Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55007 |
| ensemblid | ENSG00000100376.12 |
| hgncid | 1313 |
| symbol | FAM118A |
| name | family with sequence similarity 118 member A |
| refseq_nuc | NM_017911.4 |
| refseq_prot | NP_060381.2 |
| ensembl_nuc | ENST00000441876.7 |
| ensembl_prot | ENSP00000395892.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 45309934 |
| end | 45341955 |
| strand | + |
| ver | v1.2 |
| region | chr22:45309934-45341955 |
| region5000 | chr22:45304934-45346955 |
| regionname0 | FAM118A_chr22_45309934_45341955 |
| regionname5000 | FAM118A_chr22_45304934_45346955 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 161 | 227 | 79 | 35 | 93 | 4 | 15 | 70 | FAM118A_chr22_45304934_45346955 | FAM118A | MDSVE others(156): Show |
chr22 | 45304934 | 45346955 |
| a0002 | 1/0 | 357 | 177 | 12 | 37 | 89 | 14 | 24 | 69 | FAM118A_chr22_45304934_45346955 | FAM118A | MDSVE others(352): Show |
chr22 | 45304934 | 45346955 |
| a0003 | 0/0 | 161 | 7 | 3 | 1 | 1 | 0 | 2 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | MDSVE others(156): Show |
chr22 | 45304934 | 45346955 |
| a0004 | 0/0 | 357 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | MDSVE others(352): Show |
chr22 | 45304934 | 45346955 |
| a0005 | 0/0 | 203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | MDSVE others(198): Show |
chr22 | 45304934 | 45346955 |
| a0006 | 0/0 | 161 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | MDSVE others(156): Show |
chr22 | 45304934 | 45346955 |
| a0007 | 0/0 | 357 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | MDSVE others(352): Show |
chr22 | 45304934 | 45346955 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1007 | 225 | 79 | 34 | 92 | 4 | 15 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1002): Show |
chr22 | 45304934 | 45346955 | ||
| a0001c0007 | 0/0 | 1007 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1002): Show |
chr22 | 45304934 | 45346955 | ||
| a0001c0009 | 0/0 | 1007 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1002): Show |
chr22 | 45304934 | 45346955 | ||
| a0002c0002 | 0/0 | 1071 | 124 | 4 | 34 | 57 | 14 | 15 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1066): Show |
chr22 | 45304934 | 45346955 | ||
| a0002c0003 | 1/0 | 1071 | 51 | 8 | 3 | 30 | 0 | 9 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1066): Show |
chr22 | 45304934 | 45346955 | ||
| a0002c0006 | 0/0 | 1071 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1066): Show |
chr22 | 45304934 | 45346955 | ||
| a0003c0004 | 0/0 | 1007 | 7 | 3 | 1 | 1 | 0 | 2 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1002): Show |
chr22 | 45304934 | 45346955 | ||
| a0004c0005 | 0/0 | 1071 | 2 | 1 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1066): Show |
chr22 | 45304934 | 45346955 | ||
| a0005c0010 | 0/0 | 1153 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1148): Show |
chr22 | 45304934 | 45346955 | ||
| a0006c0008 | 0/0 | 1007 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1002): Show |
chr22 | 45304934 | 45346955 | ||
| a0007c0011 | 0/0 | 1071 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | ATGGA others(1066): Show |
chr22 | 45304934 | 45346955 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2819 | 138 | 56 | 17 | 50 | 3 | 11 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0002 | 0/0 | 2819 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0003 | 0/0 | 2819 | 3 | 0 | 3 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0004 | 0/0 | 2819 | 53 | 9 | 12 | 28 | 1 | 3 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0005 | 0/0 | 2818 | 21 | 10 | 1 | 9 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2813): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0007 | 0/0 | 2819 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0008 | 0/0 | 2819 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0011 | 0/0 | 2819 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0013 | 0/0 | 2819 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0015 | 0/0 | 2819 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0016 | 0/0 | 2819 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0001t0017 | 0/0 | 2819 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0007t0001 | 0/0 | 2819 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0001c0009t0001 | 0/0 | 2819 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0002c0002t0001 | 0/0 | 2883 | 3 | 0 | 0 | 1 | 2 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0002c0002t0002 | 0/0 | 2883 | 120 | 4 | 34 | 56 | 11 | 15 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0002c0002t0009 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0002c0003t0003 | 1/0 | 2883 | 46 | 6 | 3 | 27 | 0 | 9 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0002c0003t0006 | 0/0 | 2883 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0002c0003t0012 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0002c0003t0014 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0002c0006t0002 | 0/0 | 2883 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0003c0004t0001 | 0/0 | 2819 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0003c0004t0003 | 0/0 | 2819 | 3 | 1 | 1 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0003c0004t0010 | 0/0 | 2819 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0003c0004t0018 | 0/0 | 2819 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0004c0005t0003 | 0/0 | 2883 | 2 | 1 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| a0005c0010t0003 | 0/0 | 2965 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2960): Show |
chr22 | 45304934 | 45346955 |
| a0006c0008t0001 | 0/0 | 2819 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2814): Show |
chr22 | 45304934 | 45346955 |
| a0007c0011t0002 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | GCGGC others(2878): Show |
chr22 | 45304934 | 45346955 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0011g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0013g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0016g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0001t0017g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0007t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0001c0009t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0002t0009g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0003t0014g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0006t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0002c0006t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0003c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0003c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0003c0004t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0003c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0003c0004t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0003c0004t0010g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0003c0004t0018g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0004c0005t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0004c0005t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0005c0010t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0006c0008t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| a0007c0011t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0080 | EUR | GBR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0062 | EUR | GBR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0065 | EUR | GBR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0071 | EUR | GBR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0083 | EUR | FIN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | FIN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0141 | EUR | FIN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00408 | hp1 | a0001 | c0009 | t0001 | g0284 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00408 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00423 | hp1 | a0002 | c0003 | t0003 | g0230 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00597 | hp2 | a0002 | c0003 | t0003 | g0032 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00609 | hp1 | a0002 | c0003 | t0003 | g0205 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0121 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00639 | hp2 | a0001 | c0007 | t0001 | g0047 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | CHS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0078 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG00741 | hp2 | a0001 | c0001 | t0016 | g0025 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0142 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0095 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0146 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0097 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0169 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0111 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0193 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0253 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01257 | hp2 | a0002 | c0003 | t0003 | g0028 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01258 | hp2 | a0002 | c0003 | t0003 | g0028 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0144 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0068 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0064 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0052 | EUR | IBS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0020 | EUR | IBS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0061 | EUR | IBS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0166 | EUR | IBS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0020 | EUR | IBS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0167 | EUR | IBS | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01884 | hp2 | a0002 | c0003 | t0003 | g0330 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0108 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01928 | hp2 | a0003 | c0004 | t0003 | g0226 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0091 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0149 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01975 | hp1 | a0005 | c0010 | t0003 | g0232 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0067 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0090 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0070 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0152 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02004 | hp2 | a0002 | c0003 | t0003 | g0011 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02027 | hp1 | a0002 | c0003 | t0003 | g0235 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02055 | hp2 | a0002 | c0003 | t0003 | g0329 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02074 | hp2 | a0002 | c0003 | t0003 | g0236 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0206 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02132 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02135 | hp1 | a0003 | c0004 | t0018 | g0225 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0107 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | CDX | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02165 | hp2 | a0002 | c0003 | t0003 | g0031 | EAS | CDX | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02257 | hp1 | a0003 | c0004 | t0001 | g0173 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02258 | hp1 | a0002 | c0003 | t0012 | g0282 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0328 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02280 | hp2 | a0002 | c0003 | t0003 | g0030 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0100 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02451 | hp1 | a0002 | c0003 | t0003 | g0208 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02523 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | KHV | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02602 | hp2 | a0003 | c0004 | t0010 | g0227 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02698 | hp2 | a0002 | c0003 | t0003 | g0250 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02717 | hp1 | a0002 | c0003 | t0014 | g0201 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02717 | hp2 | a0003 | c0004 | t0001 | g0172 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0133 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02738 | hp1 | a0002 | c0003 | t0003 | g0034 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0145 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0332 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02886 | hp1 | a0001 | c0001 | t0017 | g0203 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02970 | hp1 | a0006 | c0008 | t0001 | g0016 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02976 | hp1 | a0003 | c0004 | t0003 | g0248 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0207 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03130 | hp1 | a0002 | c0003 | t0003 | g0030 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0056 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0094 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03492 | hp2 | a0002 | c0003 | t0003 | g0320 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0079 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03669 | hp1 | a0002 | c0003 | t0003 | g0229 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | STU | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03688 | hp2 | a0002 | c0003 | t0003 | g0234 | SAS | STU | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0128 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0096 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0093 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03710 | hp2 | a0002 | c0003 | t0003 | g0212 | SAS | PJL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03831 | hp1 | a0002 | c0003 | t0003 | g0035 | SAS | BEB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | BEB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0099 | SAS | BEB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03834 | hp2 | a0004 | c0005 | t0003 | g0240 | SAS | BEB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03942 | hp1 | a0003 | c0004 | t0003 | g0247 | SAS | BEB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0283 | SAS | BEB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0143 | SAS | STU | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0252 | SAS | STU | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | STU | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | STU | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | CHB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | CHB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0170 | AFR | YRI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18941 | hp1 | a0007 | c0011 | t0002 | g0002 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18943 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18944 | hp1 | a0002 | c0003 | t0003 | g0033 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18945 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18952 | hp1 | a0002 | c0003 | t0003 | g0287 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18957 | hp1 | a0002 | c0003 | t0003 | g0286 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0335 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18959 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18966 | hp2 | a0002 | c0003 | t0003 | g0228 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18970 | hp2 | a0002 | c0003 | t0003 | g0204 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18971 | hp1 | a0002 | c0006 | t0002 | g0140 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0336 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18977 | hp2 | a0002 | c0003 | t0003 | g0033 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18983 | hp2 | a0002 | c0003 | t0006 | g0032 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18984 | hp1 | a0002 | c0006 | t0002 | g0126 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18989 | hp1 | a0002 | c0003 | t0003 | g0251 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19005 | hp2 | a0002 | c0003 | t0003 | g0237 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | LWK | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19054 | hp1 | a0002 | c0003 | t0003 | g0031 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0241 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19064 | hp1 | a0002 | c0003 | t0006 | g0035 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19068 | hp2 | a0002 | c0003 | t0006 | g0233 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19074 | hp1 | a0002 | c0003 | t0003 | g0242 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19078 | hp1 | a0001 | c0001 | t0008 | g0202 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19079 | hp2 | a0002 | c0003 | t0003 | g0238 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19085 | hp1 | a0001 | c0001 | t0011 | g0306 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19089 | hp1 | a0002 | c0003 | t0003 | g0231 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ASW | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ASW | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0085 | EUR | TSI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20752 | hp2 | a0002 | c0002 | t0009 | g0057 | EUR | TSI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0086 | EUR | TSI | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20905 | hp1 | a0002 | c0003 | t0003 | g0034 | SAS | GIH | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | GIH | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0289 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0112 | AMR | CLM | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0087 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | MSL | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG06807 | hp1 | a0004 | c0005 | t0003 | g0239 | AFR | USA | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0249 | AFR | USA | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | USA | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | LWK | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0266 | REF | REF | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0003 | g0224 | REF | REF | FAM118A_chr22_45304934_45346955 | FAM118A | chr22 | 45304934 | 45346955 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45327926 | G | C | 3 | a0001 a0004 a0006 |
229 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
missense_variant | MODERATE | c.385G>C | p.Val129Leu | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/9 | 644/2883 | 385/1074 | 129/357 | chr22 | 45327926 | |||
| chr22:45327965 | G | A | 1 | a0006 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.424G>A | p.Ala142Thr | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/9 | 683/2883 | 424/1074 | 142/357 | chr22 | 45327965 | |||
| chr22:45327998 | C | A | 1 | a0007 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.457C>A | p.Leu153Met | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/9 | 716/2883 | 457/1074 | 153/357 | chr22 | 45327998 | |||
| chr22:45328021 | G | C | 1 | a0002 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.480G>C | p.Gln160His | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/9 | 739/2883 | 480/1074 | 160/357 | chr22 | 45328021 | |||
| chr22:45332489 | G | A | 2 | a0001 a0006 |
226 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(223): Show |
missense_variant | MODERATE | c.716G>A | p.Arg239His | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/9 | 975/2883 | 716/1074 | 239/357 | chr22 | 45332489 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45323223 | G | A | 1 | a0001c0007 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.96G>A | p.Leu32Leu | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/9 | 355/2883 | 96/1074 | 32/357 | chr22 | 45323223 | |||
| chr22:45327898 | C | T | 1 | a0002c0006 | 2 | NA18971.hp1 NA18984.hp1 |
synonymous_variant | LOW | c.357C>T | p.Asp119Asp | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/9 | 616/2883 | 357/1074 | 119/357 | chr22 | 45327898 | |||
| chr22:45327961 | G | A | 5 | a0001c0001 a0001c0007 a0001c0009 others(2): Show |
229 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
synonymous_variant | LOW | c.420G>A | p.Arg140Arg | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/9 | 679/2883 | 420/1074 | 140/357 | chr22 | 45327961 | |||
| chr22:45327973 | C | G | 3 | a0002c0002 a0002c0006 a0007c0011 |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
synonymous_variant | LOW | c.432C>G | p.Val144Val | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/9 | 691/2883 | 432/1074 | 144/357 | chr22 | 45327973 | |||
| chr22:45328039 | C | T | 1 | a0002c0002 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.498C>T | p.Ser166Ser | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/9 | 757/2883 | 498/1074 | 166/357 | chr22 | 45328039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45310123 | C | T | 1 | a0003c0004t0018 | 1 | HG02135.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/9 | chr22 | 45310123 | |||||||
| chr22:45340446 | T | G | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*41T>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 41 | chr22 | 45340446 | ||||||
| chr22:45340553 | C | G | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(12): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*148C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 148 | chr22 | 45340553 | ||||||
| chr22:45340604 | C | T | 7 | a0001c0001t0002 a0001c0001t0011 a0002c0002t0002 others(4): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*199C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 199 | chr22 | 45340604 | ||||||
| chr22:45340634 | G | T | 1 | a0001c0001t0017 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*229G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 229 | chr22 | 45340634 | ||||||
| chr22:45340808 | CT | C | 1 | a0001c0001t0005 | 21 | HG00558.hp2 HG01257.hp1 HG02559.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*414delT | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 414 | INFO_REALIGN_3_PRIME | chr22 | 45340808 | |||||
| chr22:45340886 | A | G | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(19): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*481A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 481 | chr22 | 45340886 | ||||||
| chr22:45340990 | T | C | 5 | a0001c0001t0002 a0001c0001t0011 a0002c0002t0002 others(2): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*585T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 585 | chr22 | 45340990 | ||||||
| chr22:45341049 | C | T | 1 | a0001c0001t0016 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 644 | chr22 | 45341049 | ||||||
| chr22:45341409 | G | A | 7 | a0001c0001t0002 a0001c0001t0011 a0002c0002t0002 others(4): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1004 | chr22 | 45341409 | ||||||
| chr22:45341429 | A | G | 16 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(13): Show |
228 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1024A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1024 | chr22 | 45341429 | ||||||
| chr22:45341600 | T | C | 16 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(13): Show |
228 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1195T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1195 | chr22 | 45341600 | ||||||
| chr22:45341606 | G | A | 6 | a0001c0001t0002 a0001c0001t0011 a0002c0002t0002 others(3): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1201G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1201 | chr22 | 45341606 | ||||||
| chr22:45341634 | G | A | 1 | a0001c0001t0013 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1229G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1229 | chr22 | 45341634 | ||||||
| chr22:45341659 | G | T | 1 | a0001c0001t0007 | 2 | HG02280.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1254G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1254 | chr22 | 45341659 | ||||||
| chr22:45341819 | A | G | 1 | a0001c0001t0015 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1414A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1414 | chr22 | 45341819 | ||||||
| chr22:45341856 | T | G | 1 | a0002c0003t0014 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1451T>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1451 | chr22 | 45341856 | ||||||
| chr22:45341906 | A | G | 3 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0016 |
55 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1501A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1501 | chr22 | 45341906 | ||||||
| chr22:45341936 | A | T | 1 | a0001c0001t0011 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 9/9 | 1531 | chr22 | 45341936 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45310188 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.-10+5G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45310188 | |||||||
| chr22:45310234 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10+51C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45310234 | |||||||
| chr22:45310278 | G | T | 1 | a0001c0001t0001g0337 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+95G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45310278 | |||||||
| chr22:45310398 | T | C | 2 | a0001c0001t0004g0052 a0001c0001t0004g0053 |
2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-10+215T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45310398 | |||||||
| chr22:45310633 | C | A | 1 | a0001c0001t0004g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-10+450C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45310633 | |||||||
| chr22:45310840 | C | G | 4 | a0002c0002t0002g0333 a0002c0002t0002g0334 a0002c0002t0002g0335 others(1): Show |
4 | HG02015.hp1 NA18952.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+657C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45310840 | |||||||
| chr22:45310860 | T | TTAGG | 5 | a0001c0001t0001g0331 a0001c0001t0007g0328 a0001c0001t0007g0332 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+678_-10+681dup others(4): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 45310860 | ||||||
| chr22:45310896 | C | A | 123 | a0001c0001t0001g0060 a0002c0002t0001g0085 a0002c0002t0001g0086 others(120): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-10+713C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45310896 | |||||||
| chr22:45310923 | A | C | 1 | a0002c0002t0002g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-10+740A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45310923 | |||||||
| chr22:45311034 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0013g0170 |
3 | HG03130.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-10+851T>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311034 | |||||||
| chr22:45311113 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(60): Show |
88 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-10+930A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311113 | |||||||
| chr22:45311200 | C | T | 2 | a0002c0003t0003g0286 a0002c0003t0003g0287 |
2 | NA18952.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-10+1017C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311200 | |||||||
| chr22:45311247 | G | A | 1 | a0002c0002t0002g0055 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-10+1064G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311247 | |||||||
| chr22:45311319 | C | T | 2 | a0002c0002t0002g0166 a0002c0002t0002g0167 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-10+1136C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311319 | |||||||
| chr22:45311344 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0171 |
7 | HG02647.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+1161G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311344 | |||||||
| chr22:45311630 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-10+1447A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311630 | |||||||
| chr22:45311639 | G | T | 124 | a0001c0001t0001g0060 a0001c0009t0001g0284 a0002c0002t0001g0085 others(121): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.-10+1456G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311639 | |||||||
| chr22:45311782 | G | C | 2 | a0003c0004t0001g0172 a0003c0004t0001g0173 |
2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-10+1599G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311782 | |||||||
| chr22:45311856 | C | G | 124 | a0001c0001t0001g0060 a0001c0009t0001g0284 a0002c0002t0001g0085 others(121): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.-10+1673C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311856 | |||||||
| chr22:45311913 | C | G | 1 | a0001c0001t0004g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-10+1730C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45311913 | |||||||
| chr22:45312006 | G | T | 1 | a0001c0001t0007g0332 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-10+1823G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312006 | |||||||
| chr22:45312021 | G | T | 13 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0002g0156 others(10): Show |
13 | HG00621.hp2 NA18940.hp2 NA18955.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+1838G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312021 | |||||||
| chr22:45312035 | T | C | 44 | a0001c0001t0001g0195 a0001c0001t0001g0288 a0001c0001t0004g0005 others(41): Show |
52 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-10+1852T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312035 | |||||||
| chr22:45312162 | C | T | 1 | a0001c0001t0008g0202 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-10+1979C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312162 | |||||||
| chr22:45312215 | C | A | 1 | a0002c0002t0002g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10+2032C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312215 | |||||||
| chr22:45312216 | A | T | 1 | a0002c0002t0002g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10+2033A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312216 | |||||||
| chr22:45312259 | A | C | 1 | a0001c0001t0005g0040 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-10+2076A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312259 | |||||||
| chr22:45312405 | G | A | 1 | a0001c0001t0017g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-10+2222G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312405 | |||||||
| chr22:45312470 | C | T | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-10+2287C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312470 | |||||||
| chr22:45312518 | C | CAA | 6 | a0002c0003t0003g0009 a0002c0003t0003g0204 a0002c0003t0003g0205 others(3): Show |
8 | HG00408.hp2 HG00609.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+2340_-10+2341d others(4): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 45312518 | ||||||
