Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 646851 |
| ensemblid | ENSG00000184949.18 |
| hgncid | 44197 |
| symbol | FAM227A |
| name | family with sequence similarity 227 member A |
| refseq_nuc | NM_001013647.2 |
| refseq_prot | NP_001013669.1 |
| ensembl_nuc | ENST00000535113.7 |
| ensembl_prot | ENSP00000445093.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 38578118 |
| end | 38656392 |
| strand | - |
| ver | v1.2 |
| region | chr22:38578118-38656392 |
| region5000 | chr22:38573118-38661392 |
| regionname0 | FAM227A_chr22_38578118_38656392 |
| regionname5000 | FAM227A_chr22_38573118_38661392 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 570 | 284 | 73 | 52 | 118 | 14 | 25 | 88 | FAM227A_chr22_38573118_38661392 | FAM227A | MNHFR others(565): Show |
chr22 | 38573118 | 38661392 |
| a0002 | 0/0 | 570 | 43 | 9 | 0 | 33 | 0 | 1 | 29 | FAM227A_chr22_38573118_38661392 | FAM227A | MNHFR others(565): Show |
chr22 | 38573118 | 38661392 |
| a0003 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | MNHFR others(565): Show |
chr22 | 38573118 | 38661392 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1710 | 277 | 66 | 52 | 118 | 14 | 25 | FAM227A_chr22_38573118_38661392 | FAM227A | ATGAA others(1705): Show |
chr22 | 38573118 | 38661392 | ||
| a0001c0003 | 0/0 | 1710 | 5 | 5 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | ATGAA others(1705): Show |
chr22 | 38573118 | 38661392 | ||
| a0001c0006 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | ATGAA others(1705): Show |
chr22 | 38573118 | 38661392 | ||
| a0001c0007 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | ATGAA others(1705): Show |
chr22 | 38573118 | 38661392 | ||
| a0002c0002 | 0/0 | 1710 | 42 | 8 | 0 | 33 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | ATGAA others(1705): Show |
chr22 | 38573118 | 38661392 | ||
| a0002c0004 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | ATGAA others(1705): Show |
chr22 | 38573118 | 38661392 | ||
| a0003c0005 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | ATGAA others(1705): Show |
chr22 | 38573118 | 38661392 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 10087 | 87 | 8 | 16 | 45 | 8 | 9 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0002 | 0/0 | 10092 | 39 | 0 | 4 | 31 | 0 | 4 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10087): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0003 | 0/0 | 10093 | 38 | 7 | 2 | 23 | 2 | 4 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0005 | 0/0 | 10088 | 12 | 2 | 7 | 0 | 1 | 2 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0006 | 0/0 | 10088 | 10 | 9 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0007 | 0/0 | 10088 | 10 | 6 | 1 | 2 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0008 | 0/0 | 10088 | 8 | 6 | 2 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0009 | 0/0 | 10093 | 9 | 9 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0010 | 0/0 | 10088 | 7 | 0 | 2 | 3 | 1 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0013 | 0/0 | 10088 | 5 | 0 | 4 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0015 | 0/0 | 10093 | 4 | 4 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0016 | 0/1 | 10093 | 4 | 1 | 1 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0017 | 0/0 | 10089 | 3 | 3 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10084): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0018 | 0/0 | 10087 | 3 | 0 | 3 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0020 | 0/0 | 10094 | 3 | 1 | 1 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10089): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0021 | 0/0 | 10094 | 3 | 0 | 0 | 2 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10089): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0022 | 0/0 | 10089 | 2 | 2 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10084): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0023 | 0/0 | 10087 | 2 | 0 | 2 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0026 | 0/0 | 10093 | 2 | 1 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0027 | 0/0 | 10087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0028 | 0/0 | 10087 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0029 | 0/0 | 10088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0030 | 0/0 | 10087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0032 | 0/0 | 10088 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0033 | 0/0 | 10088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0034 | 0/0 | 10089 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10084): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0035 | 0/0 | 10088 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0036 | 0/0 | 10088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0037 | 0/0 | 10088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0038 | 0/0 | 10088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0039 | 0/0 | 10087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0040 | 0/0 | 10087 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0041 | 0/0 | 10087 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0042 | 0/0 | 10087 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0043 | 0/0 | 10087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10082): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0044 | 0/0 | 10088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0049 | 0/0 | 10092 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10087): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0050 | 0/0 | 10093 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0051 | 0/0 | 10093 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0052 | 0/0 | 10093 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0053 | 0/0 | 10093 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0054 | 0/0 | 10093 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0055 | 0/0 | 10092 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10087): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0056 | 0/0 | 10093 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0001t0057 | 0/0 | 10093 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0001c0003t0012 | 0/0 | 10090 | 4 | 4 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10085): Show |
chr22 | 38573118 | 38661392 |
| a0001c0003t0031 | 0/0 | 10091 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10086): Show |
chr22 | 38573118 | 38661392 |
| a0001c0006t0008 | 0/0 | 10088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10083): Show |
chr22 | 38573118 | 38661392 |
| a0001c0007t0012 | 0/0 | 10090 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10085): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0004 | 0/0 | 10094 | 20 | 0 | 0 | 19 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10089): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0011 | 0/0 | 10094 | 7 | 7 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10089): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0014 | 0/0 | 10093 | 5 | 0 | 0 | 5 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10088): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0019 | 0/0 | 10094 | 3 | 0 | 0 | 3 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10089): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0024 | 0/0 | 10095 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10090): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0025 | 0/0 | 10091 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10086): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0046 | 0/0 | 10094 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10089): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0047 | 0/0 | 10094 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10089): Show |
chr22 | 38573118 | 38661392 |
| a0002c0002t0048 | 0/0 | 10091 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10086): Show |
chr22 | 38573118 | 38661392 |
| a0002c0004t0045 | 0/0 | 10095 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10090): Show |
chr22 | 38573118 | 38661392 |
| a0003c0005t0004 | 0/0 | 10094 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | GACAA others(10089): Show |
chr22 | 38573118 | 38661392 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0010g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0010g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0013g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0013g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0013g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0013g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0013g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0015g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0015g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0015g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0015g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0016g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0016g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0016g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0016g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0017g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0018g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0018g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0018g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0020g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0020g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0020g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0021g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0021g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0021g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0022g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0022g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0023g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0023g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0026g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0026g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0027g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0028g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0029g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0030g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0032g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0033g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0034g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0035g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0036g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0037g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0038g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0039g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0040g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0041g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0042g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0043g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0044g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0049g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0050g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0051g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0052g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0053g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0054g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0055g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0056g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0001t0057g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0003t0012g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0003t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0003t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0003t0031g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0006t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0001c0007t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0011g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0011g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0014g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0014g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0019g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0019g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0019g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0024g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0024g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0025g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0025g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0046g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0047g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0002t0048g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0002c0004t0045g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| a0003c0005t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0013 | g0166 | EUR | GBR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00280 | hp1 | a0001 | c0001 | t0016 | g0279 | EUR | FIN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0245 | EUR | FIN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00408 | hp2 | a0002 | c0002 | t0024 | g0192 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00423 | hp2 | a0001 | c0001 | t0026 | g0261 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00642 | hp1 | a0001 | c0001 | t0050 | g0273 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00673 | hp2 | a0002 | c0002 | t0004 | g0198 | EAS | CHS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0142 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00735 | hp2 | a0001 | c0001 | t0013 | g0164 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00738 | hp2 | a0001 | c0001 | t0018 | g0136 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00741 | hp1 | a0001 | c0001 | t0010 | g0103 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01069 | hp1 | a0001 | c0001 | t0023 | g0102 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01069 | hp2 | a0001 | c0001 | t0013 | g0165 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01071 | hp2 | a0001 | c0001 | t0023 | g0101 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01074 | hp2 | a0001 | c0001 | t0018 | g0137 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0095 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0133 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01243 | hp1 | a0001 | c0001 | t0040 | g0053 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0040 | AMR | PUR | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0162 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01256 | hp2 | a0001 | c0001 | t0042 | g0074 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01258 | hp1 | a0001 | c0001 | t0013 | g0163 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01261 | hp2 | a0001 | c0001 | t0035 | g0138 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01346 | hp1 | a0001 | c0001 | t0020 | g0253 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01433 | hp1 | a0001 | c0001 | t0016 | g0284 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0044 | AMR | CLM | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0038 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01891 | hp1 | a0001 | c0001 | t0057 | g0307 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01891 | hp2 | a0002 | c0002 | t0011 | g0205 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0143 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01934 | hp1 | a0001 | c0001 | t0018 | g0139 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01981 | hp2 | a0001 | c0001 | t0041 | g0146 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02015 | hp2 | a0002 | c0002 | t0004 | g0190 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02027 | hp1 | a0001 | c0001 | t0021 | g0244 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02027 | hp2 | a0001 | c0001 | t0037 | g0154 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0034 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0290 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02056 | hp2 | a0001 | c0001 | t0043 | g0144 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02083 | hp2 | a0002 | c0002 | t0004 | g0196 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02129 | hp1 | a0001 | c0001 | t0010 | g0149 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02135 | hp2 | a0001 | c0001 | t0056 | g0269 | EAS | KHV | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02145 | hp1 | a0002 | c0002 | t0011 | g0172 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02155 | hp1 | a0001 | c0001 | t0049 | g0268 | EAS | CDX | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CDX | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02258 | hp1 | a0001 | c0001 | t0044 | g0128 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02258 | hp2 | a0001 | c0003 | t0012 | g0005 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02280 | hp1 | a0001 | c0001 | t0017 | g0167 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02300 | hp2 | a0001 | c0001 | t0028 | g0134 | AMR | PEL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02451 | hp2 | a0001 | c0001 | t0020 | g0254 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0305 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02698 | hp2 | a0001 | c0001 | t0020 | g0255 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02717 | hp1 | a0001 | c0007 | t0012 | g0158 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02717 | hp2 | a0002 | c0004 | t0045 | g0207 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02886 | hp1 | a0001 | c0001 | t0017 | g0168 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0319 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0214 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02896 | hp2 | a0002 | c0002 | t0011 | g0174 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0215 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0306 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02922 | hp2 | a0001 | c0001 | t0022 | g0141 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0065 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0169 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02976 | hp2 | a0001 | c0001 | t0022 | g0033 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0308 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03041 | hp2 | a0001 | c0001 | t0034 | g0130 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03098 | hp1 | a0001 | c0003 | t0031 | g0157 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03098 | hp2 | a0001 | c0001 | t0026 | g0298 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0310 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03139 | hp2 | a0002 | c0002 | t0011 | g0200 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03195 | hp1 | a0001 | c0001 | t0055 | g0274 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03195 | hp2 | a0001 | c0001 | t0029 | g0039 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03209 | hp2 | a0001 | c0001 | t0033 | g0161 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0093 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03225 | hp2 | a0001 | c0001 | t0015 | g0292 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03453 | hp1 | a0002 | c0002 | t0011 | g0199 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0309 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03516 | hp2 | a0002 | c0002 | t0011 | g0202 | AFR | ESN | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03540 | hp2 | a0001 | c0003 | t0012 | g0159 | AFR | GWD | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0302 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03669 | hp1 | a0001 | c0001 | t0032 | g0156 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | STU | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | STU | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0097 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03834 | hp2 | a0001 | c0001 | t0051 | g0249 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03927 | hp1 | a0001 | c0001 | t0021 | g0241 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0080 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | STU | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0213 | SAS | STU | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG04184 | hp1 | a0002 | c0002 | t0004 | g0211 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18522 | hp1 | a0001 | c0006 | t0008 | g0035 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | CHB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CHB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0288 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18939 | hp2 | a0001 | c0001 | t0030 | g0155 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18943 | hp1 | a0002 | c0002 | t0004 | g0201 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18944 | hp1 | a0002 | c0002 | t0019 | g0173 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18948 | hp2 | a0001 | c0001 | t0027 | g0075 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18952 | hp2 | a0002 | c0002 | t0014 | g0006 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18960 | hp1 | a0002 | c0002 | t0024 | g0191 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18960 | hp2 | a0001 | c0001 | t0053 | g0239 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18962 | hp1 | a0002 | c0002 | t0004 | g0180 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18963 | hp2 | a0001 | c0001 | t0010 | g0062 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18964 | hp2 | a0002 | c0002 | t0019 | g0185 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18974 | hp2 | a0002 | c0002 | t0004 | g0208 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18979 | hp2 | a0002 | c0002 | t0004 | g0170 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18980 | hp1 | a0002 | c0002 | t0004 | g0182 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18982 | hp1 | a0003 | c0005 | t0004 | g0178 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18983 | hp2 | a0002 | c0002 | t0046 | g0189 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0186 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18990 | hp1 | a0002 | c0002 | t0004 | g0209 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18991 | hp1 | a0002 | c0002 | t0004 | g0177 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0183 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18994 | hp2 | a0002 | c0002 | t0025 | g0194 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18995 | hp1 | a0001 | c0001 | t0036 | g0131 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0151 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19011 | hp1 | a0001 | c0001 | t0039 | g0012 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19012 | hp1 | a0002 | c0002 | t0004 | g0184 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0315 | AFR | LWK | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19057 | hp1 | a0002 | c0002 | t0004 | g0181 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19060 | hp2 | a0002 | c0002 | t0014 | g0187 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19062 | hp1 | a0001 | c0001 | t0052 | g0318 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19064 | hp1 | a0002 | c0002 | t0025 | g0193 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19064 | hp2 | a0001 | c0001 | t0038 | g0081 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19065 | hp2 | a0002 | c0002 | t0004 | g0197 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19067 | hp1 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19068 | hp2 | a0002 | c0002 | t0004 | g0210 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19076 | hp2 | a0002 | c0002 | t0014 | g0206 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19079 | hp1 | a0002 | c0002 | t0004 | g0171 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19080 | hp1 | a0002 | c0002 | t0004 | g0179 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19082 | hp2 | a0001 | c0001 | t0010 | g0060 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19084 | hp2 | a0002 | c0002 | t0047 | g0175 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19085 | hp1 | a0002 | c0002 | t0019 | g0195 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19086 | hp1 | a0002 | c0002 | t0014 | g0176 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19086 | hp2 | a0001 | c0001 | t0021 | g0219 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19087 | hp2 | a0002 | c0002 | t0004 | g0188 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19088 | hp1 | a0002 | c0002 | t0014 | g0006 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA19240 | hp2 | a0002 | c0002 | t0048 | g0204 | AFR | YRI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ASW | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA20129 | hp2 | a0002 | c0002 | t0011 | g0203 | AFR | ASW | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0096 | EUR | TSI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0312 | EUR | TSI | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | GIH | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0032 | SAS | GIH | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02109 | hp2 | a0001 | c0003 | t0012 | g0160 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0291 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | ACB | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03471 | hp1 | a0001 | c0001 | t0054 | g0300 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | MSL | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | USA | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| HG06807 | hp2 | a0001 | c0003 | t0012 | g0005 | AFR | USA | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | USA | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | LWK | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0016 | g0293 | REF | REF | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0099 | REF | REF | FAM227A_chr22_38573118_38661392 | FAM227A | chr22 | 38573118 | 38661392 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:38597330 | A | T | 1 | a0003 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1406T>A | p.Val469Asp | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/17 | 1773/10087 | 1406/1713 | 469/570 | chr22 | 38597330 | |||
| chr22:38638781 | C | T | 2 | a0002 a0003 |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
missense_variant | MODERATE | c.337G>A | p.Glu113Lys | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/17 | 704/10087 | 337/1713 | 113/570 | chr22 | 38638781 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:38599826 | G | A | 1 | a0001c0006 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1317C>T | p.Ala439Ala | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/17 | 1684/10087 | 1317/1713 | 439/570 | chr22 | 38599826 | |||
| chr22:38599874 | G | A | 1 | a0001c0007 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1269C>T | p.Asn423Asn | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/17 | 1636/10087 | 1269/1713 | 423/570 | chr22 | 38599874 | |||
| chr22:38623236 | C | T | 1 | a0002c0004 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.894G>A | p.Ser298Ser | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/17 | 1261/10087 | 894/1713 | 298/570 | chr22 | 38623236 | |||
| chr22:38638776 | G | A | 1 | a0001c0003 | 5 | HG02109.hp2 HG02258.hp2 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.342C>T | p.Leu114Leu | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/17 | 709/10087 | 342/1713 | 114/570 | chr22 | 38638776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:38578149 | C | A | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(26): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*7976G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7976 | chr22 | 38578149 | ||||||
| chr22:38578504 | T | C | 1 | a0001c0001t0023 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7621A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7621 | chr22 | 38578504 | ||||||
| chr22:38578564 | T | C | 8 | a0002c0002t0004 a0002c0002t0014 a0002c0002t0019 others(5): Show |
