Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54097 |
| ensemblid | ENSG00000183844.17 |
| hgncid | 1253 |
| symbol | FAM3B |
| name | FAM3 metabolism regulating signaling molecule B |
| refseq_nuc | NM_058186.4 |
| refseq_prot | NP_478066.3 |
| ensembl_nuc | ENST00000357985.7 |
| ensembl_prot | ENSP00000350673.2 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 41316801 |
| end | 41357727 |
| strand | + |
| ver | v1.2 |
| region | chr21:41316801-41357727 |
| region5000 | chr21:41311801-41362727 |
| regionname0 | FAM3B_chr21_41316801_41357727 |
| regionname5000 | FAM3B_chr21_41311801_41362727 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 235 | 284 | 69 | 61 | 103 | 14 | 35 | 72 | FAM3B_chr21_41311801_41362727 | FAM3B | MRPLA others(230): Show |
chr21 | 41311801 | 41362727 |
| a0002 | 0/0 | 235 | 27 | 21 | 4 | 1 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | MRPLA others(230): Show |
chr21 | 41311801 | 41362727 |
| a0003 | 0/0 | 235 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | MRPLA others(230): Show |
chr21 | 41311801 | 41362727 |
| a0004 | 0/0 | 136 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | MRPLA others(131): Show |
chr21 | 41311801 | 41362727 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 705 | 238 | 66 | 45 | 85 | 12 | 30 | FAM3B_chr21_41311801_41362727 | FAM3B | ATGCG others(700): Show |
chr21 | 41311801 | 41362727 | ||
| a0001c0002 | 1/1 | 705 | 41 | 0 | 15 | 18 | 2 | 4 | FAM3B_chr21_41311801_41362727 | FAM3B | ATGCG others(700): Show |
chr21 | 41311801 | 41362727 | ||
| a0001c0004 | 0/0 | 705 | 4 | 3 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | ATGCG others(700): Show |
chr21 | 41311801 | 41362727 | ||
| a0001c0006 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | ATGCG others(700): Show |
chr21 | 41311801 | 41362727 | ||
| a0002c0003 | 0/0 | 705 | 27 | 21 | 4 | 1 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | ATGCG others(700): Show |
chr21 | 41311801 | 41362727 | ||
| a0003c0005 | 0/0 | 705 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | ATGCG others(700): Show |
chr21 | 41311801 | 41362727 | ||
| a0004c0007 | 0/0 | 484 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | ATGCG others(479): Show |
chr21 | 41311801 | 41362727 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1317 | 181 | 29 | 39 | 79 | 9 | 25 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0001t0002 | 0/0 | 1317 | 51 | 32 | 6 | 5 | 3 | 5 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0001t0003 | 0/0 | 1317 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0001t0004 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0001t0005 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0001t0006 | 0/0 | 1317 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0002t0001 | 1/1 | 1317 | 41 | 0 | 15 | 18 | 2 | 4 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0004t0001 | 0/0 | 1317 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0004t0002 | 0/0 | 1317 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0001c0006t0001 | 0/0 | 1317 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0002c0003t0001 | 0/0 | 1317 | 13 | 9 | 2 | 1 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0002c0003t0002 | 0/0 | 1317 | 12 | 10 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0002c0003t0004 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0002c0003t0007 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0003c0005t0001 | 0/0 | 1317 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1312): Show |
chr21 | 41311801 | 41362727 |
| a0004c0007t0001 | 0/0 | 1096 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | CTTCC others(1091): Show |
chr21 | 41311801 | 41362727 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 3 | 9 | 1 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0002 | 0/0 | 13 | 2 | 3 | 6 | 1 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0002t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0004t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0004t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0001c0006t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0002c0003t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0003c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0003c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| a0004c0007t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | GBR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0208 | EUR | GBR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0092 | EUR | GBR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01071 | hp1 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0199 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0016 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0054 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CDX | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02293 | hp2 | a0004 | c0007 | t0001 | g0219 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02451 | hp2 | a0002 | c0003 | t0002 | g0058 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02572 | hp2 | a0002 | c0003 | t0004 | g0047 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02615 | hp2 | a0002 | c0003 | t0007 | g0100 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0225 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0016 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02886 | hp1 | a0002 | c0003 | t0002 | g0050 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0049 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0048 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02897 | hp2 | a0002 | c0003 | t0002 | g0043 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0059 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03041 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0051 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03195 | hp1 | a0002 | c0003 | t0002 | g0045 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03209 | hp1 | a0002 | c0003 | t0002 | g0056 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03579 | hp2 | a0002 | c0003 | t0002 | g0044 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03927 | hp1 | a0001 | c0006 | t0001 | g0042 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0057 | AFR | YRI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | YRI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | LWK | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19030 | hp2 | a0001 | c0004 | t0002 | g0224 | AFR | LWK | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19056 | hp1 | a0003 | c0005 | t0001 | g0201 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19065 | hp2 | a0003 | c0005 | t0001 | g0215 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19083 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ASW | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ASW | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | TSI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0141 | EUR | TSI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | GIH | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02109 | hp1 | a0002 | c0003 | t0002 | g0046 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0226 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | USA | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20300 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | USA | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0055 | AFR | LWK | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | LWK | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0230 | REF | REF | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0159 | REF | REF | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:41322943 | G | A | 1 | a0002 | 27 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(24): Show |
missense_variant | MODERATE | c.40G>A | p.Val14Met | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/8 | 119/1317 | 40/708 | 14/235 | chr21 | 41322943 | |||
| chr21:41346027 | AAAAAAAA others(5917): Show |
A | 1 | a0004 | 1 | HG02293.hp2 | exon_loss_variant | HIGH | c.397+293_618+3228de others(1): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr21 | 41346027 | ||||||
| chr21:41348652 | G | A | 1 | a0001 | 18 | HG00140.hp2 HG00558.hp1 HG01070.hp1 others(15): Show |
missense_variant | MODERATE | c.546G>A | p.Met182Ile | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/8 | 625/1317 | 546/708 | 182/235 | chr21 | 41348652 | |||
| chr21:41357190 | G | A | 1 | a0003 | 2 | NA19056.hp1 NA19065.hp2 |
missense_variant | MODERATE | c.701G>A | p.Arg234Gln | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 780/1317 | 701/708 | 234/235 | chr21 | 41357190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:41322951 | C | T | 1 | a0001c0004 | 4 | HG01106.hp1 HG02559.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.48C>T | p.Phe16Phe | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/8 | 127/1317 | 48/708 | 16/235 | chr21 | 41322951 | |||
| chr21:41338403 | T | C | 1 | a0001c0006 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.189T>C | p.Cys63Cys | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/8 | 268/1317 | 189/708 | 63/235 | chr21 | 41338403 | |||
| chr21:41345735 | T | C | 6 | a0001c0001 a0001c0004 a0001c0006 others(3): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
splice_region_variant&synonymous_variant | LOW | c.396T>C | p.Gly132Gly | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/8 | 475/1317 | 396/708 | 132/235 | chr21 | 41345735 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:41316825 | G | T | 1 | a0002c0003t0007 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/8 | 55 | chr21 | 41316825 | ||||||
| chr21:41357220 | G | T | 1 | a0001c0001t0006 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 23 | chr21 | 41357220 | ||||||
| chr21:41357550 | A | G | 2 | a0001c0001t0003 a0001c0001t0005 |
4 | HG02109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*353A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 353 | chr21 | 41357550 | ||||||
| chr21:41357664 | C | G | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
72 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*467C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 467 | chr21 | 41357664 | ||||||
| chr21:41357686 | G | A | 2 | a0001c0001t0004 a0002c0003t0004 |
2 | HG02572.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*489G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 489 | chr21 | 41357686 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:41317004 | C | G | 52 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(49): Show |
69 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.19+106C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317004 | |||||||
| chr21:41317005 | GGGAGGGC others(16): Show |
G | 1 | a0001c0001t0001g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.19+110_19+132delAG others(21): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr21 | 41317005 | ||||||
| chr21:41317032 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.19+134T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317032 | |||||||
| chr21:41317130 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.19+232C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317130 | |||||||
| chr21:41317169 | G | C | 2 | a0001c0001t0001g0041 a0001c0001t0002g0040 |
2 | HG02602.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.19+271G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317169 | |||||||
| chr21:41317258 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.19+360C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317258 | |||||||
| chr21:41317310 | C | T | 1 | a0001c0002t0001g0039 | 2 | HG00673.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.19+412C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317310 | |||||||
| chr21:41317356 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(117): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.19+458T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317356 | |||||||
| chr21:41317477 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+579G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317477 | |||||||
| chr21:41317516 | G | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(73): Show |
106 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.19+618G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317516 | |||||||
| chr21:41317710 | G | T | 49 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0036 others(46): Show |
64 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.19+812G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317710 | |||||||
| chr21:41317727 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(94): Show |
132 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.19+829C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317727 | |||||||
| chr21:41317773 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(94): Show |
132 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.19+875A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317773 | |||||||
| chr21:41317801 | A | G | 2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.19+903A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317801 | |||||||
