| chr2:96962175 | A | G | 6 | a0003c0005t0001g0239 a0003c0005t0001g0240 a0003c0005t0001g0241 others(3): Show |
6 | HG00642.hp2 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-1735T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962175 | |||||||
| chr2:96962242 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.735-1802G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962242 | |||||||
| chr2:96962265 | G | A | 3 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0233 |
3 | HG03834.hp2 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.735-1825C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962265 | |||||||
| chr2:96962310 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.735-1870C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962310 | |||||||
| chr2:96962428 | CAAGA | C | 30 | a0001c0001t0001g0131 a0002c0008t0001g0159 a0002c0008t0001g0229 others(27): Show |
30 | HG00609.hp1 HG00642.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.735-1992_735-1989d others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962428 | |||||||
| chr2:96962428 | CAAGAAA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.735-1994_735-1989d others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962428 | |||||||
| chr2:96962445 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.735-2005C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962445 | |||||||
| chr2:96962461 | G | A | 14 | a0002c0002t0001g0155 a0003c0005t0001g0237 a0003c0005t0001g0238 others(11): Show |
14 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.735-2021C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962461 | |||||||
| chr2:96962494 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.735-2054G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962494 | |||||||
| chr2:96962588 | G | A | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-2148C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962588 | |||||||
| chr2:96962803 | T | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.735-2363A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962803 | |||||||
| chr2:96962929 | G | A | 2 | a0003c0011t0001g0236 a0003c0011t0001g0248 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.735-2489C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96962929 | |||||||
| chr2:96963054 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.735-2614T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963054 | |||||||
| chr2:96963055 | C | T | 1 | a0001c0003t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.735-2615G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963055 | |||||||
| chr2:96963109 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.735-2669G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963109 | |||||||
| chr2:96963119 | A | G | 1 | a0002c0023t0005g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-2679T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963119 | |||||||
| chr2:96963395 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(15): Show |
19 | HG00423.hp2 HG02602.hp1 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.735-2955A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963395 | |||||||
| chr2:96963462 | A | G | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.735-3022T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963462 | |||||||
| chr2:96963506 | G | C | 1 | a0003c0011t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.735-3066C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963506 | |||||||
| chr2:96963513 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.735-3073A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963513 | |||||||
| chr2:96963909 | C | T | 3 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.735-3469G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963909 | |||||||
| chr2:96963936 | C | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.735-3496G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963936 | |||||||
| chr2:96963967 | G | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.735-3527C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96963967 | |||||||
| chr2:96964000 | C | A | 1 | a0002c0002t0001g0219 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.734+3520G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964000 | |||||||
| chr2:96964073 | G | A | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0133 others(7): Show |
10 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.734+3447C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964073 | |||||||
| chr2:96964149 | GAC | G | 55 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
55 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.734+3369_734+3370d others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964149 | |||||||
| chr2:96964216 | CAA | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.734+3302_734+3303d others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964216 | |||||||
| chr2:96964383 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.734+3137C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964383 | |||||||
| chr2:96964426 | A | G | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.734+3094T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964426 | |||||||
| chr2:96964578 | T | C | 1 | a0005c0006t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.734+2942A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964578 | |||||||
| chr2:96964625 | G | A | 63 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
63 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.734+2895C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964625 | |||||||
| chr2:96964633 | A | ACTCT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.734+2883_734+2886d others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964633 | |||||||
| chr2:96964678 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.734+2842G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964678 | |||||||
| chr2:96964715 | C | T | 1 | a0001c0003t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.734+2805G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964715 | |||||||
| chr2:96964796 | A | G | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734+2724T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964796 | |||||||
| chr2:96964803 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.734+2717A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96964803 | |||||||
| chr2:96965023 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0052 others(1): Show |
4 | HG01123.hp2 HG01169.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.734+2497C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965023 | |||||||
| chr2:96965039 | G | T | 1 | a0003c0011t0001g0236 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.734+2481C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965039 | |||||||
