Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 160857 |
| ensemblid | ENSG00000151773.13 |
| hgncid | 26478 |
| symbol | CCDC122 |
| name | coiled-coil domain containing 122 |
| refseq_nuc | NM_144974.5 |
| refseq_prot | NP_659411.2 |
| ensembl_nuc | ENST00000444614.8 |
| ensembl_prot | ENSP00000407763.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 43836352 |
| end | 43879740 |
| strand | - |
| ver | v1.2 |
| region | chr13:43836352-43879740 |
| region5000 | chr13:43831352-43884740 |
| regionname0 | CCDC122_chr13_43836352_43879740 |
| regionname5000 | CCDC122_chr13_43831352_43884740 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 273 | 391 | 88 | 64 | 191 | 10 | 36 | 156 | CCDC122_chr13_43831352_43884740 | CCDC122 | MSDNK others(268): Show |
chr13 | 43831352 | 43884740 |
| a0002 | 0/0 | 273 | 30 | 1 | 2 | 20 | 0 | 7 | 12 | CCDC122_chr13_43831352_43884740 | CCDC122 | MSDNK others(268): Show |
chr13 | 43831352 | 43884740 |
| a0003 | 0/0 | 273 | 11 | 0 | 0 | 11 | 0 | 0 | 11 | CCDC122_chr13_43831352_43884740 | CCDC122 | MSDNK others(268): Show |
chr13 | 43831352 | 43884740 |
| a0004 | 0/0 | 273 | 7 | 0 | 2 | 0 | 2 | 3 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | MSDNK others(268): Show |
chr13 | 43831352 | 43884740 |
| a0005 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | MSDNK others(268): Show |
chr13 | 43831352 | 43884740 |
| a0006 | 0/0 | 250 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | MSDNK others(245): Show |
chr13 | 43831352 | 43884740 |
| a0007 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | MSDNK others(268): Show |
chr13 | 43831352 | 43884740 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 819 | 353 | 73 | 60 | 175 | 8 | 35 | CCDC122_chr13_43831352_43884740 | CCDC122 | ATGTC others(814): Show |
chr13 | 43831352 | 43884740 | ||
| a0001c0002 | 0/0 | 819 | 38 | 15 | 4 | 16 | 2 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | ATGTC others(814): Show |
chr13 | 43831352 | 43884740 | ||
| a0002c0003 | 0/0 | 819 | 30 | 1 | 2 | 20 | 0 | 7 | CCDC122_chr13_43831352_43884740 | CCDC122 | ATGTC others(814): Show |
chr13 | 43831352 | 43884740 | ||
| a0003c0004 | 0/0 | 819 | 11 | 0 | 0 | 11 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ATGTC others(814): Show |
chr13 | 43831352 | 43884740 | ||
| a0004c0005 | 0/0 | 819 | 7 | 0 | 2 | 0 | 2 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | ATGTC others(814): Show |
chr13 | 43831352 | 43884740 | ||
| a0005c0008 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ATGTC others(814): Show |
chr13 | 43831352 | 43884740 | ||
| a0006c0006 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ATGTC others(814): Show |
chr13 | 43831352 | 43884740 | ||
| a0007c0007 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ATGTC others(814): Show |
chr13 | 43831352 | 43884740 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2060 | 100 | 28 | 15 | 47 | 1 | 8 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0002 | 0/0 | 2060 | 50 | 2 | 13 | 22 | 3 | 10 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0003 | 1/0 | 2059 | 51 | 8 | 9 | 32 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCTA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0004 | 0/0 | 2060 | 27 | 0 | 3 | 23 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0006 | 0/0 | 2060 | 22 | 0 | 0 | 16 | 0 | 6 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0007 | 0/0 | 2060 | 19 | 0 | 5 | 12 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0008 | 0/0 | 2061 | 15 | 6 | 1 | 5 | 1 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0009 | 0/0 | 2059 | 18 | 10 | 4 | 0 | 1 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0010 | 0/0 | 2059 | 9 | 7 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0012 | 0/0 | 2061 | 7 | 0 | 3 | 3 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0013 | 0/0 | 2059 | 7 | 6 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0015 | 0/0 | 2061 | 4 | 0 | 1 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0017 | 0/0 | 2060 | 4 | 1 | 1 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCTA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0018 | 0/0 | 2060 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0019 | 0/0 | 2059 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0020 | 0/0 | 2059 | 2 | 0 | 0 | 1 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0021 | 0/0 | 2061 | 2 | 1 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0022 | 0/0 | 2059 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0024 | 0/0 | 2061 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0025 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0026 | 0/0 | 2060 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0028 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2386): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0029 | 0/0 | 2060 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0030 | 0/0 | 2060 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0031 | 0/0 | 2059 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0001t0032 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0002t0005 | 0/0 | 2061 | 25 | 5 | 3 | 14 | 2 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0002t0014 | 0/0 | 2061 | 5 | 4 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0002t0016 | 0/0 | 2061 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0002t0027 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0001c0002t0033 | 0/0 | 2059 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0001c0002t0034 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0001c0002t0035 | 0/0 | 2059 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2054): Show |
chr13 | 43831352 | 43884740 |
| a0002c0003t0001 | 0/0 | 2060 | 27 | 1 | 2 | 18 | 0 | 6 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0002c0003t0008 | 0/0 | 2061 | 2 | 0 | 0 | 1 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0002c0003t0036 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0003c0004t0011 | 0/0 | 2060 | 9 | 0 | 0 | 9 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0003c0004t0023 | 0/0 | 2061 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0004c0005t0001 | 0/0 | 2060 | 7 | 0 | 2 | 0 | 2 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0005c0008t0008 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2056): Show |
chr13 | 43831352 | 43884740 |
| a0006c0006t0001 | 0/0 | 2060 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| a0007c0007t0002 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | ACCCA others(2055): Show |
