Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 167555 |
| ensemblid | ENSG00000152380.10 |
| hgncid | 33716 |
| symbol | FAM151B |
| name | family with sequence similarity 151 member B |
| refseq_nuc | NM_205548.3 |
| refseq_prot | NP_991111.2 |
| ensembl_nuc | ENST00000282226.5 |
| ensembl_prot | ENSP00000282226.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 80488100 |
| end | 80542563 |
| strand | + |
| ver | v1.2 |
| region | chr5:80488100-80542563 |
| region5000 | chr5:80483100-80547563 |
| regionname0 | FAM151B_chr5_80488100_80542563 |
| regionname5000 | FAM151B_chr5_80483100_80547563 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 276 | 251 | 73 | 50 | 87 | 11 | 30 | 64 | FAM151B_chr5_80483100_80547563 | FAM151B | MAASA others(271): Show |
chr5 | 80483100 | 80547563 |
| a0002 | 1/1 | 276 | 103 | 14 | 19 | 55 | 1 | 12 | 44 | FAM151B_chr5_80483100_80547563 | FAM151B | MAASA others(271): Show |
chr5 | 80483100 | 80547563 |
| a0003 | 0/0 | 276 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | MAASA others(271): Show |
chr5 | 80483100 | 80547563 |
| a0004 | 0/0 | 276 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | MAASA others(271): Show |
chr5 | 80483100 | 80547563 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 828 | 241 | 72 | 45 | 87 | 9 | 28 | FAM151B_chr5_80483100_80547563 | FAM151B | ATGGC others(823): Show |
chr5 | 80483100 | 80547563 | ||
| a0001c0003 | 0/0 | 828 | 10 | 1 | 5 | 0 | 2 | 2 | FAM151B_chr5_80483100_80547563 | FAM151B | ATGGC others(823): Show |
chr5 | 80483100 | 80547563 | ||
| a0002c0002 | 1/1 | 828 | 103 | 14 | 19 | 55 | 1 | 12 | FAM151B_chr5_80483100_80547563 | FAM151B | ATGGC others(823): Show |
chr5 | 80483100 | 80547563 | ||
| a0003c0005 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | ATGGC others(823): Show |
chr5 | 80483100 | 80547563 | ||
| a0004c0004 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | ATGGC others(823): Show |
chr5 | 80483100 | 80547563 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1586 | 222 | 55 | 45 | 85 | 9 | 28 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0001c0001t0002 | 0/0 | 1586 | 14 | 14 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0001c0001t0003 | 0/0 | 1586 | 2 | 2 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0001c0001t0004 | 0/0 | 1586 | 2 | 0 | 0 | 2 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0001c0001t0006 | 0/0 | 1586 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0001c0003t0001 | 0/0 | 1586 | 10 | 1 | 5 | 0 | 2 | 2 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0002c0002t0001 | 1/1 | 1586 | 100 | 14 | 19 | 52 | 1 | 12 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0002c0002t0005 | 0/0 | 1586 | 2 | 0 | 0 | 2 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0002c0002t0007 | 0/0 | 1586 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0003c0005t0001 | 0/0 | 1586 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| a0004c0004t0001 | 0/0 | 1586 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | GCGCG others(1581): Show |
chr5 | 80483100 | 80547563 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0001t0006g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0001c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0001g0347 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0002c0002t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0003c0005t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| a0004c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0292 | EUR | FIN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0341 | EUR | FIN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0143 | EUR | FIN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00438 | hp1 | a0002 | c0002 | t0007 | g0089 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0185 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0291 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0186 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0290 | EUR | IBS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0231 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01978 | hp2 | a0003 | c0005 | t0001 | g0257 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0235 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0230 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0350 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0120 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02723 | hp1 | a0004 | c0004 | t0001 | g0322 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0293 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0273 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0342 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0140 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0282 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0106 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0048 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0103 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0343 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0288 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0244 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0017 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18978 | hp2 | a0002 | c0002 | t0005 | g0104 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19056 | hp2 | a0002 | c0002 | t0005 | g0098 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ASW | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ASW | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0326 | EUR | TSI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | GIH | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0289 | SAS | GIH | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | USA | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | USA | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | USA | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | USA | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0189 | REF | REF | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0347 | REF | REF | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80519781 | C | A | 1 | a0004 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.406C>A | p.Pro136Thr | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/6 | 430/1586 | 406/831 | 136/276 | chr5 | 80519781 | |||
| chr5:80519839 | T | C | 3 | a0001 a0003 a0004 |
253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
missense_variant | MODERATE | c.464T>C | p.Ile155Thr | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/6 | 488/1586 | 464/831 | 155/276 | chr5 | 80519839 | |||
| chr5:80522042 | G | A | 1 | a0003 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.575G>A | p.Cys192Tyr | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/6 | 599/1586 | 575/831 | 192/276 | chr5 | 80522042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80522079 | A | G | 1 | a0001c0003 | 10 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
synonymous_variant | LOW | c.612A>G | p.Arg204Arg | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/6 | 636/1586 | 612/831 | 204/276 | chr5 | 80522079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80542255 | G | A | 2 | a0001c0001t0003 a0001c0001t0006 |
3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*423G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 423 | chr5 | 80542255 | ||||||
| chr5:80542260 | G | C | 1 | a0001c0001t0006 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 428 | chr5 | 80542260 | ||||||
| chr5:80542310 | T | C | 1 | a0002c0002t0007 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*478T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 478 | chr5 | 80542310 | ||||||
| chr5:80542340 | G | A | 1 | a0001c0001t0004 | 2 | HG00438.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*508G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 508 | chr5 | 80542340 | ||||||
| chr5:80542402 | G | T | 1 | a0001c0001t0002 | 14 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 570 | chr5 | 80542402 | ||||||
| chr5:80542503 | G | A | 2 | a0001c0001t0003 a0001c0001t0006 |
3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*671G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 671 | chr5 | 80542503 | ||||||
| chr5:80542521 | C | T | 1 | a0002c0002t0005 | 2 | NA18978.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*689C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 689 | chr5 | 80542521 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80488365 | G | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
277 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.25+217G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488365 | |||||||
| chr5:80488390 | T | G | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.25+242T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488390 | |||||||
| chr5:80488543 | G | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG00408.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.25+395G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488543 | |||||||
| chr5:80488557 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.25+409C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488557 | |||||||
| chr5:80488573 | G | T | 1 | a0002c0002t0001g0273 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.25+425G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488573 | |||||||
| chr5:80488578 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | NA19062.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.25+430G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488578 | |||||||
| chr5:80489033 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.25+885G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489033 | |||||||
| chr5:80489130 | A | G | 1 | a0002c0002t0001g0272 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.25+982A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489130 | |||||||
| chr5:80489241 | G | T | 1 | a0002c0002t0001g0271 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.25+1093G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489241 | |||||||
| chr5:80489349 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | NA18948.hp1 NA18950.hp1 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+1201T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489349 | |||||||
| chr5:80489411 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.25+1263C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489411 | |||||||
| chr5:80489433 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.25+1285T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489433 | |||||||
| chr5:80489710 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0002g0280 |
3 | HG01884.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.25+1562G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489710 | |||||||
| chr5:80489872 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
278 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.25+1724C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489872 | |||||||
| chr5:80489903 | A | G | 19 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(16): Show |
19 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+1755A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489903 | |||||||
| chr5:80489937 | AC | A | 3 | a0001c0001t0001g0283 a0001c0001t0003g0281 a0002c0002t0001g0282 |
3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+1790delC | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489937 | |||||||
| chr5:80489938 | C | CAAAAACA others(6): Show |
2 | a0001c0001t0002g0284 a0001c0001t0006g0350 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.25+1795_25+1796ins others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80489938 | ||||||
| chr5:80490019 | T | TAAACACA others(3): Show |
1 | a0001c0001t0002g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25+1872_25+1873ins others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TAC | 24 | a0001c0001t0001g0234 a0001c0001t0001g0253 a0001c0001t0001g0254 others(21): Show |
24 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+1903_25+1904dup others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TACAC | 16 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(13): Show |
16 | HG01192.hp2 HG01433.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+1901_25+1904dup others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TACACAC | 18 | a0001c0001t0001g0210 a0001c0001t0001g0213 a0001c0001t0001g0214 others(15): Show |
18 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.25+1899_25+1904dup others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TACACACA others(1): Show |
39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
40 | HG00280.hp1 HG00621.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.25+1897_25+1904dup others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TACACACA others(3): Show |
122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0071 others(119): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.25+1895_25+1904dup others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TACACACA others(5): Show |
39 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0045 others(36): Show |
39 | HG00558.hp2 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.25+1893_25+1904dup others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TACACACA others(7): Show |
15 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0032 others(12): Show |
15 | HG00741.hp2 HG02071.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+1891_25+1904dup others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TACACACA others(9): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG02155.hp2 HG03704.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+1889_25+1904dup others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | T | TACACACA others(11): Show |
3 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 |
3 | HG03471.hp1 HG04115.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.25+1887_25+1904dup others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | TAC | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0239 others(13): Show |
16 | HG01099.hp1 HG01255.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.25+1903_25+1904del others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490019 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0353 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.25+1895_25+1904del others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | ||||||
| chr5:80490020 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.25+1873_25+1885dup others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490020 | ||||||
| chr5:80490053 | T | C | 3 | a0001c0003t0001g0002 a0001c0003t0001g0185 a0001c0003t0001g0186 |
4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+1905T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490053 | |||||||
| chr5:80490109 | C | T | 2 | a0001c0001t0002g0284 a0001c0001t0006g0350 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.25+1961C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490109 | |||||||
| chr5:80490413 | T | C | 2 | a0001c0001t0002g0284 a0001c0001t0006g0350 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.25+2265T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490413 | |||||||
| chr5:80490417 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.25+2269A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490417 | |||||||
| chr5:80490586 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
310 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.25+2438T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490586 | |||||||
| chr5:80490618 | T | C | 1 | a0001c0001t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.25+2470T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490618 | |||||||
| chr5:80490638 | A | G | 3 | a0002c0002t0001g0019 a0002c0002t0001g0033 a0002c0002t0001g0070 |
3 | HG00558.hp2 NA18612.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.25+2490A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490638 | |||||||
| chr5:80490698 | A | G | 1 | a0001c0001t0001g0354 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.25+2550A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490698 | |||||||
| chr5:80490849 | A | G | 6 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0003t0001g0290 others(3): Show |
6 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+2701A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490849 | |||||||
| chr5:80490906 | A | C | 1 | a0001c0001t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.25+2758A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490906 | |||||||
| chr5:80491050 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.25+2902C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491050 | |||||||
| chr5:80491102 | C | G | 21 | a0001c0001t0001g0184 a0001c0001t0001g0234 a0001c0001t0001g0252 others(18): Show |
21 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+2954C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491102 | |||||||
| chr5:80491153 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.25+3005G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491153 | |||||||
| chr5:80491202 | CTAT | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(323): Show |
328 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.25+3079_25+3081del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80491202 | ||||||
| chr5:80491227 | T | C | 2 | a0001c0001t0001g0210 a0002c0002t0001g0299 |
2 | HG01070.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.25+3079T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491227 | |||||||
| chr5:80491294 | C | T | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG01981.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.25+3146C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491294 | |||||||
| chr5:80491469 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.25+3321C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491469 | |||||||
| chr5:80491774 | G | A | 16 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0283 others(13): Show |
16 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+3626G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491774 | |||||||
| chr5:80491782 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.25+3634G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491782 | |||||||
| chr5:80491788 | C | T | 2 | a0001c0001t0001g0182 a0002c0002t0001g0183 |
2 | NA18943.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.25+3640C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491788 | |||||||
| chr5:80491821 | A | G | 11 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0304 others(8): Show |
11 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+3673A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491821 | |||||||
| chr5:80492018 | C | T | 2 | a0002c0002t0001g0342 a0002c0002t0001g0343 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.25+3870C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492018 | |||||||
| chr5:80492297 | A | G | 1 | a0001c0001t0001g0352 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.25+4149A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492297 | |||||||
| chr5:80492312 | A | C | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+4164A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492312 | |||||||
| chr5:80492330 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.25+4182G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492330 | |||||||
| chr5:80492349 | C | A | 1 | a0001c0001t0002g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25+4201C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492349 | |||||||
| chr5:80492465 | T | C | 2 | a0002c0002t0001g0033 a0002c0002t0001g0070 |
2 | HG00558.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.25+4317T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492465 | |||||||
| chr5:80492695 | G | A | 2 | a0001c0001t0001g0221 a0002c0002t0001g0273 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.25+4547G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492695 | |||||||
| chr5:80492742 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+4594C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492742 | |||||||
| chr5:80492803 | A | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.25+4655A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492803 | |||||||
| chr5:80492826 | C | T | 3 | a0001c0001t0001g0283 a0001c0001t0003g0281 a0002c0002t0001g0282 |
3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+4678C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492826 | |||||||
| chr5:80492963 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.25+4815A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492963 | |||||||
| chr5:80493015 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0003g0281 a0002c0002t0001g0282 |
3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+4867G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493015 | |||||||
| chr5:80493174 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.25+5026C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493174 | |||||||
| chr5:80493202 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.25+5054C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493202 | |||||||
| chr5:80493368 | CAT | C | 9 | a0001c0001t0001g0297 a0001c0001t0001g0304 a0001c0001t0001g0305 others(6): Show |