| chr21:41317802 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.19+904G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317802 | |||||||
| chr21:41317874 | G | A | 2 | a0002c0003t0002g0043 a0002c0003t0002g0044 |
2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.19+976G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317874 | |||||||
| chr21:41318052 | T | C | 11 | a0002c0003t0001g0048 a0002c0003t0001g0049 a0002c0003t0001g0051 others(8): Show |
13 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+1154T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318052 | |||||||
| chr21:41318169 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+1271C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318169 | |||||||
| chr21:41318218 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.19+1320G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318218 | |||||||
| chr21:41318436 | G | A | 61 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0035 others(58): Show |
80 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.19+1538G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318436 | |||||||
| chr21:41318489 | CAGAGTGG others(8): Show |
C | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.19+1594_19+1608del others(15): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr21 | 41318489 | ||||||
| chr21:41318497 | C | T | 54 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0035 others(51): Show |
72 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.19+1599C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318497 | |||||||
| chr21:41318506 | G | A | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+1608G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318506 | |||||||
| chr21:41318529 | T | G | 1 | a0001c0001t0001g0053 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.19+1631T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318529 | |||||||
| chr21:41318995 | A | C | 24 | a0001c0001t0001g0023 a0001c0001t0001g0119 a0001c0001t0001g0125 others(21): Show |
25 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.19+2097A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318995 | |||||||
| chr21:41319040 | A | G | 8 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
10 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+2142A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319040 | |||||||
| chr21:41319184 | C | G | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+2286C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319184 | |||||||
| chr21:41319189 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+2291C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319189 | |||||||
| chr21:41319311 | G | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0032 others(46): Show |
52 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.19+2413G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319311 | |||||||
| chr21:41319471 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19+2573C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319471 | |||||||
| chr21:41319520 | C | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0185 |
2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.19+2622C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319520 | |||||||
| chr21:41319552 | G | T | 9 | a0001c0001t0001g0031 a0001c0001t0001g0167 a0001c0001t0001g0171 others(6): Show |
9 | HG01255.hp1 HG01952.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2654G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319552 | |||||||
| chr21:41319574 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.19+2676C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319574 | |||||||
| chr21:41319695 | G | A | 34 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0202 others(31): Show |
48 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.19+2797G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319695 | |||||||
| chr21:41319718 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(73): Show |
106 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.19+2820T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319718 | |||||||
| chr21:41319993 | C | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(112): Show |
142 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.20-2930C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319993 | |||||||
| chr21:41319998 | G | C | 15 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0129 others(12): Show |
15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.20-2925G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319998 | |||||||
| chr21:41320143 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.20-2780C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320143 | |||||||
| chr21:41320173 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.20-2750A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320173 | |||||||
| chr21:41320231 | C | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
5 | HG00280.hp2 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-2692C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320231 | |||||||
| chr21:41320241 | T | G | 24 | a0001c0001t0001g0006 a0001c0001t0002g0197 a0002c0003t0001g0016 others(21): Show |
32 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.20-2682T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320241 | |||||||
| chr21:41320367 | C | T | 5 | a0001c0001t0001g0108 a0001c0001t0002g0104 a0001c0001t0002g0105 others(2): Show |
5 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-2556C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320367 | |||||||
| chr21:41320372 | A | G | 2 | a0001c0004t0001g0226 a0001c0004t0002g0225 |
2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.20-2551A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320372 | |||||||
| chr21:41320392 | G | T | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-2531G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320392 | |||||||
| chr21:41320536 | G | A | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-2387G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320536 | |||||||
| chr21:41320738 | T | G | 3 | a0001c0004t0001g0199 a0001c0004t0001g0226 a0001c0004t0002g0225 |
3 | HG01106.hp1 HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.20-2185T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320738 | |||||||
| chr21:41320934 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.20-1989C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320934 | |||||||
| chr21:41320935 | C | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(81): Show |
106 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.20-1988C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320935 | |||||||
| chr21:41321416 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.20-1507G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41321416 | |||||||
| chr21:41321438 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.20-1485G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41321438 | |||||||
| chr21:41321603 | C | A | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-1320C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41321603 | |||||||
| chr21:41321898 | T | TCCTTTCC others(23): Show |
1 | a0001c0001t0001g0095 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.20-1020_20-991dupT others(29): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr21 | 41321898 | ||||||
| chr21:41321906 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-1017T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41321906 | |||||||
| chr21:41322008 | A | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG00280.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.20-915A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322008 | |||||||
| chr21:41322190 | AC | A | 18 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0109 others(15): Show |
21 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.20-727delC | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr21 | 41322190 | ||||||
| chr21:41322357 | G | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(113): Show |
143 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.20-566G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322357 | |||||||
| chr21:41322405 | G | T | 8 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
10 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-518G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322405 | |||||||
| chr21:41322446 | C | T | 22 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(19): Show |
27 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.20-477C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322446 | |||||||
| chr21:41322706 | A | T | 37 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0202 others(34): Show |
51 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.20-217A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322706 | |||||||
| chr21:41322740 | T | C | 45 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0032 others(42): Show |
50 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.20-183T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322740 | |||||||
| chr21:41322758 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.20-165T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322758 | |||||||
| chr21:41323234 | A | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0109 others(14): Show |
20 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.163+168A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41323234 | |||||||
| chr21:41323518 | G | C | 120 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(117): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.163+452G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41323518 | |||||||
| chr21:41323774 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.163+708G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41323774 | |||||||
| chr21:41324214 | A | G | 15 | a0001c0001t0001g0108 a0001c0001t0001g0187 a0001c0001t0001g0189 others(12): Show |
15 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+1148A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324214 | |||||||
| chr21:41324495 | A | T | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+1429A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324495 | |||||||
| chr21:41324872 | C | T | 26 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(23): Show |
31 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.163+1806C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324872 | |||||||
| chr21:41324873 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+1807G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324873 | |||||||
| chr21:41324881 | C | A | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+1815C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324881 | |||||||
| chr21:41324960 | G | C | 12 | a0002c0003t0001g0048 a0002c0003t0001g0049 a0002c0003t0001g0051 others(9): Show |
14 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.163+1894G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324960 | |||||||
| chr21:41324963 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0094 |
3 | HG02683.hp1 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.163+1897A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324963 | |||||||
| chr21:41324982 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+1916A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324982 | |||||||
| chr21:41324988 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0002g0124 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.163+1922G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324988 | |||||||
| chr21:41324994 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.163+1928C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324994 | |||||||
| chr21:41325294 | T | G | 36 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(33): Show |
41 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.163+2228T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325294 | |||||||
| chr21:41325305 | G | A | 5 | a0001c0001t0001g0108 a0001c0001t0002g0104 a0001c0001t0002g0105 others(2): Show |
5 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+2239G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325305 | |||||||
| chr21:41325480 | T | C | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+2414T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325480 | |||||||
| chr21:41325525 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2459T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325525 | |||||||
| chr21:41325670 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0002g0172 |
2 | HG02165.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.163+2604C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325670 | |||||||
| chr21:41325787 | C | G | 87 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0032 others(84): Show |
106 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.163+2721C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325787 | |||||||