| chr22:45312629 | T | C | 2 | a0002c0003t0003g0207 a0002c0003t0003g0208 |
2 | HG02451.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-10+2446T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312629 | |||||||
| chr22:45312672 | A | C | 1 | a0001c0001t0001g0327 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-10+2489A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312672 | |||||||
| chr22:45312742 | C | T | 123 | a0001c0001t0001g0060 a0002c0002t0001g0085 a0002c0002t0001g0086 others(120): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-10+2559C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312742 | |||||||
| chr22:45312768 | G | A | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-10+2585G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312768 | |||||||
| chr22:45312923 | G | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-10+2740G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45312923 | |||||||
| chr22:45313079 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
65 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.-10+2896C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45313079 | |||||||
| chr22:45313080 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10+2897G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45313080 | |||||||
| chr22:45313319 | G | GT | 27 | a0001c0001t0001g0019 a0001c0001t0001g0195 a0001c0001t0001g0210 others(24): Show |
29 | HG00558.hp1 HG00733.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.-10+3156dupT | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 45313319 | ||||||
| chr22:45313319 | GT | G | 119 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0060 others(116): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.-10+3156delT | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 45313319 | ||||||
| chr22:45313386 | G | A | 1 | a0001c0001t0004g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-10+3203G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45313386 | |||||||
| chr22:45313588 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10+3405G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45313588 | |||||||
| chr22:45313619 | A | G | 1 | a0001c0001t0005g0276 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-10+3436A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45313619 | |||||||
| chr22:45313839 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-10+3656C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45313839 | |||||||
| chr22:45313848 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-10+3665C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45313848 | |||||||
| chr22:45313996 | G | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0006c0008t0001g0016 |
4 | HG02818.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+3813G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45313996 | |||||||
| chr22:45314031 | C | T | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-10+3848C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314031 | |||||||
| chr22:45314099 | G | T | 1 | a0002c0006t0002g0140 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-10+3916G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314099 | |||||||
| chr22:45314203 | T | C | 1 | a0001c0001t0004g0174 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-10+4020T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314203 | |||||||
| chr22:45314324 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0322 |
3 | HG00280.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-10+4141C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314324 | |||||||
| chr22:45314359 | AAAACT | A | 123 | a0001c0001t0001g0060 a0002c0002t0001g0085 a0002c0002t0001g0086 others(120): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-10+4182_-10+4186d others(7): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 45314359 | ||||||
| chr22:45314361 | A | G | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-10+4178A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314361 | |||||||
| chr22:45314385 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0006c0008t0001g0016 |
4 | HG02818.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4202T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314385 | |||||||
| chr22:45314403 | G | T | 1 | a0001c0001t0004g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-10+4220G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314403 | |||||||
| chr22:45314445 | G | C | 1 | a0001c0001t0001g0026 | 2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-10+4262G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314445 | |||||||
| chr22:45314516 | C | T | 23 | a0002c0002t0001g0139 a0002c0002t0002g0002 a0002c0002t0002g0134 others(20): Show |
26 | HG00438.hp1 HG00621.hp2 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.-10+4333C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314516 | |||||||
| chr22:45314522 | G | T | 1 | a0003c0004t0003g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-10+4339G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314522 | |||||||
| chr22:45314883 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10+4700G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314883 | |||||||
| chr22:45314933 | G | T | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-10+4750G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45314933 | |||||||
| chr22:45315104 | T | G | 1 | a0001c0001t0004g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-10+4921T>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315104 | |||||||
| chr22:45315278 | T | C | 19 | a0001c0001t0001g0042 a0001c0001t0001g0292 a0001c0001t0001g0293 others(16): Show |
26 | HG00558.hp2 HG01257.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-10+5095T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315278 | |||||||
| chr22:45315487 | G | A | 1 | a0002c0002t0002g0059 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-10+5304G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315487 | |||||||
| chr22:45315514 | T | C | 4 | a0001c0001t0004g0005 a0001c0001t0004g0175 a0001c0001t0004g0177 others(1): Show |
7 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+5331T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315514 | |||||||
| chr22:45315517 | T | A | 4 | a0001c0001t0004g0005 a0001c0001t0004g0175 a0001c0001t0004g0177 others(1): Show |
7 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+5334T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315517 | |||||||
| chr22:45315519 | A | T | 4 | a0001c0001t0004g0005 a0001c0001t0004g0175 a0001c0001t0004g0177 others(1): Show |
7 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+5336A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315519 | |||||||
| chr22:45315565 | C | T | 1 | a0002c0002t0002g0152 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-10+5382C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315565 | |||||||
| chr22:45315677 | T | TAGGTTTA others(26): Show |
3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0321 |
3 | HG02055.hp1 NA18522.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-10+5556_-10+5588d others(35): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 45315677 | ||||||
| chr22:45315738 | G | T | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01943.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+5555G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315738 | |||||||
| chr22:45315973 | G | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-10+5790G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45315973 | |||||||
| chr22:45316176 | A | G | 1 | a0002c0002t0002g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-10+5993A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45316176 | |||||||
| chr22:45316282 | C | T | 19 | a0001c0001t0001g0042 a0001c0001t0001g0292 a0001c0001t0001g0293 others(16): Show |
26 | HG00558.hp2 HG01257.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9-6089C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45316282 | |||||||
| chr22:45317013 | C | T | 2 | a0002c0003t0003g0241 a0002c0003t0003g0242 |
2 | NA19056.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-9-5358C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317013 | |||||||
| chr22:45317063 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9-5308G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317063 | |||||||
| chr22:45317103 | A | C | 1 | a0001c0001t0001g0321 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-9-5268A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317103 | |||||||
| chr22:45317139 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-9-5232A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317139 | |||||||
| chr22:45317182 | G | T | 1 | a0001c0001t0001g0319 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-9-5189G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317182 | |||||||
| chr22:45317304 | G | A | 8 | a0001c0001t0001g0060 a0002c0002t0002g0020 a0002c0002t0002g0056 others(5): Show |
9 | HG00099.hp2 HG00323.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-5067G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317304 | |||||||
| chr22:45317332 | T | C | 1 | a0002c0003t0003g0206 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-9-5039T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317332 | |||||||
| chr22:45317677 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(43): Show |
66 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-9-4694C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317677 | |||||||
| chr22:45317850 | G | A | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01943.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-4521G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317850 | |||||||
| chr22:45317883 | G | A | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-9-4488G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317883 | |||||||
| chr22:45317986 | C | T | 1 | a0001c0001t0017g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9-4385C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45317986 | |||||||
| chr22:45318169 | A | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
5 | HG01433.hp2 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-4202A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318169 | |||||||
| chr22:45318339 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-9-4032C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318339 | |||||||
| chr22:45318354 | G | A | 1 | a0002c0002t0002g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-9-4017G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318354 | |||||||
| chr22:45318420 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-9-3951G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318420 | |||||||
| chr22:45318452 | C | T | 1 | a0003c0004t0001g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9-3919C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318452 | |||||||
| chr22:45318474 | C | T | 4 | a0002c0002t0002g0130 a0002c0002t0002g0131 a0002c0002t0002g0132 others(1): Show |
4 | NA18945.hp1 NA18967.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-3897C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318474 | |||||||
| chr22:45318511 | T | C | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01943.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-3860T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318511 | |||||||
| chr22:45318517 | C | T | 341 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(338): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.-9-3854C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318517 | |||||||
| chr22:45318608 | T | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-9-3763T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45318608 | |||||||
| chr22:45319056 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
224 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9-3315T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45319056 | |||||||
| chr22:45319062 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9-3309C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45319062 | |||||||
| chr22:45319226 | G | A | 1 | a0001c0001t0017g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9-3145G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45319226 | |||||||
| chr22:45319355 | G | C | 2 | a0001c0001t0001g0022 a0001c0001t0013g0170 |
3 | HG03130.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-9-3016G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45319355 | |||||||
| chr22:45319708 | C | T | 2 | a0002c0002t0002g0128 a0002c0002t0002g0129 |
2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-9-2663C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45319708 | |||||||
| chr22:45319727 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
224 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9-2644C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45319727 | |||||||
| chr22:45319743 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
224 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9-2628A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45319743 | |||||||
| chr22:45319827 | C | T | 1 | a0002c0003t0014g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9-2544C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45319827 | |||||||
| chr22:45320006 | A | G | 127 | a0001c0001t0001g0019 a0002c0002t0001g0085 a0002c0002t0001g0086 others(124): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.-9-2365A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45320006 | |||||||
| chr22:45320099 | G | A | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-9-2272G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45320099 | |||||||
| chr22:45320516 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
229 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-9-1855A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45320516 | |||||||
| chr22:45320593 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9-1778A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45320593 | |||||||
| chr22:45320720 | G | A | 1 | a0003c0004t0003g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-9-1651G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45320720 | |||||||
| chr22:45320794 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-1577C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45320794 | |||||||
| chr22:45320795 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-1576T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45320795 | |||||||
| chr22:45320973 | CAT | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0050 others(14): Show |
21 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9-1397_-9-1396del others(2): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45320973 | |||||||
| chr22:45321052 | G | A | 1 | a0002c0002t0002g0066 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-9-1319G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321052 | |||||||
| chr22:45321109 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9-1262A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321109 | |||||||
| chr22:45321139 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0317 |
2 | HG02258.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-9-1232C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321139 | |||||||