9 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+5221_25+5222del others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493368 | |||||||
| chr5:80493423 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.25+5275G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493423 | |||||||
| chr5:80493452 | C | T | 1 | a0001c0001t0002g0296 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.25+5304C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493452 | |||||||
| chr5:80493454 | T | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | NA18955.hp1 NA18982.hp1 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+5306T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493454 | |||||||
| chr5:80493487 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.25+5339C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493487 | |||||||
| chr5:80493552 | A | G | 8 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(5): Show |
8 | HG01496.hp1 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.25+5404A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493552 | |||||||
| chr5:80493726 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
279 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.25+5578A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493726 | |||||||
| chr5:80493770 | T | G | 1 | a0001c0001t0001g0313 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.25+5622T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493770 | |||||||
| chr5:80494085 | G | A | 2 | a0002c0002t0001g0073 a0002c0002t0001g0299 |
2 | HG00408.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.25+5937G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494085 | |||||||
| chr5:80494104 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.25+5956G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494104 | |||||||
| chr5:80494105 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.25+5957T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494105 | |||||||
| chr5:80494127 | T | C | 10 | a0001c0001t0001g0297 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+5979T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494127 | |||||||
| chr5:80494442 | TTTTTCTT others(6): Show |
T | 7 | a0001c0001t0001g0075 a0001c0001t0001g0097 a0001c0001t0002g0284 others(4): Show |
7 | HG00621.hp2 HG01123.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+6311_25+6323del others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494442 | ||||||
| chr5:80494443 | T | TTTTCTTT others(1): Show |
24 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(21): Show |
24 | HG00673.hp2 HG01168.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+6303_25+6310dup others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494443 | ||||||
| chr5:80494443 | TTTTCTTT others(22): Show |
T | 1 | a0003c0005t0001g0257 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.25+6311_25+6339del others(29): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494443 | ||||||
| chr5:80494447 | CTTTCTTT others(2): Show |
C | 19 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+6311_25+6319del others(9): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494447 | ||||||
| chr5:80494451 | CTTTCT | C | 45 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0027 others(42): Show |
45 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.25+6311_25+6315del others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494451 | ||||||
| chr5:80494455 | CT | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(122): Show |
127 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.25+6311delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494455 | ||||||
| chr5:80494456 | T | TTTC | 62 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
62 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | T | TTTCTTTC others(5): Show |
9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0179 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | T | TTTCTTTC others(9): Show |
2 | a0001c0003t0001g0289 a0002c0002t0001g0076 |
2 | HG01123.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | T | TTTCTTTC others(14): Show |
2 | a0001c0001t0001g0287 a0001c0001t0002g0286 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(21): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | T | TTTCTTTC others(30): Show |
2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(37): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | T | TTTTC | 4 | a0001c0001t0001g0300 a0001c0001t0001g0312 a0001c0001t0001g0314 others(1): Show |
4 | HG02145.hp1 HG02717.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+6376_25+6379dup others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | TTTTC | T | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0321 others(9): Show |
12 | HG01243.hp2 HG01981.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.25+6376_25+6379del others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | TTTTCTTT others(1): Show |
T | 12 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.25+6372_25+6379del others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | TTTTCTTT others(5): Show |
T | 8 | a0001c0001t0001g0302 a0001c0001t0001g0311 a0001c0001t0001g0313 others(5): Show |
8 | HG02886.hp1 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+6368_25+6379del others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494456 | TTTTCTTT others(9): Show |
T | 3 | a0001c0001t0001g0303 a0001c0001t0001g0340 a0001c0001t0001g0341 |
3 | HG00323.hp1 HG03654.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.25+6364_25+6379del others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | ||||||
| chr5:80494459 | T | C | 1 | a0001c0003t0001g0292 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.25+6311T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494459 | |||||||
| chr5:80494460 | C | CT | 59 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
59 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.25+6315dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494460 | ||||||
| chr5:80494460 | C | T | 1 | a0001c0003t0001g0292 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.25+6312C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494460 | |||||||
| chr5:80494463 | T | TTC | 3 | a0001c0001t0001g0283 a0001c0001t0003g0281 a0002c0002t0001g0282 |
3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+6315_25+6316ins others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494463 | |||||||
| chr5:80494464 | C | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.25+6316C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494464 | |||||||
| chr5:80494464 | C | CT | 61 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(58): Show |
62 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.25+6319dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494464 | ||||||
| chr5:80494464 | C | T | 3 | a0001c0001t0001g0283 a0001c0001t0003g0281 a0002c0002t0001g0282 |
3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+6316C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494464 | |||||||
| chr5:80494465 | TTTC | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0060 others(57): Show |
61 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.25+6320_25+6322del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494465 | ||||||
| chr5:80494465 | TTTCTTTC others(24): Show |
T | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.25+6320_25+6350del others(31): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494465 | ||||||
| chr5:80494468 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25+6320C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494468 | |||||||
| chr5:80494468 | C | CT | 4 | a0001c0003t0001g0288 a0001c0003t0001g0290 a0001c0003t0001g0291 others(1): Show |
4 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+6323dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494468 | ||||||
| chr5:80494469 | TTTC | T | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0027 others(41): Show |
44 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+6324_25+6326del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494469 | ||||||
| chr5:80494472 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25+6324C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494472 | |||||||
| chr5:80494473 | TTTC | T | 19 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+6328_25+6330del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494473 | ||||||
| chr5:80494477 | TTTC | T | 6 | a0001c0001t0001g0097 a0001c0001t0002g0284 a0002c0002t0001g0096 others(3): Show |
6 | HG00621.hp2 HG01884.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+6332_25+6334del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494477 | ||||||
| chr5:80494480 | C | A | 2 | a0001c0001t0001g0287 a0001c0001t0002g0286 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.25+6332C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494480 | |||||||
| chr5:80494516 | CTTTCTTT others(3): Show |
C | 1 | a0001c0001t0001g0326 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.25+6372_25+6381del others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494516 | ||||||
| chr5:80494525 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.25+6377T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494525 | |||||||
| chr5:80494572 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.25+6424G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494572 | |||||||
| chr5:80494794 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+6646A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494794 | |||||||
| chr5:80494850 | AT | A | 6 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0285 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+6704delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494850 | ||||||
| chr5:80495083 | C | T | 3 | a0001c0001t0001g0206 a0002c0002t0001g0044 a0002c0002t0001g0074 |
3 | HG02559.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.26-6709C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495083 | |||||||
| chr5:80495389 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26-6403A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495389 | |||||||
| chr5:80495528 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.26-6264G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495528 | |||||||
| chr5:80495745 | G | A | 3 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0264 |
3 | HG00639.hp1 HG01346.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.26-6047G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495745 | |||||||
| chr5:80495786 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
279 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.26-6006G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495786 | |||||||
| chr5:80495797 | C | G | 1 | a0002c0002t0001g0271 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.26-5995C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495797 | |||||||
| chr5:80495809 | C | T | 2 | a0001c0001t0002g0284 a0001c0001t0006g0350 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-5983C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495809 | |||||||
| chr5:80495830 | CA | C | 27 | a0001c0001t0001g0302 a0001c0001t0001g0312 a0001c0001t0001g0313 others(24): Show |
27 | HG00323.hp1 HG01070.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.26-5933delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | ||||||
| chr5:80495830 | CAAAA | C | 21 | a0001c0001t0001g0016 a0001c0001t0001g0056 a0001c0001t0001g0060 others(18): Show |
21 | HG00280.hp2 HG01123.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.26-5936_26-5933del others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | ||||||
| chr5:80495830 | CAAAAA | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
244 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.26-5937_26-5933del others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | ||||||
| chr5:80495830 | CAAAAAA | C | 10 | a0001c0001t0001g0068 a0001c0001t0001g0134 a0001c0001t0001g0157 others(7): Show |
10 | HG01069.hp1 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-5938_26-5933del others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | ||||||
| chr5:80495830 | CAAAAAAA | C | 30 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0283 others(27): Show |
30 | HG00280.hp1 HG00741.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.26-5939_26-5933del others(7): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | ||||||
| chr5:80495830 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | NA18973.hp2 NA18977.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-5944_26-5933del others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | ||||||
| chr5:80495830 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0334 |
3 | HG01243.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-5947_26-5933del others(15): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | ||||||
| chr5:80495915 | G | A | 7 | a0001c0001t0003g0294 a0001c0003t0001g0288 a0001c0003t0001g0289 others(4): Show |
7 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-5877G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495915 | |||||||
| chr5:80496184 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.26-5608A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496184 | |||||||
| chr5:80496430 | A | C | 6 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0003t0001g0290 others(3): Show |
6 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-5362A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496430 | |||||||
| chr5:80496456 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(98): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.26-5336A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496456 | |||||||
| chr5:80496511 | A | G | 11 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0323 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-5281A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496511 | |||||||
| chr5:80496591 | A | C | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.26-5201A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496591 | |||||||
| chr5:80496771 | G | T | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.26-5021G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496771 | |||||||
| chr5:80496783 | T | A | 2 | a0001c0001t0001g0300 a0001c0001t0001g0315 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26-5009T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496783 | |||||||
| chr5:80496799 | A | AT | 10 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0001t0001g0331 others(7): Show |
10 | HG01070.hp1 HG01109.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-4964dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80496799 | ||||||
| chr5:80496799 | ATT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0071 others(30): Show |
33 | HG00544.hp1 HG00673.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.26-4965_26-4964del others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80496799 | ||||||
| chr5:80496799 | ATTT | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
253 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.26-4966_26-4964del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80496799 | ||||||
| chr5:80496799 | ATTTT | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0123 a0001c0001t0001g0136 others(14): Show |
17 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-4967_26-4964del others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80496799 | ||||||
| chr5:80496843 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.26-4949C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496843 | |||||||
| chr5:80497018 | C | A | 2 | a0002c0002t0001g0242 a0002c0002t0001g0244 |
2 | HG02735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.26-4774C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497018 | |||||||
| chr5:80497154 | G | A | 1 | a0002c0002t0001g0110 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.26-4638G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497154 | |||||||
| chr5:80497164 | G | A | 6 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0285 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-4628G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497164 | |||||||
| chr5:80497254 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.26-4538C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497254 | |||||||
| chr5:80497445 | A | G | 3 | a0001c0001t0001g0319 a0002c0002t0001g0342 a0002c0002t0001g0343 |
3 | HG03195.hp1 HG03490.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.26-4347A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497445 | |||||||
| chr5:80497472 | A | T | 1 | a0002c0002t0001g0272 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.26-4320A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497472 | |||||||
| chr5:80497770 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
279 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.26-4022A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497770 | |||||||
| chr5:80497780 | C | G | 2 | a0001c0001t0002g0284 a0001c0001t0006g0350 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-4012C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497780 | |||||||
| chr5:80497889 | A | G | 1 | a0002c0002t0001g0096 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.26-3903A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497889 | |||||||
| chr5:80497931 | T | G | 3 | a0001c0001t0001g0190 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02922.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.26-3861T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497931 | |||||||
| chr5:80497943 | T | A | 1 | a0001c0001t0003g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-3849T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497943 | |||||||
| chr5:80497963 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-3829G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497963 | |||||||
| chr5:80498017 | T | C | 2 | a0001c0001t0002g0284 a0001c0001t0006g0350 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-3775T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498017 | |||||||
| chr5:80498231 | A | G | 4 | a0001c0001t0001g0075 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG01123.hp1 HG01433.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-3561A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498231 | |||||||
| chr5:80498283 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
310 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.26-3509A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498283 | |||||||
| chr5:80498302 | G | A | 2 | a0002c0002t0001g0150 a0002c0002t0001g0166 |
2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.26-3490G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498302 | |||||||
| chr5:80498335 | A | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG01099.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.26-3457A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498335 | |||||||
| chr5:80498338 | T | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
277 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.26-3454T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498338 | |||||||
| chr5:80498351 | C | A | 1 | a0001c0001t0003g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-3441C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498351 | |||||||
| chr5:80498351 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.26-3441C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498351 | |||||||
| chr5:80498525 | G | A | 10 | a0001c0001t0001g0297 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-3267G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498525 | |||||||
| chr5:80498638 | T | A | 1 | a0001c0001t0002g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-3154T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498638 | |||||||
| chr5:80498904 | T | C | 7 | a0001c0001t0003g0294 a0001c0003t0001g0288 a0001c0003t0001g0289 others(4): Show |
7 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-2888T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498904 | |||||||
| chr5:80498914 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.26-2878A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498914 | |||||||
| chr5:80498985 | G | T | 3 | a0001c0001t0001g0303 a0001c0001t0001g0326 a0001c0001t0001g0341 |
3 | HG00323.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.26-2807G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498985 | |||||||
| chr5:80499013 | GA | G | 15 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0001t0001g0097 others(12): Show |
15 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.26-2765delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80499013 | ||||||
| chr5:80499054 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.26-2738A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499054 | |||||||
| chr5:80499061 | G | A | 1 | a0002c0002t0001g0231 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.26-2731G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499061 | |||||||
| chr5:80499131 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.26-2661T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499131 | |||||||
| chr5:80499365 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.26-2427G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499365 | |||||||