| chr21:41325791 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG01167.hp2 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+2725G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325791 | |||||||
| chr21:41325822 | C | T | 5 | a0001c0001t0001g0108 a0001c0001t0002g0104 a0001c0001t0002g0105 others(2): Show |
5 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+2756C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325822 | |||||||
| chr21:41326055 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.163+2989G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326055 | |||||||
| chr21:41326161 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+3095G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326161 | |||||||
| chr21:41326211 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.163+3145T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326211 | |||||||
| chr21:41326276 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0094 |
3 | HG02683.hp1 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.163+3210T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326276 | |||||||
| chr21:41326277 | G | A | 12 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0129 others(9): Show |
12 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+3211G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326277 | |||||||
| chr21:41326351 | C | G | 2 | a0001c0001t0001g0130 a0001c0004t0001g0199 |
2 | HG01106.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.163+3285C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326351 | |||||||
| chr21:41326463 | G | T | 5 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
7 | HG01243.hp2 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+3397G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326463 | |||||||
| chr21:41326586 | C | T | 1 | a0001c0002t0001g0029 | 2 | HG01106.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.163+3520C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326586 | |||||||
| chr21:41326733 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+3667G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326733 | |||||||
| chr21:41326785 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0130 a0001c0001t0002g0197 others(1): Show |
7 | HG01106.hp1 HG02630.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+3719T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326785 | |||||||
| chr21:41326854 | T | G | 27 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(24): Show |
32 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.163+3788T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326854 | |||||||
| chr21:41326942 | T | C | 12 | a0001c0001t0001g0126 a0001c0001t0001g0177 a0001c0001t0001g0180 others(9): Show |
14 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.163+3876T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326942 | |||||||
| chr21:41326980 | A | G | 121 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(118): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.163+3914A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326980 | |||||||
| chr21:41327198 | C | T | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.163+4132C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41327198 | |||||||
| chr21:41327468 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0185 |
2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.163+4402T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41327468 | |||||||
| chr21:41327725 | G | C | 1 | a0001c0001t0001g0011 | 3 | HG01192.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.163+4659G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41327725 | |||||||
| chr21:41327834 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0002g0031 |
2 | HG01255.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.163+4768G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41327834 | |||||||
| chr21:41328086 | G | A | 2 | a0001c0004t0001g0226 a0001c0004t0002g0225 |
2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.163+5020G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328086 | |||||||
| chr21:41328169 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163+5103G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328169 | |||||||
| chr21:41328219 | T | C | 104 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0032 others(101): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.163+5153T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328219 | |||||||
| chr21:41328351 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+5285A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328351 | |||||||
| chr21:41328468 | G | T | 1 | a0001c0002t0001g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.163+5402G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328468 | |||||||
| chr21:41328483 | A | G | 107 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0032 others(104): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.163+5417A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328483 | |||||||
| chr21:41328553 | G | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
11 | HG00558.hp1 HG01070.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+5487G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328553 | |||||||
| chr21:41328608 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163+5542G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328608 | |||||||
| chr21:41328785 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+5719G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328785 | |||||||
| chr21:41328797 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+5731G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328797 | |||||||
| chr21:41328822 | A | C | 1 | a0002c0003t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.163+5756A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328822 | |||||||
| chr21:41328860 | G | T | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+5794G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328860 | |||||||
| chr21:41329139 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.163+6073C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329139 | |||||||
| chr21:41329153 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.163+6087T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329153 | |||||||
| chr21:41329168 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0185 |
2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.163+6102C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329168 | |||||||
| chr21:41329347 | A | T | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+6281A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329347 | |||||||
| chr21:41329382 | C | T | 22 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0108 others(19): Show |
24 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.163+6316C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329382 | |||||||
| chr21:41329397 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+6331C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329397 | |||||||
| chr21:41329398 | G | A | 36 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0119 others(33): Show |
50 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.163+6332G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329398 | |||||||
| chr21:41329573 | C | CT | 12 | a0001c0001t0001g0160 a0001c0001t0001g0171 a0001c0001t0001g0218 others(9): Show |
14 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.163+6521dupT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41329573 | ||||||
| chr21:41329673 | G | A | 14 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(11): Show |
17 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.163+6607G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329673 | |||||||
| chr21:41329725 | T | A | 58 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0066 others(55): Show |
69 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.163+6659T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329725 | |||||||
| chr21:41329797 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163+6731T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329797 | |||||||
| chr21:41329887 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.163+6821A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329887 | |||||||
| chr21:41330134 | G | GA | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(142): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.163+7085dupA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41330134 | ||||||
| chr21:41330134 | G | GAA | 40 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0063 others(37): Show |
44 | HG00558.hp1 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.163+7084_163+7085d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41330134 | ||||||
| chr21:41330134 | GA | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0126 others(21): Show |
30 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.163+7085delA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41330134 | ||||||
| chr21:41330151 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+7085A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330151 | |||||||
| chr21:41330188 | A | G | 22 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0108 others(19): Show |
24 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.163+7122A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330188 | |||||||
| chr21:41330334 | C | T | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.163+7268C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330334 | |||||||
| chr21:41330443 | G | C | 4 | a0001c0001t0001g0066 a0002c0003t0001g0016 a0002c0003t0001g0054 others(1): Show |
5 | HG00280.hp1 HG01109.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+7377G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330443 | |||||||
| chr21:41330493 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.163+7427T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330493 | |||||||
| chr21:41330582 | C | T | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+7516C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330582 | |||||||
| chr21:41330603 | G | A | 1 | a0001c0001t0001g0012 | 3 | HG00733.hp2 HG01192.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.163+7537G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330603 | |||||||
| chr21:41330739 | T | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0066 others(54): Show |
68 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.164-7639T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330739 | |||||||
| chr21:41330750 | G | A | 36 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0119 others(33): Show |
50 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.164-7628G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330750 | |||||||
| chr21:41330846 | G | A | 2 | a0001c0004t0001g0226 a0001c0004t0002g0225 |
2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.164-7532G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330846 | |||||||
| chr21:41330979 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.164-7399A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330979 | |||||||
| chr21:41331459 | G | A | 60 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0032 others(57): Show |
70 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.164-6919G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331459 | |||||||
| chr21:41331550 | A | G | 10 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-6828A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331550 | |||||||
| chr21:41331575 | T | C | 1 | a0001c0001t0002g0033 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.164-6803T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331575 | |||||||
| chr21:41331680 | A | G | 5 | a0001c0001t0001g0108 a0001c0001t0002g0104 a0001c0001t0002g0105 others(2): Show |
5 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-6698A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331680 | |||||||
| chr21:41331843 | A | G | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.164-6535A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331843 | |||||||
| chr21:41331892 | A | G | 1 | a0001c0002t0001g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164-6486A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331892 | |||||||
| chr21:41331894 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-6484A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331894 | |||||||
| chr21:41332016 | C | T | 3 | a0002c0003t0002g0014 a0002c0003t0002g0015 a0002c0003t0002g0046 |
5 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-6362C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332016 | |||||||
| chr21:41332136 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0129 a0001c0001t0001g0174 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-6242G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332136 | |||||||
| chr21:41332159 | C | G | 21 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0108 others(18): Show |
23 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-6219C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332159 | |||||||