35 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*7561A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7561 | chr22 | 38578564 | ||||||
| chr22:38578675 | C | T | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(32): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*7450G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7450 | chr22 | 38578675 | ||||||
| chr22:38578755 | C | T | 1 | a0001c0001t0032 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7370G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7370 | chr22 | 38578755 | ||||||
| chr22:38578756 | G | A | 1 | a0002c0002t0046 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7369C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7369 | chr22 | 38578756 | ||||||
| chr22:38578778 | A | G | 1 | a0001c0001t0038 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7347T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7347 | chr22 | 38578778 | ||||||
| chr22:38578794 | C | G | 1 | a0001c0001t0041 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7331G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7331 | chr22 | 38578794 | ||||||
| chr22:38578848 | A | G | 1 | a0001c0001t0040 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7277T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7277 | chr22 | 38578848 | ||||||
| chr22:38579098 | C | T | 3 | a0001c0001t0018 a0001c0001t0028 a0001c0001t0035 |
5 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7027G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 7027 | chr22 | 38579098 | ||||||
| chr22:38579441 | A | G | 1 | a0001c0001t0037 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6684T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6684 | chr22 | 38579441 | ||||||
| chr22:38579506 | G | A | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(40): Show |
206 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*6619C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6619 | chr22 | 38579506 | ||||||
| chr22:38579540 | G | A | 1 | a0002c0002t0047 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6585C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6585 | chr22 | 38579540 | ||||||
| chr22:38580039 | G | A | 1 | a0001c0001t0042 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6086C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6086 | chr22 | 38580039 | ||||||
| chr22:38580096 | T | TTTTA | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(26): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6028_*6029insTAAA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 6028 | chr22 | 38580096 | ||||||
| chr22:38580130 | G | A | 3 | a0001c0001t0005 a0001c0001t0034 a0001c0001t0036 |
14 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5995C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5995 | chr22 | 38580130 | ||||||
| chr22:38580345 | T | C | 1 | a0001c0001t0053 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5780A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5780 | chr22 | 38580345 | ||||||
| chr22:38580508 | CTGTT | C | 1 | a0001c0001t0017 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5613_*5616delAACA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5613 | chr22 | 38580508 | ||||||
| chr22:38580814 | C | G | 1 | a0002c0002t0019 | 3 | NA18944.hp1 NA18964.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5311G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5311 | chr22 | 38580814 | ||||||
| chr22:38580954 | T | C | 1 | a0001c0001t0054 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5171A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5171 | chr22 | 38580954 | ||||||
| chr22:38581036 | C | T | 1 | a0001c0001t0039 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5089G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5089 | chr22 | 38581036 | ||||||
| chr22:38581068 | C | T | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0034 others(1): Show |
24 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5057G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5057 | chr22 | 38581068 | ||||||
| chr22:38581093 | T | A | 1 | a0001c0001t0043 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5032A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 5032 | chr22 | 38581093 | ||||||
| chr22:38581742 | G | GT | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(19): Show |
126 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*4382dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4382 | chr22 | 38581742 | ||||||
| chr22:38581742 | G | GTT | 5 | a0001c0001t0021 a0001c0001t0026 a0001c0001t0056 others(2): Show |
12 | HG00423.hp2 HG02027.hp1 HG02135.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4381_*4382dupAA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4382 | chr22 | 38581742 | ||||||
| chr22:38581742 | G | GTTT | 8 | a0002c0002t0004 a0002c0002t0011 a0002c0002t0019 others(5): Show |
36 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4380_*4382dupAAA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4382 | chr22 | 38581742 | ||||||
| chr22:38581845 | C | T | 1 | a0001c0001t0017 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4280G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4280 | chr22 | 38581845 | ||||||
| chr22:38581846 | G | A | 1 | a0001c0001t0044 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4279C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4279 | chr22 | 38581846 | ||||||
| chr22:38581885 | G | C | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0016 others(11): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4240C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4240 | chr22 | 38581885 | ||||||
| chr22:38582072 | G | C | 2 | a0001c0001t0009 a0001c0001t0057 |
10 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4053C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 4053 | chr22 | 38582072 | ||||||
| chr22:38582164 | A | G | 6 | a0001c0001t0013 a0001c0001t0032 a0001c0001t0033 others(3): Show |
13 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3961T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3961 | chr22 | 38582164 | ||||||
| chr22:38582257 | G | T | 1 | a0001c0001t0052 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3868C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3868 | chr22 | 38582257 | ||||||
| chr22:38582504 | G | A | 1 | a0001c0001t0036 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3621C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3621 | chr22 | 38582504 | ||||||
| chr22:38582861 | C | T | 1 | a0001c0001t0006 | 10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3264G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3264 | chr22 | 38582861 | ||||||
| chr22:38582969 | G | A | 1 | a0001c0001t0056 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3156C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3156 | chr22 | 38582969 | ||||||
| chr22:38583013 | C | G | 1 | a0001c0001t0051 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3112G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3112 | chr22 | 38583013 | ||||||
| chr22:38583115 | C | T | 1 | a0001c0001t0013 | 5 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3010G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 3010 | chr22 | 38583115 | ||||||
| chr22:38583171 | C | CT | 26 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(23): Show |
118 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2953dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2953 | chr22 | 38583171 | ||||||
| chr22:38583171 | C | CTT | 5 | a0001c0001t0020 a0001c0001t0022 a0001c0003t0012 others(2): Show |
11 | HG01346.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2952_*2953dupAA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2953 | chr22 | 38583171 | ||||||
| chr22:38583204 | C | T | 1 | a0001c0001t0030 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2921G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2921 | chr22 | 38583204 | ||||||
| chr22:38583230 | T | C | 6 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0026 others(3): Show |
47 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2895A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2895 | chr22 | 38583230 | ||||||
| chr22:38583809 | C | T | 1 | a0001c0001t0029 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2316G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 2316 | chr22 | 38583809 | ||||||
| chr22:38584407 | C | G | 1 | a0001c0001t0028 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1718G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1718 | chr22 | 38584407 | ||||||
| chr22:38584466 | C | T | 1 | a0001c0001t0017 | 3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1659G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1659 | chr22 | 38584466 | ||||||
| chr22:38584797 | A | T | 2 | a0001c0001t0001 a0001c0001t0002 |
7 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1328T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1328 | chr22 | 38584797 | ||||||
| chr22:38585005 | C | T | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0015 others(12): Show |
100 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1120G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1120 | chr22 | 38585005 | ||||||
| chr22:38585037 | T | C | 1 | a0001c0001t0050 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1088A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1088 | chr22 | 38585037 | ||||||
| chr22:38585044 | T | C | 1 | a0001c0001t0050 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1081A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1081 | chr22 | 38585044 | ||||||
| chr22:38585047 | A | G | 1 | a0001c0001t0050 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1078T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1078 | chr22 | 38585047 | ||||||
| chr22:38585110 | T | G | 1 | a0001c0001t0057 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 1015 | chr22 | 38585110 | ||||||
| chr22:38585371 | C | T | 1 | a0001c0001t0027 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 754 | chr22 | 38585371 | ||||||
| chr22:38585720 | C | T | 1 | a0001c0001t0049 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 405 | chr22 | 38585720 | ||||||
| chr22:38586026 | C | A | 11 | a0002c0002t0004 a0002c0002t0011 a0002c0002t0014 others(8): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*99G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 17/17 | 99 | chr22 | 38586026 | ||||||
| chr22:38656150 | G | A | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(14): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-125C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/17 | chr22 | 38656150 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:38586316 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1639-117A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586316 | |||||||
| chr22:38586353 | C | G | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1639-154G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586353 | |||||||
| chr22:38586436 | G | A | 1 | a0001c0001t0036g0131 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1639-237C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586436 | |||||||
| chr22:38586437 | T | A | 99 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(96): Show |
100 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1639-238A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586437 | |||||||
| chr22:38586654 | G | A | 8 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639-455C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586654 | |||||||
| chr22:38586738 | A | G | 191 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(188): Show |
195 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1639-539T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586738 | |||||||
| chr22:38586839 | G | GT | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639-641dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586839 | |||||||
| chr22:38586913 | C | T | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639-714G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586913 | |||||||
| chr22:38586914 | G | A | 8 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639-715C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38586914 | |||||||
| chr22:38587089 | AAC | A | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1639-892_1639-891d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587089 | |||||||
| chr22:38587174 | A | G | 7 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0306 others(4): Show |
7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1639-975T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587174 | |||||||
| chr22:38587553 | A | G | 4 | a0001c0001t0008g0040 a0001c0001t0008g0042 a0001c0001t0008g0043 others(1): Show |
4 | HG01243.hp2 HG01433.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639-1354T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587553 | |||||||
| chr22:38587696 | T | C | 1 | a0001c0001t0003g0230 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1639-1497A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587696 | |||||||
| chr22:38587704 | G | GT | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1639-1506dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38587704 | |||||||
| chr22:38588475 | C | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639-2276G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588475 | |||||||
| chr22:38588480 | G | A | 3 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0026 |
4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639-2281C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588480 | |||||||
| chr22:38588499 | G | C | 1 | a0001c0001t0039g0012 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1639-2300C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588499 | |||||||
| chr22:38588615 | T | TA | 50 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0001t0001g0058 others(47): Show |
50 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1639-2417dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588615 | |||||||
| chr22:38588615 | TA | T | 6 | a0001c0001t0001g0112 a0001c0001t0001g0124 a0001c0001t0001g0145 others(3): Show |
6 | HG00323.hp1 HG01346.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639-2417delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588615 | |||||||
| chr22:38588764 | C | CA | 6 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0152 others(3): Show |
6 | HG00140.hp1 HG00438.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639-2566dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588764 | |||||||
| chr22:38588764 | CA | C | 148 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(145): Show |
150 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1639-2566delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588764 | |||||||
| chr22:38588780 | T | A | 23 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(20): Show |
24 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1639-2581A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588780 | |||||||
| chr22:38588841 | T | C | 7 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0306 others(4): Show |
7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1638+2594A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588841 | |||||||
| chr22:38588945 | A | G | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1638+2490T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38588945 | |||||||
| chr22:38589060 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1638+2375A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589060 | |||||||
| chr22:38589254 | G | C | 1 | a0002c0002t0004g0181 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1638+2181C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589254 | |||||||
| chr22:38589309 | TGGACTTC | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1638+2119_1638+212 others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589309 | |||||||
| chr22:38589352 | T | C | 1 | a0001c0001t0003g0312 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1638+2083A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589352 | |||||||
| chr22:38589698 | T | C | 1 | a0002c0004t0045g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1638+1737A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589698 | |||||||
| chr22:38589813 | A | C | 95 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1638+1622T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589813 | |||||||
| chr22:38589944 | T | C | 1 | a0003c0005t0004g0178 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1638+1491A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38589944 | |||||||
| chr22:38590086 | C | CACAAA | 139 | a0001c0001t0001g0052 a0001c0001t0002g0218 a0001c0001t0002g0225 others(136): Show |
141 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1638+1344_1638+134 others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | |||||||
| chr22:38590086 | C | CACAAAAC others(3): Show |
17 | a0001c0001t0002g0217 a0001c0001t0002g0226 a0001c0001t0002g0227 others(14): Show |
17 | HG02135.hp2 HG02165.hp2 HG02896.hp1 others(14): Show |
intron_variant | MODIFIER | c.1638+1339_1638+134 others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | |||||||
| chr22:38590086 | C | CACAAAAC others(8): Show |
1 | a0001c0001t0002g0283 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1638+1334_1638+134 others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | |||||||
| chr22:38590086 | C | CACAAAAC others(13): Show |
2 | a0001c0001t0017g0168 a0001c0001t0017g0169 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1638+1329_1638+134 others(24): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | |||||||
| chr22:38590086 | CACAAAAC others(3): Show |
C | 1 | a0001c0001t0010g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1638+1339_1638+134 others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590086 | |||||||
| chr22:38590243 | G | A | 158 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(155): Show |
160 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1638+1192C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590243 | |||||||
| chr22:38590279 | CA | C | 102 | a0001c0001t0001g0013 a0001c0001t0001g0124 a0001c0001t0002g0217 others(99): Show |
103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1638+1155delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590279 | |||||||
| chr22:38590279 | CAA | C | 8 | a0001c0001t0002g0276 a0001c0001t0002g0283 a0001c0001t0002g0303 others(5): Show |
8 | HG02895.hp1 HG02922.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638+1154_1638+115 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38590279 | |||||||
| chr22:38591290 | C | G | 1 | a0001c0001t0009g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1638+145G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38591290 | |||||||
| chr22:38591407 | T | G | 3 | a0001c0001t0002g0262 a0001c0001t0003g0236 a0001c0001t0003g0250 |
3 | HG00558.hp1 NA18975.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1638+28A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 16/16 | chr22 | 38591407 | |||||||
| chr22:38591631 | C | T | 1 | a0001c0001t0005g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1533-91G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38591631 | |||||||
| chr22:38591722 | T | C | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1533-182A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38591722 | |||||||
| chr22:38591747 | C | T | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1533-207G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38591747 | |||||||
| chr22:38591874 | G | A | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1533-334C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38591874 | |||||||
| chr22:38592066 | A | C | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-526T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592066 | |||||||
| chr22:38592110 | A | G | 169 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(166): Show |
171 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1533-570T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592110 | |||||||
| chr22:38592339 | C | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(314): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1533-799G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592339 | |||||||
| chr22:38592380 | C | T | 1 | a0002c0002t0004g0184 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1533-840G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592380 | |||||||
| chr22:38592472 | G | T | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-932C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592472 | |||||||
| chr22:38592514 | G | T | 1 | a0001c0001t0017g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1533-974C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592514 | |||||||
| chr22:38592605 | TTAAATCA others(11): Show |
T | 2 | a0001c0001t0022g0033 a0001c0001t0022g0141 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1533-1083_1533-106 others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592605 | |||||||
| chr22:38592622 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1533-1082C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38592622 | |||||||
| chr22:38593002 | C | G | 99 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(96): Show |
100 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1533-1462G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593002 | |||||||
| chr22:38593361 | C | T | 1 | a0002c0002t0011g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1533-1821G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593361 | |||||||
| chr22:38593379 | C | T | 2 | a0002c0002t0004g0177 a0002c0002t0014g0206 |
2 | NA18991.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1533-1839G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593379 | |||||||
| chr22:38593499 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0072 |
2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1533-1959G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593499 | |||||||
| chr22:38593600 | A | G | 2 | a0001c0001t0022g0033 a0001c0001t0022g0141 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1533-2060T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593600 | |||||||
| chr22:38593622 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01071.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1533-2082G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593622 | |||||||
| chr22:38593641 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1533-2101A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593641 | |||||||
| chr22:38593808 | A | G | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1533-2268T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593808 | |||||||
| chr22:38593857 | A | G | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1533-2317T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38593857 | |||||||
| chr22:38594657 | G | A | 166 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(163): Show |
169 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1532+2547C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38594657 | |||||||
| chr22:38594677 | T | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0264 a0001c0001t0002g0270 |
3 | NA18939.hp1 NA18975.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1532+2527A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38594677 | |||||||
| chr22:38594690 | C | T | 3 | a0001c0001t0020g0253 a0001c0001t0020g0254 a0001c0001t0020g0255 |
3 | HG01346.hp1 HG02451.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1532+2514G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38594690 | |||||||
| chr22:38594733 | C | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1532+2471G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38594733 | |||||||
| chr22:38595350 | C | T | 23 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(20): Show |
24 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1532+1854G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595350 | |||||||
| chr22:38595388 | G | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1532+1816C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595388 | |||||||
| chr22:38595492 | G | A | 7 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(4): Show |
7 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1532+1712C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595492 | |||||||
| chr22:38595710 | C | T | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1532+1494G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595710 | |||||||
| chr22:38595746 | T | C | 1 | a0002c0002t0025g0194 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1532+1458A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595746 | |||||||
| chr22:38595871 | T | C | 4 | a0001c0001t0003g0296 a0001c0001t0003g0301 a0001c0001t0003g0320 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1532+1333A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595871 | |||||||
| chr22:38595885 | A | G | 1 | a0001c0001t0027g0075 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1532+1319T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595885 | |||||||
| chr22:38595896 | A | T | 1 | a0001c0001t0040g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1532+1308T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595896 | |||||||
| chr22:38595970 | AG | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(288): Show |
297 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1532+1233delC | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595970 | |||||||
| chr22:38595972 | G | C | 5 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0306 others(2): Show |
5 | HG00642.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1532+1232C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595972 | |||||||
| chr22:38595973 | G | C | 104 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(101): Show |
105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1532+1231C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38595973 | |||||||
| chr22:38596178 | G | A | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1532+1026C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596178 | |||||||
| chr22:38596226 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1532+978G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596226 | |||||||
| chr22:38596368 | G | A | 1 | a0001c0001t0002g0285 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1532+836C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596368 | |||||||
| chr22:38596444 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1532+760C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596444 | |||||||
| chr22:38596962 | G | A | 2 | a0001c0001t0017g0168 a0001c0001t0017g0169 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1532+242C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 15/16 | chr22 | 38596962 | |||||||
| chr22:38597365 | C | T | 95 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1380-9G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597365 | |||||||
| chr22:38597397 | G | A | 1 | a0001c0001t0055g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1380-41C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597397 | |||||||
| chr22:38597462 | A | G | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1380-106T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597462 | |||||||
| chr22:38597471 | A | G | 12 | a0002c0002t0004g0177 a0002c0002t0004g0190 a0002c0002t0004g0196 others(9): Show |
12 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380-115T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597471 | |||||||
| chr22:38597512 | G | A | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1380-156C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597512 | |||||||
| chr22:38597942 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1380-586G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597942 | |||||||