| chr5:80499389 | T | C | 9 | a0001c0001t0001g0297 a0001c0001t0001g0304 a0001c0001t0001g0305 others(6): Show |
9 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-2403T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499389 | |||||||
| chr5:80499588 | G | C | 4 | a0001c0003t0001g0288 a0001c0003t0001g0290 a0001c0003t0001g0291 others(1): Show |
4 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-2204G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499588 | |||||||
| chr5:80499594 | G | A | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.26-2198G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499594 | |||||||
| chr5:80499668 | T | G | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.26-2124T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499668 | |||||||
| chr5:80499669 | A | G | 18 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0283 others(15): Show |
18 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.26-2123A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499669 | |||||||
| chr5:80499671 | G | A | 1 | a0001c0001t0003g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-2121G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499671 | |||||||
| chr5:80499778 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.26-2014G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499778 | |||||||
| chr5:80499853 | A | AT | 9 | a0001c0001t0001g0099 a0001c0001t0001g0351 a0001c0003t0001g0288 others(6): Show |
9 | HG00280.hp1 HG01109.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-1922dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80499853 | ||||||
| chr5:80499950 | C | G | 3 | a0002c0002t0001g0122 a0002c0002t0001g0135 a0002c0002t0001g0147 |
3 | NA18983.hp2 NA19000.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.26-1842C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499950 | |||||||
| chr5:80499979 | G | A | 2 | a0001c0001t0002g0284 a0001c0001t0006g0350 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-1813G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499979 | |||||||
| chr5:80500060 | A | G | 3 | a0001c0001t0001g0283 a0001c0001t0003g0281 a0002c0002t0001g0282 |
3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.26-1732A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500060 | |||||||
| chr5:80500215 | T | C | 3 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0245 |
3 | HG00642.hp1 HG01099.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.26-1577T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500215 | |||||||
| chr5:80500242 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.26-1550G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500242 | |||||||
| chr5:80500360 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-1432G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500360 | |||||||
| chr5:80500646 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.26-1146G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500646 | |||||||
| chr5:80500713 | T | C | 1 | a0002c0002t0001g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.26-1079T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500713 | |||||||
| chr5:80500777 | T | C | 9 | a0001c0001t0001g0297 a0001c0001t0001g0304 a0001c0001t0001g0305 others(6): Show |
9 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-1015T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500777 | |||||||
| chr5:80500797 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-995C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500797 | |||||||
| chr5:80500807 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.26-985G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500807 | |||||||
| chr5:80500937 | A | C | 1 | a0002c0002t0001g0192 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26-855A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500937 | |||||||
| chr5:80501040 | G | C | 1 | a0001c0001t0003g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-752G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501040 | |||||||
| chr5:80501180 | A | AT | 8 | a0001c0001t0002g0277 a0001c0003t0001g0288 a0001c0003t0001g0289 others(5): Show |
8 | HG00280.hp1 HG00408.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-599dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80501180 | ||||||
| chr5:80501193 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG02071.hp1 HG02155.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-599T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501193 | |||||||
| chr5:80501389 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.26-403G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501389 | |||||||
| chr5:80501414 | T | G | 15 | a0001c0001t0001g0045 a0001c0001t0001g0081 a0001c0001t0001g0119 others(12): Show |
16 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.26-378T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501414 | |||||||
| chr5:80501465 | GA | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
267 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.26-306delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80501465 | ||||||
| chr5:80501465 | GAA | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0214 others(7): Show |
10 | HG02897.hp1 HG02965.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-307_26-306delAA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80501465 | ||||||
| chr5:80501600 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.26-192A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501600 | |||||||
| chr5:80501676 | A | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0297 a0002c0002t0001g0076 |
3 | HG01123.hp2 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.26-116A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501676 | |||||||
| chr5:80501983 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.151+66T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80501983 | |||||||
| chr5:80502173 | C | T | 2 | a0001c0001t0002g0284 a0001c0001t0006g0350 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.151+256C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502173 | |||||||
| chr5:80502182 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.151+265T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502182 | |||||||
| chr5:80502226 | C | G | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.151+309C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502226 | |||||||
| chr5:80502263 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.151+346G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502263 | |||||||
| chr5:80502279 | T | C | 18 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0283 others(15): Show |
18 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.151+362T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502279 | |||||||
| chr5:80502668 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
310 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.151+751T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502668 | |||||||
| chr5:80502860 | A | C | 5 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0285 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+943A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502860 | |||||||
| chr5:80503087 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.151+1170A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80503087 | |||||||
| chr5:80503096 | G | A | 3 | a0001c0001t0002g0236 a0001c0001t0002g0237 a0001c0001t0002g0280 |
3 | HG03098.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.151+1179G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80503096 | |||||||
| chr5:80503258 | A | T | 10 | a0002c0002t0001g0163 a0002c0002t0001g0222 a0002c0002t0001g0225 others(7): Show |
10 | HG01433.hp1 HG01943.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+1341A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80503258 | |||||||
| chr5:80504111 | C | T | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.151+2194C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504111 | |||||||
| chr5:80504119 | G | A | 1 | a0003c0005t0001g0257 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.151+2202G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504119 | |||||||
| chr5:80504201 | A | G | 3 | a0001c0001t0001g0319 a0002c0002t0001g0342 a0002c0002t0001g0343 |
3 | HG03195.hp1 HG03490.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.151+2284A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504201 | |||||||
| chr5:80504255 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151+2338G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504255 | |||||||
| chr5:80504292 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.151+2375T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504292 | |||||||
| chr5:80504380 | T | C | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.151+2463T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504380 | |||||||
| chr5:80504503 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
289 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.151+2586C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504503 | |||||||
| chr5:80504514 | CT | C | 14 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0283 others(11): Show |
14 | HG00741.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.151+2622delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80504514 | ||||||
| chr5:80504514 | CTT | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(55): Show |
59 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.151+2621_151+2622d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80504514 | ||||||
| chr5:80504514 | CTTT | C | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
211 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.151+2620_151+2622d others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80504514 | ||||||
| chr5:80504514 | CTTTT | C | 17 | a0001c0001t0001g0232 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00639.hp1 HG00735.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+2619_151+2622d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80504514 | ||||||
| chr5:80504583 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.151+2666C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504583 | |||||||
| chr5:80504614 | G | A | 10 | a0001c0001t0001g0247 a0001c0001t0001g0297 a0001c0001t0001g0304 others(7): Show |
10 | HG01192.hp2 HG01255.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+2697G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504614 | |||||||
| chr5:80504660 | T | C | 207 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
207 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.151+2743T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504660 | |||||||
| chr5:80504668 | T | C | 3 | a0001c0001t0001g0303 a0001c0001t0001g0326 a0001c0001t0001g0341 |
3 | HG00323.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.151+2751T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504668 | |||||||
| chr5:80504676 | T | C | 5 | a0001c0001t0003g0294 a0002c0002t0001g0211 a0002c0002t0001g0212 others(2): Show |
5 | HG02257.hp1 NA18955.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+2759T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504676 | |||||||
| chr5:80504708 | T | C | 1 | a0001c0001t0002g0296 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.151+2791T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504708 | |||||||
| chr5:80504728 | T | C | 34 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0053 others(31): Show |
34 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.151+2811T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504728 | |||||||
| chr5:80504732 | A | C | 1 | a0001c0001t0003g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151+2815A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504732 | |||||||
| chr5:80504788 | G | A | 2 | a0001c0001t0001g0344 a0002c0002t0001g0017 |
2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.151+2871G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504788 | |||||||
| chr5:80504915 | C | G | 1 | a0001c0001t0001g0337 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151+2998C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504915 | |||||||
| chr5:80504996 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+3079C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504996 | |||||||
| chr5:80505051 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0128 others(2): Show |
5 | HG00408.hp2 HG02129.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+3134G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505051 | |||||||
| chr5:80505391 | G | A | 5 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0139 others(2): Show |
5 | HG00642.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+3474G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505391 | |||||||
| chr5:80505394 | C | CT | 7 | a0001c0001t0002g0146 a0001c0001t0002g0286 a0001c0001t0003g0281 others(4): Show |
7 | HG01099.hp1 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+3488dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505394 | ||||||
| chr5:80505405 | TC | T | 41 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0303 others(38): Show |
41 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.151+3489delC | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505405 | |||||||
| chr5:80505406 | C | T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0084 others(108): Show |
111 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.151+3489C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505406 | |||||||
| chr5:80505457 | C | T | 4 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3540C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505457 | |||||||
| chr5:80505481 | G | A | 4 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0287 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3564G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505481 | |||||||
| chr5:80505487 | T | C | 2 | a0001c0001t0003g0281 a0002c0002t0001g0282 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.151+3570T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505487 | |||||||
| chr5:80505491 | T | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0084 others(153): Show |
156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.151+3574T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505491 | |||||||
| chr5:80505548 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.151+3631T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505548 | |||||||
| chr5:80505646 | G | A | 4 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3729G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505646 | |||||||
| chr5:80505701 | T | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0020 others(152): Show |
155 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.151+3784T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505701 | |||||||
| chr5:80505749 | A | AT | 28 | a0001c0001t0001g0077 a0001c0001t0001g0090 a0001c0001t0001g0126 others(25): Show |
28 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.151+3857dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | ||||||
| chr5:80505749 | A | ATT | 121 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0020 others(118): Show |
121 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.151+3856_151+3857d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | ||||||
| chr5:80505749 | A | ATTT | 21 | a0001c0001t0001g0221 a0001c0001t0001g0251 a0001c0001t0001g0300 others(18): Show |
21 | HG01167.hp2 HG02083.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.151+3855_151+3857d others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | ||||||
| chr5:80505749 | AT | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0123 others(17): Show |
20 | HG01496.hp1 HG01884.hp1 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.151+3857delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | ||||||
| chr5:80505749 | ATT | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(46): Show |
50 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.151+3856_151+3857d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | ||||||
| chr5:80505821 | A | G | 1 | a0001c0001t0001g0352 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.151+3904A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505821 | |||||||
| chr5:80505858 | G | A | 10 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(7): Show |
10 | HG00735.hp1 HG01261.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+3941G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505858 | |||||||
| chr5:80505891 | G | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0287 |
3 | HG01884.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.151+3974G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505891 | |||||||
| chr5:80505908 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.151+3991C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505908 | |||||||
| chr5:80506013 | C | G | 4 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0031 others(1): Show |
4 | HG02135.hp2 NA18946.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+4096C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506013 | |||||||
| chr5:80506015 | C | T | 1 | a0001c0001t0002g0318 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.151+4098C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506015 | |||||||
| chr5:80506016 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.151+4099G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506016 | |||||||
| chr5:80506183 | T | C | 6 | a0001c0001t0001g0354 a0001c0001t0002g0207 a0001c0001t0002g0209 others(3): Show |
6 | HG00741.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+4266T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506183 | |||||||
| chr5:80506318 | G | A | 8 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0102 others(5): Show |
8 | NA18950.hp2 NA18955.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+4401G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506318 | |||||||
| chr5:80506520 | C | T | 2 | a0001c0001t0004g0092 a0001c0001t0004g0093 |
2 | HG00438.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.151+4603C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506520 | |||||||
| chr5:80506521 | G | A | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.151+4604G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506521 | |||||||
| chr5:80506672 | G | T | 1 | a0002c0002t0001g0145 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.151+4755G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506672 | |||||||
| chr5:80506826 | T | A | 2 | a0001c0001t0001g0354 a0002c0002t0001g0074 |
2 | HG00741.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.151+4909T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506826 | |||||||
| chr5:80506888 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151+4971C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506888 | |||||||
| chr5:80507051 | A | C | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.151+5134A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507051 | |||||||
| chr5:80507052 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.151+5135G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507052 | |||||||
| chr5:80507118 | C | CA | 31 | a0001c0001t0001g0011 a0001c0001t0001g0075 a0001c0001t0001g0082 others(28): Show |
31 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.151+5220dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80507118 | ||||||
| chr5:80507118 | CA | C | 114 | a0001c0001t0001g0014 a0001c0001t0001g0064 a0001c0001t0001g0078 others(111): Show |
114 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.151+5220delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80507118 | ||||||
| chr5:80507118 | CAA | C | 39 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0303 others(36): Show |
39 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.151+5219_151+5220d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80507118 | ||||||
| chr5:80507137 | A | T | 4 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0287 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+5220A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507137 | |||||||
| chr5:80507359 | T | C | 1 | a0002c0002t0001g0163 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.151+5442T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507359 | |||||||
| chr5:80507419 | G | A | 4 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+5502G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507419 | |||||||
| chr5:80507580 | C | T | 1 | a0001c0001t0002g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.151+5663C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507580 | |||||||
| chr5:80507709 | T | C | 2 | a0002c0002t0001g0103 a0002c0002t0001g0106 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.151+5792T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507709 | |||||||
| chr5:80507865 | C | T | 9 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0323 others(6): Show |
9 | HG01109.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-5739C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507865 | |||||||
| chr5:80507952 | C | T | 2 | a0002c0002t0001g0103 a0002c0002t0001g0106 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.152-5652C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507952 | |||||||