| chr21:41332325 | T | C | 1 | a0002c0003t0007g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.164-6053T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332325 | |||||||
| chr21:41332563 | T | A | 13 | a0001c0001t0001g0031 a0001c0001t0001g0118 a0001c0001t0001g0167 others(10): Show |
13 | HG00140.hp2 HG00642.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-5815T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332563 | |||||||
| chr21:41332781 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.164-5597G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332781 | |||||||
| chr21:41332874 | C | CA | 69 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(66): Show |
91 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.164-5498dupA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41332874 | ||||||
| chr21:41333020 | T | C | 118 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(115): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.164-5358T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333020 | |||||||
| chr21:41333024 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.164-5354A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333024 | |||||||
| chr21:41333056 | C | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0177 others(14): Show |
20 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.164-5322C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333056 | |||||||
| chr21:41333078 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-5300T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333078 | |||||||
| chr21:41333131 | G | GT | 69 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(66): Show |
91 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.164-5234dupT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41333131 | ||||||
| chr21:41333131 | G | GTT | 13 | a0001c0001t0001g0125 a0001c0001t0001g0187 a0001c0001t0001g0189 others(10): Show |
13 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-5235_164-5234d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41333131 | ||||||
| chr21:41333151 | A | T | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.164-5227A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333151 | |||||||
| chr21:41333194 | A | G | 118 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(115): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.164-5184A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333194 | |||||||
| chr21:41333397 | T | G | 119 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(116): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.164-4981T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333397 | |||||||
| chr21:41333478 | T | C | 35 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(32): Show |
39 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.164-4900T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333478 | |||||||
| chr21:41333523 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0004g0134 |
2 | HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.164-4855T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333523 | |||||||
| chr21:41333762 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-4616A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333762 | |||||||
| chr21:41334013 | A | T | 21 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0108 others(18): Show |
23 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-4365A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334013 | |||||||
| chr21:41334035 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.164-4343G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334035 | |||||||
| chr21:41334047 | T | G | 2 | a0001c0001t0001g0125 a0001c0001t0002g0124 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.164-4331T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334047 | |||||||
| chr21:41334303 | T | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0066 a0001c0001t0001g0113 others(25): Show |
36 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.164-4075T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334303 | |||||||
| chr21:41334362 | G | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0066 others(54): Show |
68 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.164-4016G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334362 | |||||||
| chr21:41334376 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.164-4002A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334376 | |||||||
| chr21:41334384 | A | G | 26 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(23): Show |
31 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.164-3994A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334384 | |||||||
| chr21:41334573 | G | T | 1 | a0001c0001t0001g0008 | 3 | HG00609.hp1 HG00621.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.164-3805G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334573 | |||||||
| chr21:41334682 | G | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0108 others(18): Show |
23 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-3696G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334682 | |||||||
| chr21:41334737 | G | T | 1 | a0001c0001t0001g0028 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.164-3641G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334737 | |||||||
| chr21:41334794 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-3584C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334794 | |||||||
| chr21:41334844 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.164-3534G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334844 | |||||||
| chr21:41334846 | A | G | 126 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(123): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.164-3532A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334846 | |||||||
| chr21:41335146 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.164-3232G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335146 | |||||||
| chr21:41335239 | A | G | 85 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0035 others(82): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.164-3139A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335239 | |||||||
| chr21:41335399 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-2979G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335399 | |||||||
| chr21:41335679 | G | T | 1 | a0001c0001t0002g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.164-2699G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335679 | |||||||
| chr21:41335705 | G | T | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-2673G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335705 | |||||||
| chr21:41335802 | T | G | 1 | a0001c0001t0002g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.164-2576T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335802 | |||||||
| chr21:41335989 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.164-2389T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335989 | |||||||
| chr21:41336064 | TC | T | 3 | a0001c0001t0001g0171 a0001c0001t0002g0092 a0001c0001t0002g0170 |
3 | HG00140.hp2 HG02895.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.164-2313delC | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336064 | |||||||
| chr21:41336073 | G | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0108 others(19): Show |
24 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.164-2305G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336073 | |||||||
| chr21:41336086 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0075 others(11): Show |
19 | HG01255.hp2 HG01257.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.164-2292G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336086 | |||||||
| chr21:41336207 | T | G | 1 | a0001c0001t0002g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-2171T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336207 | |||||||
| chr21:41336233 | A | T | 4 | a0001c0001t0001g0126 a0001c0001t0002g0102 a0001c0001t0002g0103 others(1): Show |
4 | HG02723.hp1 HG03139.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-2145A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336233 | |||||||
| chr21:41336558 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-1820A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336558 | |||||||
| chr21:41336658 | A | G | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.164-1720A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336658 | |||||||
| chr21:41336829 | C | T | 1 | a0002c0003t0002g0014 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.164-1549C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336829 | |||||||
| chr21:41336859 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1519G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336859 | |||||||
| chr21:41336913 | A | G | 1 | a0001c0001t0002g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.164-1465A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336913 | |||||||
| chr21:41336926 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1452G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336926 | |||||||
| chr21:41336958 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.164-1420A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336958 | |||||||
| chr21:41336969 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.164-1409C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336969 | |||||||
| chr21:41337058 | T | A | 7 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
9 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-1320T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337058 | |||||||
| chr21:41337077 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.164-1301G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337077 | |||||||
| chr21:41337201 | C | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1177C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337201 | |||||||
| chr21:41337331 | C | T | 12 | a0001c0001t0001g0182 a0001c0001t0002g0140 a0002c0003t0001g0048 others(9): Show |
14 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-1047C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337331 | |||||||
| chr21:41337669 | G | T | 53 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0032 others(50): Show |
58 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.164-709G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337669 | |||||||
| chr21:41337682 | C | G | 1 | a0001c0006t0001g0042 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.164-696C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337682 | |||||||
| chr21:41337720 | T | C | 15 | a0001c0001t0001g0035 a0001c0001t0001g0187 a0001c0001t0001g0189 others(12): Show |
16 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-658T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337720 | |||||||
| chr21:41337729 | T | C | 7 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
9 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-649T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337729 | |||||||
| chr21:41337731 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
8 | HG03669.hp1 HG03710.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-647C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337731 | |||||||
| chr21:41337810 | G | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0023 others(47): Show |
70 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.164-568G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337810 | |||||||
| chr21:41337837 | G | A | 1 | a0001c0002t0001g0038 | 2 | HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.164-541G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337837 | |||||||
| chr21:41337883 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0197 |
5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-495G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337883 | |||||||
| chr21:41338027 | C | G | 1 | a0002c0003t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164-351C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41338027 | |||||||
| chr21:41338138 | C | T | 11 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(8): Show |
14 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.164-240C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41338138 | |||||||
| chr21:41338248 | T | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(100): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.164-130T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41338248 | |||||||
| chr21:41338308 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.164-70G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41338308 | |||||||
| chr21:41338533 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.287+32C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338533 | |||||||
| chr21:41338595 | A | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18964.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.287+94A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338595 | |||||||
| chr21:41338609 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.287+108T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338609 | |||||||