| chr22:38597958 | G | A | 95 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1380-602C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597958 | |||||||
| chr22:38597971 | A | C | 95 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1380-615T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38597971 | |||||||
| chr22:38598042 | C | CAAAAAA | 68 | a0001c0001t0002g0218 a0001c0001t0002g0225 a0001c0001t0002g0229 others(65): Show |
69 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1380-692_1380-687d others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | |||||||
| chr22:38598042 | C | CAAAAAAA | 34 | a0001c0001t0002g0217 a0001c0001t0002g0226 a0001c0001t0002g0228 others(31): Show |
34 | HG01175.hp1 HG01891.hp1 HG02135.hp2 others(31): Show |
intron_variant | MODIFIER | c.1380-693_1380-687d others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | |||||||
| chr22:38598042 | C | CAAAAAAA others(1): Show |
42 | a0001c0001t0002g0227 a0001c0001t0002g0283 a0001c0001t0009g0302 others(39): Show |
43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.1380-694_1380-687d others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | |||||||
| chr22:38598042 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0015g0290 a0002c0002t0004g0210 a0002c0002t0011g0172 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1380-695_1380-687d others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | |||||||
| chr22:38598042 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1380-696_1380-687d others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598042 | |||||||
| chr22:38598135 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0076 others(1): Show |
4 | NA18959.hp2 NA18965.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380-779C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598135 | |||||||
| chr22:38598572 | C | T | 167 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1379+1192G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598572 | |||||||
| chr22:38598761 | C | T | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+1003G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598761 | |||||||
| chr22:38598824 | A | T | 1 | a0001c0001t0007g0065 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1379+940T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598824 | |||||||
| chr22:38598851 | T | C | 5 | a0001c0001t0002g0217 a0001c0001t0002g0226 a0001c0001t0002g0227 others(2): Show |
5 | NA18980.hp2 NA18983.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379+913A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598851 | |||||||
| chr22:38598957 | C | CT | 74 | a0001c0001t0001g0090 a0001c0001t0002g0217 a0001c0001t0002g0218 others(71): Show |
75 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1379+806dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598957 | |||||||
| chr22:38598957 | CT | C | 6 | a0001c0001t0003g0248 a0001c0001t0013g0162 a0001c0001t0013g0163 others(3): Show |
6 | HG00558.hp2 HG00735.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1379+806delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38598957 | |||||||
| chr22:38599047 | C | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1379+717G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599047 | |||||||
| chr22:38599121 | G | T | 2 | a0001c0001t0003g0236 a0001c0001t0003g0250 |
2 | HG00558.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1379+643C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599121 | |||||||
| chr22:38599214 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0090 |
2 | NA19009.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1379+550C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599214 | |||||||
| chr22:38599345 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1379+419G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599345 | |||||||
| chr22:38599380 | G | T | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1379+384C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599380 | |||||||
| chr22:38599385 | A | G | 2 | a0002c0002t0024g0191 a0002c0002t0024g0192 |
2 | HG00408.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1379+379T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599385 | |||||||
| chr22:38599392 | T | C | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+372A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599392 | |||||||
| chr22:38599539 | A | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0076 others(1): Show |
4 | NA18959.hp2 NA18965.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379+225T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599539 | |||||||
| chr22:38599566 | C | T | 14 | a0001c0001t0003g0220 a0001c0001t0003g0221 a0001c0001t0003g0222 others(11): Show |
14 | HG00609.hp2 HG01099.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.1379+198G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599566 | |||||||
| chr22:38599621 | G | A | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1379+143C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599621 | |||||||
| chr22:38599676 | C | A | 13 | a0001c0001t0003g0220 a0001c0001t0003g0221 a0001c0001t0003g0222 others(10): Show |
13 | HG00609.hp2 HG01099.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.1379+88G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599676 | |||||||
| chr22:38599685 | C | T | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+79G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599685 | |||||||
| chr22:38599753 | G | C | 1 | a0001c0001t0021g0244 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1379+11C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 14/16 | chr22 | 38599753 | |||||||
| chr22:38600308 | G | C | 1 | a0002c0004t0045g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1222-387C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600308 | |||||||
| chr22:38600316 | G | GTA | 76 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(73): Show |
78 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1222-397_1222-396d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600316 | |||||||
| chr22:38600316 | G | GTATA | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222-399_1222-396d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600316 | |||||||
| chr22:38600316 | GTA | G | 9 | a0001c0001t0001g0067 a0001c0001t0001g0119 a0001c0001t0007g0003 others(6): Show |
10 | HG01175.hp2 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1222-397_1222-396d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600316 | |||||||
| chr22:38600648 | T | C | 2 | a0001c0001t0002g0229 a0001c0001t0002g0264 |
2 | NA18939.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1222-727A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600648 | |||||||
| chr22:38600723 | C | T | 3 | a0001c0001t0020g0253 a0001c0001t0020g0254 a0001c0001t0020g0255 |
3 | HG01346.hp1 HG02451.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1222-802G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600723 | |||||||
| chr22:38600860 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0082 |
3 | HG01516.hp2 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1222-939C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600860 | |||||||
| chr22:38600900 | C | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1222-979G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600900 | |||||||
| chr22:38600929 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1222-1008G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600929 | |||||||
| chr22:38600950 | C | CA | 23 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(20): Show |
24 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.1222-1030dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600950 | |||||||
| chr22:38600950 | CA | C | 11 | a0001c0001t0009g0214 a0001c0001t0009g0215 a0001c0001t0009g0288 others(8): Show |
11 | HG01891.hp1 HG02451.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222-1030delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38600950 | |||||||
| chr22:38601011 | C | T | 1 | a0001c0001t0016g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1222-1090G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601011 | |||||||
| chr22:38601109 | C | T | 1 | a0001c0001t0003g0238 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1222-1188G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601109 | |||||||
| chr22:38601264 | C | G | 191 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(188): Show |
195 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1222-1343G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601264 | |||||||
| chr22:38601878 | A | G | 8 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-1957T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601878 | |||||||
| chr22:38601953 | G | T | 1 | a0001c0001t0003g0271 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1222-2032C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38601953 | |||||||
| chr22:38602060 | G | C | 46 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(43): Show |
46 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1222-2139C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602060 | |||||||
| chr22:38602206 | C | G | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222-2285G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602206 | |||||||
| chr22:38602408 | A | G | 1 | a0001c0001t0003g0222 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1222-2487T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602408 | |||||||
| chr22:38602514 | C | A | 152 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(149): Show |
154 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1222-2593G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602514 | |||||||
| chr22:38602777 | C | T | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1221+2477G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602777 | |||||||
| chr22:38602801 | C | T | 1 | a0001c0001t0008g0037 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1221+2453G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38602801 | |||||||
| chr22:38603071 | G | A | 1 | a0001c0001t0050g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1221+2183C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603071 | |||||||
| chr22:38603116 | T | C | 190 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(187): Show |
194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1221+2138A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603116 | |||||||
| chr22:38603230 | C | T | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1221+2024G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603230 | |||||||
| chr22:38603487 | C | CA | 138 | a0001c0001t0001g0079 a0001c0001t0002g0217 a0001c0001t0002g0218 others(135): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1221+1766dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603487 | |||||||
| chr22:38603487 | C | CAA | 12 | a0001c0001t0002g0227 a0001c0001t0003g0304 a0001c0001t0009g0214 others(9): Show |
12 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1221+1765_1221+176 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603487 | |||||||
| chr22:38603801 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0140 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1221+1453C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603801 | |||||||
| chr22:38603817 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1221+1437A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603817 | |||||||
| chr22:38603921 | T | C | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1221+1333A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38603921 | |||||||
| chr22:38604392 | G | A | 97 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(94): Show |
98 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1221+862C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604392 | |||||||
| chr22:38604514 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1221+740C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604514 | |||||||
| chr22:38604655 | T | A | 44 | a0001c0001t0009g0288 a0002c0002t0004g0170 a0002c0002t0004g0171 others(41): Show |
45 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.1221+599A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604655 | |||||||
| chr22:38604971 | T | C | 1 | a0002c0002t0011g0202 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1221+283A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604971 | |||||||
| chr22:38604991 | A | T | 6 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(3): Show |
6 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1221+263T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38604991 | |||||||
| chr22:38605156 | T | C | 1 | a0001c0001t0043g0144 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1221+98A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 13/16 | chr22 | 38605156 | |||||||
| chr22:38605747 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1127-399C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38605747 | |||||||
| chr22:38606019 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1127-671T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38606019 | |||||||
| chr22:38606044 | T | C | 1 | a0001c0001t0017g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1127-696A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38606044 | |||||||
| chr22:38606623 | G | T | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1126+766C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38606623 | |||||||
| chr22:38606968 | G | C | 1 | a0001c0001t0008g0044 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1126+421C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38606968 | |||||||
| chr22:38607076 | T | C | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1126+313A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607076 | |||||||
| chr22:38607092 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1126+297C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607092 | |||||||
| chr22:38607123 | G | A | 1 | a0001c0001t0016g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1126+266C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607123 | |||||||
| chr22:38607176 | C | CA | 42 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0057 others(39): Show |
42 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1126+212dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607176 | |||||||
| chr22:38607176 | CA | C | 20 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0150 others(17): Show |
20 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1126+212delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607176 | |||||||
| chr22:38607176 | CAA | C | 32 | a0002c0002t0004g0170 a0002c0002t0004g0177 a0002c0002t0004g0179 others(29): Show |
33 | HG01891.hp2 HG02145.hp1 HG02896.hp2 others(30): Show |
intron_variant | MODIFIER | c.1126+211_1126+212d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607176 | |||||||
| chr22:38607292 | G | C | 1 | a0001c0001t0001g0010 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1126+97C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607292 | |||||||
| chr22:38607325 | C | T | 1 | a0001c0001t0033g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1126+64G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 12/16 | chr22 | 38607325 | |||||||
| chr22:38607490 | G | A | 153 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(150): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1039-14C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607490 | |||||||
| chr22:38607513 | C | A | 2 | a0001c0001t0003g0213 a0001c0001t0051g0249 |
2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1039-37G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607513 | |||||||
| chr22:38607514 | G | A | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1039-38C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607514 | |||||||
| chr22:38607768 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0072 |
2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1039-292A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607768 | |||||||
| chr22:38607771 | C | G | 1 | a0001c0001t0003g0311 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1039-295G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607771 | |||||||
| chr22:38607771 | C | T | 1 | a0002c0002t0004g0181 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1039-295G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38607771 | |||||||
| chr22:38608014 | A | G | 1 | a0001c0001t0003g0311 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1039-538T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608014 | |||||||
| chr22:38608065 | A | G | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-589T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608065 | |||||||
| chr22:38608080 | A | G | 1 | a0001c0001t0002g0317 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1039-604T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608080 | |||||||
| chr22:38608096 | A | C | 1 | a0001c0001t0003g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1039-620T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608096 | |||||||
| chr22:38608113 | C | A | 1 | a0001c0001t0003g0236 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-637G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608113 | |||||||
| chr22:38608155 | C | CA | 22 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0085 others(19): Show |
22 | HG01175.hp2 HG01346.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.1039-680dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608155 | |||||||
| chr22:38608155 | CA | C | 118 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0127 others(115): Show |
121 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1039-680delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608155 | |||||||
| chr22:38608155 | CAA | C | 13 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(10): Show |
13 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039-681_1039-680d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608155 | |||||||
| chr22:38608155 | CAAAAAAA others(4): Show |
C | 1 | a0001c0007t0012g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1039-690_1039-680d others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608155 | |||||||
| chr22:38608191 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1039-715C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608191 | |||||||
| chr22:38608214 | G | T | 1 | a0001c0001t0035g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1039-738C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608214 | |||||||
| chr22:38608572 | A | C | 94 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(91): Show |
95 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1039-1096T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608572 | |||||||
| chr22:38608701 | G | C | 1 | a0001c0001t0010g0060 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1039-1225C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608701 | |||||||
| chr22:38608793 | C | CT | 7 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0084 others(4): Show |
7 | HG00741.hp1 HG01175.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-1318dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608793 | |||||||
| chr22:38608793 | CT | C | 191 | a0001c0001t0001g0061 a0001c0001t0001g0066 a0001c0001t0001g0116 others(188): Show |
195 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1039-1318delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608793 | |||||||
| chr22:38608832 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1039-1356C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608832 | |||||||
| chr22:38608859 | G | C | 1 | a0001c0001t0009g0310 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1039-1383C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608859 | |||||||
| chr22:38608958 | G | A | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-1482C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38608958 | |||||||
| chr22:38609021 | A | G | 189 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(186): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1039-1545T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609021 | |||||||
| chr22:38609057 | A | T | 154 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1039-1581T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609057 | |||||||
| chr22:38609276 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1039-1800G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609276 | |||||||
| chr22:38609398 | GT | G | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-1923delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609398 | |||||||
| chr22:38609522 | A | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG01515.hp1 HG01517.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1039-2046T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609522 | |||||||
| chr22:38609743 | G | T | 1 | a0001c0001t0003g0320 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1039-2267C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609743 | |||||||
| chr22:38609785 | G | C | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1039-2309C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609785 | |||||||
| chr22:38609821 | G | C | 1 | a0001c0001t0003g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1039-2345C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609821 | |||||||
| chr22:38609833 | G | A | 10 | a0001c0001t0009g0214 a0001c0001t0009g0215 a0001c0001t0009g0288 others(7): Show |
10 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1039-2357C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609833 | |||||||
| chr22:38609865 | A | G | 316 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(313): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1039-2389T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609865 | |||||||
| chr22:38609992 | C | T | 9 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0025 others(6): Show |
10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1039-2516G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38609992 | |||||||
| chr22:38610183 | T | A | 41 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(38): Show |
42 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1039-2707A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610183 | |||||||
| chr22:38610184 | A | T | 1 | a0001c0001t0002g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039-2708T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610184 | |||||||
| chr22:38610192 | A | T | 12 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(9): Show |
13 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039-2716T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610192 | |||||||
| chr22:38610193 | T | A | 1 | a0002c0002t0014g0176 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1039-2717A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610193 | |||||||
| chr22:38610273 | C | T | 1 | a0001c0001t0026g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1039-2797G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610273 | |||||||
| chr22:38610527 | C | CCT | 154 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1039-3052_1039-305 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610527 | |||||||
| chr22:38610628 | G | A | 2 | a0002c0002t0004g0177 a0002c0002t0014g0206 |
2 | NA18991.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1039-3152C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610628 | |||||||
| chr22:38610743 | T | C | 4 | a0002c0002t0004g0186 a0002c0002t0004g0197 a0002c0002t0004g0208 others(1): Show |
4 | HG04184.hp1 NA18974.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-3267A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610743 | |||||||
| chr22:38610791 | G | A | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1039-3315C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610791 | |||||||
| chr22:38610912 | T | C | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-3436A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610912 | |||||||
| chr22:38610929 | A | G | 189 | a0001c0001t0001g0110 a0001c0001t0002g0217 a0001c0001t0002g0218 others(186): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1039-3453T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610929 | |||||||
| chr22:38610984 | C | T | 1 | a0002c0002t0004g0197 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1039-3508G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610984 | |||||||
| chr22:38610985 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1039-3509C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38610985 | |||||||
| chr22:38611055 | G | A | 8 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-3579C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611055 | |||||||
| chr22:38611067 | GAAA | G | 12 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(9): Show |
13 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039-3594_1039-359 others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611067 | |||||||
| chr22:38611096 | C | T | 3 | a0001c0001t0008g0042 a0001c0001t0008g0043 a0001c0001t0008g0044 |
3 | HG01433.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1039-3620G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611096 | |||||||
| chr22:38611158 | G | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1039-3682C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611158 | |||||||
| chr22:38611169 | A | C | 161 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0147 others(158): Show |
164 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1039-3693T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611169 | |||||||
| chr22:38611187 | C | G | 1 | a0001c0001t0057g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1039-3711G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611187 | |||||||
| chr22:38611262 | T | TGA | 9 | a0001c0001t0001g0067 a0001c0001t0001g0119 a0001c0001t0007g0003 others(6): Show |
10 | HG01175.hp2 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1039-3788_1039-378 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611262 | |||||||
| chr22:38611303 | G | A | 10 | a0001c0001t0009g0214 a0001c0001t0009g0215 a0001c0001t0009g0288 others(7): Show |
10 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1039-3827C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611303 | |||||||
| chr22:38611321 | A | G | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-3845T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611321 | |||||||
| chr22:38611353 | C | A | 2 | a0002c0002t0011g0172 a0002c0002t0011g0199 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1039-3877G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611353 | |||||||
| chr22:38611396 | G | A | 22 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(19): Show |
23 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.1039-3920C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611396 | |||||||
| chr22:38611445 | A | G | 2 | a0002c0002t0011g0202 a0002c0002t0048g0204 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1039-3969T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611445 | |||||||
| chr22:38611510 | T | C | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1039-4034A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611510 | |||||||
| chr22:38611650 | G | A | 2 | a0001c0001t0003g0280 a0001c0001t0003g0281 |
2 | NA18942.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1039-4174C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611650 | |||||||
| chr22:38611658 | T | C | 1 | a0001c0001t0006g0028 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1039-4182A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611658 | |||||||
| chr22:38611775 | T | G | 1 | a0001c0001t0003g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1039-4299A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611775 | |||||||