| chr22:45321179 | C | T | 1 | a0002c0002t0002g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-9-1192C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321179 | |||||||
| chr22:45321319 | G | A | 1 | a0001c0001t0017g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9-1052G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321319 | |||||||
| chr22:45321388 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-9-983C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321388 | |||||||
| chr22:45321405 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-966T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321405 | |||||||
| chr22:45321406 | A | T | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-965A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321406 | |||||||
| chr22:45321411 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-960T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321411 | |||||||
| chr22:45321416 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-955T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321416 | |||||||
| chr22:45321457 | G | A | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-9-914G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321457 | |||||||
| chr22:45321631 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0278 |
2 | HG01261.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-9-740G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321631 | |||||||
| chr22:45321643 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
224 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9-728C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321643 | |||||||
| chr22:45321721 | G | T | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-650G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321721 | |||||||
| chr22:45321723 | A | G | 2 | a0002c0002t0002g0166 a0002c0002t0002g0167 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-9-648A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321723 | |||||||
| chr22:45321969 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-402T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321969 | |||||||
| chr22:45321978 | C | A | 1 | a0001c0001t0001g0318 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-9-393C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321978 | |||||||
| chr22:45321978 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
223 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.-9-393C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45321978 | |||||||
| chr22:45322077 | G | A | 1 | a0001c0001t0004g0179 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-9-294G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45322077 | |||||||
| chr22:45322160 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
226 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-9-211A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 1/8 | chr22 | 45322160 | |||||||
| chr22:45322746 | G | A | 123 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(120): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.47+320G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | chr22 | 45322746 | |||||||
| chr22:45322862 | A | G | 123 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(120): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.48-313A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | chr22 | 45322862 | |||||||
| chr22:45323041 | C | CTG | 66 | a0001c0001t0001g0042 a0001c0001t0001g0215 a0001c0001t0001g0293 others(63): Show |
70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.48-100_48-99dupGT | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | C | CTGTG | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(108): Show |
132 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.48-102_48-99dupGTG others(1): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | C | CTGTGTG | 28 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(25): Show |
39 | HG00639.hp2 HG00642.hp1 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.48-104_48-99dupGTG others(3): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | C | CTGTGTGT others(1): Show |
31 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(28): Show |
44 | HG00323.hp2 HG00673.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.48-106_48-99dupGTG others(5): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | C | CTGTGTGT others(3): Show |
39 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0039 others(36): Show |
48 | HG00733.hp1 HG00735.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.48-108_48-99dupGTG others(7): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | C | CTGTGTGT others(5): Show |
10 | a0001c0001t0001g0210 a0001c0001t0001g0337 a0001c0001t0004g0008 others(7): Show |
12 | HG00558.hp1 HG00609.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.48-110_48-99dupGTG others(9): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | C | CTGTGTGT others(7): Show |
3 | a0001c0001t0001g0209 a0001c0001t0001g0275 a0001c0001t0017g0203 |
3 | HG02647.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.48-112_48-99dupGTG others(11): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | CTGTG | C | 2 | a0001c0001t0001g0026 a0003c0004t0018g0225 |
3 | HG02135.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.48-102_48-99delGTG others(1): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | CTGTGTG | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0297 a0006c0008t0001g0016 |
4 | HG02258.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-104_48-99delGTG others(3): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | CTGTGTGT others(9): Show |
C | 1 | a0002c0002t0002g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.48-114_48-99delGTG others(13): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323041 | CTGTGTGT others(13): Show |
C | 1 | a0002c0002t0002g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.48-118_48-99delGTG others(17): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 45323041 | ||||||
| chr22:45323134 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.48-41C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | chr22 | 45323134 | |||||||
| chr22:45323616 | C | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.300+189C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45323616 | |||||||
| chr22:45323622 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.300+195C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45323622 | |||||||
| chr22:45323753 | C | T | 122 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(119): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.300+326C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45323753 | |||||||
| chr22:45323773 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.300+346C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45323773 | |||||||
| chr22:45323930 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(3): Show |
11 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+503C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45323930 | |||||||
| chr22:45323936 | G | T | 122 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(119): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.300+509G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45323936 | |||||||
| chr22:45323942 | T | G | 1 | a0001c0001t0017g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.300+515T>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45323942 | |||||||
| chr22:45323986 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0312 a0001c0001t0001g0314 others(2): Show |
8 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+559A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45323986 | |||||||
| chr22:45324062 | T | C | 2 | a0001c0001t0007g0328 a0001c0001t0007g0332 |
2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.300+635T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324062 | |||||||
| chr22:45324106 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0050 others(13): Show |
20 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.300+679G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324106 | |||||||
| chr22:45324217 | A | G | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.300+790A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324217 | |||||||
| chr22:45324291 | G | A | 1 | a0003c0004t0001g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.300+864G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324291 | |||||||
| chr22:45324353 | C | T | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.300+926C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324353 | |||||||
| chr22:45324370 | T | A | 1 | a0001c0001t0004g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.300+943T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324370 | |||||||
| chr22:45324379 | G | A | 1 | a0001c0001t0003g0289 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.300+952G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324379 | |||||||
| chr22:45324380 | C | G | 1 | a0002c0003t0003g0250 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.300+953C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324380 | |||||||
| chr22:45324654 | C | T | 1 | a0001c0001t0004g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.300+1227C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324654 | |||||||
| chr22:45324677 | C | T | 1 | a0002c0003t0003g0028 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.300+1250C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324677 | |||||||
| chr22:45324773 | G | A | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.300+1346G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324773 | |||||||
| chr22:45324784 | C | T | 1 | a0002c0002t0002g0097 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.300+1357C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324784 | |||||||
| chr22:45324812 | C | T | 2 | a0001c0001t0001g0016 a0006c0008t0001g0016 |
3 | HG02965.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.300+1385C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324812 | |||||||
| chr22:45324817 | C | A | 2 | a0001c0001t0001g0016 a0006c0008t0001g0016 |
3 | HG02965.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.300+1390C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324817 | |||||||
| chr22:45324818 | A | G | 2 | a0001c0001t0001g0016 a0006c0008t0001g0016 |
3 | HG02965.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.300+1391A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324818 | |||||||
| chr22:45324859 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.300+1432C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324859 | |||||||
| chr22:45324920 | G | T | 1 | a0001c0001t0001g0337 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.300+1493G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45324920 | |||||||
| chr22:45325013 | C | T | 122 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(119): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.300+1586C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325013 | |||||||
| chr22:45325015 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.300+1588C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325015 | |||||||
| chr22:45325246 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.300+1819A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325246 | |||||||
| chr22:45325304 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.300+1877G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325304 | |||||||
| chr22:45325315 | C | T | 121 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(118): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.300+1888C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325315 | |||||||
| chr22:45325403 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.300+1976T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325403 | |||||||
| chr22:45325417 | G | A | 1 | a0001c0001t0004g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.300+1990G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325417 | |||||||
| chr22:45325542 | C | CAT | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.300+2116_300+2117i others(4): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 45325542 | ||||||
| chr22:45325570 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.300+2143A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325570 | |||||||
| chr22:45325666 | G | C | 45 | a0001c0001t0001g0195 a0001c0001t0004g0005 a0001c0001t0004g0007 others(42): Show |
56 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.301-2176G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325666 | |||||||
| chr22:45325752 | A | G | 1 | a0002c0002t0002g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.301-2090A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325752 | |||||||
| chr22:45325767 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.301-2075A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325767 | |||||||
| chr22:45325965 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.301-1877G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325965 | |||||||
| chr22:45325970 | A | G | 12 | a0002c0003t0003g0031 a0002c0003t0003g0032 a0002c0003t0003g0033 others(9): Show |
14 | HG00597.hp2 HG02027.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.301-1872A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45325970 | |||||||
| chr22:45326056 | A | G | 1 | a0002c0002t0002g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.301-1786A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45326056 | |||||||
| chr22:45326153 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0300 others(3): Show |
8 | HG00673.hp1 HG01934.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-1689C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45326153 | |||||||
| chr22:45326166 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.301-1676T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45326166 | |||||||
| chr22:45326284 | GCTGTCAA others(19): Show |
G | 1 | a0001c0001t0001g0321 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.301-1546_301-1521d others(28): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 45326284 | ||||||
| chr22:45326324 | C | T | 1 | a0002c0002t0002g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.301-1518C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45326324 | |||||||
| chr22:45326386 | A | T | 1 | a0002c0006t0002g0126 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.301-1456A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45326386 | |||||||
| chr22:45326404 | C | T | 1 | a0001c0001t0004g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.301-1438C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45326404 | |||||||
| chr22:45326824 | C | CA | 48 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0042 others(45): Show |
60 | HG00280.hp2 HG00558.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.301-995dupA | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 45326824 | ||||||
| chr22:45326824 | CA | C | 7 | a0001c0001t0001g0263 a0001c0001t0001g0318 a0001c0001t0004g0200 others(4): Show |
7 | HG00558.hp1 HG00609.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-995delA | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 45326824 | ||||||
| chr22:45326872 | GGTGT | G | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(311): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.301-964_301-961del others(4): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 45326872 | ||||||