| chr21:41338639 | A | G | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
44 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.287+138A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338639 | |||||||
| chr21:41338709 | CT | C | 15 | a0001c0001t0001g0133 a0001c0001t0001g0177 a0001c0001t0001g0180 others(12): Show |
15 | HG01167.hp2 HG01243.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.287+210delT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr21 | 41338709 | ||||||
| chr21:41338745 | A | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
6 | HG02027.hp1 HG02132.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.287+244A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338745 | |||||||
| chr21:41338795 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.287+294C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338795 | |||||||
| chr21:41339012 | G | A | 13 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(10): Show |
16 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.287+511G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339012 | |||||||
| chr21:41339063 | G | T | 1 | a0001c0002t0001g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.287+562G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339063 | |||||||
| chr21:41339280 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.287+779C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339280 | |||||||
| chr21:41339352 | C | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0035 others(81): Show |
91 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.287+851C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339352 | |||||||
| chr21:41339529 | G | A | 98 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0031 others(95): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.287+1028G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339529 | |||||||
| chr21:41339592 | A | T | 26 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0029 others(23): Show |
39 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.287+1091A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339592 | |||||||
| chr21:41339751 | T | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(162): Show |
228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.287+1250T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339751 | |||||||
| chr21:41339758 | G | A | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.287+1257G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339758 | |||||||
| chr21:41339786 | C | T | 40 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0108 others(37): Show |
41 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.287+1285C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339786 | |||||||
| chr21:41339862 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0129 a0001c0001t0001g0174 others(4): Show |
8 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.287+1361G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339862 | |||||||
| chr21:41339885 | A | G | 1 | a0001c0004t0001g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287+1384A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339885 | |||||||
| chr21:41339966 | G | C | 3 | a0001c0001t0002g0034 a0001c0004t0002g0225 a0002c0003t0001g0051 |
4 | HG02717.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1465G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339966 | |||||||
| chr21:41340009 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.287+1508T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340009 | |||||||
| chr21:41340054 | G | A | 22 | a0001c0001t0001g0031 a0001c0001t0001g0118 a0001c0001t0001g0125 others(19): Show |
22 | HG00140.hp2 HG00642.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.287+1553G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340054 | |||||||
| chr21:41340074 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.287+1573T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340074 | |||||||
| chr21:41340099 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287+1598G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340099 | |||||||
| chr21:41340152 | C | CT | 13 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0125 others(10): Show |
13 | HG02258.hp1 HG02300.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.287+1671dupT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr21 | 41340152 | ||||||
| chr21:41340152 | CTT | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0109 others(11): Show |
16 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.287+1670_287+1671d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr21 | 41340152 | ||||||
| chr21:41340215 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.287+1714G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340215 | |||||||
| chr21:41340223 | G | A | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.287+1722G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340223 | |||||||
| chr21:41340388 | A | G | 14 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0129 others(11): Show |
16 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.287+1887A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340388 | |||||||
| chr21:41340590 | A | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0129 others(12): Show |
17 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.287+2089A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340590 | |||||||
| chr21:41340592 | C | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0129 others(12): Show |
17 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.287+2091C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340592 | |||||||
| chr21:41340696 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.287+2195G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340696 | |||||||
| chr21:41341003 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.287+2502T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341003 | |||||||
| chr21:41341069 | A | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0129 others(12): Show |
17 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.287+2568A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341069 | |||||||
| chr21:41341142 | G | GTTAATAG others(27): Show |
1 | a0001c0001t0001g0079 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.287+2644_287+2677d others(36): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr21 | 41341142 | ||||||
| chr21:41341163 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.287+2662T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341163 | |||||||
| chr21:41341237 | T | G | 1 | a0001c0001t0002g0024 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.287+2736T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341237 | |||||||
| chr21:41341444 | C | T | 26 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0029 others(23): Show |
39 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.287+2943C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341444 | |||||||
| chr21:41341595 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.288-2881A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341595 | |||||||
| chr21:41341936 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0002g0121 a0001c0001t0002g0122 others(3): Show |
7 | HG00099.hp1 HG01074.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-2540G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341936 | |||||||
| chr21:41341985 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.288-2491G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341985 | |||||||
| chr21:41342021 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.288-2455A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342021 | |||||||
| chr21:41342161 | T | C | 21 | a0001c0001t0001g0031 a0001c0001t0001g0118 a0001c0001t0001g0125 others(18): Show |
21 | HG00140.hp2 HG00642.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.288-2315T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342161 | |||||||
| chr21:41342181 | G | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0174 others(12): Show |
17 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.288-2295G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342181 | |||||||
| chr21:41342210 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.288-2266C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342210 | |||||||
| chr21:41342226 | C | T | 1 | a0001c0001t0002g0033 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.288-2250C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342226 | |||||||
| chr21:41342361 | T | A | 135 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0031 others(132): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.288-2115T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342361 | |||||||
| chr21:41342544 | A | C | 1 | a0001c0001t0002g0111 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.288-1932A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342544 | |||||||
| chr21:41342547 | A | G | 43 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0063 others(40): Show |
58 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.288-1929A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342547 | |||||||
| chr21:41342556 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.288-1920G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342556 | |||||||
| chr21:41342605 | C | T | 4 | a0001c0001t0004g0134 a0002c0003t0001g0048 a0002c0003t0001g0049 others(1): Show |
4 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-1871C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342605 | |||||||
| chr21:41342640 | A | G | 44 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0063 others(41): Show |
60 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.288-1836A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342640 | |||||||
| chr21:41342709 | A | G | 1 | a0001c0001t0002g0033 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.288-1767A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342709 | |||||||
| chr21:41342764 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0109 others(10): Show |
15 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.288-1712T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342764 | |||||||
| chr21:41342781 | T | C | 14 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(11): Show |
17 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-1695T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342781 | |||||||
| chr21:41342858 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.288-1618G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342858 | |||||||
| chr21:41342872 | G | A | 27 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(24): Show |
30 | HG00280.hp1 HG01109.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.288-1604G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342872 | |||||||
| chr21:41342910 | A | G | 7 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0001g0136 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.288-1566A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342910 | |||||||
| chr21:41342992 | A | G | 29 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(26): Show |
42 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.288-1484A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342992 | |||||||
| chr21:41343351 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02040.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.288-1125T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343351 | |||||||
| chr21:41343355 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.288-1121G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343355 | |||||||
| chr21:41343367 | ATCTTTAA others(7): Show |
A | 1 | a0001c0002t0001g0206 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.288-1108_288-1095d others(16): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343367 | |||||||
| chr21:41343389 | A | C | 15 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(12): Show |
18 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.288-1087A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343389 | |||||||
| chr21:41343422 | A | G | 4 | a0001c0001t0004g0134 a0002c0003t0001g0048 a0002c0003t0001g0049 others(1): Show |
4 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-1054A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343422 | |||||||
| chr21:41343480 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.288-996A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343480 | |||||||
| chr21:41343548 | A | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0109 others(10): Show |
15 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.288-928A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343548 | |||||||
| chr21:41343763 | G | A | 14 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(11): Show |
17 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-713G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343763 | |||||||
| chr21:41343770 | G | A | 1 | a0001c0002t0001g0207 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.288-706G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343770 | |||||||