| chr2:96965105 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.734+2415A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965105 | |||||||
| chr2:96965133 | G | A | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.734+2387C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965133 | |||||||
| chr2:96965181 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0052 others(1): Show |
4 | HG01123.hp2 HG01169.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.734+2339C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965181 | |||||||
| chr2:96965226 | C | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(7): Show |
10 | HG01261.hp2 HG01358.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.734+2294G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965226 | |||||||
| chr2:96965300 | T | A | 1 | a0014c0020t0001g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.734+2220A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965300 | |||||||
| chr2:96965319 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.734+2201C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965319 | |||||||
| chr2:96965466 | AT | A | 11 | a0001c0001t0001g0117 a0001c0003t0001g0118 a0002c0008t0001g0229 others(8): Show |
11 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.734+2053delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965466 | |||||||
| chr2:96965471 | T | G | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.734+2049A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965471 | |||||||
| chr2:96965825 | G | T | 5 | a0002c0008t0001g0159 a0002c0010t0001g0144 a0002c0010t0001g0158 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.734+1695C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965825 | |||||||
| chr2:96965848 | A | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.734+1672T>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96965848 | |||||||
| chr2:96966145 | C | T | 60 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(57): Show |
60 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.734+1375G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966145 | |||||||
| chr2:96966175 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.734+1345C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966175 | |||||||
| chr2:96966245 | T | C | 62 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(59): Show |
62 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.734+1275A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966245 | |||||||
| chr2:96966267 | C | A | 1 | a0004c0004t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.734+1253G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966267 | |||||||
| chr2:96966274 | C | G | 9 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.734+1246G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966274 | |||||||
| chr2:96966517 | T | TC | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.734+1002_734+1003i others(3): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966517 | |||||||
| chr2:96966534 | T | C | 1 | a0002c0002t0001g0177 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.734+986A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966534 | |||||||
| chr2:96966564 | G | A | 2 | a0009c0016t0001g0226 a0009c0016t0001g0227 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.734+956C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966564 | |||||||
| chr2:96966712 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(74): Show |
78 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.734+808C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966712 | |||||||
| chr2:96966713 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(74): Show |
78 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.734+807C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966713 | |||||||
| chr2:96966894 | G | A | 1 | a0002c0002t0001g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.734+626C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96966894 | |||||||
| chr2:96967018 | T | C | 6 | a0002c0008t0001g0159 a0002c0010t0001g0144 a0002c0010t0001g0158 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.734+502A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96967018 | |||||||
| chr2:96967234 | C | CAA | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.734+285_734+286ins others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96967234 | |||||||
| chr2:96967276 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.734+244T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 5/16 | chr2 | 96967276 | |||||||
| chr2:96967906 | T | G | 2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.627-279A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967906 | |||||||
| chr2:96967911 | C | CT | 24 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0134 others(21): Show |
24 | HG00544.hp2 HG00558.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.627-285dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTT | 7 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0017t0001g0142 others(4): Show |
7 | HG00597.hp2 HG02027.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.627-286_627-285dup others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0107 others(3): Show |
6 | HG01261.hp2 HG02895.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-292_627-285dup others(8): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0064 others(2): Show |
5 | HG02451.hp2 HG02717.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-294_627-285dup others(10): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(4): Show |
26 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0047 others(23): Show |
26 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.627-295_627-285dup others(11): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(5): Show |
21 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0035 others(18): Show |
21 | HG00642.hp1 HG00741.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.627-296_627-285dup others(12): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0052 others(2): Show |
5 | HG01099.hp2 HG01123.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.627-297_627-285dup others(13): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.627-299_627-285dup others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(9): Show |
1 | a0001c0003t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.627-300_627-285dup others(16): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0136 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627-301_627-285dup others(17): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(12): Show |
1 | a0001c0003t0001g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.627-303_627-285dup others(19): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | C | CTTTTTTT others(19): Show |