chr13 | 43831352 | 43884740 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 20 | 2 | 3 | 9 | 0 | 6 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0003 | 0/0 | 16 | 1 | 3 | 12 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0001 | 0/0 | 26 | 0 | 6 | 12 | 3 | 5 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0031 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0064 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0015 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0010g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0010g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0010g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0012g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0012g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0012g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0012g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0013g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0013g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0015g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0015g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0015g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0017g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0017g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0017g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0017g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0018g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0018g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0019g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0019g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0020g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0020g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0021g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0021g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0022g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0022g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0024g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0025g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0026g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0028g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0029g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0030g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0031g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0001t0032g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0004 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0060 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0014g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0014g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0014g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0016g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0016g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0027g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0033g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0034g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0001c0002t0035g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0018 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0008g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0002c0003t0036g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0003c0004t0011g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0003c0004t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0003c0004t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0003c0004t0023g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0004c0005t0001g0007 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0004c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0005c0008t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0006c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| a0007c0007t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0200 | EUR | FIN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0116 | EUR | FIN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00323 | hp2 | a0004 | c0005 | t0001 | g0007 | EUR | FIN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0107 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0180 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0211 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00609 | hp2 | a0002 | c0003 | t0001 | g0177 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00642 | hp1 | a0001 | c0001 | t0029 | g0109 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0112 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0004 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00735 | hp1 | a0001 | c0001 | t0015 | g0115 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00735 | hp2 | a0004 | c0005 | t0001 | g0007 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00738 | hp2 | a0001 | c0001 | t0009 | g0127 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00741 | hp1 | a0001 | c0002 | t0005 | g0221 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0058 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0092 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01109 | hp2 | a0001 | c0001 | t0012 | g0106 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0058 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0020 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01243 | hp2 | a0001 | c0002 | t0014 | g0113 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0104 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01346 | hp1 | a0004 | c0005 | t0001 | g0007 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01346 | hp2 | a0001 | c0001 | t0017 | g0256 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01361 | hp1 | a0001 | c0001 | t0009 | g0046 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0204 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01496 | hp2 | a0001 | c0001 | t0028 | g0074 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01515 | hp1 | a0001 | c0002 | t0005 | g0060 | EUR | IBS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01515 | hp2 | a0001 | c0001 | t0020 | g0071 | EUR | IBS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01516 | hp2 | a0001 | c0002 | t0005 | g0004 | EUR | IBS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01891 | hp1 | a0001 | c0002 | t0014 | g0223 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0101 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01952 | hp2 | a0001 | c0001 | t0012 | g0036 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01993 | hp1 | a0001 | c0001 | t0012 | g0100 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0174 