| chr22:45327081 | A | T | 2 | a0002c0003t0003g0329 a0002c0003t0003g0330 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.301-761A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327081 | |||||||
| chr22:45327082 | A | G | 3 | a0001c0001t0001g0265 a0001c0001t0001g0270 a0001c0001t0001g0273 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.301-760A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327082 | |||||||
| chr22:45327182 | G | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0003g0048 others(2): Show |
7 | HG00639.hp2 HG01123.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-660G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327182 | |||||||
| chr22:45327200 | A | G | 1 | a0001c0001t0004g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.301-642A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327200 | |||||||
| chr22:45327235 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
229 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.301-607A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327235 | |||||||
| chr22:45327300 | A | G | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.301-542A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327300 | |||||||
| chr22:45327372 | A | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.301-470A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327372 | |||||||
| chr22:45327409 | C | T | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG01943.hp2 HG02486.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-433C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327409 | |||||||
| chr22:45327439 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.301-403C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327439 | |||||||
| chr22:45327445 | C | G | 123 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(120): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.301-397C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327445 | |||||||
| chr22:45327486 | C | G | 1 | a0002c0003t0003g0238 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.301-356C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327486 | |||||||
| chr22:45327584 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.301-258A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327584 | |||||||
| chr22:45327621 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0046 others(5): Show |
11 | HG00673.hp1 HG01934.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-221G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327621 | |||||||
| chr22:45327645 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.301-197T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327645 | |||||||
| chr22:45327703 | G | A | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.301-139G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327703 | |||||||
| chr22:45327711 | C | T | 1 | a0002c0002t0002g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.301-131C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327711 | |||||||
| chr22:45327815 | G | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
232 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.301-27G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327815 | |||||||
| chr22:45327815 | G | T | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.301-27G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 3/8 | chr22 | 45327815 | |||||||
| chr22:45327999 | T | TGGAGGCC others(75): Show |
1 | a0005c0010t0003g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.522+24_522+105dupC others(81): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45327999 | ||||||
| chr22:45327999 | TGGAGGCC others(75): Show |
T | 7 | a0003c0004t0001g0172 a0003c0004t0001g0173 a0003c0004t0003g0226 others(4): Show |
7 | HG01928.hp2 HG02135.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.522+24_522+105delC others(81): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45327999 | ||||||
| chr22:45327999 | TGGAGGCC others(321): Show |
T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
splice_region_variant&intron_variant | LOW | c.522+3_522+330del | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45327999 | ||||||
| chr22:45328005 | CCTTTGGC others(239): Show |
C | 1 | a0002c0003t0003g0032 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.522+85_522+330del | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328005 | ||||||
| chr22:45328039 | C | CCTGGACT others(977): Show |
1 | a0007c0011t0002g0002 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.522+15_522+16insAC others(982): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328039 | ||||||
| chr22:45328039 | C | CCTGGACT others(1141): Show |
1 | a0002c0002t0002g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.522+15_522+16insAC others(1146): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328039 | ||||||
| chr22:45328039 | C | CCTGGACT others(1387): Show |
1 | a0002c0002t0002g0002 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.522+15_522+16insAC others(1392): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328039 | ||||||
| chr22:45328039 | C | CCTGGACT others(1715): Show |
1 | a0002c0002t0002g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.522+15_522+16insAC others(1720): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328039 | ||||||
| chr22:45328066 | A | ATGGGCTG others(1633): Show |
1 | a0002c0002t0002g0002 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.522+15_522+16insAC others(1638): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328066 | ||||||
| chr22:45328066 | A | ATGGGCTG others(2371): Show |
1 | a0002c0002t0002g0002 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.522+15_522+16insAC others(2376): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328066 | ||||||
| chr22:45328066 | A | ATGGGCTG others(1551): Show |
1 | a0002c0002t0002g0002 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.522+15_522+16insAC others(1556): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328066 | ||||||
| chr22:45328066 | A | ATGGGCTG others(813): Show |
1 | a0002c0002t0002g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.522+15_522+16insAC others(818): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328066 | ||||||
| chr22:45328066 | A | ATGGGCTG others(75): Show |
1 | a0002c0003t0012g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.522+23_522+24insTC others(80): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328066 | ||||||
| chr22:45328066 | A | G | 1 | a0002c0002t0002g0105 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.522+3A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328066 | |||||||
| chr22:45328067 | T | C | 4 | a0002c0002t0002g0130 a0002c0002t0002g0131 a0002c0002t0002g0132 others(1): Show |
4 | NA18945.hp1 NA18967.hp2 NA18990.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.522+4T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328067 | |||||||
| chr22:45328067 | T | TGGGCTGG others(567): Show |
1 | a0002c0002t0002g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.522+15_522+16insAC others(572): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328067 | ||||||
| chr22:45328067 | T | TGGGCTGG others(1797): Show |
1 | a0002c0002t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.522+15_522+16insAC others(1802): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328067 | ||||||
| chr22:45328079 | G | A | 107 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0002g0020 others(104): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.522+16G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328079 | |||||||
| chr22:45328087 | C | T | 112 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0002g0020 others(109): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.522+24C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328087 | |||||||
| chr22:45328087 | CCTTTGGC others(75): Show |
C | 24 | a0002c0003t0003g0009 a0002c0003t0003g0011 a0002c0003t0003g0030 others(21): Show |
29 | HG00408.hp2 HG00609.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.522+188_522+269del others(82): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328087 | ||||||
| chr22:45328087 | CCTTTGGC others(157): Show |
C | 1 | a0002c0003t0003g0230 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.522+106_522+269del | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328087 | ||||||
| chr22:45328099 | G | A | 5 | a0002c0002t0002g0096 a0002c0002t0002g0104 a0002c0002t0002g0162 others(2): Show |
5 | HG02258.hp1 HG03704.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.522+36G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328099 | |||||||
| chr22:45328103 | G | C | 1 | a0002c0003t0014g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.522+40G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328103 | |||||||
| chr22:45328121 | C | T | 119 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0002g0020 others(116): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.522+58C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328121 | |||||||
| chr22:45328148 | A | G | 13 | a0002c0002t0001g0139 a0002c0002t0002g0002 a0002c0002t0002g0104 others(10): Show |
16 | HG02129.hp2 HG02258.hp1 NA18942.hp2 others(13): Show |
intron_variant | MODIFIER | c.522+85A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328148 | |||||||
| chr22:45328149 | T | C | 1 | a0002c0002t0009g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.522+86T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328149 | |||||||
| chr22:45328161 | G | A | 108 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0002g0020 others(105): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.522+98G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328161 | |||||||
| chr22:45328169 | T | C | 119 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0002g0020 others(116): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.522+106T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328169 | |||||||
| chr22:45328169 | T | TCTTTGGC others(75): Show |
1 | a0002c0003t0003g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.522+187_522+188ins others(82): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328169 | ||||||
| chr22:45328177 | C | T | 1 | a0002c0002t0002g0097 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.522+114C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328177 | |||||||
| chr22:45328181 | G | A | 9 | a0002c0002t0001g0139 a0002c0002t0002g0002 a0002c0002t0002g0104 others(6): Show |
9 | HG02129.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.522+118G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328181 | |||||||
| chr22:45328185 | G | C | 1 | a0003c0004t0003g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.522+122G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328185 | |||||||
| chr22:45328203 | C | T | 15 | a0002c0002t0001g0139 a0002c0002t0002g0002 a0002c0002t0002g0055 others(12): Show |
15 | HG02129.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.522+140C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328203 | |||||||
| chr22:45328230 | A | ATGGGCTG others(1469): Show |
1 | a0002c0002t0002g0138 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.522+179_522+180ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328230 | ||||||
| chr22:45328230 | A | ATGGGCTG others(2125): Show |
1 | a0002c0002t0002g0021 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.522+179_522+180ins others(2132): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328230 | ||||||
| chr22:45328230 | A | G | 9 | a0002c0002t0001g0139 a0002c0002t0002g0002 a0002c0002t0002g0055 others(6): Show |
12 | HG00738.hp2 HG02129.hp2 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.522+167A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328230 | |||||||
| chr22:45328230 | ATGGGCTG others(157): Show |
A | 1 | a0002c0003t0014g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.522+178_522+341del | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328230 | ||||||
| chr22:45328231 | T | C | 8 | a0002c0002t0002g0096 a0002c0002t0002g0130 a0002c0002t0002g0131 others(5): Show |
8 | HG02258.hp1 HG03704.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.522+168T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328231 | |||||||
| chr22:45328243 | G | A | 100 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0002g0020 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.522+180G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328243 | |||||||
| chr22:45328245 | G | T | 1 | a0002c0002t0002g0164 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.522+182G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328245 | |||||||
| chr22:45328251 | T | C | 119 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0002g0020 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.522+188T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328251 | |||||||
| chr22:45328263 | G | A | 18 | a0002c0002t0001g0139 a0002c0002t0002g0002 a0002c0002t0002g0021 others(15): Show |
22 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.522+200G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328263 | |||||||
| chr22:45328263 | G | GGCAGAAC others(1797): Show |
1 | a0002c0002t0002g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.522+221_522+222ins others(1804): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328263 | ||||||
| chr22:45328267 | G | C | 2 | a0002c0003t0003g0329 a0002c0003t0003g0330 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.522+204G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328267 | |||||||
| chr22:45328285 | C | T | 112 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(109): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.522+222C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328285 | |||||||
| chr22:45328312 | A | ATGGGCTG others(75): Show |
2 | a0002c0003t0003g0329 a0002c0003t0003g0330 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.522+269_522+270ins others(82): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328312 | ||||||
| chr22:45328312 | A | G | 115 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(112): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.522+249A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328312 | |||||||
| chr22:45328312 | ATGGGCTG others(75): Show |
A | 2 | a0003c0004t0001g0172 a0003c0004t0001g0173 |
2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.522+260_522+341del others(82): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328312 | ||||||
| chr22:45328313 | T | C | 5 | a0002c0002t0002g0055 a0002c0002t0002g0101 a0002c0002t0002g0102 others(2): Show |
5 | NA18965.hp1 NA18982.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+250T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328313 | |||||||
| chr22:45328325 | G | A | 2 | a0002c0002t0002g0056 a0002c0002t0002g0065 |
2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.522+262G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328325 | |||||||
| chr22:45328327 | G | T | 1 | a0002c0002t0002g0076 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.522+264G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328327 | |||||||
| chr22:45328333 | C | CCTTTGGC others(75): Show |
1 | a0002c0003t0012g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.522+281_522+282ins others(82): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328333 | ||||||
| chr22:45328333 | C | T | 7 | a0002c0002t0001g0139 a0002c0002t0002g0002 a0002c0002t0002g0096 others(4): Show |