1 | a0001c0003t0001g0069 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.627-310_627-285dup others(26): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | CT | C | 10 | a0001c0001t0001g0112 a0001c0003t0001g0223 a0002c0002t0001g0149 others(7): Show |
10 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.627-285delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | CTT | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(38): Show |
42 | HG00423.hp2 HG01884.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.627-286_627-285del others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96967911 | CTTTTTT | C | 24 | a0001c0001t0001g0076 a0003c0005t0001g0237 a0003c0005t0001g0238 others(21): Show |
24 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.627-290_627-285del others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96967911 | |||||||
| chr2:96968008 | C | A | 1 | a0003c0005t0001g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.627-381G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968008 | |||||||
| chr2:96968009 | G | A | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.627-382C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968009 | |||||||
| chr2:96968035 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.627-408T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968035 | |||||||
| chr2:96968077 | C | A | 55 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
55 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.627-450G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968077 | |||||||
| chr2:96968308 | G | A | 2 | a0009c0016t0001g0226 a0009c0016t0001g0227 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.627-681C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968308 | |||||||
| chr2:96968374 | T | C | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.627-747A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968374 | |||||||
| chr2:96968469 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.627-842A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968469 | |||||||
| chr2:96968532 | C | CCCCAGG | 9 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(6): Show |
9 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.627-911_627-906dup others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968532 | |||||||
| chr2:96968612 | C | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.627-985G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968612 | |||||||
| chr2:96968693 | G | GC | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.627-1067dupG | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968693 | |||||||
| chr2:96968697 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.627-1070C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968697 | |||||||
| chr2:96968751 | T | C | 9 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(6): Show |
9 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.627-1124A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968751 | |||||||
| chr2:96968793 | T | C | 2 | a0003c0011t0001g0236 a0003c0011t0001g0248 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.627-1166A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968793 | |||||||
| chr2:96968935 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.627-1308T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968935 | |||||||
| chr2:96968938 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.627-1311G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96968938 | |||||||
| chr2:96969116 | T | G | 7 | a0002c0002t0001g0146 a0002c0002t0001g0174 a0002c0002t0001g0193 others(4): Show |
7 | HG00438.hp2 HG00544.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.627-1489A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969116 | |||||||
| chr2:96969210 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.626+1506C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969210 | |||||||
| chr2:96969220 | C | A | 6 | a0002c0002t0001g0146 a0002c0002t0001g0174 a0002c0002t0001g0193 others(3): Show |
6 | HG00438.hp2 HG00544.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+1496G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969220 | |||||||
| chr2:96969577 | G | A | 61 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(58): Show |
61 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.626+1139C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969577 | |||||||
| chr2:96969761 | G | A | 11 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.626+955C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969761 | |||||||
| chr2:96969781 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.626+935G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969781 | |||||||
| chr2:96969783 | C | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(22): Show |
26 | HG00423.hp2 HG02559.hp1 HG02572.hp2 others(23): Show |
intron_variant | MODIFIER | c.626+933G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969783 | |||||||
| chr2:96969784 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.626+932T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969784 | |||||||
| chr2:96969812 | C | T | 1 | a0015c0022t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.626+904G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969812 | |||||||
| chr2:96969990 | C | T | 2 | a0002c0010t0001g0158 a0002c0010t0001g0160 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.626+726G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96969990 | |||||||
| chr2:96970103 | C | T | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.626+613G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96970103 | |||||||
| chr2:96970314 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.626+402G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96970314 | |||||||
| chr2:96970458 | G | C | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.626+258C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96970458 | |||||||
| chr2:96970501 | G | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.626+215C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96970501 | |||||||
| chr2:96970580 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.626+136G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96970580 | |||||||
| chr2:96970671 | C | T | 1 | a0007c0014t0001g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.626+45G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 4/16 | chr2 | 96970671 | |||||||
| chr2:96971163 | AT | A | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.565-387delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/16 | chr2 | 96971163 | |||||||
| chr2:96971186 | C | T | 3 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.565-409G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/16 | chr2 | 96971186 | |||||||
| chr2:96971281 | T | TTCCCTCT others(8): Show |