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0099 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0060 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0080 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02056 | hp1 | a0001 | c0001 | t0012 | g0108 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02056 | hp2 | a0005 | c0008 | t0008 | g0214 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02071 | hp1 | a0002 | c0003 | t0008 | g0183 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02074 | hp1 | a0001 | c0002 | t0005 | g0228 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02080 | hp1 | a0002 | c0003 | t0001 | g0190 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0176 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0091 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0130 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0161 | EAS | CDX | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | CDX | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02258 | hp1 | a0001 | c0002 | t0016 | g0057 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02273 | hp2 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0089 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02280 | hp2 | a0001 | c0002 | t0014 | g0220 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02300 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02300 | hp2 | a0001 | c0001 | t0030 | g0213 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0088 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02572 | hp1 | a0001 | c0002 | t0016 | g0224 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02615 | hp2 | a0001 | c0001 | t0018 | g0139 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0059 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02683 | hp2 | a0004 | c0005 | t0001 | g0007 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02717 | hp1 | a0001 | c0002 | t0016 | g0235 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02735 | hp2 | a0004 | c0005 | t0001 | g0007 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02809 | hp2 | a0006 | c0006 | t0001 | g0155 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0020 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02886 | hp2 | a0001 | c0002 | t0035 | g0229 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02897 | hp1 | a0001 | c0001 | t0031 | g0149 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0137 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02970 | hp1 | a0001 | c0002 | t0027 | g0110 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03017 | hp1 | a0002 | c0003 | t0001 | g0181 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03139 | hp2 | a0001 | c0001 | t0018 | g0133 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0138 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0150 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0253 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03225 | hp2 | a0001 | c0002 | t0005 | g0227 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0022 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0178 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0131 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0093 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0087 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0134 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0111 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03579 | hp2 | a0001 | c0002 | t0016 | g0057 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0051 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0015 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0015 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0022 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0018 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03710 | hp2 | a0004 | c0005 | t0001 | g0160 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0168 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0018 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03927 | hp1 | a0001 | c0001 | t0008 | g0196 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03942 | hp1 | a0002 | c0003 | t0008 | g0179 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03942 | hp2 | a0001 | c0001 | t0026 | g0066 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04115 | hp2 | a0001 | c0001 | t0012 | g0096 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04184 | hp1 | a0001 | c0002 | t0005 | g0004 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04184 | hp2 | a0001 | c0001 | t0009 | g0129 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04199 | hp2 | a0001 | c0001 | t0009 | g0044 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0128 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0022 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG04228 | hp2 | a0001 | c0001 | t0021 | g0073 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18522 | hp1 | a0001 | c0002 | t0014 | g0056 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | CHB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | CHB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0059 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18939 | hp1 | a0003 | c0004 | t0011 | g0143 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18940 | hp1 | a0001 | c0002 | t0005 | g0233 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18941 | hp1 | a0001 | c0002 | t0005 | g0232 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18941 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18942 | hp1 | a0001 | c0001 | t0025 | g0072 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18942 | hp2 | a0001 | c0002 | t0005 | g0027 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18944 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0097 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18947 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18947 | hp2 | a0007 | c0007 | t0002 | g0068 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18953 | hp1 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18956 | hp1 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0234 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18960 | hp1 | a0001 | c0002 | t0005 | g0027 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18961 | hp1 | a0001 | c0001 | t0015 | g0054 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18962 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18966 | hp1 | a0003 | c0004 | t0011 | g0142 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18967 | hp1 | a0001 | c0001 | t0008 | g0049 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18969 | hp2 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18972 | hp1 | a0001 | c0001 | t0017 | g0246 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18974 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0094 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18978 | hp1 | a0001 | c0001 | t0024 | g0042 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18978 | hp2 | a0001 | c0001 | t0017 | g0250 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18980 | hp2 | a0001 | c0001 | t0007 | g0102 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18982 | hp2 | a0001 | c0001 | t0012 | g0098 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18984 | hp2 | a0001 | c0001 | t0015 | g0054 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18985 | hp2 | a0001 | c0001 | t0019 | g0095 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18986 | hp1 | a0001 | c0001 | t0013 | g0086 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18987 | hp2 | a0001 | c0001 | t0020 | g0084 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18988 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18991 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18992 | hp1 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18995 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19000 | hp1 | a0001 | c0001 | t0022 | g0192 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19001 | hp1 | a0001 | c0002 | t0033 | g0231 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19005 | hp2 | a0002 | c0003 | t0001 | g0121 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19006 | hp1 | a0003 | c0004 | t0023 | g0047 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19006 | hp2 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19010 | hp1 | a0001 | c0001 | t0012 | g0036 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19011 | hp1 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19012 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0135 | AFR | LWK | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0187 | AFR | LWK | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19056 | hp1 | a0001 | c0001 | t0022 | g0120 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19057 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19059 | hp1 | a0001 | c0002 | t0034 | g0222 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19059 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19060 | hp2 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19064 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19065 | hp2 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19067 | hp2 | a0003 | c0004 | t0023 | g0047 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19070 | hp2 | a0001 | c0001 | t0032 | g0207 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19072 | hp1 | a0001 | c0002 | t0005 | g0225 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19074 | hp1 | a0002 | c0003 | t0001 | g0172 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19075 | hp2 | a0001 | c0001 | t0019 | g0105 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19079 | hp2 | a0002 | c0003 | t0036 | g0175 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19082 | hp2 | a0001 | c0001 | t0024 | g0042 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19083 | hp1 | a0001 | c0001 | t0015 | g0194 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19085 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19086 | hp1 | a0001 | c0001 | t0008 | g0049 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19088 | hp1 | a0001 | c0002 | t0005 | g0027 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19091 | hp2 | a0001 | c0002 | t0005 | g0226 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19240 | hp1 | a0001 | c0002 | t0014 | g0056 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0132 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ASW | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA20805 | hp1 | a0004 | c0005 | t0001 | g0007 | EUR | TSI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA20805 | hp2 | a0001 | c0001 | t0009 | g0044 | EUR | TSI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0125 | SAS | GIH | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0051 | SAS | GIH | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0230 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0147 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0202 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0136 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0154 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0146 | AFR | USA | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA20300 | hp1 | a0002 | c0003 | t0001 | g0173 | AFR | USA | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | USA | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0158 | REF | REF | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0064 | REF | REF | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:43837285 | C | T | 1 | a0004 | 7 | HG00323.hp2 HG00735.hp2 HG01346.hp1 others(4): Show |
missense_variant | MODERATE | c.817G>A | p.Glu273Lys | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 1126/2059 | 817/822 | 273/273 | chr13 | 43837285 | |||
| chr13:43837296 | A | G | 1 | a0002 | 30 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(27): Show |
missense_variant | MODERATE | c.806T>C | p.Ile269Thr | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 1115/2059 | 806/822 | 269/273 | chr13 | 43837296 | |||
| chr13:43837350 | C | T | 1 | a0006 | 1 | HG02809.hp2 | stop_gained | HIGH | c.752G>A | p.Trp251* | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 1061/2059 | 752/822 | 251/273 | chr13 | 43837350 | |||
| chr13:43858837 | T | C | 1 | a0007 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.616A>G | p.Thr206Ala | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/7 | 925/2059 | 616/822 | 206/273 | chr13 | 43858837 | |||
| chr13:43859905 | T | G | 1 | a0005 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.322A>C | p.Lys108Gln | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/7 | 631/2059 | 322/822 | 108/273 | chr13 | 43859905 | |||
| chr13:43868738 | C | T | 1 | a0003 | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
missense_variant | MODERATE | c.112G>A | p.Ala38Thr | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/7 | 421/2059 | 112/822 | 38/273 | chr13 | 43868738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:43837427 | T | C | 1 | a0001c0002 | 38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