| chr5:80508169 | T | C | 7 | a0001c0001t0003g0294 a0001c0003t0001g0288 a0001c0003t0001g0289 others(4): Show |
7 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-5435T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508169 | |||||||
| chr5:80508209 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-5395A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508209 | |||||||
| chr5:80508221 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0285 |
2 | HG02965.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152-5383G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508221 | |||||||
| chr5:80508311 | C | T | 159 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0102 others(156): Show |
159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.152-5293C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508311 | |||||||
| chr5:80508350 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152-5254A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508350 | |||||||
| chr5:80508445 | CT | C | 10 | a0001c0001t0001g0190 a0001c0001t0001g0199 a0001c0001t0001g0200 others(7): Show |
10 | HG01070.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-5148delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80508445 | ||||||
| chr5:80508456 | T | A | 1 | a0002c0002t0001g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-5148T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508456 | |||||||
| chr5:80508575 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-5029T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508575 | |||||||
| chr5:80508698 | A | C | 1 | a0001c0001t0001g0202 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.152-4906A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508698 | |||||||
| chr5:80508920 | G | A | 1 | a0001c0001t0003g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152-4684G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508920 | |||||||
| chr5:80509026 | T | C | 1 | a0002c0002t0001g0135 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.152-4578T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509026 | |||||||
| chr5:80509034 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-4570C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509034 | |||||||
| chr5:80509094 | C | T | 6 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0003t0001g0290 others(3): Show |
6 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-4510C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509094 | |||||||
| chr5:80509399 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.152-4205G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509399 | |||||||
| chr5:80509492 | C | G | 4 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-4112C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509492 | |||||||
| chr5:80509522 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152-4082C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509522 | |||||||
| chr5:80509946 | G | A | 158 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0102 others(155): Show |
158 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.152-3658G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509946 | |||||||
| chr5:80509961 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.152-3643C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509961 | |||||||
| chr5:80510394 | T | C | 1 | a0002c0002t0001g0145 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.152-3210T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80510394 | |||||||
| chr5:80510912 | C | T | 1 | a0002c0002t0001g0135 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.152-2692C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80510912 | |||||||
| chr5:80511221 | T | C | 2 | a0001c0001t0001g0354 a0002c0002t0001g0074 |
2 | HG00741.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.152-2383T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511221 | |||||||
| chr5:80511353 | A | T | 2 | a0001c0001t0001g0354 a0002c0002t0001g0074 |
2 | HG00741.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.152-2251A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511353 | |||||||
| chr5:80511399 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.152-2205A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511399 | |||||||
| chr5:80511407 | C | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(224): Show |
228 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.152-2197C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511407 | |||||||
| chr5:80511435 | C | CA | 16 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0117 others(13): Show |
16 | HG01109.hp2 HG01361.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.152-2144dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80511435 | ||||||
| chr5:80511435 | CA | C | 136 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0084 others(133): Show |
136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.152-2144delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80511435 | ||||||
| chr5:80511435 | CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0001g0212 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.152-2154_152-2144d others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80511435 | ||||||
| chr5:80511501 | C | T | 10 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-2103C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511501 | |||||||
| chr5:80511525 | C | T | 1 | a0002c0002t0001g0235 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.152-2079C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511525 | |||||||
| chr5:80511615 | T | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(42): Show |
46 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.152-1989T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511615 | |||||||
| chr5:80511692 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.152-1912C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511692 | |||||||
| chr5:80511693 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0240 others(3): Show |
6 | NA18954.hp2 NA18975.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-1911G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511693 | |||||||
| chr5:80511795 | C | T | 2 | a0001c0001t0003g0281 a0002c0002t0001g0282 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.152-1809C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511795 | |||||||
| chr5:80511941 | T | A | 2 | a0001c0001t0001g0354 a0002c0002t0001g0074 |
2 | HG00741.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.152-1663T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511941 | |||||||
| chr5:80511979 | T | C | 4 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1625T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511979 | |||||||
| chr5:80512121 | C | T | 1 | a0002c0002t0001g0299 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.152-1483C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512121 | |||||||
| chr5:80512273 | T | C | 155 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(152): Show |
155 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.152-1331T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512273 | |||||||
| chr5:80512577 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.152-1027C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512577 | |||||||
| chr5:80512625 | TA | T | 350 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(347): Show |
352 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.152-972delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512625 | ||||||
| chr5:80512771 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0001g0315 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.152-833C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512771 | |||||||
| chr5:80512780 | T | TAA | 11 | a0001c0001t0003g0294 a0001c0001t0006g0350 a0001c0003t0001g0288 others(8): Show |
11 | HG00280.hp1 HG00639.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-810_152-809dup others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512780 | ||||||
| chr5:80512780 | T | TAAA | 133 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(130): Show |
133 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.152-811_152-809dup others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512780 | ||||||
| chr5:80512780 | T | TAAAA | 12 | a0001c0001t0001g0300 a0001c0001t0001g0315 a0001c0001t0001g0317 others(9): Show |
12 | HG01168.hp2 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-812_152-809dup others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512780 | ||||||
| chr5:80512780 | TA | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0047 others(8): Show |
11 | HG01070.hp1 HG01070.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-809delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512780 | ||||||
| chr5:80512809 | A | G | 1 | a0002c0002t0001g0299 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.152-795A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512809 | |||||||
| chr5:80512817 | A | G | 3 | a0001c0001t0002g0236 a0001c0001t0002g0237 a0001c0001t0002g0280 |
3 | HG03098.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.152-787A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512817 | |||||||
| chr5:80512967 | G | C | 1 | a0001c0001t0002g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.152-637G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512967 | |||||||
| chr5:80513050 | G | A | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.152-554G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513050 | |||||||
| chr5:80513394 | A | G | 1 | a0001c0001t0003g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.152-210A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513394 | |||||||
| chr5:80513448 | G | C | 2 | a0001c0001t0001g0349 a0001c0001t0001g0353 |
2 | NA18948.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.152-156G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513448 | |||||||
| chr5:80513479 | G | A | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-125G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513479 | |||||||
| chr5:80513522 | C | T | 10 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-82C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513522 | |||||||
| chr5:80513574 | G | A | 1 | a0002c0002t0001g0273 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152-30G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513574 | |||||||
| chr5:80513807 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0287 |
3 | HG01884.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.317+38G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80513807 | |||||||
| chr5:80513839 | A | T | 186 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(183): Show |
186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.317+70A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80513839 | |||||||
| chr5:80514097 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.317+328G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514097 | |||||||
| chr5:80514106 | A | G | 156 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(153): Show |
156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.317+337A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514106 | |||||||
| chr5:80514348 | G | A | 3 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG01099.hp2 HG02280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.317+579G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514348 | |||||||
| chr5:80514432 | G | A | 1 | a0001c0001t0003g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.317+663G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514432 | |||||||
| chr5:80514476 | A | AAAT | 51 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0001g0067 others(48): Show |
51 | HG00544.hp2 HG00738.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.317+751_317+753dup others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | ||||||
| chr5:80514476 | A | AAATAAT | 10 | a0001c0001t0001g0274 a0001c0001t0001g0278 a0001c0001t0002g0295 others(7): Show |
10 | HG00558.hp2 HG01070.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+748_317+753dup others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | ||||||
| chr5:80514476 | AAAT | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.317+751_317+753del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | ||||||
| chr5:80514476 | AAATAAT | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0095 others(17): Show |
20 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.317+748_317+753del others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | ||||||
| chr5:80514476 | AAATAATA others(2): Show |
A | 5 | a0001c0001t0001g0127 a0001c0001t0001g0218 a0001c0001t0001g0354 others(2): Show |
5 | HG00741.hp2 HG01109.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+745_317+753del others(9): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | ||||||
| chr5:80514476 | AAATAATA others(5): Show |
A | 1 | a0002c0002t0001g0135 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.317+742_317+753del others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | ||||||
| chr5:80514611 | A | G | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.317+842A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514611 | |||||||
| chr5:80514836 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.317+1067C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514836 | |||||||
| chr5:80514900 | T | C | 2 | a0002c0002t0001g0342 a0002c0002t0001g0343 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.317+1131T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514900 | |||||||
| chr5:80514957 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0121 |
2 | NA19067.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.317+1188C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514957 | |||||||
| chr5:80515010 | C | T | 2 | a0001c0001t0001g0331 a0001c0001t0006g0350 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.317+1241C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515010 | |||||||
| chr5:80515194 | T | C | 167 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(164): Show |
168 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.317+1425T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515194 | |||||||
| chr5:80515216 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.317+1447G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515216 | |||||||
| chr5:80515267 | T | TA | 165 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(162): Show |
166 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.317+1504dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80515267 | ||||||
| chr5:80515276 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317+1507A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515276 | |||||||
| chr5:80515296 | A | G | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317+1527A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515296 | |||||||
| chr5:80515501 | C | T | 10 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0152 others(7): Show |
10 | HG00741.hp2 HG01515.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+1732C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515501 | |||||||
| chr5:80515810 | T | C | 5 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+2041T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515810 | |||||||
| chr5:80515843 | G | A | 192 | a0001c0001t0001g0040 a0001c0001t0001g0069 a0001c0001t0001g0075 others(189): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.317+2074G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515843 | |||||||
| chr5:80515846 | G | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+2077G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515846 | |||||||
| chr5:80515958 | T | C | 13 | a0001c0001t0001g0040 a0001c0001t0001g0075 a0001c0001t0001g0113 others(10): Show |
13 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.317+2189T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515958 | |||||||
| chr5:80516106 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.317+2337C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516106 | |||||||
| chr5:80516139 | A | G | 2 | a0001c0001t0003g0281 a0001c0001t0006g0350 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.317+2370A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516139 | |||||||
| chr5:80516448 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.317+2679G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516448 | |||||||
| chr5:80516524 | A | G | 29 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(26): Show |
30 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.317+2755A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516524 | |||||||
| chr5:80516657 | A | G | 2 | a0002c0002t0001g0038 a0002c0002t0001g0062 |
2 | HG01255.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.317+2888A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516657 | |||||||
| chr5:80516847 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.318-2846A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516847 | |||||||
| chr5:80517181 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.318-2512A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517181 | |||||||
| chr5:80517190 | T | C | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.318-2503T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517190 | |||||||
| chr5:80517197 | A | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0002g0280 |
3 | HG01884.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.318-2496A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517197 | |||||||
| chr5:80517295 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.318-2398A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517295 | |||||||
| chr5:80517393 | AT | A | 4 | a0001c0001t0001g0287 a0001c0001t0001g0324 a0001c0001t0001g0325 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-2296delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80517393 | ||||||
| chr5:80517484 | TCAAGTTT others(11): Show |
T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0157 |
2 | NA19056.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.318-2208_318-2191d others(20): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517484 | |||||||
| chr5:80517537 | G | A | 19 | a0001c0001t0001g0234 a0001c0001t0001g0252 a0001c0001t0001g0253 others(16): Show |
19 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.318-2156G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517537 | |||||||
| chr5:80517558 | C | T | 53 | a0001c0001t0001g0027 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
53 | HG00323.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.318-2135C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517558 | |||||||
| chr5:80517564 | T | TTTTGTTT others(6): Show |
247 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.318-2126_318-2125i others(15): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80517564 | ||||||
| chr5:80517564 | T | TTTTGTTT others(1766): Show |
1 | a0001c0001t0002g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.318-2126_318-2125i others(1775): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80517564 | ||||||
| chr5:80517639 | A | G | 2 | a0002c0002t0001g0103 a0002c0002t0001g0106 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.318-2054A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517639 | |||||||
| chr5:80517653 | C | T | 2 | a0001c0001t0003g0281 a0001c0001t0006g0350 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.318-2040C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517653 | |||||||
| chr5:80517711 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.318-1982C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517711 | |||||||
| chr5:80517946 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
155 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.318-1747C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517946 | |||||||
| chr5:80518032 | G | C | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.318-1661G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518032 | |||||||
| chr5:80518059 | G | A | 1 | a0002c0002t0001g0299 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.318-1634G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518059 | |||||||
| chr5:80518075 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0232 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.318-1618G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518075 | |||||||
| chr5:80518075 | G | GA | 6 | a0001c0001t0001g0184 a0001c0001t0001g0266 a0001c0001t0002g0141 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.318-1599dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80518075 | ||||||
| chr5:80518075 | GA | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.318-1599delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80518075 | ||||||
| chr5:80518138 | A | T | 4 | a0001c0001t0001g0287 a0001c0001t0001g0324 a0001c0001t0001g0325 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-1555A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518138 | |||||||
| chr5:80518240 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.318-1453C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518240 | |||||||
| chr5:80518446 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.318-1247T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518446 | |||||||