1 | a0001c0001t0001g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.565-505_565-504ins others(15): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/16 | chr2 | 96971281 | |||||||
| chr2:96971286 | T | C | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.565-509A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/16 | chr2 | 96971286 | |||||||
| chr2:96971290 | T | TC | 7 | a0001c0001t0001g0035 a0001c0003t0001g0223 a0002c0008t0001g0230 others(4): Show |
7 | HG01981.hp1 HG02055.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-514dupG | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/16 | chr2 | 96971290 | |||||||
| chr2:96971294 | A | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.565-517T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/16 | chr2 | 96971294 | |||||||
| chr2:96971647 | C | T | 1 | a0003c0005t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.564+254G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/16 | chr2 | 96971647 | |||||||
| chr2:96971779 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(154): Show |
158 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.564+122A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 3/16 | chr2 | 96971779 | |||||||
| chr2:96972758 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.74-152C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96972758 | |||||||
| chr2:96972848 | C | T | 1 | a0003c0011t0001g0236 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.74-242G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96972848 | |||||||
| chr2:96972942 | C | G | 3 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0177 |
3 | HG02135.hp1 HG02148.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.74-336G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96972942 | |||||||
| chr2:96972976 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.74-370C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96972976 | |||||||
| chr2:96973065 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.74-459G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973065 | |||||||
| chr2:96973070 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.74-464C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973070 | |||||||
| chr2:96973074 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.74-468G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973074 | |||||||
| chr2:96973075 | G | A | 1 | a0002c0002t0001g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.74-469C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973075 | |||||||
| chr2:96973086 | T | C | 4 | a0001c0001t0001g0099 a0001c0003t0001g0101 a0001c0003t0001g0102 others(1): Show |
4 | HG03139.hp1 HG03225.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-480A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973086 | |||||||
| chr2:96973147 | G | A | 1 | a0001c0003t0001g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.74-541C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973147 | |||||||
| chr2:96973206 | CA | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.74-601delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973206 | |||||||
| chr2:96973237 | A | G | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.74-631T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973237 | |||||||
| chr2:96973398 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.74-792A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973398 | |||||||
| chr2:96973873 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.74-1267G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96973873 | |||||||
| chr2:96974116 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.74-1510G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974116 | |||||||
| chr2:96974305 | C | T | 1 | a0002c0002t0001g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.74-1699G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974305 | |||||||
| chr2:96974370 | A | G | 1 | a0006c0007t0002g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.74-1764T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974370 | |||||||
| chr2:96974381 | C | CA | 17 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0001g0088 others(14): Show |
17 | HG00423.hp1 HG01106.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.74-1776dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974381 | |||||||
| chr2:96974381 | CA | C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0082 a0001c0001t0001g0105 others(6): Show |
9 | HG01070.hp2 HG02071.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.74-1776delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974381 | |||||||
| chr2:96974480 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0091 others(3): Show |
7 | HG00423.hp2 HG02602.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-1874T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974480 | |||||||
| chr2:96974765 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.74-2159A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974765 | |||||||
| chr2:96974897 | C | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0068 |
2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.74-2291G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974897 | |||||||
| chr2:96974927 | C | T | 1 | a0002c0008t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.74-2321G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974927 | |||||||
| chr2:96974934 | T | C | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.74-2328A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974934 | |||||||
| chr2:96974984 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.74-2378C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96974984 | |||||||
| chr2:96975094 | C | CA | 84 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(81): Show |
84 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.74-2489dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96975094 | |||||||
| chr2:96975094 | C | CAA | 24 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(21): Show |
24 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.74-2490_74-2489dup others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96975094 | |||||||
| chr2:96975094 | CA | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0099 a0001c0001t0001g0134 others(7): Show |
10 | HG01243.hp1 HG02165.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.74-2489delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96975094 | |||||||
| chr2:96975127 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.74-2521G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96975127 | |||||||
| chr2:96975260 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.74-2654T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96975260 | |||||||
| chr2:96975338 | C | G | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.74-2732G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96975338 | |||||||