| chr22:38611813 | C | G | 6 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(3): Show |
6 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-4337G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611813 | |||||||
| chr22:38611926 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1039-4450C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611926 | |||||||
| chr22:38611950 | C | T | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1039-4474G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38611950 | |||||||
| chr22:38612021 | C | G | 1 | a0001c0001t0010g0060 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1039-4545G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38612021 | |||||||
| chr22:38612419 | C | A | 34 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(31): Show |
35 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.1039-4943G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38612419 | |||||||
| chr22:38612778 | A | T | 1 | a0002c0004t0045g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1039-5302T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38612778 | |||||||
| chr22:38612873 | G | C | 1 | a0002c0004t0045g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1039-5397C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38612873 | |||||||
| chr22:38613012 | A | C | 4 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(1): Show |
4 | HG00735.hp2 HG01069.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5536T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613012 | |||||||
| chr22:38613012 | A | G | 154 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1039-5536T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613012 | |||||||
| chr22:38613042 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1039-5566A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613042 | |||||||
| chr22:38613042 | T | TTATATAT others(35): Show |
4 | a0001c0001t0003g0216 a0001c0001t0003g0271 a0001c0001t0003g0272 others(1): Show |
4 | HG02922.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5608_1039-556 others(46): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613042 | |||||||
| chr22:38613054 | T | A | 1 | a0001c0001t0003g0280 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1039-5578A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613054 | |||||||
| chr22:38613055 | A | T | 1 | a0001c0001t0003g0280 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1039-5579T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613055 | |||||||
| chr22:38613066 | AATATATT others(37): Show |
A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0092 a0001c0001t0001g0098 others(1): Show |
4 | HG01928.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5634_1039-559 others(48): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613066 | |||||||
| chr22:38613082 | TTA | T | 20 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0076 others(17): Show |
20 | HG01346.hp1 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039-5608_1039-560 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613082 | |||||||
| chr22:38613084 | A | ATATATAT others(12): Show |
22 | a0002c0002t0004g0170 a0002c0002t0004g0177 a0002c0002t0004g0184 others(19): Show |
22 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-5609_1039-560 others(23): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613084 | |||||||
| chr22:38613084 | A | ATATATAT others(33): Show |
4 | a0002c0002t0019g0173 a0002c0002t0019g0195 a0002c0002t0047g0175 others(1): Show |
4 | NA18944.hp1 NA18982.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5609_1039-560 others(44): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613084 | |||||||
| chr22:38613084 | A | ATATATAT others(54): Show |
6 | a0002c0002t0004g0179 a0002c0002t0004g0180 a0002c0002t0004g0181 others(3): Show |
6 | NA18962.hp1 NA18980.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-5609_1039-560 others(65): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613084 | |||||||
| chr22:38613084 | A | ATATATAT others(11): Show |
1 | a0002c0002t0011g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1039-5609_1039-560 others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613084 | |||||||
| chr22:38613086 | A | ATATATTA others(69): Show |
5 | a0001c0001t0018g0136 a0001c0001t0018g0137 a0001c0001t0018g0139 others(2): Show |
5 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-5611_1039-561 others(80): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613086 | |||||||
| chr22:38613088 | A | ATATATTA others(8): Show |
1 | a0002c0002t0011g0202 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1039-5613_1039-561 others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613088 | |||||||
| chr22:38613094 | A | G | 2 | a0002c0002t0004g0170 a0002c0002t0025g0193 |
2 | NA18979.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1039-5618T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613094 | |||||||
| chr22:38613105 | TTATA | T | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5633_1039-563 others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613105 | |||||||
| chr22:38613116 | T | TATAATTA others(6): Show |
3 | a0002c0002t0011g0199 a0002c0002t0011g0203 a0002c0002t0011g0205 |
3 | HG01891.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1039-5641_1039-564 others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613116 | |||||||
| chr22:38613116 | T | TATATAAT others(8): Show |
2 | a0002c0002t0011g0172 a0002c0002t0011g0174 |
2 | HG02145.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1039-5641_1039-564 others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613116 | |||||||
| chr22:38613116 | T | TATATAAT others(10): Show |
1 | a0002c0002t0048g0204 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1039-5641_1039-564 others(21): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613116 | |||||||
| chr22:38613122 | ATAAT | A | 4 | a0001c0001t0003g0296 a0001c0001t0003g0301 a0001c0001t0003g0320 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5650_1039-564 others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613122 | |||||||
| chr22:38613130 | A | T | 102 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(99): Show |
103 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1039-5654T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613130 | |||||||
| chr22:38613140 | T | C | 1 | a0001c0001t0005g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1039-5664A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613140 | |||||||
| chr22:38613168 | G | GTATATAT others(27): Show |
1 | a0001c0001t0003g0238 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1039-5726_1039-569 others(38): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613168 | |||||||
| chr22:38613172 | ATATATTA others(18): Show |
A | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-5721_1039-569 others(29): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613172 | |||||||
| chr22:38613185 | AAT | A | 73 | a0001c0001t0002g0267 a0001c0001t0003g0296 a0001c0001t0003g0301 others(70): Show |
75 | HG00408.hp2 HG00673.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1039-5711_1039-571 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613185 | |||||||
| chr22:38613200 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0086 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1039-5724A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613200 | |||||||
| chr22:38613237 | T | A | 1 | a0001c0001t0042g0074 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1039-5761A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613237 | |||||||
| chr22:38613238 | A | ATC | 144 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(141): Show |
146 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1039-5763_1039-576 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613238 | |||||||
| chr22:38613238 | A | C | 53 | a0001c0001t0003g0221 a0001c0001t0005g0008 a0001c0001t0005g0017 others(50): Show |
55 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1039-5762T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613238 | |||||||
| chr22:38613239 | A | T | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5763T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613239 | |||||||
| chr22:38613240 | T | C | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5764A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613240 | |||||||
| chr22:38613246 | A | T | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5770T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613246 | |||||||
| chr22:38613247 | T | A | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5771A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613247 | |||||||
| chr22:38613254 | CATATATT | C | 5 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-5785_1039-577 others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613254 | |||||||
| chr22:38613255 | ATATAT | A | 3 | a0001c0001t0005g0022 a0001c0001t0005g0143 a0001c0001t0038g0081 |
3 | HG01928.hp2 HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1039-5784_1039-578 others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613255 | |||||||
| chr22:38613260 | T | TTATATAT others(18): Show |
3 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0026 |
4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5785_1039-578 others(29): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613260 | |||||||
| chr22:38613265 | A | T | 4 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0026 others(1): Show |
5 | HG01934.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-5789T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613265 | |||||||
| chr22:38613272 | T | A | 1 | a0001c0001t0010g0060 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1039-5796A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613272 | |||||||
| chr22:38613272 | TTATATAT others(9): Show |
T | 8 | a0001c0001t0009g0309 a0001c0001t0013g0162 a0001c0001t0013g0163 others(5): Show |
8 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-5812_1039-579 others(20): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613272 | |||||||
| chr22:38613273 | T | A | 3 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0026 |
4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5797A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613273 | |||||||
| chr22:38613280 | C | A | 3 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0026 |
4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5804G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613280 | |||||||
| chr22:38613282 | T | C | 3 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0026 |
4 | HG01934.hp2 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5806A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613282 | |||||||
| chr22:38613282 | T | TATATAAT others(23): Show |
4 | a0001c0001t0006g0025 a0001c0001t0006g0027 a0001c0001t0006g0028 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5836_1039-580 others(34): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613282 | |||||||
| chr22:38613289 | T | TATATATA others(4): Show |
1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5814_1039-581 others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613289 | |||||||
| chr22:38613295 | T | A | 1 | a0001c0001t0050g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1039-5819A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613295 | |||||||
| chr22:38613296 | C | A | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5820G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613296 | |||||||
| chr22:38613298 | T | C | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5822A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613298 | |||||||
| chr22:38613302 | T | C | 2 | a0001c0001t0002g0267 a0001c0001t0016g0284 |
2 | HG01433.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1039-5826A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613302 | |||||||
| chr22:38613308 | A | G | 1 | a0001c0001t0003g0238 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1039-5832T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613308 | |||||||
| chr22:38613310 | A | C | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5834T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613310 | |||||||
| chr22:38613312 | C | CATATAAT others(9): Show |
98 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(95): Show |
99 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1039-5852_1039-583 others(20): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | |||||||
| chr22:38613312 | C | CATATAAT others(25): Show |
42 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(39): Show |
43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.1039-5837_1039-583 others(36): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | |||||||
| chr22:38613312 | C | CATATAAT others(41): Show |
1 | a0002c0002t0004g0179 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1039-5837_1039-583 others(52): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | |||||||
| chr22:38613312 | C | CATATAAT others(7): Show |
2 | a0001c0001t0017g0168 a0001c0001t0017g0169 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1039-5837_1039-583 others(18): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | |||||||
| chr22:38613312 | C | CATATATT | 6 | a0001c0001t0001g0057 a0001c0001t0018g0136 a0001c0001t0018g0137 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-5837_1039-583 others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | |||||||
| chr22:38613312 | C | T | 3 | a0001c0001t0009g0214 a0001c0001t0009g0215 a0001c0001t0017g0167 |
3 | HG02280.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1039-5836G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613312 | |||||||
| chr22:38613341 | A | T | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1039-5865T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613341 | |||||||
| chr22:38613362 | T | TTTATAAT others(66): Show |
1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1039-5887_1039-588 others(77): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613362 | |||||||
| chr22:38613362 | T | TTTATAAT others(66): Show |
7 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0018g0136 others(4): Show |
7 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-5887_1039-588 others(77): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613362 | |||||||
| chr22:38613363 | C | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-5887G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613363 | |||||||
| chr22:38613363 | CATATATA | C | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-5894_1039-588 others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613363 | |||||||
| chr22:38613370 | A | AAT | 8 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-5896_1039-589 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613370 | |||||||
| chr22:38613370 | A | AATATATA others(109): Show |
1 | a0001c0001t0057g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1039-5895_1039-589 others(120): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613370 | |||||||
| chr22:38613379 | C | T | 7 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(4): Show |
7 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-5903G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613379 | |||||||
| chr22:38613385 | T | TTA | 9 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5911_1039-591 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613385 | |||||||
| chr22:38613396 | A | T | 9 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5920T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613396 | |||||||
| chr22:38613397 | T | A | 9 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5921A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613397 | |||||||
| chr22:38613399 | T | TCATATAT others(155): Show |
1 | a0001c0001t0005g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1039-5924_1039-592 others(166): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613399 | |||||||
| chr22:38613399 | T | TCATATAT others(149): Show |
2 | a0001c0001t0023g0101 a0001c0001t0023g0102 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1039-5924_1039-592 others(160): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613399 | |||||||
| chr22:38613400 | T | A | 9 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5924A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613400 | |||||||
| chr22:38613403 | TA | T | 3 | a0001c0001t0005g0022 a0001c0001t0023g0101 a0001c0001t0023g0102 |
3 | HG01069.hp1 HG01071.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1039-5928delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613403 | |||||||
| chr22:38613404 | A | AATATATA others(108): Show |
1 | a0001c0001t0051g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1039-5929_1039-592 others(119): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | AATATATA others(122): Show |
44 | a0001c0001t0017g0168 a0001c0001t0017g0169 a0002c0002t0004g0170 others(41): Show |
45 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(133): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | AATATATA others(157): Show |
1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039-5929_1039-592 others(168): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | AATATATA others(122): Show |
1 | a0002c0002t0004g0201 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1039-5929_1039-592 others(133): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | AATATATA others(115): Show |
87 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(84): Show |
88 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(126): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | AATATATA others(117): Show |
4 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0306 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(128): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | AATATATA others(122): Show |
9 | a0001c0001t0009g0214 a0001c0001t0009g0215 a0001c0001t0009g0305 others(6): Show |
9 | HG02055.hp2 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(133): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | AATATATA others(110): Show |
1 | a0001c0001t0003g0281 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1039-5929_1039-592 others(121): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | AATATATA others(110): Show |
4 | a0001c0001t0003g0296 a0001c0001t0003g0301 a0001c0001t0003g0320 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(121): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613404 | A | ATTAT | 9 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
9 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5929_1039-592 others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613404 | |||||||
| chr22:38613413 | G | A | 164 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0105 others(161): Show |
166 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1039-5937C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613413 | |||||||
| chr22:38613414 | A | ATATATAA others(108): Show |
1 | a0001c0001t0002g0317 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(119): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(117): Show |
7 | a0001c0001t0005g0008 a0001c0001t0005g0023 a0001c0001t0005g0024 others(4): Show |
7 | HG00735.hp1 HG01261.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(128): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(108): Show |
1 | a0001c0001t0006g0031 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(119): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(118): Show |
1 | a0001c0001t0013g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(129): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(117): Show |
23 | a0001c0001t0005g0017 a0001c0001t0005g0020 a0001c0001t0005g0021 others(20): Show |
25 | HG00735.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(128): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(115): Show |
1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(126): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(109): Show |
2 | a0001c0001t0022g0033 a0001c0001t0022g0141 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(120): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(111): Show |
8 | a0001c0001t0008g0034 a0001c0001t0008g0036 a0001c0001t0008g0037 others(5): Show |
8 | HG01433.hp2 HG02055.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(111): Show |
1 | a0001c0001t0016g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(111): Show |
107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(104): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1039-5939_1039-593 others(122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(110): Show |
1 | a0001c0001t0013g0165 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(121): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(110): Show |
1 | a0001c0001t0001g0015 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(121): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613414 | A | ATATATAT others(111): Show |
1 | a0001c0001t0008g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1039-5939_1039-593 others(122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613414 | |||||||
| chr22:38613786 | C | T | 1 | a0001c0001t0007g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1039-6310G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613786 | |||||||
| chr22:38613863 | C | A | 1 | a0001c0007t0012g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1038+6349G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613863 | |||||||
| chr22:38613918 | C | G | 1 | a0002c0002t0004g0181 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1038+6294G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613918 | |||||||
| chr22:38613924 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0073 |
2 | NA18951.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1038+6288A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38613924 | |||||||
| chr22:38614022 | C | T | 46 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(43): Show |
47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.1038+6190G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614022 | |||||||
| chr22:38614060 | T | C | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1038+6152A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614060 | |||||||
| chr22:38614537 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1038+5675C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614537 | |||||||
| chr22:38614630 | A | T | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5582T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614630 | |||||||
| chr22:38614761 | A | T | 1 | a0001c0001t0013g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1038+5451T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614761 | |||||||
| chr22:38614796 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1038+5416C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614796 | |||||||
| chr22:38614805 | A | AAGCC | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+5403_1038+540 others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614805 | |||||||
| chr22:38614871 | T | C | 1 | a0002c0002t0004g0190 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1038+5341A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614871 | |||||||
| chr22:38614900 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1038+5312T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614900 | |||||||
| chr22:38614917 | G | A | 1 | a0002c0002t0011g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1038+5295C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38614917 | |||||||
| chr22:38615068 | A | G | 1 | a0001c0001t0006g0030 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1038+5144T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38615068 | |||||||
| chr22:38615187 | T | A | 6 | a0001c0001t0005g0017 a0001c0001t0005g0020 a0001c0001t0005g0021 others(3): Show |
6 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+5025A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38615187 | |||||||
| chr22:38615315 | C | T | 6 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(3): Show |
6 | HG02055.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+4897G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38615315 | |||||||
| chr22:38616019 | G | A | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1038+4193C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616019 | |||||||
| chr22:38616491 | C | T | 1 | a0001c0001t0003g0221 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1038+3721G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616491 | |||||||
| chr22:38616509 | A | C | 12 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(9): Show |
13 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1038+3703T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616509 | |||||||
| chr22:38616666 | C | CA | 11 | a0001c0001t0001g0069 a0001c0001t0001g0126 a0001c0001t0022g0033 others(8): Show |
12 | HG00642.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1038+3545dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616666 | |||||||
| chr22:38616679 | A | T | 9 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0025 others(6): Show |
10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1038+3533T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616679 | |||||||
| chr22:38616708 | A | G | 1 | a0001c0001t0016g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1038+3504T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616708 | |||||||
| chr22:38616714 | T | G | 5 | a0001c0001t0005g0017 a0001c0001t0005g0020 a0001c0001t0005g0021 others(2): Show |
5 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+3498A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616714 | |||||||
| chr22:38616846 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1038+3366C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38616846 | |||||||
| chr22:38617065 | G | C | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1038+3147C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617065 | |||||||
| chr22:38617292 | C | CT | 13 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0059 others(10): Show |
13 | HG00408.hp1 HG00673.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1038+2919dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617292 | |||||||
| chr22:38617292 | CT | C | 144 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(141): Show |
146 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1038+2919delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617292 | |||||||
| chr22:38617292 | CTT | C | 6 | a0001c0001t0002g0283 a0001c0001t0009g0310 a0001c0001t0015g0292 others(3): Show |
6 | HG00408.hp2 HG02896.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+2918_1038+291 others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617292 | |||||||
| chr22:38617354 | G | A | 1 | a0001c0001t0005g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1038+2858C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617354 | |||||||
| chr22:38617359 | G | A | 3 | a0001c0001t0020g0253 a0001c0001t0020g0254 a0001c0001t0020g0255 |
3 | HG01346.hp1 HG02451.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1038+2853C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617359 | |||||||
| chr22:38617381 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1038+2831G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617381 | |||||||
| chr22:38617420 | C | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1038+2792G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617420 | |||||||
| chr22:38617517 | G | A | 90 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(87): Show |
91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1038+2695C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617517 | |||||||
| chr22:38617528 | C | T | 1 | a0001c0001t0051g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1038+2684G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617528 | |||||||