| chr5:80518603 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.318-1090G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518603 | |||||||
| chr5:80519027 | G | T | 2 | a0002c0002t0001g0135 a0002c0002t0007g0089 |
2 | HG00438.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.318-666G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519027 | |||||||
| chr5:80519154 | A | C | 1 | a0002c0002t0001g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.318-539A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519154 | |||||||
| chr5:80519264 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.318-429A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519264 | |||||||
| chr5:80519288 | G | A | 2 | a0001c0001t0003g0281 a0001c0001t0006g0350 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.318-405G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519288 | |||||||
| chr5:80519353 | G | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.318-340G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519353 | |||||||
| chr5:80520086 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.535+176A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520086 | |||||||
| chr5:80520095 | G | A | 32 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(29): Show |
32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.535+185G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520095 | |||||||
| chr5:80520341 | T | G | 1 | a0001c0001t0001g0346 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.535+431T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520341 | |||||||
| chr5:80520367 | G | T | 1 | a0001c0001t0001g0346 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.535+457G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520367 | |||||||
| chr5:80520391 | T | G | 5 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+481T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520391 | |||||||
| chr5:80520491 | A | G | 3 | a0002c0002t0001g0018 a0002c0002t0001g0219 a0002c0002t0001g0220 |
3 | HG02280.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535+581A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520491 | |||||||
| chr5:80520644 | C | CA | 6 | a0001c0001t0001g0184 a0001c0001t0001g0285 a0001c0001t0001g0319 others(3): Show |
6 | HG00438.hp1 HG01175.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.535+749dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520644 | ||||||
| chr5:80520644 | CA | C | 10 | a0001c0003t0001g0002 a0001c0003t0001g0185 a0001c0003t0001g0186 others(7): Show |
11 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+749delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520644 | ||||||
| chr5:80520650 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.535+740A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520650 | |||||||
| chr5:80520686 | G | GTA | 12 | a0001c0001t0002g0141 a0001c0001t0002g0146 a0001c0001t0002g0207 others(9): Show |
12 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+790_535+791dup others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520686 | ||||||
| chr5:80520698 | ATATT | A | 32 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(29): Show |
32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.535+797_535+800del others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520698 | ||||||
| chr5:80520813 | G | GT | 8 | a0001c0001t0001g0165 a0001c0001t0001g0278 a0001c0001t0001g0279 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+917dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520813 | ||||||
| chr5:80520827 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.535+917T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520827 | |||||||
| chr5:80520861 | T | G | 1 | a0001c0001t0001g0276 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.535+951T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520861 | |||||||
| chr5:80520935 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.535+1025A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520935 | |||||||
| chr5:80520957 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.536-1046C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520957 | |||||||
| chr5:80520995 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0171 |
2 | NA18978.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.536-1008T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520995 | |||||||
| chr5:80521116 | C | CT | 44 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0053 others(41): Show |
44 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.536-862dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | ||||||
| chr5:80521116 | C | CTT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.536-863_536-862dup others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | ||||||
| chr5:80521116 | C | CTTT | 32 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0014 others(29): Show |
32 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.536-864_536-862dup others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | ||||||
| chr5:80521116 | CT | C | 28 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0302 others(25): Show |
28 | HG00323.hp1 HG00323.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.536-862delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | ||||||
| chr5:80521116 | CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-877_536-862del others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | ||||||
| chr5:80521152 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.536-851G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521152 | |||||||
| chr5:80521156 | G | T | 1 | a0001c0001t0002g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.536-847G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521156 | |||||||
| chr5:80521256 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.536-747C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521256 | |||||||
| chr5:80521474 | A | G | 1 | a0002c0002t0001g0096 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.536-529A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521474 | |||||||
| chr5:80521552 | G | C | 17 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(14): Show |
18 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.536-451G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521552 | |||||||
| chr5:80521559 | A | G | 5 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.536-444A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521559 | |||||||
| chr5:80521574 | A | G | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.536-429A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521574 | |||||||
| chr5:80521708 | A | G | 31 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(28): Show |
32 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.536-295A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521708 | |||||||
| chr5:80521824 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.536-179C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521824 | |||||||
| chr5:80522261 | A | C | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+123A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522261 | |||||||
| chr5:80522326 | T | A | 1 | a0001c0001t0001g0285 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.671+188T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522326 | |||||||
| chr5:80522352 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+214C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522352 | |||||||
| chr5:80522410 | T | C | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+272T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522410 | |||||||
| chr5:80522588 | C | T | 1 | a0002c0002t0001g0036 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.671+450C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522588 | |||||||
| chr5:80522634 | C | T | 31 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(28): Show |
31 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+496C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522634 | |||||||
| chr5:80522734 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0002g0280 |
3 | HG01884.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.671+596C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522734 | |||||||
| chr5:80522783 | C | A | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+645C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522783 | |||||||
| chr5:80522838 | A | G | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.671+700A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522838 | |||||||
| chr5:80522884 | AT | A | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+755delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80522884 | ||||||
| chr5:80523134 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0002g0280 |
3 | HG01884.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.671+996G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523134 | |||||||
| chr5:80523600 | T | C | 1 | a0001c0001t0001g0340 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.671+1462T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523600 | |||||||
| chr5:80523749 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.671+1611T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523749 | |||||||
| chr5:80523757 | A | T | 1 | a0001c0001t0001g0193 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.671+1619A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523757 | |||||||
| chr5:80523899 | C | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0300 others(1): Show |
4 | HG02145.hp1 HG02922.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+1761C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523899 | |||||||
| chr5:80523981 | C | T | 1 | a0001c0001t0002g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.671+1843C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523981 | |||||||
| chr5:80524046 | T | C | 32 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(29): Show |
32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.671+1908T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524046 | |||||||
| chr5:80524099 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.671+1961G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524099 | |||||||
| chr5:80524196 | T | G | 3 | a0001c0001t0003g0281 a0001c0001t0003g0294 a0001c0001t0006g0350 |
3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+2058T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524196 | |||||||
| chr5:80524262 | C | T | 3 | a0001c0001t0003g0281 a0001c0001t0003g0294 a0001c0001t0006g0350 |
3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+2124C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524262 | |||||||
| chr5:80524310 | A | G | 1 | a0002c0002t0001g0299 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.671+2172A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524310 | |||||||
| chr5:80524361 | A | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.671+2223A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524361 | |||||||
| chr5:80524611 | G | A | 1 | a0001c0001t0003g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.671+2473G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524611 | |||||||
| chr5:80524706 | A | G | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+2568A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524706 | |||||||
| chr5:80524905 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.671+2767T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524905 | |||||||
| chr5:80525038 | G | GGTGTTTA others(14): Show |
1 | a0002c0002t0001g0163 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.671+2901_671+2921d others(23): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80525038 | ||||||
| chr5:80525086 | C | A | 1 | a0002c0002t0001g0017 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.671+2948C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525086 | |||||||
| chr5:80525224 | C | T | 1 | a0002c0002t0001g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.671+3086C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525224 | |||||||
| chr5:80525242 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.671+3104C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525242 | |||||||
| chr5:80525291 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0167 others(1): Show |
4 | HG02074.hp1 NA18954.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+3153T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525291 | |||||||
| chr5:80525370 | C | G | 3 | a0001c0001t0003g0281 a0001c0001t0003g0294 a0001c0001t0006g0350 |
3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+3232C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525370 | |||||||
| chr5:80525413 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.671+3275A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525413 | |||||||
| chr5:80525534 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.671+3396G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525534 | |||||||
| chr5:80525663 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+3525A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525663 | |||||||
| chr5:80525875 | CAT | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.671+3756_671+3757d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80525875 | ||||||
| chr5:80525977 | T | A | 1 | a0001c0001t0001g0181 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.671+3839T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525977 | |||||||
| chr5:80526058 | G | A | 7 | a0001c0001t0001g0045 a0001c0001t0001g0081 a0001c0001t0001g0119 others(4): Show |
7 | HG01515.hp2 HG01516.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.671+3920G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526058 | |||||||
| chr5:80526133 | G | C | 4 | a0001c0001t0001g0190 a0001c0001t0001g0298 a0001c0001t0001g0306 others(1): Show |
4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+3995G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526133 | |||||||
| chr5:80526214 | A | C | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+4076A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526214 | |||||||
| chr5:80526268 | G | A | 4 | a0001c0001t0001g0190 a0001c0001t0001g0298 a0001c0001t0001g0306 others(1): Show |
4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+4130G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526268 | |||||||
| chr5:80526453 | C | CA | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
159 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.671+4332dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80526453 | ||||||
| chr5:80526516 | A | G | 1 | a0002c0002t0001g0178 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.671+4378A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526516 | |||||||
| chr5:80526648 | T | A | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0300 others(1): Show |
4 | HG02145.hp1 HG02922.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+4510T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526648 | |||||||
| chr5:80527016 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0004g0092 a0001c0001t0004g0093 |
3 | HG00438.hp2 HG02083.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.671+4878G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527016 | |||||||
| chr5:80527097 | C | T | 32 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(29): Show |
32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.671+4959C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527097 | |||||||
| chr5:80527307 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.671+5169C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527307 | |||||||
| chr5:80527426 | TA | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
199 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.671+5303delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80527426 | ||||||
| chr5:80527710 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.671+5572G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527710 | |||||||
| chr5:80527807 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.671+5669A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527807 | |||||||
| chr5:80527909 | T | A | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+5771T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527909 | |||||||
| chr5:80527996 | A | G | 1 | a0001c0003t0001g0293 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.671+5858A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527996 | |||||||
| chr5:80528118 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.671+5980G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528118 | |||||||
| chr5:80528150 | A | G | 5 | a0001c0001t0001g0108 a0002c0002t0001g0211 a0002c0002t0001g0212 others(2): Show |
5 | HG02040.hp1 NA18955.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+6012A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528150 | |||||||
| chr5:80528252 | C | G | 1 | a0001c0001t0002g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.671+6114C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528252 | |||||||
| chr5:80528346 | A | C | 20 | a0001c0001t0001g0184 a0001c0001t0001g0234 a0001c0001t0001g0252 others(17): Show |
20 | HG00639.hp1 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.671+6208A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528346 | |||||||
| chr5:80528373 | A | G | 4 | a0001c0001t0001g0190 a0001c0001t0001g0298 a0001c0001t0001g0306 others(1): Show |
4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+6235A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528373 | |||||||
| chr5:80528438 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
133 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(130): Show |
intron_variant | MODIFIER | c.671+6300A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528438 | |||||||
| chr5:80528601 | A | C | 4 | a0001c0001t0001g0190 a0001c0001t0001g0298 a0001c0001t0001g0306 others(1): Show |
4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+6463A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528601 | |||||||
| chr5:80528655 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+6517G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528655 | |||||||
| chr5:80528687 | C | T | 1 | a0002c0002t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671+6549C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528687 | |||||||
| chr5:80528803 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.671+6665C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528803 | |||||||
| chr5:80528919 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.671+6781A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528919 | |||||||
| chr5:80528978 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.671+6840T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528978 | |||||||
| chr5:80529095 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(53): Show |
57 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.671+6957G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529095 | |||||||
| chr5:80529141 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0354 |
2 | HG00741.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671+7003G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529141 | |||||||
| chr5:80529217 | C | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG00642.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.671+7079C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529217 | |||||||
| chr5:80529241 | T | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA18975.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.671+7103T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529241 | |||||||
| chr5:80529329 | T | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0102 others(1): Show |
4 | HG02074.hp1 NA18950.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+7191T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529329 | |||||||
| chr5:80529434 | G | T | 17 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(14): Show |
18 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.671+7296G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529434 | |||||||
| chr5:80529485 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0354 |
2 | HG00741.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671+7347C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529485 | |||||||
| chr5:80529508 | A | G | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+7370A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529508 | |||||||
| chr5:80529531 | C | T | 1 | a0002c0002t0001g0033 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.671+7393C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529531 | |||||||
| chr5:80529551 | C | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG03491.hp2 NA18948.hp1 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.671+7413C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529551 | |||||||
| chr5:80529551 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.671+7413C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529551 | |||||||
| chr5:80529626 | G | T | 2 | a0001c0001t0001g0279 a0001c0001t0003g0281 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+7488G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529626 | |||||||