| chr2:96975530 | T | G | 65 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(62): Show |
65 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.74-2924A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96975530 | |||||||
| chr2:96975972 | T | A | 1 | a0002c0002t0001g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.74-3366A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96975972 | |||||||
| chr2:96976097 | C | CT | 12 | a0002c0002t0001g0146 a0003c0005t0001g0237 a0003c0005t0001g0238 others(9): Show |
12 | HG00642.hp2 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.74-3492dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976097 | |||||||
| chr2:96976097 | CT | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0038 others(19): Show |
23 | HG00423.hp2 HG01070.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.74-3492delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976097 | |||||||
| chr2:96976111 | T | G | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.74-3505A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976111 | |||||||
| chr2:96976112 | T | A | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.74-3506A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976112 | |||||||
| chr2:96976125 | T | G | 1 | a0002c0002t0001g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.74-3519A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976125 | |||||||
| chr2:96976186 | C | T | 2 | a0009c0016t0001g0226 a0009c0016t0001g0227 |
2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.74-3580G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976186 | |||||||
| chr2:96976208 | C | T | 1 | a0011c0021t0001g0225 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.74-3602G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976208 | |||||||
| chr2:96976477 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.74-3871T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976477 | |||||||
| chr2:96976624 | C | T | 2 | a0003c0011t0001g0236 a0003c0011t0001g0248 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.74-4018G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976624 | |||||||
| chr2:96976804 | T | C | 2 | a0002c0002t0001g0198 a0002c0002t0001g0199 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.74-4198A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96976804 | |||||||
| chr2:96977073 | G | T | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.74-4467C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977073 | |||||||
| chr2:96977092 | C | T | 1 | a0006c0007t0002g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.74-4486G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977092 | |||||||
| chr2:96977117 | C | G | 1 | a0003c0011t0001g0236 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.74-4511G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977117 | |||||||
| chr2:96977178 | G | C | 2 | a0002c0015t0003g0003 a0002c0015t0003g0004 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.74-4572C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977178 | |||||||
| chr2:96977194 | C | CA | 34 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0088 others(31): Show |
34 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.74-4589dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977194 | |||||||
| chr2:96977194 | CA | C | 55 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(52): Show |
55 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.74-4589delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977194 | |||||||
| chr2:96977194 | CAAAA | C | 9 | a0002c0002t0001g0017 a0002c0002t0001g0170 a0002c0002t0001g0171 others(6): Show |
9 | HG00642.hp2 HG01169.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.74-4592_74-4589del others(4): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977194 | |||||||
| chr2:96977363 | C | T | 1 | a0003c0005t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.74-4757G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977363 | |||||||
| chr2:96977380 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.74-4774C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977380 | |||||||
| chr2:96977384 | C | CA | 16 | a0001c0001t0001g0047 a0001c0003t0001g0039 a0001c0003t0001g0075 others(13): Show |
16 | HG00639.hp1 HG01175.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.74-4779dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977384 | |||||||
| chr2:96977384 | CA | C | 6 | a0001c0001t0001g0008 a0001c0003t0001g0024 a0001c0003t0001g0025 others(3): Show |
6 | HG02004.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-4779delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977384 | |||||||
| chr2:96977436 | A | G | 1 | a0001c0003t0001g0049 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.74-4830T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977436 | |||||||
| chr2:96977452 | A | AT | 15 | a0001c0001t0001g0040 a0001c0001t0001g0085 a0001c0003t0001g0029 others(12): Show |
15 | HG01192.hp2 HG01243.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.74-4847dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977452 | |||||||
| chr2:96977698 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.74-5092C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977698 | |||||||
| chr2:96977784 | G | T | 1 | a0005c0006t0001g0048 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.74-5178C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977784 | |||||||
| chr2:96977839 | T | C | 62 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(59): Show |
62 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.74-5233A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977839 | |||||||
| chr2:96977926 | T | TTCA | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-5323_74-5321dup others(3): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977926 | |||||||
| chr2:96977943 | G | C | 12 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(9): Show |
12 | HG00609.hp1 HG00642.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.74-5337C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977943 | |||||||
| chr2:96977947 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(23): Show |
27 | HG00423.hp2 HG02145.hp1 HG02559.hp1 others(24): Show |
intron_variant | MODIFIER | c.74-5341C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96977947 | |||||||
| chr2:96978119 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0091 others(3): Show |
7 | HG00423.hp2 HG02602.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-5513T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978119 | |||||||
| chr2:96978278 | C | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0085 others(23): Show |
27 | HG00423.hp2 HG02145.hp1 HG02559.hp1 others(24): Show |
intron_variant | MODIFIER | c.74-5672G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978278 | |||||||