| chr22:38617545 | T | C | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+2667A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617545 | |||||||
| chr22:38617565 | G | A | 6 | a0001c0001t0002g0225 a0001c0001t0002g0275 a0001c0001t0002g0276 others(3): Show |
6 | HG00609.hp1 NA18951.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1038+2647C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617565 | |||||||
| chr22:38617568 | T | C | 1 | a0001c0001t0002g0282 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1038+2644A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617568 | |||||||
| chr22:38617591 | G | A | 1 | a0002c0002t0011g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1038+2621C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617591 | |||||||
| chr22:38617763 | C | T | 7 | a0002c0002t0004g0179 a0002c0002t0004g0180 a0002c0002t0004g0181 others(4): Show |
7 | NA18962.hp1 NA18980.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+2449G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617763 | |||||||
| chr22:38617825 | T | C | 152 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(149): Show |
154 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1038+2387A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617825 | |||||||
| chr22:38617972 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0121 |
2 | NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1038+2240T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38617972 | |||||||
| chr22:38618046 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1038+2166A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618046 | |||||||
| chr22:38618368 | C | T | 1 | a0001c0001t0036g0131 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1038+1844G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618368 | |||||||
| chr22:38618666 | AG | A | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+1545delC | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618666 | |||||||
| chr22:38618777 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1038+1435G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618777 | |||||||
| chr22:38618805 | G | A | 1 | a0001c0001t0055g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1038+1407C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618805 | |||||||
| chr22:38618939 | C | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0092 a0001c0001t0001g0098 others(1): Show |
4 | HG01928.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+1273G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618939 | |||||||
| chr22:38618971 | G | GA | 17 | a0001c0001t0001g0055 a0001c0001t0001g0105 a0001c0001t0001g0122 others(14): Show |
17 | HG00735.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1038+1240dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38618971 | |||||||
| chr22:38619297 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1038+915A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38619297 | |||||||
| chr22:38619313 | C | CTTAT | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1038+895_1038+898d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38619313 | |||||||
| chr22:38619492 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1038+720A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38619492 | |||||||
| chr22:38620177 | T | C | 167 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1038+35A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38620177 | |||||||
| chr22:38620203 | C | G | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+9G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 11/16 | chr22 | 38620203 | |||||||
| chr22:38620398 | A | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0094 others(32): Show |
36 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.959-107T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620398 | |||||||
| chr22:38620424 | A | G | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.959-133T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620424 | |||||||
| chr22:38620458 | T | TAA | 3 | a0001c0001t0001g0057 a0001c0001t0001g0087 a0001c0001t0001g0127 |
3 | NA18950.hp1 NA18961.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.959-168_959-167ins others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620458 | |||||||
| chr22:38620638 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.959-347G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620638 | |||||||
| chr22:38620678 | G | A | 45 | a0001c0001t0017g0168 a0001c0001t0017g0169 a0002c0002t0004g0170 others(42): Show |
46 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.959-387C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620678 | |||||||
| chr22:38620808 | C | G | 1 | a0001c0001t0002g0317 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.959-517G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620808 | |||||||
| chr22:38620869 | C | A | 1 | a0001c0001t0001g0011 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.959-578G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620869 | |||||||
| chr22:38620998 | A | G | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.959-707T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38620998 | |||||||
| chr22:38621074 | C | T | 1 | a0001c0001t0010g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.959-783G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621074 | |||||||
| chr22:38621316 | C | G | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.959-1025G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621316 | |||||||
| chr22:38621349 | C | CA | 105 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(102): Show |
106 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.959-1059dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621349 | |||||||
| chr22:38621498 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.959-1207C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621498 | |||||||
| chr22:38621634 | C | G | 1 | a0001c0001t0020g0255 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.959-1343G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621634 | |||||||
| chr22:38621666 | C | T | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.959-1375G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621666 | |||||||
| chr22:38621888 | C | T | 1 | a0001c0001t0005g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.958+1284G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621888 | |||||||
| chr22:38621934 | G | A | 1 | a0001c0001t0037g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.958+1238C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38621934 | |||||||
| chr22:38622174 | T | A | 238 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0088 others(235): Show |
243 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.958+998A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622174 | |||||||
| chr22:38622329 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.958+843A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622329 | |||||||
| chr22:38622404 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.958+768G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622404 | |||||||
| chr22:38622568 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.958+604C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622568 | |||||||
| chr22:38622824 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.958+348G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622824 | |||||||
| chr22:38622873 | C | CA | 21 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0058 others(18): Show |
21 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.958+298dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622873 | |||||||
| chr22:38622873 | CA | C | 145 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0018 others(142): Show |
147 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.958+298delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622873 | |||||||
| chr22:38622873 | CAA | C | 38 | a0001c0001t0002g0283 a0001c0001t0002g0285 a0001c0001t0003g0007 others(35): Show |
40 | HG00140.hp1 HG00408.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.958+297_958+298del others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622873 | |||||||
| chr22:38622873 | CAAA | C | 12 | a0001c0001t0013g0165 a0002c0002t0004g0197 a0002c0002t0004g0208 others(9): Show |
12 | HG01069.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.958+296_958+298del others(3): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38622873 | |||||||
| chr22:38623027 | C | T | 23 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(20): Show |
24 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+145G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 10/16 | chr22 | 38623027 | |||||||
| chr22:38623359 | G | T | 1 | a0001c0001t0055g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.851-80C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623359 | |||||||
| chr22:38623363 | GAGGATTG others(60): Show |
G | 1 | a0001c0001t0003g0280 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.851-151_851-85delT others(66): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623363 | |||||||
| chr22:38623368 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851-89A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623368 | |||||||
| chr22:38623431 | A | T | 1 | a0001c0001t0003g0280 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.851-152T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623431 | |||||||
| chr22:38623433 | T | A | 1 | a0001c0001t0003g0280 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.851-154A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623433 | |||||||
| chr22:38623444 | T | C | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.851-165A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623444 | |||||||
| chr22:38623600 | G | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.851-321C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623600 | |||||||
| chr22:38623609 | C | A | 1 | a0001c0001t0002g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.851-330G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623609 | |||||||
| chr22:38623848 | C | T | 36 | a0001c0001t0003g0007 a0001c0001t0003g0213 a0001c0001t0003g0220 others(33): Show |
37 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.851-569G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623848 | |||||||
| chr22:38623876 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0106 |
2 | NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.851-597C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38623876 | |||||||
| chr22:38624031 | G | A | 2 | a0001c0001t0023g0101 a0001c0001t0023g0102 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.851-752C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624031 | |||||||
| chr22:38624203 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.851-924C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624203 | |||||||
| chr22:38624261 | C | A | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.851-982G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624261 | |||||||
| chr22:38624389 | C | CA | 10 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0066 others(7): Show |
11 | HG00733.hp1 HG01516.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.851-1111dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624389 | |||||||
| chr22:38624643 | G | GGTGTCTA others(24): Show |
1 | a0001c0001t0003g0280 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.851-1395_851-1365d others(33): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624643 | |||||||
| chr22:38624802 | C | T | 14 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(11): Show |
14 | HG00735.hp1 HG01261.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.850+1378G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38624802 | |||||||
| chr22:38625012 | G | A | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+1168C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625012 | |||||||
| chr22:38625160 | T | C | 160 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(157): Show |
163 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.850+1020A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625160 | |||||||
| chr22:38625175 | G | A | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850+1005C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625175 | |||||||
| chr22:38625304 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.850+876C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625304 | |||||||
| chr22:38625320 | C | T | 1 | a0001c0001t0006g0031 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.850+860G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625320 | |||||||
| chr22:38625321 | T | G | 190 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(187): Show |
194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.850+859A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625321 | |||||||
| chr22:38625368 | G | A | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850+812C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625368 | |||||||
| chr22:38625385 | C | T | 7 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0306 others(4): Show |
7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+795G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625385 | |||||||
| chr22:38625387 | C | CA | 18 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0147 others(15): Show |
19 | HG01099.hp1 HG01516.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.850+792dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625387 | |||||||
| chr22:38625387 | CA | C | 8 | a0001c0001t0001g0120 a0001c0001t0002g0229 a0001c0001t0002g0282 others(5): Show |
9 | HG02735.hp1 HG02895.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.850+792delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625387 | |||||||
| chr22:38625517 | G | A | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.850+663C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625517 | |||||||
| chr22:38625712 | G | A | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.850+468C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625712 | |||||||
| chr22:38625830 | G | GC | 160 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(157): Show |
163 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.850+349_850+350ins others(1): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625830 | |||||||
| chr22:38625926 | G | A | 3 | a0002c0002t0014g0006 a0002c0002t0014g0176 a0002c0002t0014g0187 |
4 | NA18952.hp2 NA19060.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+254C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625926 | |||||||
| chr22:38625930 | G | A | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+250C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625930 | |||||||
| chr22:38625943 | C | CA | 35 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0079 others(32): Show |
36 | HG00140.hp1 HG00438.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.850+236dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625943 | |||||||
| chr22:38625943 | C | CAA | 41 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(38): Show |
42 | HG00408.hp2 HG00673.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+235_850+236dup others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625943 | |||||||
| chr22:38625993 | T | C | 1 | a0001c0001t0041g0146 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.850+187A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38625993 | |||||||
| chr22:38626060 | G | A | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.850+120C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38626060 | |||||||
| chr22:38626156 | C | A | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.850+24G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38626156 | |||||||
| chr22:38626174 | T | G | 1 | a0001c0001t0002g0260 | 1 | HG00733.hp2 | splice_region_variant&intron_variant | LOW | c.850+6A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 9/16 | chr22 | 38626174 | |||||||
| chr22:38626548 | C | A | 3 | a0001c0001t0020g0253 a0001c0001t0020g0254 a0001c0001t0020g0255 |
3 | HG01346.hp1 HG02451.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.727-245G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626548 | |||||||
| chr22:38626796 | C | T | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.727-493G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626796 | |||||||
| chr22:38626838 | A | G | 1 | a0002c0002t0004g0190 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.727-535T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626838 | |||||||
| chr22:38626865 | C | CA | 24 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0055 others(21): Show |
24 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.727-563dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626865 | |||||||
| chr22:38626865 | C | CAA | 16 | a0001c0001t0001g0089 a0001c0001t0001g0127 a0001c0001t0005g0017 others(13): Show |
17 | HG01261.hp1 HG01928.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.727-564_727-563dup others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626865 | |||||||
| chr22:38626865 | CA | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0124 others(4): Show |
7 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-563delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626865 | |||||||
| chr22:38626882 | AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18971.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.727-590_727-580del others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626882 | |||||||
| chr22:38626885 | A | T | 1 | a0001c0001t0003g0221 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.727-582T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626885 | |||||||
| chr22:38626887 | A | T | 1 | a0001c0001t0003g0221 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.727-584T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626887 | |||||||
| chr22:38626889 | A | AATATATA others(7): Show |
1 | a0001c0003t0012g0160 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.727-587_727-586ins others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626889 | |||||||
| chr22:38626889 | A | ATATATAT others(8): Show |
1 | a0002c0002t0004g0180 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.727-587_727-586ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626889 | |||||||
| chr22:38626889 | A | T | 7 | a0001c0001t0001g0140 a0001c0001t0003g0221 a0001c0001t0013g0162 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.727-586T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626889 | |||||||
| chr22:38626891 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0002g0313 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(32): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0003g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0056g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0002g0317 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(7): Show |
3 | a0001c0001t0002g0218 a0001c0001t0003g0243 a0001c0001t0016g0284 |
3 | HG00741.hp2 HG01099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0003g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0002g0314 a0001c0001t0003g0213 |
2 | HG04115.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(6): Show |
3 | a0001c0001t0002g0227 a0001c0001t0002g0260 a0001c0001t0002g0267 |
3 | HG00733.hp2 HG03654.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(8): Show |
3 | a0001c0001t0002g0232 a0001c0001t0002g0283 a0002c0002t0004g0177 |
3 | NA18959.hp1 NA18979.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(5): Show |
13 | a0001c0001t0002g0217 a0001c0001t0002g0225 a0001c0001t0002g0226 others(10): Show |
13 | HG00609.hp1 HG01993.hp2 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(7): Show |
5 | a0001c0001t0002g0262 a0001c0001t0002g0286 a0001c0001t0002g0303 others(2): Show |
5 | HG01346.hp1 HG02040.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAA others(17): Show |
1 | a0002c0002t0004g0197 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(24): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAT | 7 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0306 others(4): Show |
7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAT others(4): Show |
5 | a0001c0001t0002g0257 a0001c0001t0003g0238 a0001c0001t0003g0250 others(2): Show |
5 | HG00423.hp2 HG00558.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAT others(6): Show |
7 | a0001c0001t0002g0258 a0001c0001t0003g0223 a0001c0001t0003g0236 others(4): Show |
7 | HG02165.hp2 HG02698.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAT others(8): Show |
3 | a0001c0001t0003g0287 a0002c0002t0004g0201 a0002c0002t0014g0206 |
3 | NA18906.hp1 NA18943.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAT others(10): Show |
2 | a0001c0001t0003g0272 a0002c0004t0045g0207 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAT others(12): Show |
1 | a0002c0002t0004g0184 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(19): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAAAT others(16): Show |
2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(23): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAATA others(3): Show |
2 | a0001c0001t0015g0290 a0001c0001t0051g0249 |
2 | HG02055.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAATA others(5): Show |
9 | a0001c0001t0002g0228 a0001c0001t0002g0233 a0001c0001t0002g0275 others(6): Show |
9 | HG00280.hp1 HG03041.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAATA others(7): Show |
3 | a0001c0001t0002g0265 a0001c0001t0003g0252 a0001c0001t0049g0268 |
3 | HG02155.hp1 HG03688.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAATA others(9): Show |
2 | a0001c0001t0002g0259 a0001c0001t0050g0273 |
2 | HG00642.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAATA others(11): Show |
2 | a0002c0002t0004g0171 a0002c0002t0046g0189 |
2 | NA18983.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(18): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAATA others(15): Show |
1 | a0002c0002t0004g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAAATA others(17): Show |
1 | a0002c0002t0004g0186 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(24): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAATAT others(4): Show |
13 | a0001c0001t0003g0220 a0001c0001t0003g0222 a0001c0001t0003g0224 others(10): Show |
13 | HG00609.hp2 NA18942.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAATAT others(6): Show |
7 | a0001c0001t0002g0231 a0001c0001t0002g0289 a0001c0001t0003g0246 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAATAT others(8): Show |
2 | a0002c0002t0004g0196 a0002c0002t0004g0198 |
2 | HG00673.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAATAT others(10): Show |
4 | a0001c0001t0003g0271 a0002c0002t0004g0209 a0002c0002t0024g0191 others(1): Show |
4 | HG02922.hp1 NA18960.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAATAT others(14): Show |
2 | a0002c0002t0004g0208 a0002c0002t0011g0200 |
2 | HG03139.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(21): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAAATAT others(16): Show |
1 | a0002c0002t0014g0176 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(23): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAATATA others(3): Show |
1 | a0001c0001t0002g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAATATA others(5): Show |
7 | a0001c0001t0002g0229 a0001c0001t0002g0264 a0001c0001t0002g0266 others(4): Show |
7 | HG02895.hp1 HG02970.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAATATA others(9): Show |
6 | a0002c0002t0004g0190 a0002c0002t0004g0210 a0002c0002t0019g0173 others(3): Show |
6 | HG02015.hp2 NA18944.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAATATA others(11): Show |
1 | a0002c0002t0025g0194 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(18): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAAATATA others(15): Show |
1 | a0002c0002t0014g0006 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.727-589_727-588ins others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAATATAT others(4): Show |
2 | a0001c0001t0003g0248 a0001c0001t0003g0321 |
2 | HG00558.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAATATAT others(6): Show |
1 | a0001c0001t0026g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(13): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAATATAT others(8): Show |
4 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0031g0157 others(1): Show |
4 | HG00408.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AAATATAT others(10): Show |
3 | a0002c0002t0004g0170 a0002c0002t0004g0182 a0002c0002t0004g0188 |
3 | NA18979.hp2 NA18980.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.727-589_727-588ins others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AATATATA others(7): Show |
1 | a0002c0002t0004g0183 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.727-602_727-589dup others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AATATATA others(9): Show |
2 | a0002c0002t0004g0179 a0002c0002t0004g0181 |
2 | NA19057.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.727-604_727-589dup others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AATATATA others(15): Show |
1 | a0002c0002t0014g0006 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.727-610_727-589dup others(22): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AATATATA others(17): Show |
1 | a0002c0002t0014g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(24): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | AT | 4 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0152 others(1): Show |
4 | HG00140.hp2 HG02056.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-589_727-588ins others(1): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | ATATATAT others(8): Show |
1 | a0001c0003t0012g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.727-589_727-588ins others(15): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | ATATATAT others(10): Show |
2 | a0001c0007t0012g0158 a0002c0002t0025g0193 |
2 | HG02717.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.727-589_727-588ins others(17): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626891 | A | T | 16 | a0001c0001t0001g0067 a0001c0001t0001g0123 a0001c0001t0001g0124 others(13): Show |
16 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.727-588T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626891 | |||||||
| chr22:38626892 | AT | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0073 others(9): Show |
13 | HG01175.hp2 HG02015.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.727-590delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626892 | |||||||
| chr22:38626893 | T | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(86): Show |
91 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.727-590A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626893 | |||||||
| chr22:38626895 | T | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(32): Show |
38 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.727-592A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626895 | |||||||
| chr22:38626897 | T | A | 1 | a0001c0001t0007g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.727-594A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626897 | |||||||
| chr22:38626913 | T | C | 101 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(98): Show |
102 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.727-610A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626913 | |||||||
| chr22:38626913 | T | TATATATA others(3): Show |
2 | a0001c0001t0003g0007 a0001c0001t0003g0294 |
3 | HG03490.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.727-611_727-610ins others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626913 | |||||||
| chr22:38626938 | G | T | 2 | a0001c0001t0008g0040 a0002c0002t0004g0196 |
2 | HG01243.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.727-635C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38626938 | |||||||