| chr21:41343771 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.288-705G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343771 | |||||||
| chr21:41343947 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.288-529G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343947 | |||||||
| chr21:41343961 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.288-515A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343961 | |||||||
| chr21:41343962 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.288-514T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343962 | |||||||
| chr21:41343963 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.288-513T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343963 | |||||||
| chr21:41344059 | G | T | 25 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0029 others(22): Show |
38 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.288-417G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344059 | |||||||
| chr21:41344064 | G | A | 1 | a0001c0001t0001g0019 | 2 | NA18940.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.288-412G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344064 | |||||||
| chr21:41344267 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.288-209G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344267 | |||||||
| chr21:41344324 | C | T | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.288-152C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344324 | |||||||
| chr21:41344330 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.288-146C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344330 | |||||||
| chr21:41344348 | G | A | 43 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0108 others(40): Show |
45 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.288-128G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344348 | |||||||
| chr21:41344360 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.288-116T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344360 | |||||||
| chr21:41344379 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0109 others(12): Show |
17 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-97C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344379 | |||||||
| chr21:41344434 | G | A | 10 | a0001c0001t0002g0025 a0001c0001t0002g0140 a0001c0001t0002g0229 others(7): Show |
13 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.288-42G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344434 | |||||||
| chr21:41344468 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19010.hp2 | splice_region_variant&intron_variant | LOW | c.288-8C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344468 | |||||||
| chr21:41344621 | G | A | 43 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0108 others(40): Show |
45 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.346+87G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344621 | |||||||
| chr21:41344765 | G | C | 13 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(10): Show |
16 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.346+231G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344765 | |||||||
| chr21:41344780 | A | T | 1 | a0001c0001t0001g0027 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.346+246A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344780 | |||||||
| chr21:41344804 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0167 |
2 | HG00642.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.346+270C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344804 | |||||||
| chr21:41344820 | G | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0083 |
2 | NA18979.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.346+286G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344820 | |||||||
| chr21:41344933 | G | A | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.346+399G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344933 | |||||||
| chr21:41345040 | G | A | 40 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0108 others(37): Show |
41 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.346+506G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345040 | |||||||
| chr21:41345070 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.346+536C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345070 | |||||||
| chr21:41345136 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.347-550A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345136 | |||||||
| chr21:41345152 | A | AGGCTGAG others(85): Show |
2 | a0001c0002t0001g0208 a0001c0002t0001g0223 |
2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.347-457_347-366dup others(92): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | 41345152 | ||||||
| chr21:41345183 | TGAGGCGG others(39): Show |
T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.347-457_347-412del others(46): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | 41345183 | ||||||
| chr21:41345229 | A | AGAGGCGG others(39): Show |
2 | a0001c0001t0002g0025 a0001c0001t0002g0229 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.347-348_347-303dup others(46): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | 41345229 | ||||||
| chr21:41345229 | AGAGGCGG others(39): Show |
A | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.347-348_347-303del others(46): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | 41345229 | ||||||
| chr21:41345234 | C | T | 43 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0108 others(40): Show |
45 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.347-452C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345234 | |||||||
| chr21:41345280 | C | T | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.347-406C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345280 | |||||||
| chr21:41345338 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.347-348G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345338 | |||||||
| chr21:41345339 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.347-347C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345339 | |||||||
| chr21:41345372 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0152 a0001c0001t0001g0158 |
5 | HG01358.hp2 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-314C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345372 | |||||||
| chr21:41345539 | C | T | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.347-147C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345539 | |||||||
| chr21:41345631 | A | G | 11 | a0001c0001t0001g0035 a0001c0001t0001g0119 a0001c0001t0001g0189 others(8): Show |
12 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-55A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345631 | |||||||
| chr21:41345649 | G | A | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.347-37G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345649 | |||||||
| chr21:41345683 | C | T | 2 | a0002c0003t0001g0048 a0002c0003t0001g0049 |
2 | HG02895.hp2 HG02897.hp1 |
splice_region_variant&intron_variant | LOW | c.347-3C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345683 | |||||||
| chr21:41345753 | T | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
7 | HG01256.hp2 HG01361.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+17T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41345753 | |||||||
| chr21:41345866 | T | C | 1 | a0001c0006t0001g0042 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.397+130T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41345866 | |||||||
| chr21:41345992 | TATA | T | 18 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0001g0119 others(15): Show |
19 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.397+261_397+263del others(3): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41345992 | ||||||
| chr21:41346014 | C | CT | 28 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0127 others(25): Show |
41 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+286dupT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41346014 | ||||||
| chr21:41346021 | T | A | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.397+285T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346021 | |||||||
| chr21:41346022 | T | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0161 a0001c0001t0002g0205 others(1): Show |
5 | HG01106.hp1 HG01346.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+286T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346022 | |||||||
| chr21:41346022 | T | TA | 48 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(45): Show |
51 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.397+300dupA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41346022 | ||||||
| chr21:41346022 | T | TAA | 12 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0062 others(9): Show |
15 | HG00558.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.397+299_397+300dup others(2): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41346022 | ||||||
| chr21:41346022 | TA | T | 9 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0146 others(6): Show |
10 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.397+300delA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41346022 | ||||||
| chr21:41346023 | A | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0133 a0001c0001t0001g0155 others(4): Show |
8 | HG00673.hp2 HG01167.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+287A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346023 | |||||||
| chr21:41346035 | A | G | 5 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0183 others(2): Show |
5 | HG00099.hp1 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+299A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346035 | |||||||
| chr21:41346149 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.397+413G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346149 | |||||||
| chr21:41346193 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.397+457G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346193 | |||||||
| chr21:41346235 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.397+499G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346235 | |||||||
| chr21:41346335 | C | T | 40 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0108 others(37): Show |
41 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+599C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346335 | |||||||
| chr21:41346402 | G | A | 1 | a0002c0003t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.398-611G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346402 | |||||||
| chr21:41346559 | C | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0141 |
2 | HG03688.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.398-454C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346559 | |||||||
| chr21:41346588 | C | T | 31 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(28): Show |
44 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-425C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346588 | |||||||
| chr21:41346640 | C | G | 31 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(28): Show |
44 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-373C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346640 | |||||||
| chr21:41346782 | G | C | 1 | a0002c0003t0001g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.398-231G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346782 | |||||||
| chr21:41346786 | C | A | 1 | a0001c0002t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.398-227C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346786 | |||||||
| chr21:41346827 | A | G | 3 | a0001c0001t0002g0034 a0001c0004t0002g0225 a0002c0003t0001g0051 |
4 | HG02717.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-186A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346827 | |||||||
| chr21:41346912 | C | A | 2 | a0001c0002t0001g0029 a0001c0002t0001g0123 |
3 | HG01106.hp2 HG01175.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.398-101C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346912 | |||||||
| chr21:41347140 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.485+40A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347140 | |||||||
| chr21:41347210 | C | A | 31 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(28): Show |
44 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.485+110C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347210 | |||||||
| chr21:41347522 | A | C | 1 | a0001c0001t0002g0205 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.485+422A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347522 | |||||||
| chr21:41347580 | T | G | 1 | a0001c0001t0002g0205 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.485+480T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347580 | |||||||
| chr21:41347723 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.485+623A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347723 | |||||||
| chr21:41347737 | G | C | 1 | a0001c0001t0002g0005 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.485+637G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347737 | |||||||