splice_region_variant&synonymous_variant | LOW | c.675A>G | p.Val225Val | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 984/2059 | 675/822 | 225/273 | chr13 | 43837427 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:43836417 | G | A | 9 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0020 others(6): Show |
82 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*863C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 863 | chr13 | 43836417 | ||||||
| chr13:43836472 | C | A | 1 | a0001c0001t0026 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 808 | chr13 | 43836472 | ||||||
| chr13:43836476 | G | T | 1 | a0001c0001t0032 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*804C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 804 | chr13 | 43836476 | ||||||
| chr13:43836533 | T | C | 18 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(15): Show |
141 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*747A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 747 | chr13 | 43836533 | ||||||
| chr13:43836622 | G | A | 3 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0022 |
33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*658C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 658 | chr13 | 43836622 | ||||||
| chr13:43836712 | C | T | 4 | a0001c0002t0005 a0001c0002t0027 a0001c0002t0033 others(1): Show |
28 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*568G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 568 | chr13 | 43836712 | ||||||
| chr13:43836774 | C | T | 1 | a0001c0001t0025 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*506G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 506 | chr13 | 43836774 | ||||||
| chr13:43836775 | A | G | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*505T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 505 | chr13 | 43836775 | ||||||
| chr13:43836826 | C | T | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(15): Show |
218 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*454G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 454 | chr13 | 43836826 | ||||||
| chr13:43836856 | C | CA | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(17): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*423dupT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 423 | chr13 | 43836856 | ||||||
| chr13:43836856 | C | CAA | 12 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0015 others(9): Show |
70 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*423dupTT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 423 | chr13 | 43836856 | ||||||
| chr13:43836923 | G | T | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*357C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 357 | chr13 | 43836923 | ||||||
| chr13:43837009 | C | T | 1 | a0001c0001t0030 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 271 | chr13 | 43837009 | ||||||
| chr13:43837011 | T | C | 2 | a0001c0002t0016 a0001c0002t0035 |
5 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*269A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 269 | chr13 | 43837011 | ||||||
| chr13:43837013 | T | G | 7 | a0001c0002t0005 a0001c0002t0014 a0001c0002t0016 others(4): Show |
38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*267A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 267 | chr13 | 43837013 | ||||||
| chr13:43837121 | G | C | 1 | a0002c0003t0036 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 159 | chr13 | 43837121 | ||||||
| chr13:43837164 | T | TAAGACAG others(324): Show |
1 | a0001c0001t0028 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115_*116insTTTTTT others(325): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 115 | chr13 | 43837164 | ||||||
| chr13:43837274 | G | A | 2 | a0001c0001t0009 a0001c0001t0018 |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 6 | chr13 | 43837274 | ||||||
| chr13:43869426 | C | A | 1 | a0001c0001t0010 | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-50G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/7 | 50 | chr13 | 43869426 | ||||||
| chr13:43869475 | T | C | 1 | a0001c0001t0029 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-99A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/7 | 99 | chr13 | 43869475 | ||||||
| chr13:43879647 | G | A | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(23): Show |
282 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(279): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-216C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/7 | chr13 | 43879647 | |||||||
| chr13:43879737 | A | G | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(37): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
5_prime_UTR_variant | MODIFIER | c.-306T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/7 | 10361 | chr13 | 43879737 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:43837548 | ATAAT | A | 2 | a0001c0001t0010g0020 a0001c0001t0010g0111 |
4 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-123_673-120del others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837548 | |||||||
| chr13:43837637 | T | TAATTAAA others(327): Show |
1 | a0001c0001t0009g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.673-209_673-208ins others(334): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837637 | |||||||
| chr13:43837637 | T | TAATTAAA others(328): Show |
1 | a0001c0001t0009g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.673-209_673-208ins others(335): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837637 | |||||||
| chr13:43837637 | T | TAATTAAA others(329): Show |
4 | a0001c0001t0009g0045 a0001c0001t0009g0046 a0001c0001t0009g0132 others(1): Show |
6 | HG01361.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-209_673-208ins others(336): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837637 | |||||||
| chr13:43837637 | T | TAATTAAA others(334): Show |
4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-209_673-208ins others(341): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837637 | |||||||
| chr13:43837652 | AAC | A | 78 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(75): Show |
141 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.673-225_673-224del others(2): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837652 | |||||||
| chr13:43837760 | T | C | 2 | a0001c0001t0007g0094 a0001c0001t0007g0097 |
2 | NA18945.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.673-331A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837760 | |||||||