| chr22:38627053 | C | T | 5 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(2): Show |
5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-750G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627053 | |||||||
| chr22:38627185 | C | A | 1 | a0001c0001t0055g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727-882G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627185 | |||||||
| chr22:38627498 | T | C | 1 | a0001c0001t0005g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.726+740A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627498 | |||||||
| chr22:38627596 | G | GT | 11 | a0001c0001t0003g0221 a0001c0001t0003g0240 a0001c0001t0003g0280 others(8): Show |
11 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.726+641dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627596 | |||||||
| chr22:38627698 | G | A | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.726+540C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627698 | |||||||
| chr22:38627784 | A | T | 1 | a0001c0001t0002g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.726+454T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 8/16 | chr22 | 38627784 | |||||||
| chr22:38628441 | A | T | 1 | a0001c0001t0003g0280 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.622-99T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 7/16 | chr22 | 38628441 | |||||||
| chr22:38628528 | A | T | 1 | a0001c0001t0044g0128 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.622-186T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 7/16 | chr22 | 38628528 | |||||||
| chr22:38628619 | C | T | 1 | a0002c0004t0045g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.621+215G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 7/16 | chr22 | 38628619 | |||||||
| chr22:38628941 | A | G | 1 | a0001c0001t0009g0305 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.520-6T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38628941 | |||||||
| chr22:38628954 | CAGT | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0063 others(3): Show |
6 | NA18943.hp2 NA18951.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-22_520-20delAC others(1): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38628954 | |||||||
| chr22:38628956 | G | T | 311 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(308): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.520-21C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38628956 | |||||||
| chr22:38628967 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0063 others(3): Show |
6 | NA18943.hp2 NA18951.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-32C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38628967 | |||||||
| chr22:38629272 | T | C | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.520-337A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629272 | |||||||
| chr22:38629290 | T | C | 2 | a0001c0001t0005g0023 a0001c0001t0005g0142 |
2 | HG00735.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.520-355A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629290 | |||||||
| chr22:38629336 | A | G | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.520-401T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629336 | |||||||
| chr22:38629393 | C | T | 1 | a0001c0001t0016g0279 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.520-458G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629393 | |||||||
| chr22:38629607 | A | G | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.520-672T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629607 | |||||||
| chr22:38629620 | T | C | 1 | a0001c0001t0003g0281 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.520-685A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629620 | |||||||
| chr22:38629629 | G | A | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-694C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629629 | |||||||
| chr22:38629645 | G | GACTCACA others(50): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0072 |
2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.520-767_520-711dup others(57): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629645 | |||||||
| chr22:38629645 | GACTCACA others(50): Show |
G | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-767_520-711del others(57): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629645 | |||||||
| chr22:38629754 | A | G | 1 | a0001c0001t0057g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.520-819T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629754 | |||||||
| chr22:38629814 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0106 |
2 | NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.520-879T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629814 | |||||||
| chr22:38629867 | T | TA | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.520-933dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629867 | |||||||
| chr22:38629890 | C | T | 2 | a0001c0001t0017g0168 a0001c0001t0017g0169 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.520-955G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629890 | |||||||
| chr22:38629932 | A | C | 8 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-997T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629932 | |||||||
| chr22:38629938 | C | G | 2 | a0002c0002t0011g0203 a0002c0002t0011g0205 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.520-1003G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38629938 | |||||||
| chr22:38630006 | T | C | 44 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(41): Show |
44 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.520-1071A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630006 | |||||||
| chr22:38630044 | GCCATCAC others(51): Show |
G | 2 | a0001c0001t0009g0306 a0001c0001t0009g0319 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.520-1167_520-1110d others(60): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630044 | |||||||
| chr22:38630181 | C | T | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-1246G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630181 | |||||||
| chr22:38630227 | G | A | 1 | a0001c0001t0010g0060 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.520-1292C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630227 | |||||||
| chr22:38630269 | G | A | 1 | a0001c0001t0003g0246 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.520-1334C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630269 | |||||||
| chr22:38630280 | C | T | 1 | a0002c0002t0011g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-1345G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630280 | |||||||
| chr22:38630483 | C | T | 1 | a0001c0001t0042g0074 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.520-1548G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630483 | |||||||
| chr22:38630484 | G | C | 1 | a0001c0001t0008g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.520-1549C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630484 | |||||||
| chr22:38630659 | A | C | 2 | a0002c0002t0004g0170 a0002c0002t0025g0193 |
2 | NA18979.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.520-1724T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630659 | |||||||
| chr22:38630734 | C | T | 44 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(41): Show |
44 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.520-1799G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630734 | |||||||
| chr22:38630773 | C | T | 2 | a0001c0001t0005g0008 a0001c0001t0005g0032 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.520-1838G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630773 | |||||||
| chr22:38630791 | G | C | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.520-1856C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630791 | |||||||
| chr22:38630842 | C | A | 5 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(2): Show |
5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-1907G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630842 | |||||||
| chr22:38630867 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-1932G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630867 | |||||||
| chr22:38630906 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0091 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.520-1971C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38630906 | |||||||
| chr22:38631107 | G | A | 1 | a0002c0002t0011g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.520-2172C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631107 | |||||||
| chr22:38631281 | CAG | C | 135 | a0001c0001t0001g0014 a0001c0001t0001g0094 a0001c0001t0001g0114 others(132): Show |
136 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.520-2348_520-2347d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631281 | |||||||
| chr22:38631325 | G | A | 1 | a0001c0001t0006g0030 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.520-2390C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631325 | |||||||
| chr22:38631607 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.520-2672C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631607 | |||||||
| chr22:38631629 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0079 a0001c0001t0001g0145 others(1): Show |
4 | HG00408.hp1 HG00438.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-2694G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631629 | |||||||
| chr22:38631759 | CA | C | 6 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0025 others(3): Show |
7 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-2825delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631759 | |||||||
| chr22:38631760 | AG | A | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-2826delC | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38631760 | |||||||
| chr22:38632007 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.520-3072G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632007 | |||||||
| chr22:38632089 | T | C | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.520-3154A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632089 | |||||||
| chr22:38632091 | G | GA | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.520-3157dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632091 | |||||||
| chr22:38632135 | A | C | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.520-3200T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632135 | |||||||
| chr22:38632178 | A | C | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.520-3243T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632178 | |||||||
| chr22:38632426 | G | A | 4 | a0001c0001t0008g0034 a0001c0001t0008g0036 a0001c0001t0008g0037 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3491C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632426 | |||||||
| chr22:38632427 | C | T | 8 | a0002c0002t0011g0172 a0002c0002t0011g0174 a0002c0002t0011g0199 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-3492G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632427 | |||||||
| chr22:38632692 | G | T | 1 | a0002c0002t0011g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-3757C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632692 | |||||||
| chr22:38632817 | C | T | 5 | a0001c0001t0005g0017 a0001c0001t0005g0020 a0001c0001t0005g0021 others(2): Show |
5 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+3634G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632817 | |||||||
| chr22:38632908 | C | T | 202 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(199): Show |
206 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.519+3543G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632908 | |||||||
| chr22:38632984 | G | A | 2 | a0001c0001t0017g0168 a0001c0001t0017g0169 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.519+3467C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38632984 | |||||||
| chr22:38633306 | G | GT | 8 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+3144dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38633306 | |||||||
| chr22:38633471 | A | G | 1 | a0001c0001t0055g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.519+2980T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38633471 | |||||||
| chr22:38633647 | T | C | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.519+2804A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38633647 | |||||||
| chr22:38633690 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.519+2761A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38633690 | |||||||
| chr22:38634199 | G | T | 5 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(2): Show |
5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+2252C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634199 | |||||||
| chr22:38634200 | A | T | 5 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(2): Show |
5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+2251T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634200 | |||||||
| chr22:38634221 | C | CA | 85 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0002g0217 others(82): Show |
86 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.519+2229dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634221 | |||||||
| chr22:38634221 | C | CAA | 18 | a0001c0001t0002g0257 a0001c0001t0002g0265 a0001c0001t0002g0316 others(15): Show |
18 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.519+2228_519+2229d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634221 | |||||||
| chr22:38634221 | CA | C | 46 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0049 others(43): Show |
47 | HG00408.hp2 HG00673.hp2 HG01515.hp2 others(44): Show |
intron_variant | MODIFIER | c.519+2229delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634221 | |||||||
| chr22:38634254 | TAG | T | 3 | a0001c0003t0012g0005 a0001c0003t0012g0160 a0001c0003t0031g0157 |
4 | HG02109.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2195_519+2196d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634254 | |||||||
| chr22:38634396 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.519+2055A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634396 | |||||||
| chr22:38634410 | T | G | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.519+2041A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634410 | |||||||
| chr22:38634851 | G | A | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+1600C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634851 | |||||||
| chr22:38634894 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+1557A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634894 | |||||||
| chr22:38634947 | A | G | 9 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0025 others(6): Show |
10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+1504T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38634947 | |||||||
| chr22:38635157 | C | T | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.519+1294G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635157 | |||||||
| chr22:38635181 | G | A | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.519+1270C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635181 | |||||||
| chr22:38635182 | C | T | 1 | a0001c0001t0027g0075 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.519+1269G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635182 | |||||||
| chr22:38635190 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.519+1261G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635190 | |||||||
| chr22:38635228 | C | CA | 19 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0001c0001t0001g0086 others(16): Show |
20 | HG01433.hp2 HG01934.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.519+1222dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635228 | |||||||
| chr22:38635228 | CA | C | 154 | a0001c0001t0001g0124 a0001c0001t0001g0145 a0001c0001t0001g0148 others(151): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.519+1222delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635228 | |||||||
| chr22:38635657 | A | G | 1 | a0001c0001t0002g0262 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.519+794T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635657 | |||||||
| chr22:38635894 | G | C | 7 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0002g0233 others(4): Show |
7 | NA18939.hp1 NA18961.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+557C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635894 | |||||||
| chr22:38635896 | C | T | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+555G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38635896 | |||||||
| chr22:38636055 | GGAAA | G | 7 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0002g0233 others(4): Show |
7 | NA18939.hp1 NA18961.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+392_519+395del others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636055 | |||||||
| chr22:38636107 | C | CAGAAA | 136 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(133): Show |
139 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.519+339_519+343dup others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636107 | |||||||
| chr22:38636122 | A | AAG | 45 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(42): Show |
46 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.519+328_519+329ins others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636122 | |||||||
| chr22:38636126 | G | A | 45 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(42): Show |
46 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.519+325C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636126 | |||||||
| chr22:38636160 | T | C | 6 | a0002c0002t0004g0171 a0002c0002t0004g0184 a0002c0002t0004g0188 others(3): Show |
6 | NA18983.hp2 NA18994.hp2 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+291A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636160 | |||||||
| chr22:38636247 | T | C | 1 | a0001c0001t0003g0297 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.519+204A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636247 | |||||||
| chr22:38636265 | C | T | 236 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0094 others(233): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.519+186G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636265 | |||||||
| chr22:38636343 | C | T | 54 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(51): Show |
54 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.519+108G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 6/16 | chr22 | 38636343 | |||||||
| chr22:38636671 | C | T | 3 | a0001c0001t0002g0225 a0001c0001t0002g0277 a0001c0001t0002g0278 |
3 | HG00609.hp1 NA18951.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.373-74G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636671 | |||||||
| chr22:38636685 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.373-88G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636685 | |||||||
| chr22:38636728 | T | C | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.373-131A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636728 | |||||||
| chr22:38636766 | ATTTCT | A | 34 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(31): Show |
35 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.373-174_373-170del others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636766 | |||||||
| chr22:38636766 | ATTTCTT | A | 10 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(7): Show |
10 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-175_373-170del others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636766 | |||||||
| chr22:38636770 | CT | C | 111 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0045 others(108): Show |
112 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.373-174delA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636770 | |||||||
| chr22:38636774 | T | A | 3 | a0002c0002t0019g0173 a0002c0002t0019g0185 a0002c0002t0019g0195 |
3 | NA18944.hp1 NA18964.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.373-177A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636774 | |||||||
| chr22:38636775 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.373-178A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636775 | |||||||
| chr22:38636920 | G | A | 1 | a0001c0001t0009g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.373-323C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38636920 | |||||||
| chr22:38637043 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.373-446C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637043 | |||||||
| chr22:38637115 | A | G | 4 | a0001c0001t0003g0236 a0001c0001t0003g0250 a0001c0001t0003g0280 others(1): Show |
4 | HG00558.hp1 NA18942.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-518T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637115 | |||||||
| chr22:38637193 | G | A | 1 | a0001c0001t0026g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.373-596C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637193 | |||||||
| chr22:38637306 | T | C | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.373-709A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637306 | |||||||
| chr22:38637613 | C | A | 2 | a0001c0001t0017g0168 a0001c0001t0017g0169 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.373-1016G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637613 | |||||||
| chr22:38637663 | G | A | 1 | a0001c0001t0051g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.373-1066C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637663 | |||||||
| chr22:38637969 | C | T | 4 | a0001c0001t0003g0296 a0001c0001t0003g0301 a0001c0001t0003g0320 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+777G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38637969 | |||||||
| chr22:38638670 | C | G | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.372+76G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 5/16 | chr22 | 38638670 | |||||||
| chr22:38638862 | G | A | 95 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.296-40C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38638862 | |||||||
| chr22:38639408 | C | CG | 48 | a0001c0001t0002g0225 a0001c0001t0002g0229 a0001c0001t0002g0233 others(45): Show |
49 | HG00408.hp2 HG01243.hp2 HG01891.hp2 others(46): Show |
intron_variant | MODIFIER | c.295+246dupC | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639408 | |||||||
| chr22:38639409 | G | GA | 6 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0017g0168 others(3): Show |
6 | HG02027.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+245dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639409 | |||||||
| chr22:38639409 | GA | G | 39 | a0001c0001t0001g0013 a0001c0001t0001g0123 a0001c0001t0002g0232 others(36): Show |
41 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.295+245delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639409 | |||||||
| chr22:38639410 | A | G | 85 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(82): Show |
86 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.295+245T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639410 | |||||||
| chr22:38639411 | A | G | 3 | a0001c0001t0002g0232 a0001c0001t0002g0303 a0001c0001t0003g0312 |
3 | NA18979.hp1 NA19068.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.295+244T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639411 | |||||||
| chr22:38639462 | T | C | 4 | a0002c0002t0011g0172 a0002c0002t0011g0199 a0002c0002t0011g0202 others(1): Show |
4 | HG02145.hp1 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+193A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639462 | |||||||
| chr22:38639574 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.295+81C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 4/16 | chr22 | 38639574 | |||||||
| chr22:38639755 | G | A | 6 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-31C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38639755 | |||||||
| chr22:38639848 | G | C | 2 | a0002c0002t0011g0203 a0002c0002t0011g0205 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.226-124C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38639848 | |||||||
| chr22:38640137 | C | A | 1 | a0001c0001t0002g0286 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.226-413G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640137 | |||||||
| chr22:38640263 | G | A | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.226-539C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640263 | |||||||
| chr22:38640275 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.226-551A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640275 | |||||||
| chr22:38640293 | A | G | 1 | a0001c0001t0005g0017 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.226-569T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640293 | |||||||
| chr22:38640324 | C | T | 22 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(19): Show |
23 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.226-600G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640324 | |||||||
| chr22:38640455 | A | C | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.226-731T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640455 | |||||||
| chr22:38640764 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.226-1040A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640764 | |||||||
| chr22:38640927 | G | T | 1 | a0001c0001t0036g0131 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.226-1203C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38640927 | |||||||
| chr22:38641125 | GGA | G | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.226-1403_226-1402d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641125 | |||||||
| chr22:38641422 | C | T | 1 | a0001c0001t0002g0285 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.226-1698G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641422 | |||||||
| chr22:38641512 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.226-1788A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641512 | |||||||
| chr22:38641547 | A | G | 201 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(198): Show |
205 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.226-1823T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641547 | |||||||
| chr22:38641551 | C | CA | 10 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0090 others(7): Show |
10 | HG00741.hp1 HG02015.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-1828dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641551 | |||||||
| chr22:38641551 | CA | C | 196 | a0001c0001t0001g0092 a0001c0001t0002g0217 a0001c0001t0002g0225 others(193): Show |
200 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.226-1828delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641551 | |||||||
| chr22:38641559 | A | C | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.226-1835T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641559 | |||||||
| chr22:38641564 | A | C | 46 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(43): Show |
47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.226-1840T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641564 | |||||||
| chr22:38641699 | T | TGTTG | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.226-1979_226-1976d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641699 | |||||||
| chr22:38641868 | C | T | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-2144G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641868 | |||||||
| chr22:38641917 | C | G | 2 | a0001c0001t0018g0136 a0001c0001t0018g0137 |
2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.226-2193G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641917 | |||||||
| chr22:38641948 | G | GAT | 23 | a0001c0001t0003g0321 a0001c0001t0017g0168 a0001c0001t0017g0169 others(20): Show |
23 | HG00408.hp2 HG00673.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.226-2225_226-2224i others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | |||||||
| chr22:38641948 | G | GATGT | 14 | a0002c0002t0004g0171 a0002c0002t0004g0179 a0002c0002t0004g0180 others(11): Show |