| chr21:41347749 | C | CA | 5 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0021 others(2): Show |
7 | HG00673.hp1 HG02027.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+669dupA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | ||||||
| chr21:41347749 | C | CAA | 15 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.485+668_485+669dup others(2): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | ||||||
| chr21:41347749 | C | CAAA | 27 | a0001c0001t0002g0092 a0001c0001t0002g0205 a0001c0002t0001g0003 others(24): Show |
39 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.485+667_485+669dup others(3): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | ||||||
| chr21:41347749 | CA | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0066 others(9): Show |
13 | HG00280.hp1 HG01069.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.485+669delA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | ||||||
| chr21:41347749 | CAAAAAAA others(4): Show |
C | 40 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0108 others(37): Show |
42 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+659_485+669del others(11): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | ||||||
| chr21:41347795 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0028 others(8): Show |
19 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+695C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347795 | |||||||
| chr21:41347797 | TAC | T | 40 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0108 others(37): Show |
42 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+701_485+702del others(2): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347797 | ||||||
| chr21:41348274 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0229 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.486-318C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41348274 | |||||||
| chr21:41348284 | A | G | 92 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0031 others(89): Show |
110 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.486-308A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41348284 | |||||||
| chr21:41348290 | TGA | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00140.hp2 HG00558.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-300_486-299del others(2): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41348290 | ||||||
| chr21:41348493 | C | T | 7 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0001g0136 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-99C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41348493 | |||||||
| chr21:41348764 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618+40T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41348764 | |||||||
| chr21:41349098 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.618+374C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349098 | |||||||
| chr21:41349180 | A | C | 43 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(40): Show |
45 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.618+456A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349180 | |||||||
| chr21:41349378 | ATGCTGCA others(8): Show |
A | 1 | a0001c0001t0001g0001 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.618+673_618+687del others(15): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41349378 | ||||||
| chr21:41349406 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.618+682C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349406 | |||||||
| chr21:41349462 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.618+738A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349462 | |||||||
| chr21:41349609 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.618+885C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349609 | |||||||
| chr21:41349646 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0033 |
4 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+922G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349646 | |||||||
| chr21:41349694 | G | A | 17 | a0001c0001t0001g0031 a0001c0001t0001g0118 a0001c0001t0001g0126 others(14): Show |
17 | HG00642.hp2 HG01255.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.618+970G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349694 | |||||||
| chr21:41349704 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.618+980C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349704 | |||||||
| chr21:41349793 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618+1069C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349793 | |||||||
| chr21:41349857 | C | T | 28 | a0001c0001t0001g0147 a0001c0001t0001g0175 a0001c0001t0001g0176 others(25): Show |
41 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.618+1133C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349857 | |||||||
| chr21:41349912 | T | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0185 |
2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.618+1188T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349912 | |||||||
| chr21:41349915 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.618+1191C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349915 | |||||||
| chr21:41349919 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0033 |
4 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+1195G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349919 | |||||||
| chr21:41349942 | C | T | 43 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(40): Show |
45 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.618+1218C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349942 | |||||||
| chr21:41349949 | C | T | 126 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0031 others(123): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.618+1225C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349949 | |||||||
| chr21:41349983 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0069 others(4): Show |
8 | HG02040.hp1 HG02523.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+1259C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349983 | |||||||
| chr21:41350043 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.618+1319C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350043 | |||||||
| chr21:41350103 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.618+1379G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350103 | |||||||
| chr21:41350141 | C | T | 27 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0033 others(24): Show |
40 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.618+1417C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350141 | |||||||
| chr21:41350240 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG01243.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+1516G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350240 | |||||||
| chr21:41350250 | C | G | 1 | a0001c0002t0001g0029 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.618+1526C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350250 | |||||||
| chr21:41350463 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.618+1739G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350463 | |||||||
| chr21:41350523 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618+1799G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350523 | |||||||
| chr21:41350633 | G | A | 5 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0205 others(2): Show |
5 | HG01884.hp1 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+1909G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350633 | |||||||
| chr21:41350699 | C | T | 4 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0004t0002g0225 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+1975C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350699 | |||||||
| chr21:41350737 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.618+2013A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350737 | |||||||
| chr21:41350912 | G | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0062 others(12): Show |
18 | HG00140.hp2 HG00558.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.618+2188G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350912 | |||||||
| chr21:41350962 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.618+2238G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350962 | |||||||
| chr21:41350996 | C | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0110 others(4): Show |
9 | HG00558.hp1 HG02080.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.618+2272C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350996 | |||||||
| chr21:41351025 | TG | T | 27 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0033 others(24): Show |
40 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.618+2303delG | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41351025 | ||||||
| chr21:41351028 | T | C | 27 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0033 others(24): Show |
40 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.618+2304T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351028 | |||||||
| chr21:41351045 | T | A | 3 | a0001c0001t0001g0066 a0002c0003t0001g0016 a0002c0003t0001g0055 |
4 | HG00280.hp1 HG01109.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+2321T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351045 | |||||||
| chr21:41351133 | G | A | 1 | a0002c0003t0002g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.618+2409G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351133 | |||||||
| chr21:41351133 | G | T | 1 | a0001c0001t0001g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.618+2409G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351133 | |||||||
| chr21:41351164 | A | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0119 a0001c0001t0001g0135 others(8): Show |
12 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.618+2440A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351164 | |||||||
| chr21:41351397 | A | G | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+2673A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351397 | |||||||
| chr21:41351572 | G | C | 33 | a0001c0001t0001g0066 a0001c0001t0001g0133 a0001c0001t0001g0177 others(30): Show |
37 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.618+2848G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351572 | |||||||
| chr21:41351644 | A | C | 17 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0118 others(14): Show |
17 | HG00642.hp2 HG01255.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.618+2920A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351644 | |||||||
| chr21:41351666 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0094 |
3 | HG02683.hp1 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.618+2942G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351666 | |||||||
| chr21:41351923 | C | T | 4 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0004t0002g0225 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+3199C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351923 | |||||||
| chr21:41351953 | T | G | 1 | a0004c0007t0001g0219 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.618+3229T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351953 | |||||||
| chr21:41352013 | G | A | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+3289G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352013 | |||||||
| chr21:41352030 | T | C | 45 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0062 others(42): Show |
60 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.618+3306T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352030 | |||||||
| chr21:41352121 | A | G | 1 | a0001c0001t0002g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618+3397A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352121 | |||||||
| chr21:41352141 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.618+3417A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352141 | |||||||
| chr21:41352238 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0002g0102 |
2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.618+3514C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352238 | |||||||
| chr21:41352263 | T | C | 1 | a0001c0001t0002g0034 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.618+3539T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352263 | |||||||
| chr21:41352771 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.618+4047G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352771 | |||||||
| chr21:41352820 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.618+4096T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352820 | |||||||
| chr21:41352820 | T | TAAATAAA others(1): Show |
102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(99): Show |
154 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(10): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | ||||||
| chr21:41352820 | T | TAAATAAA others(5): Show |
31 | a0001c0001t0001g0066 a0001c0001t0001g0133 a0001c0001t0001g0177 others(28): Show |
36 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(14): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | ||||||
| chr21:41352820 | T | TAAATAAA others(5): Show |