| chr5:80529716 | T | C | 32 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(29): Show |
32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.671+7578T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529716 | |||||||
| chr5:80529790 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.671+7652G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529790 | |||||||
| chr5:80529894 | G | A | 1 | a0002c0002t0001g0178 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.671+7756G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529894 | |||||||
| chr5:80529907 | T | TACCAAAG others(53): Show |
29 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(26): Show |
30 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.671+7770_671+7829d others(62): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80529907 | ||||||
| chr5:80529958 | G | GTGATGAA others(53): Show |
1 | a0001c0001t0002g0296 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.671+7829_671+7830i others(62): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80529958 | ||||||
| chr5:80529970 | G | A | 3 | a0001c0001t0003g0281 a0001c0001t0003g0294 a0001c0001t0006g0350 |
3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+7832G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529970 | |||||||
| chr5:80530151 | T | C | 4 | a0001c0001t0001g0190 a0001c0001t0001g0298 a0001c0001t0001g0306 others(1): Show |
4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+8013T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530151 | |||||||
| chr5:80530176 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.671+8038A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530176 | |||||||
| chr5:80530368 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(54): Show |
58 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.671+8230G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530368 | |||||||
| chr5:80530462 | G | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0121 |
2 | NA19067.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.671+8324G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530462 | |||||||
| chr5:80530472 | T | A | 34 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(31): Show |
34 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.671+8334T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530472 | |||||||
| chr5:80530501 | C | T | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+8363C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530501 | |||||||
| chr5:80530520 | T | A | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+8382T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530520 | |||||||
| chr5:80530826 | T | G | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+8688T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530826 | |||||||
| chr5:80530827 | G | A | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+8689G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530827 | |||||||
| chr5:80530840 | A | C | 20 | a0001c0001t0001g0184 a0001c0001t0001g0234 a0001c0001t0001g0252 others(17): Show |
20 | HG00639.hp1 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.671+8702A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530840 | |||||||
| chr5:80530882 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.671+8744A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530882 | |||||||
| chr5:80531267 | C | T | 5 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+9129C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531267 | |||||||
| chr5:80531273 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+9135C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531273 | |||||||
| chr5:80531359 | T | C | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+9221T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531359 | |||||||
| chr5:80531427 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.671+9289A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531427 | |||||||
| chr5:80531558 | C | G | 19 | a0001c0001t0001g0234 a0001c0001t0001g0252 a0001c0001t0001g0253 others(16): Show |
19 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.671+9420C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531558 | |||||||
| chr5:80531565 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671+9427A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531565 | |||||||
| chr5:80531569 | T | C | 1 | a0002c0002t0001g0299 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.671+9431T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531569 | |||||||
| chr5:80531577 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.671+9439G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531577 | |||||||
| chr5:80531895 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0354 |
2 | HG00741.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671+9757C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531895 | |||||||
| chr5:80532017 | GA | G | 32 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(29): Show |
32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-9652delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80532017 | ||||||
| chr5:80532035 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.672-9638C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532035 | |||||||
| chr5:80532127 | C | A | 20 | a0001c0001t0001g0184 a0001c0001t0001g0234 a0001c0001t0001g0252 others(17): Show |
20 | HG00639.hp1 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.672-9546C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532127 | |||||||
| chr5:80532137 | T | C | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-9536T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532137 | |||||||
| chr5:80532217 | T | A | 4 | a0001c0001t0001g0190 a0001c0001t0001g0298 a0001c0001t0001g0306 others(1): Show |
4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-9456T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532217 | |||||||
| chr5:80532230 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.672-9443G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532230 | |||||||
| chr5:80532370 | A | T | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-9303A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532370 | |||||||
| chr5:80532464 | A | G | 1 | a0002c0002t0001g0034 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.672-9209A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532464 | |||||||
| chr5:80532539 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.672-9134A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532539 | |||||||
| chr5:80532759 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
162 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.672-8914A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532759 | |||||||
| chr5:80532889 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.672-8784C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532889 | |||||||
| chr5:80533038 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(47): Show |
51 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.672-8635C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533038 | |||||||
| chr5:80533192 | A | G | 2 | a0002c0002t0001g0103 a0002c0002t0001g0106 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.672-8481A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533192 | |||||||
| chr5:80533309 | G | A | 19 | a0001c0001t0001g0234 a0001c0001t0001g0252 a0001c0001t0001g0253 others(16): Show |
19 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.672-8364G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533309 | |||||||
| chr5:80533325 | C | T | 3 | a0002c0002t0001g0018 a0002c0002t0001g0219 a0002c0002t0001g0220 |
3 | HG02280.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.672-8348C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533325 | |||||||
| chr5:80533371 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-8302C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533371 | |||||||
| chr5:80533427 | A | AAACCCAA others(4): Show |
1 | a0001c0001t0001g0210 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672-8244_672-8234d others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533427 | ||||||
| chr5:80533471 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.672-8202G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533471 | |||||||
| chr5:80533609 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.672-8064G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533609 | |||||||
| chr5:80533621 | G | A | 32 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(29): Show |
32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-8052G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533621 | |||||||
| chr5:80533660 | G | T | 9 | a0001c0003t0001g0002 a0001c0003t0001g0185 a0001c0003t0001g0186 others(6): Show |
10 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-8013G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533660 | |||||||
| chr5:80533698 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.672-7975C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533698 | |||||||
| chr5:80533702 | A | T | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-7971A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533702 | |||||||
| chr5:80533736 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0171 |
2 | NA18978.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.672-7937C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533736 | |||||||
| chr5:80533749 | C | CA | 36 | a0001c0001t0001g0063 a0001c0001t0001g0255 a0001c0001t0001g0278 others(33): Show |
36 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.672-7905dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | ||||||
| chr5:80533749 | C | CAA | 24 | a0001c0001t0001g0097 a0001c0001t0001g0199 a0001c0001t0001g0234 others(21): Show |
24 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.672-7906_672-7905d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | ||||||
| chr5:80533749 | C | CAAA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(55): Show |
59 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.672-7907_672-7905d others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | ||||||
| chr5:80533749 | C | CAAAA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.672-7908_672-7905d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | ||||||
| chr5:80533749 | CA | C | 24 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
25 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.672-7905delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | ||||||
| chr5:80533769 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.672-7904G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533769 | |||||||
| chr5:80533934 | T | A | 1 | a0001c0001t0002g0318 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672-7739T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533934 | |||||||
| chr5:80533952 | G | C | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-7721G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533952 | |||||||
| chr5:80534036 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.672-7637C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534036 | |||||||
| chr5:80534148 | G | T | 5 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-7525G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534148 | |||||||
| chr5:80534296 | C | G | 5 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0139 others(2): Show |
5 | HG00642.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-7377C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534296 | |||||||
| chr5:80534352 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
190 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.672-7321C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534352 | |||||||
| chr5:80534490 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-7183C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534490 | |||||||
| chr5:80534723 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.672-6950C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534723 | |||||||
| chr5:80534806 | A | G | 1 | a0002c0002t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.672-6867A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534806 | |||||||
| chr5:80534858 | C | T | 1 | a0001c0001t0001g0353 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.672-6815C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534858 | |||||||
| chr5:80534939 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.672-6734G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534939 | |||||||
| chr5:80535137 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-6536G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535137 | |||||||
| chr5:80535175 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.672-6498C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535175 | |||||||
| chr5:80535280 | A | C | 2 | a0001c0001t0002g0146 a0001c0001t0002g0286 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.672-6393A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535280 | |||||||
| chr5:80535443 | G | A | 34 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0287 others(31): Show |
34 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.672-6230G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535443 | |||||||
| chr5:80535480 | C | T | 2 | a0002c0002t0001g0139 a0002c0002t0001g0191 |
2 | HG01258.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.672-6193C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535480 | |||||||
| chr5:80535562 | G | A | 1 | a0002c0002t0001g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.672-6111G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535562 | |||||||
| chr5:80535658 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-6015C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535658 | |||||||
| chr5:80535663 | G | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.672-6010G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535663 | |||||||
| chr5:80535768 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.672-5905C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535768 | |||||||
| chr5:80536074 | A | C | 1 | a0001c0001t0002g0295 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.672-5599A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536074 | |||||||
| chr5:80536141 | T | TTTTAG | 5 | a0001c0001t0002g0146 a0001c0001t0002g0286 a0001c0001t0002g0301 others(2): Show |
5 | HG02451.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-5513_672-5509d others(7): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80536141 | ||||||
| chr5:80536141 | TTTTAG | T | 9 | a0001c0003t0001g0002 a0001c0003t0001g0185 a0001c0003t0001g0186 others(6): Show |
10 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-5513_672-5509d others(7): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80536141 | ||||||
| chr5:80536160 | A | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0002c0002t0001g0120 |
3 | HG02622.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.672-5513A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536160 | |||||||
| chr5:80536160 | AGTTTTGT others(3): Show |
A | 1 | a0002c0002t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.672-5497_672-5488d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80536160 | ||||||
| chr5:80536165 | T | A | 3 | a0002c0002t0001g0273 a0002c0002t0001g0342 a0002c0002t0001g0343 |
3 | HG03041.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.672-5508T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536165 | |||||||
| chr5:80536216 | G | A | 32 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0303 others(29): Show |
32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-5457G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536216 | |||||||
| chr5:80536219 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(51): Show |
55 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.672-5454G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536219 | |||||||
| chr5:80536231 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-5442C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536231 | |||||||
| chr5:80536273 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.672-5400C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536273 | |||||||
| chr5:80536316 | G | A | 3 | a0001c0001t0003g0281 a0001c0001t0003g0294 a0001c0001t0006g0350 |
3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.672-5357G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536316 | |||||||
| chr5:80536337 | A | AT | 31 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(28): Show |
32 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-5326dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80536337 | ||||||
| chr5:80536398 | A | C | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-5275A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536398 | |||||||
| chr5:80536418 | T | C | 33 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(30): Show |
34 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.672-5255T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536418 | |||||||
| chr5:80536474 | A | T | 1 | a0002c0002t0001g0039 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.672-5199A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536474 | |||||||
| chr5:80536489 | TTGAGGAA others(14): Show |
T | 1 | a0001c0001t0001g0232 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.672-5183_672-5163d others(23): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536489 | |||||||
| chr5:80536542 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672-5131C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536542 | |||||||
| chr5:80536699 | A | G | 1 | a0002c0002t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.672-4974A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536699 | |||||||
| chr5:80536942 | A | G | 1 | a0002c0002t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.672-4731A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536942 | |||||||
| chr5:80537230 | A | C | 1 | a0002c0002t0001g0192 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.672-4443A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537230 | |||||||
| chr5:80537467 | G | C | 1 | a0002c0002t0001g0195 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.672-4206G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537467 | |||||||
| chr5:80537482 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(55): Show |
59 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.672-4191G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537482 | |||||||
| chr5:80537794 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.672-3879C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537794 | |||||||
| chr5:80537910 | TAATAG | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(56): Show |
60 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.672-3758_672-3754d others(7): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80537910 | ||||||
| chr5:80537954 | A | C | 1 | a0001c0003t0001g0288 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.672-3719A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537954 | |||||||
| chr5:80538002 | A | G | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-3671A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538002 | |||||||
| chr5:80538006 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.672-3667A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538006 | |||||||
| chr5:80538014 | G | A | 1 | a0002c0002t0001g0233 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.672-3659G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538014 | |||||||
| chr5:80538073 | A | AT | 6 | a0001c0001t0001g0184 a0001c0001t0001g0252 a0001c0001t0001g0261 others(3): Show |
6 | HG01070.hp1 HG01175.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-3587dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538073 | ||||||
| chr5:80538073 | AT | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
230 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.672-3587delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538073 | ||||||
| chr5:80538103 | C | T | 2 | a0002c0002t0001g0103 a0002c0002t0001g0106 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.672-3570C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538103 | |||||||
| chr5:80538136 | C | T | 3 | a0002c0002t0001g0017 a0002c0002t0001g0085 a0002c0002t0001g0142 |
3 | HG04115.hp2 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.672-3537C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538136 | |||||||
| chr5:80538146 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.672-3527C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538146 | |||||||
| chr5:80538153 | C | T | 3 | a0002c0002t0001g0150 a0002c0002t0001g0166 a0002c0002t0001g0201 |
3 | HG01943.hp2 HG01975.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.672-3520C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538153 | |||||||
| chr5:80538245 | T | C | 3 | a0002c0002t0001g0150 a0002c0002t0001g0166 a0002c0002t0001g0201 |
3 | HG01943.hp2 HG01975.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.672-3428T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538245 | |||||||
| chr5:80538284 | A | G | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-3389A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538284 | |||||||