15 | NA18952.hp2 NA18962.hp1 NA18980.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-2225_226-2224i others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | |||||||
| chr22:38641948 | G | GGT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(60): Show |
65 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.226-2226_226-2225d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | |||||||
| chr22:38641948 | G | GGTGT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0049 a0001c0001t0001g0054 others(9): Show |
12 | HG00423.hp1 HG01167.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-2228_226-2225d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | |||||||
| chr22:38641948 | G | GGTGTGT | 5 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(2): Show |
5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-2230_226-2225d others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | |||||||
| chr22:38641948 | GGT | G | 18 | a0001c0001t0002g0225 a0001c0001t0002g0258 a0001c0001t0002g0263 others(15): Show |
18 | HG00609.hp1 HG02135.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.226-2226_226-2225d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | |||||||
| chr22:38641948 | GGTGTGTG others(7): Show |
G | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-2238_226-2225d others(16): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641948 | |||||||
| chr22:38641949 | G | A | 99 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(96): Show |
100 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.226-2225C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641949 | |||||||
| chr22:38641951 | G | A | 18 | a0001c0001t0002g0225 a0001c0001t0002g0258 a0001c0001t0002g0263 others(15): Show |
18 | HG00609.hp1 HG02135.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.226-2227C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641951 | |||||||
| chr22:38641957 | G | A | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.226-2233C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641957 | |||||||
| chr22:38641964 | TGTGTGTG others(9): Show |
T | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226-2256_226-2241d others(18): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641964 | |||||||
| chr22:38641972 | T | C | 4 | a0001c0001t0003g0222 a0001c0001t0003g0296 a0001c0001t0003g0312 others(1): Show |
4 | HG00642.hp1 HG02280.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-2248A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641972 | |||||||
| chr22:38641974 | T | C | 114 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(111): Show |
115 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.226-2250A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641974 | |||||||
| chr22:38641974 | T | TGC | 28 | a0001c0001t0001g0014 a0001c0001t0001g0094 a0001c0001t0001g0100 others(25): Show |
28 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.226-2252_226-2251d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641974 | |||||||
| chr22:38641974 | T | TGTGC | 17 | a0001c0001t0001g0098 a0001c0001t0001g0140 a0001c0001t0005g0008 others(14): Show |
18 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.226-2251_226-2250i others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641974 | |||||||
| chr22:38641974 | T | TGTGTGC | 11 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0005g0022 others(8): Show |
11 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.226-2251_226-2250i others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641974 | |||||||
| chr22:38641976 | CGCACGTG others(5): Show |
C | 8 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0305 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-2264_226-2253d others(14): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641976 | |||||||
| chr22:38641979 | A | G | 181 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(178): Show |
185 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.226-2255T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38641979 | |||||||
| chr22:38642044 | C | T | 4 | a0001c0001t0003g0296 a0001c0001t0003g0301 a0001c0001t0003g0320 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-2320G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642044 | |||||||
| chr22:38642141 | A | G | 1 | a0001c0001t0051g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.226-2417T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642141 | |||||||
| chr22:38642152 | C | T | 1 | a0001c0001t0040g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.226-2428G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642152 | |||||||
| chr22:38642263 | T | C | 1 | a0001c0001t0037g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.226-2539A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642263 | |||||||
| chr22:38642341 | C | T | 6 | a0001c0001t0002g0225 a0001c0001t0002g0275 a0001c0001t0002g0276 others(3): Show |
6 | HG00609.hp1 NA18951.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-2617G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642341 | |||||||
| chr22:38642705 | G | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.225+2858C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642705 | |||||||
| chr22:38642785 | A | C | 105 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(102): Show |
106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.225+2778T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642785 | |||||||
| chr22:38642791 | T | C | 189 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(186): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.225+2772A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642791 | |||||||
| chr22:38642993 | T | C | 42 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(39): Show |
43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.225+2570A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38642993 | |||||||
| chr22:38643036 | T | A | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.225+2527A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643036 | |||||||
| chr22:38643159 | A | G | 4 | a0002c0002t0004g0179 a0002c0002t0004g0180 a0002c0002t0004g0209 others(1): Show |
4 | NA18962.hp1 NA18982.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+2404T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643159 | |||||||
| chr22:38643181 | T | C | 4 | a0001c0001t0008g0034 a0001c0001t0008g0036 a0001c0001t0008g0037 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+2382A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643181 | |||||||
| chr22:38643201 | A | G | 6 | a0001c0001t0005g0008 a0001c0001t0005g0023 a0001c0001t0005g0032 others(3): Show |
6 | HG00735.hp1 HG01261.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+2362T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643201 | |||||||
| chr22:38643315 | C | CA | 42 | a0001c0001t0036g0131 a0002c0002t0004g0170 a0002c0002t0004g0171 others(39): Show |
43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.225+2247dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643315 | |||||||
| chr22:38643328 | ATAG | A | 4 | a0001c0001t0003g0007 a0001c0001t0003g0294 a0001c0001t0009g0214 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+2232_225+2234d others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643328 | |||||||
| chr22:38643329 | TAGTG | T | 106 | a0001c0001t0001g0091 a0001c0001t0002g0217 a0001c0001t0002g0218 others(103): Show |
106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.225+2230_225+2233d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643329 | |||||||
| chr22:38643332 | T | A | 4 | a0001c0001t0003g0007 a0001c0001t0003g0294 a0001c0001t0009g0214 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+2231A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643332 | |||||||
| chr22:38643333 | G | T | 4 | a0001c0001t0003g0007 a0001c0001t0003g0294 a0001c0001t0009g0214 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+2230C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643333 | |||||||
| chr22:38643400 | C | T | 4 | a0001c0001t0002g0217 a0001c0001t0002g0226 a0001c0001t0002g0227 others(1): Show |
4 | NA18983.hp1 NA19012.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+2163G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643400 | |||||||
| chr22:38643449 | G | C | 6 | a0001c0001t0005g0017 a0001c0001t0005g0020 a0001c0001t0005g0021 others(3): Show |
6 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+2114C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643449 | |||||||
| chr22:38643465 | G | A | 7 | a0001c0001t0001g0068 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG02165.hp1 HG04184.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+2098C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643465 | |||||||
| chr22:38643615 | T | A | 2 | a0001c0001t0009g0309 a0001c0001t0009g0310 |
2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+1948A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643615 | |||||||
| chr22:38643704 | C | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.225+1859G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643704 | |||||||
| chr22:38643850 | G | C | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.225+1713C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643850 | |||||||
| chr22:38643962 | A | G | 4 | a0001c0001t0008g0034 a0001c0001t0008g0036 a0001c0001t0008g0037 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1601T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38643962 | |||||||
| chr22:38644008 | G | A | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1555C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644008 | |||||||
| chr22:38644015 | C | T | 1 | a0001c0001t0003g0235 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.225+1548G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644015 | |||||||
| chr22:38644019 | C | T | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.225+1544G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644019 | |||||||
| chr22:38644038 | C | T | 5 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(2): Show |
5 | HG01243.hp2 HG01433.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+1525G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644038 | |||||||
| chr22:38644095 | G | A | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.225+1468C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644095 | |||||||
| chr22:38644145 | C | CA | 57 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0051 others(54): Show |
58 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.225+1417dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644145 | |||||||
| chr22:38644145 | C | CAA | 32 | a0002c0002t0004g0171 a0002c0002t0004g0177 a0002c0002t0004g0186 others(29): Show |
33 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.225+1416_225+1417d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644145 | |||||||
| chr22:38644145 | CA | C | 11 | a0001c0001t0001g0052 a0001c0001t0002g0257 a0001c0001t0002g0260 others(8): Show |
11 | HG00408.hp1 HG00733.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.225+1417delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644145 | |||||||
| chr22:38644145 | CAAAAAAA | C | 6 | a0002c0002t0004g0179 a0002c0002t0004g0180 a0002c0002t0004g0181 others(3): Show |
6 | NA18962.hp1 NA18980.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+1411_225+1417d others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644145 | |||||||
| chr22:38644274 | G | A | 167 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.225+1289C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644274 | |||||||
| chr22:38644315 | A | AAAAGAGG others(78): Show |
6 | a0001c0001t0001g0073 a0001c0001t0005g0017 a0001c0001t0005g0020 others(3): Show |
6 | HG01928.hp2 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+1163_225+1247d others(87): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644315 | A | AAAAGAGG others(4328): Show |
2 | a0001c0001t0002g0278 a0001c0001t0002g0316 |
2 | HG00609.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.225+1247_225+1248i others(4337): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644315 | A | AAAAGAGG others(4328): Show |
1 | a0001c0001t0002g0275 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.225+1247_225+1248i others(4337): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644315 | A | AAAAGAGG others(4243): Show |
1 | a0001c0001t0002g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.225+1247_225+1248i others(4252): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644315 | A | AAAAGAGG others(1608): Show |
1 | a0001c0001t0003g0248 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.225+1247_225+1248i others(1617): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644315 | A | AAAAGAGG others(3053): Show |
1 | a0001c0001t0003g0230 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.225+1247_225+1248i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644315 | A | AAAAGAGG others(4838): Show |
1 | a0001c0001t0003g0247 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.225+1247_225+1248i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644315 | A | AAAAGAGG others(2033): Show |
1 | a0001c0001t0003g0321 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.225+1247_225+1248i others(2042): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644315 | AAAAGAGG others(78): Show |
A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0043g0144 |
3 | HG02056.hp2 NA19002.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.225+1163_225+1247d others(87): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644315 | |||||||
| chr22:38644337 | A | ACAGAGGA others(78): Show |
2 | a0001c0001t0017g0168 a0001c0001t0017g0169 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.225+1225_225+1226i others(87): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644337 | |||||||
| chr22:38644337 | A | ACAGAGGA others(4413): Show |
1 | a0001c0001t0002g0277 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.225+1225_225+1226i others(4422): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644337 | |||||||
| chr22:38644337 | A | G | 109 | a0001c0001t0001g0072 a0001c0001t0002g0217 a0001c0001t0002g0218 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.225+1226T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644337 | |||||||
| chr22:38644341 | AGGACTGT others(3): Show |
A | 42 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(39): Show |
43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.225+1212_225+1221d others(12): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644341 | |||||||
| chr22:38644370 | T | C | 93 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(90): Show |
94 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.225+1193A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | |||||||
| chr22:38644370 | T | CGTGACAC others(3562): Show |
1 | a0001c0001t0009g0215 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.225+1193_225+1194i others(3571): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | |||||||
| chr22:38644370 | T | CGTGACAC others(3563): Show |
1 | a0001c0001t0009g0214 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.225+1193_225+1194i others(3572): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | |||||||
| chr22:38644370 | T | CGTGACAC others(6368): Show |
2 | a0001c0001t0002g0263 a0001c0001t0002g0299 |
2 | NA18942.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.225+1193_225+1194i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | |||||||
| chr22:38644370 | T | CGTGACAC others(5093): Show |
1 | a0001c0001t0016g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225+1193_225+1194i others(5102): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644370 | |||||||
| chr22:38644395 | G | A | 2 | a0001c0001t0016g0279 a0001c0001t0050g0273 |
2 | HG00280.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.225+1168C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644395 | |||||||
| chr22:38644404 | G | C | 1 | a0001c0001t0003g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225+1159C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644404 | |||||||
| chr22:38644415 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.225+1148C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644415 | |||||||
| chr22:38644422 | A | G | 111 | a0001c0001t0001g0071 a0001c0001t0001g0135 a0001c0001t0002g0217 others(108): Show |
112 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.225+1141T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644422 | |||||||
| chr22:38644423 | C | AAGAGGAC others(4328): Show |
1 | a0001c0001t0002g0225 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.225+1140_225+1141i others(4337): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644423 | |||||||
| chr22:38644446 | A | ACTATGCT others(3567): Show |
1 | a0001c0001t0002g0233 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3576): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(3053): Show |
1 | a0001c0001t0050g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4668): Show |
1 | a0001c0001t0055g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4677): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4838): Show |
1 | a0001c0001t0003g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5960): Show |
1 | a0001c0001t0002g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5969): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5943): Show |
1 | a0001c0001t0002g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5952): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(3138): Show |
1 | a0001c0001t0053g0239 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3147): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5263): Show |
1 | a0001c0001t0003g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5272): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(3053): Show |
2 | a0001c0001t0003g0240 a0001c0001t0021g0241 |
2 | HG03927.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4923): Show |
1 | a0001c0001t0003g0250 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4753): Show |
1 | a0001c0001t0003g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4762): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4413): Show |
1 | a0001c0001t0003g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4422): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4413): Show |
1 | a0001c0001t0003g0007 | 2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(4422): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4923): Show |
1 | a0001c0001t0003g0235 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(2373): Show |
7 | a0001c0001t0009g0288 a0001c0001t0009g0302 a0001c0001t0009g0306 others(4): Show |
7 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1116_225+1117i others(2382): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(2373): Show |
1 | a0001c0001t0009g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(2382): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4835): Show |
2 | a0001c0001t0015g0290 a0001c0001t0015g0292 |
2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(4844): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6453): Show |
1 | a0001c0001t0002g0317 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6462): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(3138): Show |
1 | a0001c0001t0003g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3147): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(3053): Show |
9 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0223 others(6): Show |
9 | HG01099.hp1 HG02027.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+1116_225+1117i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(3053): Show |
1 | a0001c0001t0003g0220 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(3062): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4923): Show |
1 | a0001c0001t0003g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5008): Show |
1 | a0001c0001t0054g0300 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5017): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4923): Show |
1 | a0001c0001t0003g0320 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4838): Show |
1 | a0001c0001t0003g0236 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6538): Show |
1 | a0001c0001t0002g0226 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6547): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5008): Show |
1 | a0001c0001t0051g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5017): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5688): Show |
1 | a0001c0001t0003g0280 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5697): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4838): Show |
1 | a0001c0001t0003g0281 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4921): Show |
1 | a0001c0001t0003g0312 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4930): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4838): Show |
2 | a0001c0001t0003g0237 a0001c0001t0052g0318 |
2 | NA19009.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4750): Show |
1 | a0001c0001t0015g0308 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4759): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5603): Show |
1 | a0001c0001t0003g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5612): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5688): Show |
1 | a0001c0001t0003g0272 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5697): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4923): Show |
1 | a0001c0001t0003g0297 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4838): Show |
1 | a0001c0001t0003g0246 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4838): Show |
1 | a0001c0001t0003g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4847): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4923): Show |
1 | a0001c0001t0003g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4932): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6198): Show |
1 | a0001c0001t0003g0271 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6207): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(3393): Show |
2 | a0001c0001t0002g0285 a0001c0001t0002g0286 |
2 | HG02040.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(3402): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5603): Show |
1 | a0001c0001t0003g0287 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5612): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6368): Show |
2 | a0001c0001t0002g0232 a0001c0001t0002g0303 |
2 | NA18979.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6368): Show |
3 | a0001c0001t0016g0284 a0001c0001t0049g0268 a0001c0001t0056g0269 |
3 | HG01433.hp1 HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6453): Show |
1 | a0001c0001t0002g0258 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6462): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6368): Show |
6 | a0001c0001t0002g0217 a0001c0001t0002g0227 a0001c0001t0002g0228 others(3): Show |
6 | NA18959.hp1 NA18980.hp2 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6113): Show |
1 | a0001c0001t0002g0313 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6122): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5603): Show |
1 | a0001c0001t0002g0282 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5612): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6368): Show |
2 | a0001c0001t0002g0218 a0001c0001t0002g0265 |
2 | HG00741.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5858): Show |
1 | a0001c0001t0002g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5867): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6368): Show |
1 | a0001c0001t0002g0267 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6368): Show |
1 | a0001c0001t0002g0314 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6368): Show |
1 | a0001c0001t0026g0261 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6377): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4668): Show |
1 | a0001c0001t0002g0256 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4677): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6538): Show |
1 | a0001c0001t0020g0253 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6547): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6538): Show |
1 | a0001c0001t0020g0255 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6547): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5943): Show |
1 | a0001c0001t0002g0266 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5952): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5858): Show |
1 | a0001c0001t0002g0270 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5867): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4583): Show |
1 | a0001c0001t0003g0238 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4592): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6198): Show |
1 | a0001c0001t0002g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6207): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4413): Show |
1 | a0001c0001t0002g0257 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4422): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6453): Show |
1 | a0001c0001t0016g0279 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6462): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6453): Show |
1 | a0001c0001t0020g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6462): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(5858): Show |
1 | a0001c0001t0002g0289 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(5867): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6573): Show |
1 | a0001c0001t0002g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6582): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6198): Show |
1 | a0001c0001t0002g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6207): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(4835): Show |
1 | a0001c0001t0015g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.225+1116_225+1117i others(4844): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | ACTATGCT others(6538): Show |
1 | a0001c0001t0026g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.225+1116_225+1117i others(6547): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644446 | A | C | 7 | a0001c0001t0002g0263 a0001c0001t0002g0299 a0001c0001t0003g0230 others(4): Show |
7 | HG00558.hp2 NA18942.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1117T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644446 | |||||||
| chr22:38644455 | T | C | 6 | a0001c0001t0002g0225 a0001c0001t0002g0275 a0001c0001t0002g0276 others(3): Show |
6 | HG00609.hp1 NA18951.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+1108A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644455 | |||||||
| chr22:38644462 | C | G | 4 | a0001c0001t0003g0236 a0001c0001t0020g0253 a0001c0001t0020g0254 others(1): Show |
4 | HG01346.hp1 HG02451.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+1101G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644462 | |||||||
| chr22:38644507 | A | ACAGAGGA others(78): Show |
2 | a0001c0001t0001g0071 a0001c0001t0001g0135 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.225+1055_225+1056i others(87): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644507 | |||||||
| chr22:38644507 | A | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.225+1056T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644507 | |||||||
| chr22:38644520 | G | A | 46 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(43): Show |
47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.225+1043C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644520 | |||||||
| chr22:38644527 | C | T | 2 | a0001c0001t0002g0256 a0001c0001t0002g0257 |
2 | HG01074.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.225+1036G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644527 | |||||||
| chr22:38644532 | C | G | 1 | a0001c0001t0003g0235 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.225+1031G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644532 | |||||||