| chr2:96978485 | C | G | 3 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.74-5879G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978485 | |||||||
| chr2:96978549 | A | C | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.74-5943T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978549 | |||||||
| chr2:96978628 | C | CT | 11 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0133 others(8): Show |
11 | HG00597.hp2 HG03098.hp2 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.74-6023dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978628 | |||||||
| chr2:96978628 | CT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.74-6023delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978628 | |||||||
| chr2:96978883 | TCAAAGTG others(343): Show |
T | 1 | a0002c0009t0001g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.74-6627_74-6278del | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978883 | |||||||
| chr2:96978892 | T | G | 4 | a0001c0003t0001g0100 a0006c0007t0002g0041 a0006c0007t0002g0095 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-6286A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978892 | |||||||
| chr2:96978949 | A | G | 1 | a0002c0002t0001g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.74-6343T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978949 | |||||||
| chr2:96978973 | A | ACT | 19 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0040 others(16): Show |
19 | HG00438.hp1 HG00558.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.74-6369_74-6368dup others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978973 | |||||||
| chr2:96978974 | CT | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
148 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.74-6369delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978974 | |||||||
| chr2:96978974 | CTT | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG01257.hp1 HG02165.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-6370_74-6369del others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978974 | |||||||
| chr2:96978975 | T | TC | 41 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(38): Show |
41 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.74-6370_74-6369ins others(1): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978975 | |||||||
| chr2:96978976 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.74-6370A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96978976 | |||||||
| chr2:96979117 | C | T | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.74-6511G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979117 | |||||||
| chr2:96979125 | C | T | 2 | a0003c0005t0001g0240 a0003c0005t0001g0245 |
2 | HG00642.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.74-6519G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979125 | |||||||
| chr2:96979130 | C | T | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.74-6524G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979130 | |||||||
| chr2:96979275 | A | AT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(154): Show |
158 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.74-6670dupA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979275 | |||||||
| chr2:96979275 | A | ATT | 15 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(12): Show |
15 | HG00609.hp1 HG00639.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.74-6671_74-6670dup others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979275 | |||||||
| chr2:96979342 | C | T | 1 | a0002c0002t0001g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.74-6736G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979342 | |||||||
| chr2:96979343 | G | C | 65 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(62): Show |
65 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.74-6737C>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979343 | |||||||
| chr2:96979542 | CTTAGGTT others(180): Show |
C | 1 | a0006c0007t0002g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.73+6512_73+6698del | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979542 | |||||||
| chr2:96979579 | G | A | 5 | a0002c0008t0001g0159 a0002c0010t0001g0144 a0002c0010t0001g0158 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+6662C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979579 | |||||||
| chr2:96979731 | T | A | 1 | a0006c0007t0002g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.73+6510A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979731 | |||||||
| chr2:96979733 | A | C | 1 | a0006c0007t0002g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.73+6508T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979733 | |||||||
| chr2:96979735 | T | G | 1 | a0006c0007t0002g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.73+6506A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979735 | |||||||
| chr2:96979737 | A | G | 1 | a0006c0007t0002g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.73+6504T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979737 | |||||||
| chr2:96979738 | C | T | 1 | a0006c0007t0002g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.73+6503G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979738 | |||||||
| chr2:96979750 | CTG | C | 12 | a0004c0004t0001g0043 a0004c0004t0001g0121 a0004c0004t0001g0122 others(9): Show |
12 | HG00099.hp2 HG01099.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.73+6489_73+6490del others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979750 | |||||||
| chr2:96979937 | A | G | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0133 others(7): Show |
10 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.73+6304T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96979937 | |||||||
| chr2:96980013 | T | C | 1 | a0002c0002t0001g0204 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.73+6228A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980013 | |||||||
| chr2:96980031 | T | C | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.73+6210A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980031 | |||||||
| chr2:96980048 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.73+6193G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980048 | |||||||
| chr2:96980106 | C | G | 1 | a0005c0006t0001g0045 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.73+6135G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980106 | |||||||
| chr2:96980137 | G | A | 1 | a0003c0011t0001g0247 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+6104C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980137 | |||||||
| chr2:96980169 | C | T | 1 | a0002c0009t0001g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.73+6072G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980169 | |||||||
| chr2:96980170 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.73+6071C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980170 | |||||||