10 | HG02129.hp2 HG03704.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+270C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328333 | |||||||
| chr22:45328345 | G | A | 24 | a0002c0002t0001g0139 a0002c0002t0002g0002 a0002c0002t0002g0021 others(21): Show |
28 | HG01070.hp1 HG01071.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.522+282G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328345 | |||||||
| chr22:45328345 | G | GGCAGAAC others(895): Show |
1 | a0002c0002t0002g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(902): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2289): Show |
1 | a0002c0002t0002g0153 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2296): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2453): Show |
1 | a0002c0002t0002g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2460): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2125): Show |
1 | a0002c0002t0002g0075 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2132): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(977): Show |
1 | a0002c0002t0002g0076 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(984): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0107 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1879): Show |
1 | a0002c0002t0002g0157 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1886): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1223): Show |
1 | a0002c0006t0002g0126 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1230): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0002g0158 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0125 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1141): Show |
1 | a0002c0002t0002g0152 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1148): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2043): Show |
1 | a0002c0002t0002g0146 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2050): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(731): Show |
1 | a0002c0002t0002g0142 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(738): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1305): Show |
1 | a0002c0002t0002g0077 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1312): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0002g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1633): Show |
1 | a0002c0002t0002g0159 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1640): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2780): Show |
1 | a0002c0002t0002g0147 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2787): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2371): Show |
1 | a0002c0002t0002g0109 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2378): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1059): Show |
1 | a0002c0002t0002g0110 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1066): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(813): Show |
1 | a0002c0002t0002g0078 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(820): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0069 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1961): Show |
1 | a0002c0002t0002g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1968): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(977): Show |
1 | a0002c0002t0002g0080 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(984): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2043): Show |
1 | a0002c0002t0002g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2050): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2371): Show |
1 | a0002c0002t0002g0144 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2378): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0009g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(3765): Show |
1 | a0002c0002t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(3772): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2125): Show |
1 | a0002c0002t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2132): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2453): Show |
1 | a0002c0002t0002g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2460): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0002g0160 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2453): Show |
1 | a0002c0002t0002g0111 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2460): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2535): Show |
1 | a0002c0002t0002g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2542): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2699): Show |
1 | a0002c0002t0002g0149 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2706): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2125): Show |
1 | a0002c0002t0002g0113 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2132): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2207): Show |
1 | a0002c0002t0002g0114 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2214): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(3191): Show |
1 | a0002c0002t0002g0115 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(3198): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2781): Show |
1 | a0002c0002t0002g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2788): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2371): Show |
1 | a0002c0002t0002g0098 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2378): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2945): Show |
1 | a0002c0002t0002g0148 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2952): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1879): Show |
1 | a0002c0002t0002g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1886): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1387): Show |
1 | a0002c0002t0002g0116 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1394): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1879): Show |
1 | a0002c0002t0002g0117 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1886): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0002g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1633): Show |
1 | a0002c0002t0002g0083 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1640): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(895): Show |
1 | a0002c0002t0002g0084 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(902): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1141): Show |
1 | a0002c0002t0002g0155 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1148): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0006t0002g0140 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0135 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2207): Show |
1 | a0002c0002t0002g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2214): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2535): Show |
1 | a0002c0002t0002g0066 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2542): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(649): Show |
1 | a0002c0002t0002g0136 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(656): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(3519): Show |
1 | a0002c0002t0001g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(3526): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(3683): Show |
1 | a0002c0002t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(3690): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1223): Show |
1 | a0002c0002t0002g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1230): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1797): Show |
1 | a0002c0002t0002g0089 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1804): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0090 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0091 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0092 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2125): Show |
1 | a0002c0002t0002g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2132): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0119 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1223): Show |
1 | a0002c0002t0002g0120 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1230): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0150 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1141): Show |
2 | a0002c0002t0002g0166 a0002c0002t0002g0167 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.522+303_522+304ins others(1148): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2207): Show |
1 | a0002c0002t0002g0121 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2214): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0059 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1141): Show |
1 | a0002c0002t0002g0154 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1148): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(649): Show |
1 | a0002c0002t0002g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(656): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2043): Show |
1 | a0002c0002t0002g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(2050): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0002g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1059): Show |
1 | a0002c0002t0002g0020 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.522+303_522+304ins others(1066): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1223): Show |
1 | a0002c0002t0002g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1230): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1141): Show |
1 | a0002c0002t0002g0141 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1148): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1059): Show |
1 | a0002c0002t0002g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1066): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0002g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0002g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0161 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1387): Show |
1 | a0002c0002t0002g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1394): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1551): Show |
1 | a0002c0002t0002g0333 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(2125): Show |
1 | a0002c0002t0002g0335 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(2132): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(895): Show |
1 | a0002c0002t0002g0122 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(902): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1715): Show |
1 | a0002c0002t0002g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1722): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1879): Show |
1 | a0002c0002t0002g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.522+303_522+304ins others(1886): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1797): Show |
1 | a0002c0002t0002g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1804): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328345 | G | GGCAGAAC others(1469): Show |
1 | a0002c0002t0002g0123 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.522+303_522+304ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328345 | ||||||
| chr22:45328367 | C | CCTGGACT others(731): Show |
1 | a0002c0002t0002g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.522+330_522+331ins others(738): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1961): Show |
1 | a0002c0002t0002g0134 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.522+330_522+331ins others(1968): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1551): Show |
1 | a0002c0002t0002g0097 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.522+330_522+331ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1223): Show |
1 | a0002c0002t0002g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.522+330_522+331ins others(1230): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1223): Show |
1 | a0002c0002t0002g0164 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.522+341_522+342ins others(1230): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1223): Show |
1 | a0002c0002t0002g0100 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.522+341_522+342ins others(1230): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(403): Show |
1 | a0002c0002t0002g0156 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.522+341_522+342ins others(410): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1141): Show |
1 | a0002c0002t0002g0101 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.522+341_522+342ins others(1148): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(977): Show |
1 | a0002c0002t0002g0105 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.522+341_522+342ins others(984): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(895): Show |
1 | a0002c0002t0002g0055 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.522+341_522+342ins others(902): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1059): Show |
1 | a0002c0002t0002g0334 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.522+341_522+342ins others(1066): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1141): Show |
1 | a0002c0002t0002g0102 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.522+341_522+342ins others(1148): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1469): Show |
1 | a0002c0002t0002g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.522+341_522+342ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1551): Show |
1 | a0002c0002t0002g0103 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.522+341_522+342ins others(1558): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1961): Show |
1 | a0002c0002t0002g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.522+341_522+342ins others(1968): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(1305): Show |
1 | a0002c0002t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.522+341_522+342ins others(1312): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | CCTGGACT others(731): Show |
1 | a0002c0002t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.522+341_522+342ins others(738): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328367 | ||||||
| chr22:45328367 | C | T | 103 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0139 others(100): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.522+304C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328367 | |||||||
| chr22:45328374 | T | TTGAAGGA others(2945): Show |
2 | a0002c0002t0002g0130 a0002c0002t0002g0151 |
2 | NA18990.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.522+341_522+342ins others(2952): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328374 | ||||||
| chr22:45328374 | T | TTGAAGGA others(2863): Show |
1 | a0002c0002t0002g0131 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.522+341_522+342ins others(2870): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328374 | ||||||
| chr22:45328374 | T | TTGAAGGA others(1469): Show |
1 | a0002c0002t0002g0132 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.522+341_522+342ins others(1476): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328374 | ||||||
| chr22:45328518 | G | A | 3 | a0002c0002t0002g0118 a0002c0002t0002g0119 a0002c0002t0002g0125 |
3 | NA19002.hp1 NA19054.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.522+455G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328518 | |||||||