| chr22:38644583 | T | A | 4 | a0001c0001t0003g0296 a0001c0001t0003g0301 a0001c0001t0003g0320 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+980A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644583 | |||||||
| chr22:38644591 | T | C | 9 | a0001c0001t0006g0001 a0001c0001t0006g0019 a0001c0001t0006g0025 others(6): Show |
10 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.225+972A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644591 | |||||||
| chr22:38644593 | TACA | T | 105 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(102): Show |
106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.225+967_225+969del others(3): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644593 | |||||||
| chr22:38644597 | A | C | 46 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(43): Show |
47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.225+966T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644597 | |||||||
| chr22:38644612 | T | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.225+951A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644612 | |||||||
| chr22:38644728 | G | A | 106 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(103): Show |
107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.225+835C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644728 | |||||||
| chr22:38644758 | T | C | 5 | a0001c0003t0012g0005 a0001c0003t0012g0159 a0001c0003t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+805A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644758 | |||||||
| chr22:38644809 | C | T | 4 | a0001c0001t0008g0034 a0001c0001t0008g0036 a0001c0001t0008g0037 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+754G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644809 | |||||||
| chr22:38644810 | G | A | 1 | a0001c0001t0003g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.225+753C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644810 | |||||||
| chr22:38644820 | G | A | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.225+743C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644820 | |||||||
| chr22:38644840 | C | G | 36 | a0001c0001t0003g0007 a0001c0001t0003g0213 a0001c0001t0003g0220 others(33): Show |
37 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.225+723G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644840 | |||||||
| chr22:38644885 | T | C | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.225+678A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38644885 | |||||||
| chr22:38645019 | G | T | 1 | a0001c0001t0006g0031 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.225+544C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645019 | |||||||
| chr22:38645030 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+533A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645030 | |||||||
| chr22:38645036 | A | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.225+527T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645036 | |||||||
| chr22:38645080 | T | C | 1 | a0001c0001t0006g0031 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.225+483A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645080 | |||||||
| chr22:38645087 | AAAAT | A | 111 | a0001c0001t0001g0119 a0001c0001t0002g0217 a0001c0001t0002g0218 others(108): Show |
112 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.225+472_225+475del others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645087 | |||||||
| chr22:38645087 | AAAATAAA others(1): Show |
A | 42 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(39): Show |
43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.225+468_225+475del others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645087 | |||||||
| chr22:38645141 | T | C | 1 | a0001c0001t0007g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.225+422A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645141 | |||||||
| chr22:38645252 | A | G | 4 | a0001c0001t0015g0290 a0001c0001t0015g0291 a0001c0001t0015g0292 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+311T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645252 | |||||||
| chr22:38645284 | G | A | 2 | a0001c0001t0002g0317 a0001c0001t0016g0279 |
2 | HG00280.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.225+279C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645284 | |||||||
| chr22:38645483 | AGGGCACT others(21): Show |
A | 2 | a0001c0001t0005g0008 a0001c0001t0005g0032 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.225+52_225+79delCG others(26): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | 38645483 | |||||||
| chr22:38645783 | ATTTC | A | 4 | a0001c0001t0005g0142 a0001c0001t0017g0167 a0001c0001t0017g0168 others(1): Show |
4 | HG00735.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-142_143-139del others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38645783 | |||||||
| chr22:38646209 | C | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-564G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646209 | |||||||
| chr22:38646214 | C | G | 46 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(43): Show |
47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.143-569G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646214 | |||||||
| chr22:38646216 | G | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-571C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646216 | |||||||
| chr22:38646248 | C | CT | 28 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(25): Show |
28 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.143-604dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | |||||||
| chr22:38646248 | C | CTTTTT | 9 | a0001c0001t0008g0042 a0001c0001t0013g0164 a0001c0001t0013g0165 others(6): Show |
10 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-608_143-604dup others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | |||||||
| chr22:38646248 | C | CTTTTTTT | 6 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0013g0162 others(3): Show |
6 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-610_143-604dup others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | |||||||
| chr22:38646248 | CTTTTTTT | C | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0002g0232 others(9): Show |
12 | HG02055.hp2 HG02129.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.143-610_143-604del others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | |||||||
| chr22:38646248 | CTTTTTTT others(1): Show |
C | 116 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(113): Show |
118 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.143-611_143-604del others(8): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | |||||||
| chr22:38646248 | CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0002g0282 a0001c0001t0002g0289 a0001c0001t0003g0280 others(6): Show |
9 | HG02897.hp1 HG03516.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-612_143-604del others(9): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | |||||||
| chr22:38646248 | CTTTTTTT others(3): Show |
C | 38 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0179 others(35): Show |
39 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.143-613_143-604del others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | |||||||
| chr22:38646248 | CTTTTTTT others(4): Show |
C | 1 | a0002c0004t0045g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.143-614_143-604del others(11): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646248 | |||||||
| chr22:38646292 | C | T | 1 | a0001c0001t0017g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.143-647G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646292 | |||||||
| chr22:38646299 | G | A | 2 | a0001c0001t0005g0008 a0001c0001t0005g0032 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.143-654C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646299 | |||||||
| chr22:38646299 | G | T | 1 | a0001c0001t0036g0131 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.143-654C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646299 | |||||||
| chr22:38646320 | C | T | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.143-675G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646320 | |||||||
| chr22:38646328 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.143-683G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646328 | |||||||
| chr22:38646416 | C | T | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02027.hp2 HG02056.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-771G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646416 | |||||||
| chr22:38646423 | C | T | 1 | a0001c0001t0003g0230 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.143-778G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646423 | |||||||
| chr22:38646426 | ATTT | A | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-784_143-782del others(3): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646426 | |||||||
| chr22:38646541 | C | T | 1 | a0002c0002t0014g0176 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.143-896G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646541 | |||||||
| chr22:38646556 | C | T | 1 | a0001c0001t0003g0312 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.143-911G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646556 | |||||||
| chr22:38646657 | A | T | 6 | a0001c0001t0003g0321 a0001c0001t0015g0290 a0001c0001t0015g0291 others(3): Show |
6 | HG02055.hp2 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-1012T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646657 | |||||||
| chr22:38646660 | T | A | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143-1015A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646660 | |||||||
| chr22:38646769 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-1124T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646769 | |||||||
| chr22:38646813 | C | A | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-1168G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38646813 | |||||||
| chr22:38647016 | G | A | 105 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(102): Show |
106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.143-1371C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647016 | |||||||
| chr22:38647132 | G | A | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.143-1487C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647132 | |||||||
| chr22:38647153 | ATAAAT | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-1513_143-1509d others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647153 | |||||||
| chr22:38647154 | TAAATA | T | 108 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(105): Show |
109 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-1514_143-1510d others(7): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647154 | |||||||
| chr22:38647169 | A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-1524T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647169 | |||||||
| chr22:38647193 | G | A | 1 | a0001c0001t0003g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.143-1548C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647193 | |||||||
| chr22:38647471 | C | CA | 8 | a0001c0001t0002g0289 a0001c0001t0013g0162 a0001c0001t0013g0163 others(5): Show |
8 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-1827dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647471 | |||||||
| chr22:38647486 | T | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-1841A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38647486 | |||||||
| chr22:38648078 | G | A | 22 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(19): Show |
23 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.142+1949C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648078 | |||||||
| chr22:38648094 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.142+1933C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648094 | |||||||
| chr22:38648146 | T | C | 1 | a0001c0003t0012g0160 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.142+1881A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648146 | |||||||
| chr22:38648147 | G | C | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+1880C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648147 | |||||||
| chr22:38648305 | T | TA | 43 | a0001c0001t0005g0032 a0001c0001t0041g0146 a0002c0002t0004g0170 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.142+1721dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648305 | |||||||
| chr22:38648305 | TA | T | 113 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(110): Show |
115 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.142+1721delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648305 | |||||||
| chr22:38648357 | AAGCACTT others(358): Show |
A | 7 | a0001c0001t0013g0162 a0001c0001t0013g0163 a0001c0001t0013g0164 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.142+1305_142+1669d others(2): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648357 | |||||||
| chr22:38648422 | A | C | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+1605T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648422 | |||||||
| chr22:38648443 | T | C | 4 | a0002c0002t0004g0186 a0002c0002t0004g0197 a0002c0002t0004g0208 others(1): Show |
4 | HG04184.hp1 NA18974.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+1584A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648443 | |||||||
| chr22:38648531 | C | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+1496G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648531 | |||||||
| chr22:38648555 | C | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+1472G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648555 | |||||||
| chr22:38648608 | G | GAAAC | 108 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(105): Show |
109 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.142+1415_142+1418d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648608 | |||||||
| chr22:38648649 | G | A | 42 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(39): Show |
43 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.142+1378C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648649 | |||||||
| chr22:38648700 | C | T | 1 | a0001c0001t0005g0020 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.142+1327G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648700 | |||||||
| chr22:38648801 | C | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+1226G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648801 | |||||||
| chr22:38648873 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.142+1154C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648873 | |||||||
| chr22:38648971 | C | CA | 6 | a0001c0001t0029g0039 a0001c0001t0044g0128 a0002c0002t0011g0202 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+1055dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648971 | |||||||
| chr22:38648971 | CA | C | 103 | a0001c0001t0001g0049 a0001c0001t0002g0217 a0001c0001t0002g0218 others(100): Show |
104 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.142+1055delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38648971 | |||||||
| chr22:38649094 | T | C | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.142+933A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649094 | |||||||
| chr22:38649335 | C | G | 1 | a0001c0001t0002g0289 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.142+692G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649335 | |||||||
| chr22:38649336 | G | C | 1 | a0001c0001t0002g0289 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.142+691C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649336 | |||||||
| chr22:38649427 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.142+600T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649427 | |||||||
| chr22:38649456 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.142+571G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649456 | |||||||
| chr22:38649565 | C | CA | 9 | a0001c0001t0001g0004 a0001c0001t0015g0290 a0001c0001t0015g0291 others(6): Show |
10 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+461dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649565 | |||||||
| chr22:38649787 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.142+240C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649787 | |||||||
| chr22:38649879 | AGAAAG | A | 105 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(102): Show |
106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.142+143_142+147del others(5): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649879 | |||||||
| chr22:38649879 | AGAAAGAA others(3): Show |
A | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.142+138_142+147del others(10): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649879 | |||||||
| chr22:38649889 | G | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.142+138C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649889 | |||||||
| chr22:38649890 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.142+137T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38649890 | |||||||
| chr22:38650023 | A | G | 1 | a0001c0001t0003g0296 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.142+4T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 2/16 | chr22 | 38650023 | |||||||
| chr22:38650322 | T | C | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-94-60A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38650322 | |||||||
| chr22:38650695 | A | C | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-94-433T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38650695 | |||||||
| chr22:38650715 | C | T | 5 | a0001c0001t0002g0217 a0001c0001t0002g0226 a0001c0001t0002g0227 others(2): Show |
5 | NA18980.hp2 NA18983.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.-94-453G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38650715 | |||||||
| chr22:38650849 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-94-587A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38650849 | |||||||
| chr22:38651273 | C | G | 1 | a0002c0004t0045g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-94-1011G>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651273 | |||||||
| chr22:38651430 | G | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-94-1168C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651430 | |||||||
| chr22:38651438 | A | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-94-1176T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651438 | |||||||
| chr22:38651523 | G | A | 1 | a0001c0001t0013g0165 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-94-1261C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651523 | |||||||
| chr22:38651795 | G | GCT | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-94-1534_-94-1533i others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651795 | |||||||
| chr22:38651886 | T | C | 1 | a0001c0001t0029g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-94-1624A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651886 | |||||||
| chr22:38651989 | C | T | 46 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(43): Show |
47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.-94-1727G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38651989 | |||||||
| chr22:38652186 | AAAAT | A | 46 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 others(43): Show |
47 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.-94-1928_-94-1925d others(6): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652186 | |||||||
| chr22:38652281 | A | T | 1 | a0001c0001t0001g0047 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-94-2019T>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652281 | |||||||
| chr22:38652311 | A | G | 155 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-94-2049T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652311 | |||||||
| chr22:38652444 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01071.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-94-2182G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652444 | |||||||
| chr22:38652609 | G | A | 6 | a0001c0001t0007g0133 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94-2347C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652609 | |||||||
| chr22:38652713 | C | T | 22 | a0001c0001t0005g0008 a0001c0001t0005g0017 a0001c0001t0005g0020 others(19): Show |
23 | HG00735.hp1 HG01261.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.-94-2451G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652713 | |||||||
| chr22:38652738 | G | A | 2 | a0001c0001t0003g0007 a0001c0001t0003g0294 |
3 | HG03490.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-94-2476C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652738 | |||||||
| chr22:38652750 | T | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-94-2488A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652750 | |||||||
| chr22:38652800 | C | T | 1 | a0001c0001t0003g0321 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-94-2538G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652800 | |||||||
| chr22:38652872 | A | G | 203 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(200): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.-94-2610T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652872 | |||||||
| chr22:38652876 | C | CA | 17 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0147 others(14): Show |
17 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.-94-2615dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652876 | |||||||
| chr22:38652876 | CA | C | 12 | a0001c0001t0001g0016 a0001c0001t0002g0295 a0001c0001t0002g0299 others(9): Show |
12 | HG01175.hp1 HG02280.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-94-2615delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652876 | |||||||
| chr22:38652876 | CAA | C | 98 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(95): Show |
99 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-94-2616_-94-2615d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652876 | |||||||
| chr22:38652900 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-94-2638G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38652900 | |||||||
| chr22:38653037 | T | C | 1 | a0001c0001t0022g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-94-2775A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653037 | |||||||
| chr22:38653051 | T | C | 1 | a0001c0001t0030g0155 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-94-2789A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653051 | |||||||
| chr22:38653225 | A | C | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-95+2895T>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653225 | |||||||
| chr22:38653312 | A | G | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-95+2808T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653312 | |||||||
| chr22:38653337 | T | C | 1 | a0001c0001t0005g0142 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-95+2783A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653337 | |||||||
| chr22:38653377 | C | CT | 96 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(93): Show |
97 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-95+2742dupA | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653377 | |||||||
| chr22:38653377 | C | CTT | 10 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(7): Show |
10 | HG00609.hp2 HG00741.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-95+2741_-95+2742d others(4): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653377 | |||||||
| chr22:38653587 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-95+2533C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653587 | |||||||
| chr22:38653607 | C | T | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-95+2513G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653607 | |||||||
| chr22:38653889 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-95+2231T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38653889 | |||||||
| chr22:38654114 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-95+2006G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654114 | |||||||
| chr22:38654145 | C | T | 1 | a0001c0001t0003g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-95+1975G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654145 | |||||||
| chr22:38654226 | T | C | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.-95+1894A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654226 | |||||||
| chr22:38654241 | T | G | 2 | a0001c0001t0009g0309 a0001c0001t0009g0310 |
2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-95+1879A>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654241 | |||||||
| chr22:38654775 | C | CA | 8 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0005g0143 others(5): Show |
8 | HG00140.hp1 HG01928.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95+1344dupT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654775 | |||||||
| chr22:38654775 | CA | C | 140 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(137): Show |
142 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-95+1344delT | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38654775 | |||||||
| chr22:38655009 | G | A | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02280.hp1 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-95+1111C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655009 | |||||||
| chr22:38655119 | G | A | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-95+1001C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655119 | |||||||
| chr22:38655306 | G | C | 43 | a0002c0002t0004g0170 a0002c0002t0004g0171 a0002c0002t0004g0177 others(40): Show |
44 | HG00408.hp2 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.-95+814C>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655306 | |||||||
| chr22:38655339 | G | A | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-95+781C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655339 | |||||||
| chr22:38655356 | G | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02027.hp2 HG02056.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.-95+764C>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655356 | |||||||
| chr22:38655392 | A | G | 2 | a0001c0001t0009g0214 a0001c0001t0009g0215 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-95+728T>C | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655392 | |||||||
| chr22:38655423 | T | C | 167 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-95+697A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655423 | |||||||
| chr22:38655671 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-95+449A>G | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655671 | |||||||
| chr22:38655700 | C | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-95+420G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655700 | |||||||
| chr22:38655785 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-95+335G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38655785 | |||||||
| chr22:38656006 | C | A | 1 | a0001c0001t0003g0321 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-95+114G>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656006 | |||||||
| chr22:38656037 | T | A | 1 | a0001c0001t0001g0009 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-95+83A>T | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656037 | |||||||
| chr22:38656045 | G | T | 1 | a0001c0001t0001g0009 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-95+75C>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656045 | |||||||
| chr22:38656081 | C | T | 1 | a0001c0001t0005g0008 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-95+39G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656081 | |||||||
| chr22:38656111 | C | T | 109 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0225 others(106): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-95+9G>A | FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 1/16 | chr22 | 38656111 |