| chr13:43837834 | A | G | 24 | a0001c0002t0005g0004 a0001c0002t0005g0027 a0001c0002t0005g0058 others(21): Show |
38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.673-405T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837834 | |||||||
| chr13:43837855 | T | G | 1 | a0001c0002t0005g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.673-426A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837855 | |||||||
| chr13:43838330 | T | A | 37 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(34): Show |
82 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.673-901A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43838330 | |||||||
| chr13:43838552 | G | A | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-1123C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43838552 | |||||||
| chr13:43838853 | T | C | 2 | a0001c0001t0004g0191 a0001c0001t0004g0193 |
2 | HG02027.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.673-1424A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43838853 | |||||||
| chr13:43839069 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0148 a0001c0001t0008g0150 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-1640C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839069 | |||||||
| chr13:43839119 | T | C | 1 | a0001c0001t0012g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.673-1690A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839119 | |||||||
| chr13:43839240 | C | T | 6 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0090 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.673-1811G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839240 | |||||||
| chr13:43839285 | A | G | 19 | a0001c0001t0007g0005 a0001c0001t0007g0015 a0001c0001t0007g0094 others(16): Show |
29 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.673-1856T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839285 | |||||||
| chr13:43839331 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0050 others(11): Show |
41 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.673-1902A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839331 | |||||||
| chr13:43839349 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.673-1920C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839349 | |||||||
| chr13:43839360 | A | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.673-1931T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839360 | |||||||
| chr13:43839387 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.673-1958G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839387 | |||||||
| chr13:43839463 | T | C | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.673-2034A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839463 | |||||||
| chr13:43839496 | G | T | 1 | a0001c0002t0014g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.673-2067C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839496 | |||||||
| chr13:43839558 | T | A | 1 | a0001c0001t0007g0101 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.673-2129A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839558 | |||||||
| chr13:43839576 | AAT | A | 19 | a0001c0001t0007g0005 a0001c0001t0007g0015 a0001c0001t0007g0094 others(16): Show |
29 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.673-2149_673-2148d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839576 | |||||||
| chr13:43839827 | T | A | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-2398A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839827 | |||||||
| chr13:43839857 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.673-2428C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839857 | |||||||
| chr13:43839911 | C | T | 1 | a0001c0001t0003g0062 | 2 | NA19056.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.673-2482G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839911 | |||||||
| chr13:43839934 | C | T | 1 | a0004c0005t0001g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.673-2505G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839934 | |||||||
| chr13:43840054 | T | G | 1 | a0001c0001t0003g0243 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.673-2625A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840054 | |||||||
| chr13:43840065 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.673-2636G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840065 | |||||||
| chr13:43840165 | T | C | 2 | a0001c0001t0004g0017 a0001c0001t0022g0120 |
5 | NA18952.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-2736A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840165 | |||||||
| chr13:43840214 | C | T | 2 | a0001c0001t0002g0079 a0001c0001t0021g0080 |
2 | HG01074.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.673-2785G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840214 | |||||||
| chr13:43840267 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0085 |
2 | HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.673-2838G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840267 | |||||||
| chr13:43840565 | T | C | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.673-3136A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840565 | |||||||
| chr13:43840587 | A | C | 21 | a0001c0001t0001g0184 a0002c0003t0001g0012 a0002c0003t0001g0018 others(18): Show |
31 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.673-3158T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840587 | |||||||
| chr13:43840606 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.673-3177A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840606 | |||||||
| chr13:43840626 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.673-3197G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840626 | |||||||
| chr13:43840630 | C | T | 38 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0014 others(35): Show |
83 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.673-3201G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840630 | |||||||
| chr13:43840633 | T | C | 1 | a0001c0001t0010g0035 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.673-3204A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840633 | |||||||
| chr13:43840639 | G | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.673-3210C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840639 | |||||||
| chr13:43840777 | T | C | 79 | a0001c0001t0001g0219 a0001c0001t0002g0001 a0001c0001t0002g0014 others(76): Show |
142 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.673-3348A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840777 | |||||||