| chr22:45328567 | G | C | 1 | a0001c0001t0001g0317 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.522+504G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328567 | |||||||
| chr22:45328632 | TA | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
233 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.522+581delA | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 45328632 | ||||||
| chr22:45328846 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.522+783G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328846 | |||||||
| chr22:45328880 | C | T | 47 | a0001c0001t0001g0195 a0001c0001t0001g0298 a0001c0001t0004g0005 others(44): Show |
58 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.522+817C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328880 | |||||||
| chr22:45328888 | G | A | 1 | a0002c0003t0003g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.522+825G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45328888 | |||||||
| chr22:45329117 | A | G | 1 | a0003c0004t0010g0227 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.522+1054A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329117 | |||||||
| chr22:45329118 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
230 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.522+1055G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329118 | |||||||
| chr22:45329225 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.522+1162T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329225 | |||||||
| chr22:45329362 | T | C | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.523-1241T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329362 | |||||||
| chr22:45329395 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.523-1208G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329395 | |||||||
| chr22:45329511 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
230 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.523-1092T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329511 | |||||||
| chr22:45329637 | A | G | 1 | a0002c0003t0012g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.523-966A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329637 | |||||||
| chr22:45329643 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
230 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.523-960C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329643 | |||||||
| chr22:45329705 | C | T | 1 | a0002c0003t0003g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.523-898C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329705 | |||||||
| chr22:45329707 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.523-896G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329707 | |||||||
| chr22:45329719 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
231 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.523-884A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329719 | |||||||
| chr22:45329786 | A | C | 9 | a0002c0002t0002g0098 a0002c0002t0002g0105 a0002c0002t0002g0109 others(6): Show |
9 | NA18981.hp2 NA18994.hp1 NA18999.hp1 others(6): Show |
intron_variant | MODIFIER | c.523-817A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329786 | |||||||
| chr22:45329888 | C | T | 1 | a0002c0003t0012g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.523-715C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329888 | |||||||
| chr22:45329938 | C | T | 12 | a0002c0002t0002g0098 a0002c0002t0002g0101 a0002c0002t0002g0105 others(9): Show |
12 | HG01123.hp2 HG01952.hp1 NA18981.hp2 others(9): Show |
intron_variant | MODIFIER | c.523-665C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45329938 | |||||||
| chr22:45330190 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(3): Show |
11 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.523-413G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45330190 | |||||||
| chr22:45330337 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.523-266C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45330337 | |||||||
| chr22:45330339 | A | G | 46 | a0001c0001t0001g0036 a0001c0001t0001g0195 a0001c0001t0001g0288 others(43): Show |
58 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.523-264A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45330339 | |||||||
| chr22:45330411 | T | C | 1 | a0002c0002t0002g0123 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.523-192T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45330411 | |||||||
| chr22:45330464 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.523-139A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | chr22 | 45330464 | |||||||
| chr22:45330760 | C | T | 2 | a0004c0005t0003g0239 a0004c0005t0003g0240 |
2 | HG03834.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.651+29C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45330760 | |||||||
| chr22:45330912 | C | T | 1 | a0002c0002t0009g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.651+181C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45330912 | |||||||
| chr22:45331007 | C | G | 2 | a0003c0004t0001g0172 a0003c0004t0001g0173 |
2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.651+276C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331007 | |||||||
| chr22:45331012 | G | A | 1 | a0002c0002t0002g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.651+281G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331012 | |||||||
| chr22:45331024 | A | G | 341 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(338): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.651+293A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331024 | |||||||
| chr22:45331191 | G | A | 3 | a0002c0002t0002g0105 a0002c0002t0002g0109 a0002c0002t0002g0147 |
3 | NA18981.hp2 NA19074.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.651+460G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331191 | |||||||
| chr22:45331248 | C | T | 2 | a0001c0001t0004g0052 a0001c0001t0004g0053 |
2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.651+517C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331248 | |||||||
| chr22:45331299 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(43): Show |
68 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.651+568G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331299 | |||||||
| chr22:45331499 | C | T | 2 | a0003c0004t0001g0172 a0003c0004t0001g0173 |
2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.651+768C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331499 | |||||||
| chr22:45331645 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.652-780C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331645 | |||||||
| chr22:45331684 | T | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
229 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.652-741T>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331684 | |||||||
| chr22:45331800 | T | C | 1 | a0001c0001t0004g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.652-625T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331800 | |||||||
| chr22:45331807 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
228 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.652-618C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331807 | |||||||
| chr22:45331870 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
21 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.652-555C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331870 | |||||||
| chr22:45331897 | CCCT | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
229 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.652-523_652-521del others(3): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 45331897 | ||||||
| chr22:45331993 | T | A | 1 | a0002c0003t0003g0204 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.652-432T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45331993 | |||||||
| chr22:45332139 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.652-286G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | chr22 | 45332139 | |||||||
| chr22:45332282 | CCTT | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
226 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.652-140_652-138del others(3): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 45332282 | ||||||
| chr22:45332290 | CTG | C | 9 | a0001c0001t0001g0042 a0001c0001t0001g0292 a0001c0001t0001g0293 others(6): Show |
14 | HG01433.hp2 HG02559.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.652-132_652-131del others(2): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 45332290 | ||||||
| chr22:45332715 | G | A | 1 | a0002c0003t0003g0207 | 1 | HG03017.hp2 | splice_region_variant&intron_variant | LOW | c.937+5G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45332715 | |||||||
| chr22:45332751 | C | CTT | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
228 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.937+52_937+53dupTT | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 45332751 | ||||||
| chr22:45332802 | A | C | 3 | a0001c0001t0005g0259 a0001c0001t0005g0261 a0001c0001t0005g0262 |
3 | HG02886.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.937+92A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45332802 | |||||||
| chr22:45332892 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.937+182C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45332892 | |||||||
| chr22:45332894 | C | G | 1 | a0001c0001t0001g0037 | 2 | HG01081.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.937+184C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45332894 | |||||||
| chr22:45333097 | G | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.937+387G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333097 | |||||||
| chr22:45333116 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.937+406C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333116 | |||||||
| chr22:45333117 | A | G | 1 | a0002c0003t0003g0028 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.937+407A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333117 | |||||||
| chr22:45333302 | G | A | 2 | a0002c0003t0003g0329 a0002c0003t0003g0330 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.937+592G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333302 | |||||||
| chr22:45333350 | A | G | 2 | a0002c0002t0002g0079 a0002c0002t0002g0145 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.937+640A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333350 | |||||||
| chr22:45333501 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
225 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.937+791C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333501 | |||||||
| chr22:45333543 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
229 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.937+833G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333543 | |||||||
| chr22:45333674 | C | CA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
162 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.937+982dupA | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 45333674 | ||||||
| chr22:45333674 | C | CAA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0037 others(11): Show |
18 | HG00323.hp2 HG00735.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.937+981_937+982dup others(2): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 45333674 | ||||||
| chr22:45333747 | G | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG01943.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+1037G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333747 | |||||||
| chr22:45333748 | G | A | 13 | a0002c0003t0003g0030 a0002c0003t0003g0031 a0002c0003t0003g0032 others(10): Show |
15 | HG00597.hp2 HG02027.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.937+1038G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333748 | |||||||
| chr22:45333748 | G | C | 1 | a0002c0003t0003g0228 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.937+1038G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45333748 | |||||||
| chr22:45334035 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.938-1315A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45334035 | |||||||
| chr22:45334229 | C | T | 1 | a0002c0003t0003g0231 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.938-1121C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45334229 | |||||||
| chr22:45334627 | C | T | 7 | a0001c0001t0004g0010 a0001c0001t0004g0027 a0001c0001t0004g0217 others(4): Show |
10 | HG00673.hp2 HG02040.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.938-723C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45334627 | |||||||
| chr22:45334771 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0292 a0001c0001t0001g0293 |
4 | HG01433.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-579C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45334771 | |||||||
| chr22:45334828 | G | A | 2 | a0001c0001t0004g0180 a0001c0001t0004g0192 |
2 | HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.938-522G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45334828 | |||||||
| chr22:45334848 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0318 a0001c0001t0001g0323 |
4 | HG02523.hp1 NA18980.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.938-502C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45334848 | |||||||
| chr22:45334929 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.938-421G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45334929 | |||||||
| chr22:45334997 | A | G | 1 | a0002c0002t0002g0110 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.938-353A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45334997 | |||||||
| chr22:45335065 | A | G | 1 | a0002c0003t0012g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.938-285A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45335065 | |||||||
| chr22:45335169 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.938-181A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45335169 | |||||||
| chr22:45335223 | C | T | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.938-127C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45335223 | |||||||
| chr22:45335265 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.938-85C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45335265 | |||||||
| chr22:45335301 | C | T | 124 | a0001c0001t0002g0302 a0001c0001t0002g0326 a0001c0001t0011g0306 others(121): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.938-49C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45335301 | |||||||
| chr22:45335317 | C | T | 1 | a0003c0004t0001g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.938-33C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45335317 | |||||||
| chr22:45335318 | G | A | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.938-32G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 6/8 | chr22 | 45335318 | |||||||
| chr22:45335398 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.970+16C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335398 | |||||||
| chr22:45335423 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.970+41A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335423 | |||||||
| chr22:45335495 | G | A | 15 | a0001c0001t0005g0006 a0001c0001t0005g0012 a0001c0001t0005g0040 others(12): Show |
21 | HG00558.hp2 HG01257.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.970+113G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335495 | |||||||