| chr5:80538319 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(56): Show |
60 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.672-3354G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538319 | |||||||
| chr5:80538372 | T | TTTTC | 12 | a0001c0001t0001g0184 a0001c0001t0001g0234 a0001c0001t0002g0141 others(9): Show |
12 | HG01069.hp2 HG01175.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-3227_672-3224d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | ||||||
| chr5:80538372 | T | TTTTCTTT others(1): Show |
5 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0061 others(2): Show |
5 | HG00642.hp1 HG01258.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3231_672-3224d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | ||||||
| chr5:80538372 | T | TTTTCTTT others(5): Show |
3 | a0001c0001t0001g0256 a0002c0002t0001g0030 a0002c0002t0001g0194 |
3 | HG02723.hp2 NA18969.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.672-3235_672-3224d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | ||||||
| chr5:80538372 | T | TTTTCTTT others(9): Show |
2 | a0002c0002t0001g0080 a0002c0002t0001g0163 |
2 | NA18955.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.672-3239_672-3224d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | ||||||
| chr5:80538372 | TTTTC | T | 9 | a0001c0001t0001g0064 a0001c0001t0001g0208 a0002c0002t0001g0018 others(6): Show |
9 | HG01975.hp2 HG02622.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-3227_672-3224d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | ||||||
| chr5:80538372 | TTTTCTTT others(1): Show |
T | 6 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3231_672-3224d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | ||||||
| chr5:80538372 | TTTTCTTT others(5): Show |
T | 1 | a0002c0002t0001g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.672-3235_672-3224d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | ||||||
| chr5:80538372 | TTTTCTTT others(9): Show |
T | 1 | a0002c0002t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.672-3239_672-3224d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | ||||||
| chr5:80538402 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.672-3271T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538402 | |||||||
| chr5:80538418 | TTCTTTCT others(23): Show |
T | 1 | a0001c0001t0001g0298 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672-3223_672-3194d others(32): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538418 | ||||||
| chr5:80538424 | CTTTCTTT others(21): Show |
C | 1 | a0002c0002t0001g0085 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.672-3247_672-3220d others(30): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538424 | ||||||
| chr5:80538426 | T | TTCTTTCT others(3): Show |
2 | a0001c0001t0002g0236 a0001c0003t0001g0288 |
2 | HG03669.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.672-3245_672-3236d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538426 | ||||||
| chr5:80538426 | T | TTCTTTCT others(7): Show |
2 | a0001c0001t0001g0283 a0001c0001t0001g0304 |
2 | HG01496.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.672-3245_672-3232d others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538426 | ||||||
| chr5:80538426 | T | TTCTTTCT others(11): Show |
1 | a0001c0003t0001g0289 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.672-3245_672-3228d others(20): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538426 | ||||||
| chr5:80538428 | CTTTCTTT others(17): Show |
C | 1 | a0001c0001t0001g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.672-3243_672-3220d others(26): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538428 | ||||||
| chr5:80538431 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.672-3242T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538431 | |||||||
| chr5:80538432 | CTTTCTT | C | 3 | a0002c0002t0001g0094 a0002c0002t0001g0342 a0002c0002t0001g0343 |
3 | HG03195.hp1 HG03516.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.672-3239_672-3234d others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538432 | ||||||
| chr5:80538432 | CTTTCTTT others(13): Show |
C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0213 |
2 | NA18989.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.672-3239_672-3220d others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538432 | ||||||
| chr5:80538435 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.672-3238T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538435 | |||||||
| chr5:80538436 | CTT | C | 3 | a0001c0001t0001g0258 a0001c0001t0001g0278 a0002c0002t0001g0273 |
3 | HG01261.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.672-3235_672-3234d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538436 | ||||||
| chr5:80538436 | CTTTCTTT others(9): Show |
C | 8 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0066 others(5): Show |
8 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3235_672-3220d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538436 | ||||||
| chr5:80538436 | CTTTCTTT others(13): Show |
C | 1 | a0002c0002t0001g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.672-3235_672-3216d others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538436 | ||||||
| chr5:80538436 | CTTTCTTT others(17): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.672-3235_672-3212d others(26): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538436 | ||||||
| chr5:80538438 | TTCTTTCT others(3): Show |
T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02074.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.672-3223_672-3214d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538438 | ||||||
| chr5:80538440 | CTTTCTTT others(5): Show |
C | 11 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0077 others(8): Show |
11 | HG00621.hp1 HG00741.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-3231_672-3220d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538440 | ||||||
| chr5:80538440 | CTTTCTTT others(9): Show |
C | 1 | a0001c0001t0001g0326 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.672-3231_672-3216d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538440 | ||||||
| chr5:80538440 | CTTTCTTT others(13): Show |
C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0126 |
2 | HG00558.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.672-3231_672-3212d others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538440 | ||||||
| chr5:80538441 | TTTCTTTC others(39): Show |
T | 1 | a0001c0001t0001g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.672-3228_672-3183d others(48): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538441 | ||||||
| chr5:80538442 | T | C | 8 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0198 others(5): Show |
8 | HG00323.hp1 HG00738.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3231T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538442 | |||||||
| chr5:80538442 | TTCTTTC | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0167 others(6): Show |
9 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-3223_672-3218d others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538442 | ||||||
| chr5:80538444 | C | CTCTTTCT others(25): Show |
2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.672-3228_672-3227i others(34): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538444 | ||||||
| chr5:80538444 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0002g0286 a0001c0003t0001g0185 |
3 | HG00738.hp1 NA19043.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.672-3229C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538444 | |||||||
| chr5:80538444 | CTTTCTCT others(1): Show |
C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0063 others(7): Show |
10 | HG02293.hp1 HG02300.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.672-3227_672-3220d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538444 | ||||||
| chr5:80538444 | CTTTCTCT others(5): Show |
C | 2 | a0001c0001t0001g0323 a0001c0001t0001g0332 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.672-3227_672-3216d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538444 | ||||||
| chr5:80538444 | CTTTCTCT others(9): Show |
C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0095 a0001c0001t0001g0130 others(1): Show |
4 | HG02109.hp2 HG02735.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-3227_672-3212d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538444 | ||||||
| chr5:80538445 | TTTCTCTT others(35): Show |
T | 1 | a0001c0001t0001g0354 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.672-3224_672-3183d others(44): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538445 | ||||||
| chr5:80538446 | T | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0056 a0001c0001t0001g0059 others(36): Show |
39 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.672-3227T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538446 | |||||||
| chr5:80538446 | TTC | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0053 others(22): Show |
25 | HG00408.hp2 HG01070.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.672-3223_672-3222d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538446 | ||||||
| chr5:80538447 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672-3226T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538447 | |||||||
| chr5:80538448 | C | CTCTT | 7 | a0002c0002t0001g0105 a0002c0002t0001g0144 a0002c0002t0001g0195 others(4): Show |
7 | HG00621.hp2 HG00735.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-3190_672-3187d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTCTTCTT others(4): Show |
1 | a0002c0002t0001g0070 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.672-3221_672-3220i others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTT | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
43 | HG00438.hp1 HG01109.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-3224_672-3223i others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTCT others(1): Show |
5 | a0001c0001t0001g0253 a0002c0002t0001g0048 a0002c0002t0001g0183 others(2): Show |
5 | HG00639.hp1 HG03491.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3224_672-3223i others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTCT others(5): Show |
2 | a0002c0002t0001g0111 a0002c0002t0001g0271 |
2 | NA18942.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTCT others(9): Show |
1 | a0002c0002t0001g0026 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTCT others(23): Show |
1 | a0001c0003t0001g0002 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(32): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTCT others(27): Show |
1 | a0001c0003t0001g0292 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(36): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTTT others(5): Show |
3 | a0001c0001t0001g0251 a0002c0002t0001g0164 a0002c0002t0001g0228 |
3 | HG00544.hp1 HG02083.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTTT others(9): Show |
1 | a0002c0002t0001g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.672-3224_672-3223i others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTTT others(25): Show |
1 | a0002c0002t0001g0033 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.672-3224_672-3223i others(34): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTTT others(9): Show |
2 | a0001c0001t0001g0264 a0002c0002t0001g0160 |
2 | HG01346.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTTT others(13): Show |
2 | a0002c0002t0001g0110 a0002c0002t0001g0178 |
2 | HG02071.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTTT others(13): Show |
1 | a0002c0002t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTTT others(21): Show |
1 | a0002c0002t0001g0023 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(30): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | CTTTCTTT others(15): Show |
1 | a0002c0002t0001g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(24): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | C | T | 20 | a0001c0001t0001g0084 a0001c0001t0001g0266 a0001c0001t0001g0308 others(17): Show |
20 | HG00738.hp1 HG01099.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.672-3225C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538448 | |||||||
| chr5:80538448 | CTCTT | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(9): Show |
12 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-3190_672-3187d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | CTCTTTCT others(1): Show |
C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0181 a0001c0001t0001g0314 others(3): Show |
6 | HG02004.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3194_672-3187d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538448 | CTCTTTCT others(5): Show |
C | 15 | a0001c0001t0001g0046 a0001c0001t0001g0071 a0001c0001t0001g0072 others(12): Show |
15 | HG00544.hp2 HG00673.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.672-3198_672-3187d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | ||||||
| chr5:80538449 | TCTTTCTT others(31): Show |
T | 1 | a0001c0001t0001g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.672-3223_672-3186d others(40): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538449 | |||||||
| chr5:80538450 | C | CTTTCTTT others(19): Show |
1 | a0001c0003t0001g0290 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.672-3206_672-3205i others(28): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | ||||||
| chr5:80538450 | C | CTTTCTTT others(23): Show |
3 | a0001c0001t0002g0284 a0001c0003t0001g0291 a0001c0003t0001g0293 |
3 | HG01109.hp2 HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.672-3202_672-3201i others(32): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | ||||||
| chr5:80538450 | C | G | 1 | a0001c0003t0001g0292 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.672-3223C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538450 | |||||||
| chr5:80538450 | C | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0021 others(19): Show |
22 | HG00408.hp1 HG00639.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.672-3223C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538450 | |||||||
| chr5:80538450 | CTTTCTT | C | 9 | a0001c0001t0001g0165 a0001c0001t0001g0170 a0001c0001t0001g0197 others(6): Show |
9 | HG01243.hp2 HG01978.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-3221_672-3216d others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | ||||||
| chr5:80538450 | CTTTCTTT others(3): Show |
C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0158 a0001c0001t0001g0316 others(5): Show |
8 | HG01167.hp2 HG02523.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3221_672-3212d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | ||||||
| chr5:80538450 | CTTTCTTT others(7): Show |
C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0198 a0001c0001t0001g0303 others(1): Show |
4 | HG00323.hp1 HG02080.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-3221_672-3208d others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | ||||||
| chr5:80538451 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672-3222T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538451 | |||||||
| chr5:80538451 | T | C | 2 | a0001c0001t0001g0021 a0002c0002t0001g0137 |
2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.672-3222T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538451 | |||||||
| chr5:80538452 | T | C | 46 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0027 others(43): Show |
46 | HG00408.hp1 HG00673.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.672-3221T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538452 | |||||||
| chr5:80538452 | T | TTC | 9 | a0001c0001t0001g0015 a0001c0001t0001g0188 a0001c0001t0001g0239 others(6): Show |
9 | HG00438.hp1 HG01358.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-3219_672-3218d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538452 | ||||||
| chr5:80538454 | C | CTTTCTTT others(19): Show |
1 | a0001c0003t0001g0186 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.672-3202_672-3201i others(28): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538454 | ||||||
| chr5:80538454 | C | G | 2 | a0001c0001t0001g0308 a0001c0003t0001g0002 |
3 | HG01168.hp1 HG01169.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.672-3219C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538454 | |||||||
| chr5:80538454 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0247 others(3): Show |
6 | HG00673.hp1 HG01255.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3219C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538454 | |||||||
| chr5:80538454 | CTT | C | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0065 others(2): Show |
5 | HG00408.hp2 HG03490.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3217_672-3216d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538454 | ||||||
| chr5:80538456 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(83): Show |
86 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.672-3217T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538456 | |||||||
| chr5:80538456 | T | TTC | 4 | a0001c0001t0001g0248 a0001c0001t0001g0330 a0001c0001t0001g0333 others(1): Show |
4 | HG01109.hp1 HG01358.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3215_672-3214d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538456 | ||||||
| chr5:80538458 | C | G | 8 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG01496.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3215C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538458 | |||||||
| chr5:80538458 | CTT | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0032 others(16): Show |
20 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.672-3213_672-3212d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538458 | ||||||
| chr5:80538460 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
115 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.672-3213T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538460 | |||||||
| chr5:80538460 | T | TTC | 7 | a0001c0001t0001g0022 a0001c0001t0001g0082 a0001c0001t0001g0116 others(4): Show |
7 | HG00738.hp1 HG01516.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-3211_672-3210d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538460 | ||||||
| chr5:80538462 | CTT | C | 6 | a0001c0001t0001g0129 a0001c0001t0001g0199 a0001c0001t0001g0200 others(3): Show |
6 | HG02074.hp2 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3209_672-3208d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538462 | ||||||
| chr5:80538463 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.672-3210T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538463 | |||||||
| chr5:80538464 | T | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
121 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(118): Show |
intron_variant | MODIFIER | c.672-3209T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538464 | |||||||
| chr5:80538464 | T | TTC | 4 | a0001c0001t0002g0146 a0001c0001t0002g0207 a0001c0001t0002g0209 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3207_672-3206d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538464 | ||||||
| chr5:80538465 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.672-3208T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538465 | |||||||
| chr5:80538466 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.672-3207C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538466 | |||||||
| chr5:80538467 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.672-3206T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538467 | |||||||
| chr5:80538468 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
111 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(108): Show |
intron_variant | MODIFIER | c.672-3205T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538468 | |||||||
| chr5:80538468 | T | TTC | 3 | a0001c0001t0002g0141 a0001c0001t0002g0237 a0001c0001t0002g0295 |
3 | HG02622.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.672-3203_672-3202d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538468 | ||||||
| chr5:80538469 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0210 |
2 | HG03654.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.672-3204T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538469 | |||||||
| chr5:80538470 | C | G | 2 | a0001c0001t0002g0286 a0001c0003t0001g0185 |
2 | HG00738.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.672-3203C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538470 | |||||||
| chr5:80538471 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0182 a0001c0001t0001g0206 |
3 | HG02559.hp1 NA18943.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.672-3202T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538471 | |||||||
| chr5:80538472 | T | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0133 others(18): Show |
21 | HG01255.hp1 HG01358.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.672-3201T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538472 | |||||||
| chr5:80538473 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0210 |
2 | HG03654.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.672-3200T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538473 | |||||||
| chr5:80538474 | C | G | 5 | a0001c0001t0002g0146 a0001c0001t0002g0207 a0001c0001t0002g0209 others(2): Show |