| chr13:43840780 | C | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(75): Show |
141 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.673-3351G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840780 | |||||||
| chr13:43840781 | A | C | 78 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(75): Show |
141 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.673-3352T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840781 | |||||||
| chr13:43840800 | G | T | 42 | a0001c0001t0001g0219 a0001c0001t0009g0043 a0001c0001t0009g0044 others(39): Show |
60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.673-3371C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840800 | |||||||
| chr13:43840862 | A | G | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.673-3433T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840862 | |||||||
| chr13:43840960 | A | G | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-3531T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840960 | |||||||
| chr13:43840976 | T | A | 7 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0145 others(4): Show |
7 | HG01884.hp1 HG01981.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-3547A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840976 | |||||||
| chr13:43841004 | T | A | 1 | a0001c0001t0012g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.673-3575A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841004 | |||||||
| chr13:43841067 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.673-3638C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841067 | |||||||
| chr13:43841102 | C | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.673-3673G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841102 | |||||||
| chr13:43841233 | A | G | 70 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0055 others(67): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.673-3804T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841233 | |||||||
| chr13:43841260 | A | G | 1 | a0001c0001t0006g0041 | 2 | NA18979.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.673-3831T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841260 | |||||||
| chr13:43841356 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.673-3927A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841356 | |||||||
| chr13:43841462 | T | C | 6 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0090 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.673-4033A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841462 | |||||||
| chr13:43841503 | T | C | 20 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(17): Show |
33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.673-4074A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841503 | |||||||
| chr13:43841567 | T | C | 1 | a0001c0001t0003g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.673-4138A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841567 | |||||||
| chr13:43841642 | A | G | 20 | a0002c0003t0001g0012 a0002c0003t0001g0018 a0002c0003t0001g0026 others(17): Show |
30 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.673-4213T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841642 | |||||||
| chr13:43841664 | T | C | 1 | a0001c0001t0004g0037 | 2 | NA18948.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.673-4235A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841664 | |||||||
| chr13:43841692 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.673-4263A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841692 | |||||||
| chr13:43841783 | T | A | 37 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(34): Show |
82 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.673-4354A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841783 | |||||||
| chr13:43841829 | G | A | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-4400C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841829 | |||||||
| chr13:43841847 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.673-4418T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841847 | |||||||
| chr13:43841859 | C | T | 14 | a0001c0001t0003g0241 a0001c0001t0004g0016 a0001c0001t0004g0017 others(11): Show |
25 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.673-4430G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841859 | |||||||
| chr13:43841864 | T | G | 1 | a0001c0001t0002g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.673-4435A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841864 | |||||||
| chr13:43842083 | C | CT | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.673-4655dupA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842083 | |||||||
| chr13:43842141 | A | C | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-4712T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842141 | |||||||
| chr13:43842199 | G | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(36): Show |
87 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.673-4770C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842199 | |||||||
| chr13:43842265 | G | A | 1 | a0001c0001t0006g0040 | 2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.673-4836C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842265 | |||||||
| chr13:43842528 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.673-5099G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842528 | |||||||
| chr13:43842591 | A | T | 1 | a0001c0001t0003g0245 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.673-5162T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842591 | |||||||
| chr13:43842669 | T | G | 77 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0055 others(74): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.673-5240A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842669 | |||||||
| chr13:43842809 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.673-5380G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842809 | |||||||
| chr13:43842880 | A | G | 1 | a0001c0001t0013g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.673-5451T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842880 | |||||||
| chr13:43842883 | AG | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0210 others(3): Show |
6 | HG00438.hp2 NA18948.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-5455delC | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842883 | |||||||
| chr13:43842958 | T | A | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-5529A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842958 | |||||||