43 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(40): Show |
49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(14): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | ||||||
| chr21:41352820 | T | TAAATAAA others(9): Show |
5 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(18): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | ||||||
| chr21:41352820 | T | TAAATAAA others(9): Show |
20 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0119 others(17): Show |
22 | HG00558.hp1 HG01109.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(18): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | ||||||
| chr21:41352820 | T | TAAATAAA others(13): Show |
1 | a0001c0001t0002g0034 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.618+4103_618+4104i others(22): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | ||||||
| chr21:41352820 | T | TAAATAAA others(17): Show |
1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+4103_618+4104i others(26): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | ||||||
| chr21:41352820 | T | TAAATAAA others(13): Show |
5 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0002g0102 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(22): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | ||||||
| chr21:41352857 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(206): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.618+4133G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352857 | |||||||
| chr21:41352964 | C | T | 4 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0004t0002g0225 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-4144C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352964 | |||||||
| chr21:41352965 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
7 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.619-4143G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352965 | |||||||
| chr21:41353028 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.619-4080C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353028 | |||||||
| chr21:41353099 | A | G | 1 | a0001c0002t0001g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.619-4009A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353099 | |||||||
| chr21:41353225 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.619-3883A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353225 | |||||||
| chr21:41353282 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.619-3826A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353282 | |||||||
| chr21:41353453 | G | A | 126 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0031 others(123): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.619-3655G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353453 | |||||||
| chr21:41353541 | C | T | 6 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0001g0136 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-3567C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353541 | |||||||
| chr21:41353676 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.619-3432G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353676 | |||||||
| chr21:41353722 | G | T | 2 | a0001c0001t0002g0137 a0001c0001t0002g0141 |
2 | HG03688.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.619-3386G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353722 | |||||||
| chr21:41354182 | G | A | 2 | a0001c0004t0002g0225 a0002c0003t0001g0051 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.619-2926G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354182 | |||||||
| chr21:41354189 | G | A | 1 | a0001c0002t0001g0210 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.619-2919G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354189 | |||||||
| chr21:41354192 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.619-2916G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354192 | |||||||
| chr21:41354221 | CAT | C | 40 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0035 others(37): Show |
42 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.619-2886_619-2885d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354221 | |||||||
| chr21:41354310 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.619-2798T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354310 | |||||||
| chr21:41354832 | C | CT | 128 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0031 others(125): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.619-2276_619-2275i others(3): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354832 | |||||||
| chr21:41355013 | G | C | 128 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0031 others(125): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.619-2095G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355013 | |||||||
| chr21:41355370 | C | A | 6 | a0001c0001t0001g0066 a0002c0003t0001g0016 a0002c0003t0001g0055 others(3): Show |
7 | HG00280.hp1 HG01109.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.619-1738C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355370 | |||||||
| chr21:41355375 | G | A | 25 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0029 others(22): Show |
37 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.619-1733G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355375 | |||||||
| chr21:41355398 | T | C | 2 | a0002c0003t0002g0056 a0002c0003t0002g0057 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.619-1710T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355398 | |||||||
| chr21:41355488 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.619-1620C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355488 | |||||||
| chr21:41355494 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.619-1614C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355494 | |||||||
| chr21:41355556 | G | GAAAC | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.619-1530_619-1527d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41355556 | ||||||
| chr21:41355568 | C | G | 1 | a0001c0001t0002g0033 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.619-1540C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355568 | |||||||
| chr21:41355781 | A | C | 75 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(72): Show |
88 | HG00099.hp2 HG00642.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.619-1327A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355781 | |||||||
| chr21:41355848 | A | G | 18 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0001g0119 others(15): Show |
19 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.619-1260A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355848 | |||||||
| chr21:41355891 | A | G | 1 | a0001c0001t0002g0033 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.619-1217A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355891 | |||||||
| chr21:41356034 | A | AATAC | 8 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-1068_619-1065d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356034 | ||||||
| chr21:41356036 | TACATACA others(3): Show |
T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0119 a0001c0001t0001g0202 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-1068_619-1059d others(12): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356036 | ||||||
| chr21:41356036 | TACATACA others(7): Show |
T | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.619-1068_619-1055d others(16): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356036 | ||||||
| chr21:41356040 | T | TAC | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(31): Show |
43 | HG00280.hp1 HG00673.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.619-1024_619-1023d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | ||||||
| chr21:41356040 | T | TACAC | 8 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0089 others(5): Show |
10 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.619-1026_619-1023d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | ||||||
| chr21:41356040 | T | TACACAC | 6 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0026 others(3): Show |
9 | HG00642.hp1 HG01257.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.619-1028_619-1023d others(8): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | ||||||
| chr21:41356040 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0218 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.619-1034_619-1023d others(14): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | ||||||
| chr21:41356040 | TAC | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0031 others(20): Show |
25 | HG00558.hp2 HG00642.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.619-1024_619-1023d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | ||||||
| chr21:41356040 | TACAC | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0116 others(2): Show |
6 | HG01167.hp2 HG01361.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-1026_619-1023d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | ||||||
| chr21:41356040 | TACACAC | T | 12 | a0001c0001t0001g0032 a0001c0001t0001g0110 a0001c0001t0001g0125 others(9): Show |
12 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.619-1028_619-1023d others(8): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | ||||||
| chr21:41356040 | TACACACA others(1): Show |
T | 27 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0002g0106 others(24): Show |
35 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.619-1030_619-1023d others(10): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | ||||||
| chr21:41356044 | C | T | 12 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0025 others(9): Show |
16 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.619-1064C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356044 | |||||||
| chr21:41356048 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0033 |
4 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-1060C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356048 | |||||||
| chr21:41356074 | CACACACA others(5): Show |
C | 1 | a0001c0004t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.619-1032_619-1021d others(14): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356074 | ||||||
| chr21:41356076 | CACACACA others(3): Show |
C | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0033 |
4 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-1030_619-1021d others(12): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356076 | ||||||
| chr21:41356082 | CACAT | C | 6 | a0001c0001t0002g0025 a0001c0001t0002g0140 a0002c0003t0002g0014 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-1024_619-1021d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356082 | ||||||
| chr21:41356084 | CAT | C | 10 | a0001c0001t0001g0166 a0001c0001t0002g0010 a0001c0001t0002g0025 others(7): Show |
11 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.619-1022_619-1021d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356084 | ||||||
| chr21:41356086 | T | C | 24 | a0001c0001t0001g0066 a0001c0001t0001g0149 a0001c0001t0001g0177 others(21): Show |
25 | HG00280.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-1022T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356086 | |||||||
| chr21:41356506 | T | C | 45 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0032 others(42): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.619-602T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356506 | |||||||
| chr21:41356534 | T | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0026 others(82): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.619-574T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356534 | |||||||
| chr21:41356589 | C | A | 11 | a0001c0001t0002g0009 a0001c0001t0002g0077 a0001c0001t0002g0106 others(8): Show |
12 | HG02080.hp2 HG02132.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.619-519C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356589 | |||||||
| chr21:41356620 | G | A | 1 | a0001c0004t0002g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.619-488G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356620 | |||||||
| chr21:41356639 | C | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
13 | HG01255.hp2 HG01257.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.619-469C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356639 | |||||||
| chr21:41356645 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.619-463T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356645 | |||||||
| chr21:41356675 | C | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0196 |
3 | HG02723.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.619-433C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356675 | |||||||
| chr21:41356922 | A | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.619-186A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356922 | |||||||
| chr21:41356974 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.619-134G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356974 | |||||||
| chr21:41357039 | A | C | 1 | a0001c0001t0002g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.619-69A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41357039 |