5 | HG02451.hp1 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3199C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538474 | |||||||
| chr5:80538475 | T | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0154 a0001c0001t0001g0206 others(2): Show |
5 | HG01261.hp2 HG01433.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3198T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538475 | |||||||
| chr5:80538476 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-3197T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538476 | |||||||
| chr5:80538477 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.672-3196T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538477 | |||||||
| chr5:80538478 | C | G | 3 | a0001c0001t0002g0141 a0001c0001t0002g0237 a0001c0001t0002g0295 |
3 | HG02622.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.672-3195C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538478 | |||||||
| chr5:80538479 | T | C | 24 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0056 others(21): Show |
24 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.672-3194T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538479 | |||||||
| chr5:80538479 | T | TTTCCTTC others(1): Show |
5 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0260 others(2): Show |
5 | HG02280.hp2 HG02683.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3191_672-3190i others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538479 | ||||||
| chr5:80538480 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-3193T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538480 | |||||||
| chr5:80538480 | TTCTTTCC others(37): Show |
T | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672-3192_672-3149d others(46): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538480 | |||||||
| chr5:80538482 | C | G | 1 | a0001c0001t0002g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.672-3191C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538482 | |||||||
| chr5:80538483 | T | C | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
144 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.672-3190T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538483 | |||||||
| chr5:80538483 | T | TTTCCTTC others(5): Show |
2 | a0001c0001t0001g0262 a0001c0001t0001g0270 |
2 | HG01099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.672-3183_672-3172d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538483 | ||||||
| chr5:80538484 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-3189T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538484 | |||||||
| chr5:80538485 | TC | T | 13 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0002g0146 others(10): Show |
13 | HG00738.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-3186delC | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538485 | ||||||
| chr5:80538486 | C | CTTT | 8 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG01496.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3187_672-3186i others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538486 | |||||||
| chr5:80538487 | C | T | 16 | a0001c0001t0001g0149 a0001c0001t0001g0255 a0001c0001t0001g0298 others(13): Show |
17 | HG00280.hp1 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.672-3186C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538487 | |||||||
| chr5:80538490 | C | T | 22 | a0001c0001t0001g0232 a0001c0001t0001g0283 a0001c0001t0001g0304 others(19): Show |
22 | HG00738.hp1 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.672-3183C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538490 | |||||||
| chr5:80538491 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0206 a0001c0001t0001g0255 others(2): Show |
5 | HG01361.hp2 HG02559.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3182C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538491 | |||||||
| chr5:80538494 | C | T | 23 | a0001c0001t0001g0206 a0001c0001t0001g0232 a0001c0001t0001g0283 others(20): Show |
23 | HG00738.hp1 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.672-3179C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538494 | |||||||
| chr5:80538494 | CCTTCCTT others(3): Show |
C | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-3178_672-3169d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538494 | |||||||
| chr5:80538495 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0154 others(2): Show |
5 | HG01433.hp2 HG02896.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3178C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538495 | |||||||
| chr5:80538498 | C | T | 51 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(48): Show |
51 | HG00408.hp2 HG00738.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.672-3175C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538498 | |||||||
| chr5:80538500 | T | C | 1 | a0001c0003t0001g0288 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.672-3173T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538500 | |||||||
| chr5:80538500 | T | TTCC | 7 | a0001c0001t0001g0184 a0001c0001t0001g0234 a0001c0001t0001g0253 others(4): Show |
7 | HG00639.hp1 HG01175.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-3172_672-3171i others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538500 | ||||||
| chr5:80538502 | T | C | 12 | a0001c0001t0001g0084 a0001c0001t0001g0149 a0001c0001t0001g0204 others(9): Show |
12 | HG01255.hp1 HG01358.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-3171T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538502 | |||||||
| chr5:80538503 | C | T | 25 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(22): Show |
25 | HG00408.hp2 HG01123.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.672-3170C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538503 | |||||||
| chr5:80538503 | CT | C | 18 | a0001c0001t0001g0154 a0001c0001t0001g0206 a0001c0001t0001g0223 others(15): Show |
18 | HG00738.hp1 HG01433.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.672-3166delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538503 | ||||||
| chr5:80538504 | T | C | 36 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(33): Show |
36 | HG00408.hp2 HG00639.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.672-3169T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538504 | |||||||
| chr5:80538504 | T | TTTC | 4 | a0001c0001t0001g0305 a0001c0001t0001g0307 a0001c0001t0002g0141 others(1): Show |
4 | HG00639.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-3167_672-3166i others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538504 | ||||||
| chr5:80538505 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.672-3168T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538505 | |||||||
| chr5:80538505 | T | TTCC | 3 | a0001c0001t0001g0056 a0001c0001t0001g0232 a0001c0001t0003g0281 |
3 | HG02897.hp1 HG02970.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.672-3167_672-3166i others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538505 | ||||||
| chr5:80538507 | T | C | 12 | a0001c0001t0001g0149 a0001c0001t0001g0204 a0001c0001t0001g0241 others(9): Show |
12 | HG01255.hp1 HG01358.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-3166T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538507 | |||||||
| chr5:80538508 | C | CT | 8 | a0001c0001t0001g0184 a0001c0001t0001g0234 a0001c0001t0001g0253 others(5): Show |
8 | HG00639.hp1 HG01175.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3162dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538508 | ||||||
| chr5:80538508 | C | T | 9 | a0001c0001t0001g0149 a0001c0001t0001g0204 a0001c0001t0001g0241 others(6): Show |
9 | HG01255.hp1 HG01358.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-3165C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538508 | |||||||
| chr5:80538509 | T | C | 10 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0154 others(7): Show |
10 | HG00639.hp2 HG01361.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-3164T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538509 | |||||||
| chr5:80538509 | T | TTTCC | 3 | a0001c0001t0001g0045 a0001c0001t0001g0136 a0002c0002t0001g0100 |
3 | HG01516.hp1 HG02258.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.672-3161_672-3160i others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538509 | ||||||
| chr5:80538509 | TTTCTTTC others(9): Show |
T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0306 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.672-3160_672-3145d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538509 | ||||||
| chr5:80538511 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.672-3162T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538511 | |||||||
| chr5:80538513 | T | C | 42 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(39): Show |
42 | HG00408.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.672-3160T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538513 | |||||||
| chr5:80538513 | T | TTTCC | 37 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0069 others(34): Show |
37 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.672-3103_672-3100d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | T | TTTCCTTC others(1): Show |
29 | a0001c0001t0001g0109 a0001c0001t0001g0251 a0001c0001t0001g0260 others(26): Show |
29 | HG00621.hp2 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.672-3107_672-3100d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | T | TTTCCTTC others(5): Show |
5 | a0002c0002t0001g0030 a0002c0002t0001g0074 a0002c0002t0001g0233 others(2): Show |
5 | HG02735.hp2 NA18969.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3111_672-3100d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | T | TTTCCTTC others(9): Show |
5 | a0001c0001t0001g0165 a0002c0002t0001g0025 a0002c0002t0001g0048 others(2): Show |
5 | HG02135.hp1 HG02135.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3115_672-3100d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | TTTCC | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0016 others(40): Show |
43 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-3103_672-3100d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | TTTCCTTC others(1): Show |
T | 31 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0066 others(28): Show |
32 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.672-3107_672-3100d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | TTTCCTTC others(5): Show |
T | 10 | a0001c0001t0001g0071 a0001c0001t0001g0090 a0001c0001t0001g0099 others(7): Show |
10 | HG00673.hp2 HG01167.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-3111_672-3100d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | TTTCCTTC others(9): Show |
T | 11 | a0001c0001t0001g0077 a0001c0001t0001g0300 a0001c0001t0001g0303 others(8): Show |
11 | HG00323.hp1 HG00438.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-3115_672-3100d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | TTTCCTTC others(13): Show |
T | 20 | a0001c0001t0001g0287 a0001c0001t0001g0302 a0001c0001t0001g0312 others(17): Show |
20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.672-3119_672-3100d others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538513 | TTTCCTTC others(17): Show |
T | 1 | a0001c0001t0001g0338 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.672-3123_672-3100d others(26): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | ||||||
| chr5:80538516 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.672-3157C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538516 | |||||||
| chr5:80538517 | C | T | 18 | a0001c0001t0001g0149 a0001c0001t0001g0184 a0001c0001t0001g0204 others(15): Show |
18 | HG00639.hp1 HG01175.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.672-3156C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538517 | |||||||
| chr5:80538520 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-3153C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538520 | |||||||
| chr5:80538521 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0305 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.672-3150_672-3149i others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538521 | ||||||
| chr5:80538521 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0002g0280 a0001c0003t0001g0288 |
3 | HG03098.hp1 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.672-3152C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538521 | |||||||
| chr5:80538524 | C | T | 3 | a0001c0001t0002g0146 a0001c0001t0002g0286 a0001c0003t0001g0185 |
3 | HG00738.hp1 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.672-3149C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538524 | |||||||
| chr5:80538525 | C | CTT | 3 | a0001c0001t0002g0146 a0001c0001t0002g0286 a0001c0003t0001g0185 |
3 | HG00738.hp1 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.672-3147_672-3146d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538525 | ||||||
| chr5:80538525 | C | CTTTCTT | 6 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0295 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3146_672-3145i others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538525 | ||||||
| chr5:80538525 | C | CTTTCTTT others(3): Show |
2 | a0001c0001t0002g0141 a0001c0001t0003g0281 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.672-3146_672-3145i others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538525 | ||||||
| chr5:80538525 | C | CTTTCTTT others(7): Show |
5 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0307 others(2): Show |
5 | HG01496.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3146_672-3145i others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538525 | ||||||
| chr5:80538525 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0267 a0001c0001t0002g0237 others(1): Show |
4 | HG01361.hp2 HG03098.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3148C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538525 | |||||||
| chr5:80538529 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0003g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.672-3142_672-3141i others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538529 | ||||||
| chr5:80538529 | C | T | 15 | a0001c0001t0001g0255 a0001c0001t0001g0329 a0001c0001t0001g0345 others(12): Show |
15 | HG00738.hp1 HG01361.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.672-3144C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538529 | |||||||
| chr5:80538532 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0002g0277 |
2 | HG03486.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.672-3141C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538532 | |||||||
| chr5:80538533 | C | T | 11 | a0001c0001t0001g0325 a0001c0001t0001g0329 a0001c0001t0002g0146 others(8): Show |
11 | HG00738.hp1 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-3140C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538533 | |||||||
| chr5:80538541 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-3132C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538541 | |||||||
| chr5:80538545 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-3128C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538545 | |||||||
| chr5:80538570 | T | C | 2 | a0001c0001t0001g0303 a0001c0001t0001g0341 |
2 | HG00323.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.672-3103T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538570 | |||||||
| chr5:80538653 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0001g0315 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.672-3020G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538653 | |||||||
| chr5:80538745 | C | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
99 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.672-2928C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538745 | |||||||
| chr5:80538745 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-2928C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538745 | |||||||
| chr5:80538801 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-2872A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538801 | |||||||
| chr5:80538808 | A | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0300 others(1): Show |
4 | HG02145.hp1 HG02922.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-2865A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538808 | |||||||
| chr5:80538941 | C | T | 19 | a0001c0001t0001g0234 a0001c0001t0001g0252 a0001c0001t0001g0253 others(16): Show |
19 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.672-2732C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538941 | |||||||
| chr5:80538992 | CT | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.672-2664delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538992 | ||||||
| chr5:80538992 | CTT | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
128 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(125): Show |
intron_variant | MODIFIER | c.672-2665_672-2664d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538992 | ||||||
| chr5:80539226 | A | G | 17 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(14): Show |
18 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.672-2447A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539226 | |||||||
| chr5:80539370 | A | AT | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
190 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(187): Show |
intron_variant | MODIFIER | c.672-2295dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80539370 | ||||||
| chr5:80539407 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-2266G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539407 | |||||||
| chr5:80539636 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0045 others(54): Show |
57 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.672-2037C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539636 | |||||||
| chr5:80539637 | G | A | 4 | a0001c0001t0001g0190 a0001c0001t0001g0298 a0001c0001t0001g0306 others(1): Show |
4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-2036G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539637 | |||||||
| chr5:80539640 | C | T | 2 | a0001c0001t0003g0281 a0001c0001t0003g0294 |
2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.672-2033C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539640 | |||||||
| chr5:80539791 | C | CT | 7 | a0001c0001t0001g0063 a0001c0001t0001g0153 a0001c0001t0001g0352 others(4): Show |
7 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-1868dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80539791 | ||||||
| chr5:80539844 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.672-1829A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539844 | |||||||
| chr5:80540051 | C | T | 13 | a0001c0001t0002g0141 a0001c0001t0002g0146 a0001c0001t0002g0207 others(10): Show |
13 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.672-1622C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80540051 | |||||||
| chr5:80540373 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.672-1300G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80540373 | |||||||
| chr5:80540530 | G | A | 9 | a0001c0003t0001g0002 a0001c0003t0001g0185 a0001c0003t0001g0186 others(6): Show |
10 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-1143G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80540530 | |||||||
| chr5:80540835 | G | T | 1 | a0001c0001t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-838G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80540835 | |||||||
| chr5:80540939 | GGATTCT | G | 13 | a0001c0001t0001g0251 a0002c0002t0001g0094 a0002c0002t0001g0096 others(10): Show |
13 | HG00621.hp2 HG02083.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-731_672-726del others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80540939 | ||||||
| chr5:80541057 | G | A | 6 | a0002c0002t0001g0044 a0002c0002t0001g0061 a0002c0002t0001g0100 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-616G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541057 | |||||||
| chr5:80541062 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
135 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.672-611A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541062 | |||||||
| chr5:80541187 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0306 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.672-486G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541187 | |||||||
| chr5:80541225 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-448C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541225 | |||||||
| chr5:80541307 | G | C | 1 | a0001c0001t0006g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-366G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541307 | |||||||
| chr5:80541352 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.672-321A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541352 | |||||||
| chr5:80541430 | C | T | 30 | a0001c0001t0001g0283 a0001c0001t0001g0304 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-243C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541430 | |||||||
| chr5:80541608 | T | C | 1 | a0001c0001t0002g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.672-65T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541608 | |||||||
| chr5:80541635 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.672-38C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541635 |