| chr2:96980372 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.73+5869C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980372 | |||||||
| chr2:96980382 | T | C | 1 | a0004c0004t0001g0130 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.73+5859A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980382 | |||||||
| chr2:96980544 | A | G | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.73+5697T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980544 | |||||||
| chr2:96980613 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.73+5628C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980613 | |||||||
| chr2:96980708 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.73+5533G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980708 | |||||||
| chr2:96980848 | CCAATT | C | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0133 others(7): Show |
10 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.73+5388_73+5392del others(5): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980848 | |||||||
| chr2:96980929 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.73+5312G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980929 | |||||||
| chr2:96980995 | G | A | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0133 others(7): Show |
10 | HG00597.hp2 NA18941.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.73+5246C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96980995 | |||||||
| chr2:96981035 | G | A | 12 | a0004c0004t0001g0043 a0004c0004t0001g0121 a0004c0004t0001g0122 others(9): Show |
12 | HG00099.hp2 HG01099.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.73+5206C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981035 | |||||||
| chr2:96981058 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.73+5183G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981058 | |||||||
| chr2:96981093 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0081 |
3 | NA18979.hp1 NA19000.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.73+5148C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981093 | |||||||
| chr2:96981118 | A | C | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73+5123T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981118 | |||||||
| chr2:96981178 | C | T | 1 | a0007c0014t0001g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.73+5063G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981178 | |||||||
| chr2:96981193 | TGGCCTCA others(42): Show |
T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.73+4999_73+5047del others(49): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981193 | |||||||
| chr2:96981256 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73+4985C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981256 | |||||||
| chr2:96981312 | C | T | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.73+4929G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981312 | |||||||
| chr2:96981337 | C | T | 2 | a0002c0002t0001g0154 a0002c0002t0001g0163 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.73+4904G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981337 | |||||||
| chr2:96981362 | C | G | 1 | a0001c0003t0001g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73+4879G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981362 | |||||||
| chr2:96981412 | G | A | 3 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73+4829C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981412 | |||||||
| chr2:96981431 | C | A | 3 | a0001c0012t0001g0139 a0001c0012t0001g0140 a0001c0012t0001g0141 |
3 | HG02717.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.73+4810G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981431 | |||||||
| chr2:96981505 | T | C | 6 | a0002c0002t0001g0206 a0002c0002t0001g0207 a0002c0002t0001g0208 others(3): Show |
6 | HG01106.hp2 HG02602.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+4736A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981505 | |||||||
| chr2:96981709 | A | G | 1 | a0002c0002t0001g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.73+4532T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981709 | |||||||
| chr2:96981735 | C | T | 7 | a0003c0005t0001g0239 a0003c0005t0001g0240 a0003c0005t0001g0241 others(4): Show |
7 | HG00642.hp2 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+4506G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981735 | |||||||
| chr2:96981740 | C | CA | 12 | a0002c0002t0001g0154 a0002c0002t0001g0155 a0002c0002t0001g0212 others(9): Show |
12 | HG00438.hp2 HG02055.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.73+4500dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981740 | |||||||
| chr2:96981740 | C | CAAAAAA | 9 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0243 others(6): Show |
9 | HG00609.hp1 HG02040.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.73+4495_73+4500dup others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981740 | |||||||
| chr2:96981740 | CA | C | 5 | a0002c0009t0001g0161 a0002c0024t0001g0222 a0009c0016t0001g0226 others(2): Show |
5 | HG02165.hp2 HG03017.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.73+4500delT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981740 | |||||||
| chr2:96981740 | CAA | C | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.73+4499_73+4500del others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981740 | |||||||
| chr2:96981747 | A | AAAAAAG | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
69 | HG00099.hp2 HG00423.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.73+4493_73+4494ins others(6): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981747 | |||||||
| chr2:96981751 | A | AAG | 73 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(70): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.73+4489_73+4490ins others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981751 | |||||||
| chr2:96981759 | A | G | 2 | a0002c0024t0001g0222 a0012c0026t0001g0224 |
2 | HG02165.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.73+4482T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981759 | |||||||
| chr2:96981763 | G | A | 65 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(62): Show |
65 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.73+4478C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981763 | |||||||
| chr2:96981879 | C | T | 62 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(59): Show |
62 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.73+4362G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981879 | |||||||
| chr2:96981898 | C | G | 2 | a0003c0005t0001g0237 a0003c0005t0001g0238 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.73+4343G>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981898 | |||||||
| chr2:96981903 | C | CA | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0131 others(2): Show |