| chr22:45335607 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0051 others(4): Show |
11 | HG00642.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.970+225G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335607 | |||||||
| chr22:45335658 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(288): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.970+276C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335658 | |||||||
| chr22:45335697 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.970+315G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335697 | |||||||
| chr22:45335739 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.970+357T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335739 | |||||||
| chr22:45335780 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0051 others(5): Show |
12 | HG00642.hp1 HG01243.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.970+398A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335780 | |||||||
| chr22:45335849 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.970+467T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335849 | |||||||
| chr22:45335850 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.970+468G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335850 | |||||||
| chr22:45335861 | G | T | 1 | a0002c0003t0003g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.971-467G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335861 | |||||||
| chr22:45335871 | T | A | 1 | a0002c0003t0003g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.971-457T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335871 | |||||||
| chr22:45335878 | G | C | 115 | a0001c0001t0002g0302 a0001c0001t0002g0326 a0001c0001t0011g0306 others(112): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.971-450G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335878 | |||||||
| chr22:45335918 | A | G | 1 | a0002c0003t0003g0235 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.971-410A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335918 | |||||||
| chr22:45335985 | G | T | 1 | a0001c0001t0004g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.971-343G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45335985 | |||||||
| chr22:45336032 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0050 others(13): Show |
20 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.971-296A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45336032 | |||||||
| chr22:45336284 | G | A | 1 | a0002c0003t0012g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.971-44G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 7/8 | chr22 | 45336284 | |||||||
| chr22:45336447 | G | A | 129 | a0001c0001t0001g0195 a0001c0001t0002g0302 a0001c0001t0002g0326 others(126): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1054+36G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45336447 | |||||||
| chr22:45336505 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1054+94C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45336505 | |||||||
| chr22:45336539 | G | A | 1 | a0002c0002t0002g0059 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1054+128G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45336539 | |||||||
| chr22:45336771 | C | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0318 a0001c0001t0001g0323 |
4 | HG02523.hp1 NA18980.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+360C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45336771 | |||||||
| chr22:45337003 | G | T | 1 | a0001c0001t0004g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1054+592G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337003 | |||||||
| chr22:45337160 | A | C | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1054+749A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337160 | |||||||
| chr22:45337161 | C | A | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1054+750C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337161 | |||||||
| chr22:45337162 | A | C | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1054+751A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337162 | |||||||
| chr22:45337173 | A | C | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1054+762A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337173 | |||||||
| chr22:45337245 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1054+834A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337245 | |||||||
| chr22:45337311 | G | T | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1054+900G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337311 | |||||||
| chr22:45337318 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(58): Show |
86 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1054+907T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337318 | |||||||
| chr22:45337366 | C | A | 1 | a0002c0003t0003g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1054+955C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337366 | |||||||
| chr22:45337439 | A | C | 2 | a0001c0001t0007g0328 a0001c0001t0007g0332 |
2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1054+1028A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337439 | |||||||
| chr22:45337461 | G | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
6 | HG02258.hp2 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054+1050G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337461 | |||||||
| chr22:45337608 | A | T | 19 | a0001c0001t0001g0042 a0001c0001t0001g0292 a0001c0001t0001g0293 others(16): Show |
26 | HG00558.hp2 HG01257.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.1054+1197A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337608 | |||||||
| chr22:45337619 | G | C | 1 | a0001c0001t0001g0295 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1054+1208G>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337619 | |||||||
| chr22:45337712 | T | C | 1 | a0003c0004t0003g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1054+1301T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337712 | |||||||
| chr22:45337856 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1054+1445C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45337856 | |||||||
| chr22:45338208 | G | A | 1 | a0001c0001t0013g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1054+1797G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338208 | |||||||
| chr22:45338241 | A | AT | 128 | a0001c0001t0002g0302 a0001c0001t0002g0326 a0001c0001t0011g0306 others(125): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1054+1836dupT | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 45338241 | ||||||
| chr22:45338241 | A | T | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1054+1830A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338241 | |||||||
| chr22:45338242 | T | A | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1054+1831T>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338242 | |||||||
| chr22:45338292 | C | T | 1 | a0002c0002t0002g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1054+1881C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338292 | |||||||
| chr22:45338298 | C | T | 58 | a0001c0001t0001g0042 a0001c0001t0001g0292 a0001c0001t0001g0293 others(55): Show |
76 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1054+1887C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338298 | |||||||
| chr22:45338315 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1054+1904C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338315 | |||||||
| chr22:45338325 | A | G | 128 | a0001c0001t0002g0302 a0001c0001t0002g0326 a0001c0001t0011g0306 others(125): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1054+1914A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338325 | |||||||
| chr22:45338334 | G | T | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01943.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054+1923G>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338334 | |||||||
| chr22:45338374 | C | CGCA | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01943.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054+1964_1054+196 others(7): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 45338374 | ||||||
| chr22:45338378 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1054+1967C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338378 | |||||||
| chr22:45338404 | C | T | 4 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0002c0003t0012g0282 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-1982C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338404 | |||||||
| chr22:45338426 | A | G | 2 | a0003c0004t0001g0172 a0003c0004t0001g0173 |
2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1055-1960A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338426 | |||||||
| chr22:45338429 | A | G | 1 | a0001c0001t0017g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1055-1957A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338429 | |||||||
| chr22:45338445 | T | G | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1055-1941T>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338445 | |||||||
| chr22:45338522 | C | T | 3 | a0002c0003t0003g0329 a0002c0003t0003g0330 a0003c0004t0003g0248 |
3 | HG01884.hp2 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1055-1864C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338522 | |||||||
| chr22:45338571 | T | C | 2 | a0001c0001t0004g0007 a0001c0001t0004g0189 |
4 | HG02132.hp2 NA18946.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055-1815T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338571 | |||||||
| chr22:45338615 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1055-1771C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338615 | |||||||
| chr22:45338726 | T | G | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1055-1660T>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338726 | |||||||
| chr22:45338751 | A | C | 1 | a0002c0002t0002g0167 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1055-1635A>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338751 | |||||||
| chr22:45338793 | A | G | 1 | a0002c0002t0002g0135 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1055-1593A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338793 | |||||||
| chr22:45338884 | T | C | 4 | a0001c0001t0001g0215 a0002c0003t0014g0201 a0003c0004t0001g0172 others(1): Show |
4 | HG02257.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055-1502T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338884 | |||||||
| chr22:45338979 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
234 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1055-1407T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338979 | |||||||
| chr22:45338996 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1055-1390G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45338996 | |||||||
| chr22:45339050 | A | G | 182 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(179): Show |
219 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1055-1336A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339050 | |||||||
| chr22:45339142 | C | A | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1055-1244C>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339142 | |||||||
| chr22:45339143 | G | A | 3 | a0001c0001t0004g0218 a0001c0001t0004g0220 a0001c0001t0004g0221 |
3 | NA18995.hp1 NA19079.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1055-1243G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339143 | |||||||
| chr22:45339308 | A | T | 1 | a0002c0003t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1055-1078A>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339308 | |||||||
| chr22:45339377 | C | T | 14 | a0001c0001t0005g0006 a0001c0001t0005g0012 a0001c0001t0005g0040 others(11): Show |
20 | HG00558.hp2 HG01257.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1055-1009C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339377 | |||||||
| chr22:45339457 | CAT | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(16): Show |
29 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.1055-928_1055-927d others(4): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339457 | |||||||
| chr22:45339465 | A | G | 1 | a0001c0001t0004g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1055-921A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339465 | |||||||
| chr22:45339473 | C | T | 3 | a0001c0001t0004g0008 a0001c0001t0004g0174 a0001c0001t0004g0181 |
5 | HG00609.hp2 NA18962.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055-913C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339473 | |||||||
| chr22:45339504 | T | C | 3 | a0002c0003t0003g0031 a0002c0003t0003g0241 a0002c0003t0003g0242 |
4 | HG02165.hp2 NA19054.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055-882T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339504 | |||||||
| chr22:45339590 | G | A | 1 | a0001c0001t0017g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1055-796G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339590 | |||||||
| chr22:45339696 | C | T | 1 | a0001c0001t0004g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1055-690C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339696 | |||||||
| chr22:45339725 | T | C | 119 | a0001c0001t0002g0302 a0001c0001t0002g0326 a0001c0001t0004g0218 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1055-661T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339725 | |||||||
| chr22:45339824 | C | T | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1055-562C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339824 | |||||||
| chr22:45339860 | T | C | 123 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0001c0001t0001g0297 others(120): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1055-526T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339860 | |||||||
| chr22:45339908 | C | T | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1055-478C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339908 | |||||||
| chr22:45339931 | C | G | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01943.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055-455C>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45339931 | |||||||
| chr22:45340095 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1055-291T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45340095 | |||||||
| chr22:45340116 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1055-270A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45340116 | |||||||
| chr22:45340197 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0171 others(3): Show |
7 | HG02451.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1055-189C>T | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45340197 | |||||||
| chr22:45340206 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0305 a0002c0002t0001g0139 |
5 | HG02083.hp1 HG02129.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055-180A>G | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45340206 | |||||||
| chr22:45340272 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1055-114G>A | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45340272 | |||||||
| chr22:45340337 | T | C | 3 | a0002c0003t0014g0201 a0003c0004t0001g0172 a0003c0004t0001g0173 |
3 | HG02257.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1055-49T>C | FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 8/8 | chr22 | 45340337 |