5 | HG00597.hp2 HG02145.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+4337dupT | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981903 | |||||||
| chr2:96981940 | C | T | 1 | a0001c0003t0001g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.73+4301G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96981940 | |||||||
| chr2:96982260 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
69 | HG00099.hp2 HG00423.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.73+3981T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982260 | |||||||
| chr2:96982368 | T | A | 6 | a0002c0008t0001g0159 a0002c0010t0001g0144 a0002c0010t0001g0158 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+3873A>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982368 | |||||||
| chr2:96982483 | G | A | 1 | a0004c0004t0001g0143 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.73+3758C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982483 | |||||||
| chr2:96982583 | G | T | 2 | a0003c0011t0001g0236 a0003c0011t0001g0248 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.73+3658C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982583 | |||||||
| chr2:96982609 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.73+3632A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982609 | |||||||
| chr2:96982687 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.73+3554T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982687 | |||||||
| chr2:96982723 | C | T | 2 | a0001c0003t0001g0083 a0001c0003t0001g0084 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.73+3518G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982723 | |||||||
| chr2:96982735 | AT | A | 132 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0047 others(129): Show |
132 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.73+3505delA | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982735 | |||||||
| chr2:96982735 | ATT | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(68): Show |
72 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.73+3504_73+3505del others(2): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96982735 | |||||||
| chr2:96983095 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.73+3146T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96983095 | |||||||
| chr2:96983479 | C | T | 3 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73+2762G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96983479 | |||||||
| chr2:96983755 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.73+2486A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96983755 | |||||||
| chr2:96983790 | G | A | 1 | a0002c0002t0001g0219 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.73+2451C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96983790 | |||||||
| chr2:96983819 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.73+2422C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96983819 | |||||||
| chr2:96983910 | T | C | 1 | a0002c0002t0001g0221 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.73+2331A>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96983910 | |||||||
| chr2:96983917 | C | T | 4 | a0005c0006t0001g0020 a0005c0006t0001g0021 a0005c0006t0001g0022 others(1): Show |
4 | HG00642.hp1 HG01975.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.73+2324G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96983917 | |||||||
| chr2:96984072 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.73+2169G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96984072 | |||||||
| chr2:96984117 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(6): Show |
9 | HG01261.hp2 HG01358.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.73+2124C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96984117 | |||||||
| chr2:96984205 | C | T | 1 | a0002c0002t0001g0017 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.73+2036G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96984205 | |||||||
| chr2:96984282 | C | T | 1 | a0001c0003t0001g0016 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.73+1959G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96984282 | |||||||
| chr2:96984293 | G | A | 1 | a0003c0011t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.73+1948C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96984293 | |||||||
| chr2:96984375 | G | A | 1 | a0002c0024t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73+1866C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96984375 | |||||||
| chr2:96984596 | C | T | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.73+1645G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96984596 | |||||||
| chr2:96984795 | C | A | 1 | a0001c0003t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.73+1446G>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96984795 | |||||||
| chr2:96985163 | G | A | 1 | a0012c0026t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.73+1078C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96985163 | |||||||
| chr2:96985398 | G | A | 1 | a0011c0021t0001g0225 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.73+843C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96985398 | |||||||
| chr2:96985501 | T | G | 9 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(6): Show |
9 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.73+740A>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96985501 | |||||||
| chr2:96985509 | GTTTTT | G | 7 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0002c0008t0001g0232 others(4): Show |
7 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.73+727_73+731delAA others(3): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96985509 | |||||||
| chr2:96985654 | G | A | 1 | a0014c0020t0001g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.73+587C>T | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96985654 | |||||||
| chr2:96985682 | CAAGACGC others(9): Show |
C | 13 | a0003c0005t0001g0237 a0003c0005t0001g0238 a0003c0005t0001g0239 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.73+543_73+558delAG others(14): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96985682 | |||||||
| chr2:96985926 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(6): Show |
9 | HG01261.hp2 HG01358.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.73+315G>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96985926 | |||||||
| chr2:96985960 | A | C | 1 | a0002c0010t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.73+281T>G | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96985960 | |||||||
| chr2:96986029 | G | T | 1 | a0013c0025t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73+212C>A | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96986029 | |||||||
| chr2:96986049 | A | G | 1 | a0001c0003t0001g0005 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.73+192T>C | FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 1/16 | chr2 | 96986049 |