| chr13:43843254 | T | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.673-5825A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843254 | |||||||
| chr13:43843283 | C | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0148 a0001c0001t0008g0150 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-5854G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843283 | |||||||
| chr13:43843305 | G | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.673-5876C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843305 | |||||||
| chr13:43843321 | T | A | 1 | a0001c0001t0009g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.673-5892A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843321 | |||||||
| chr13:43843633 | G | A | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-6204C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843633 | |||||||
| chr13:43843824 | AT | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(198): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.673-6396delA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843824 | |||||||
| chr13:43843951 | A | G | 3 | a0001c0001t0002g0075 a0001c0001t0002g0079 a0001c0001t0021g0080 |
3 | HG01074.hp1 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.673-6522T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843951 | |||||||
| chr13:43844028 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.673-6599C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844028 | |||||||
| chr13:43844069 | CTTCT | C | 24 | a0001c0001t0001g0219 a0001c0002t0005g0004 a0001c0002t0005g0027 others(21): Show |
38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.673-6644_673-6641d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844069 | |||||||
| chr13:43844112 | G | A | 6 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0090 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.673-6683C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844112 | |||||||
| chr13:43844126 | T | C | 1 | a0001c0001t0009g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.673-6697A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844126 | |||||||
| chr13:43844224 | G | A | 1 | a0001c0002t0014g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.673-6795C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844224 | |||||||
| chr13:43844303 | G | C | 1 | a0006c0006t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.673-6874C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844303 | |||||||
| chr13:43844308 | A | G | 1 | a0001c0001t0022g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.673-6879T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844308 | |||||||
| chr13:43844639 | T | G | 4 | a0001c0001t0006g0010 a0001c0001t0006g0122 a0001c0001t0006g0123 others(1): Show |
8 | NA18953.hp2 NA18955.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.673-7210A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844639 | |||||||
| chr13:43844841 | C | G | 3 | a0001c0001t0004g0037 a0001c0001t0004g0039 a0001c0001t0004g0117 |
5 | NA18945.hp1 NA18948.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-7412G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844841 | |||||||
| chr13:43844979 | A | G | 19 | a0001c0001t0007g0005 a0001c0001t0007g0015 a0001c0001t0007g0094 others(16): Show |
29 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.673-7550T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844979 | |||||||
| chr13:43845087 | T | C | 1 | a0002c0003t0001g0176 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.673-7658A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845087 | |||||||
| chr13:43845185 | T | C | 1 | a0002c0003t0001g0174 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.673-7756A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845185 | |||||||
| chr13:43845351 | C | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-7922G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845351 | |||||||
| chr13:43845396 | A | G | 79 | a0001c0001t0001g0219 a0001c0001t0002g0001 a0001c0001t0002g0014 others(76): Show |
142 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.673-7967T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845396 | |||||||
| chr13:43845554 | T | A | 5 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0127 others(2): Show |
7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-8125A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845554 | |||||||
| chr13:43845581 | G | A | 2 | a0001c0001t0007g0107 a0001c0001t0012g0108 |
2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.673-8152C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845581 | |||||||
| chr13:43845588 | T | TATAGTCC others(25): Show |
1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8160_673-8159i others(34): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845588 | |||||||
| chr13:43845637 | G | A | 13 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(10): Show |
24 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.673-8208C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845637 | |||||||
| chr13:43845711 | A | AAAAAC | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.673-8287_673-8283d others(7): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845711 | |||||||
| chr13:43845711 | A | AAAAACAA others(3): Show |
1 | a0001c0001t0001g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.673-8292_673-8283d others(12): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845711 | |||||||
| chr13:43845769 | T | C | 1 | a0001c0002t0016g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.673-8340A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845769 | |||||||
| chr13:43845794 | T | C | 2 | a0001c0001t0003g0242 a0001c0001t0003g0244 |
2 | HG02165.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.673-8365A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845794 | |||||||
| chr13:43845967 | C | T | 1 | a0001c0002t0016g0224 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.673-8538G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845967 | |||||||
| chr13:43845985 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.673-8556A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845985 | |||||||
| chr13:43846081 | C | CT | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.673-8653dupA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846081 | |||||||
| chr13:43846094 | G | A | 2 | a0001c0001t0010g0020 a0001c0001t0010g0111 |
4 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-8665C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846094 | |||||||
| chr13:43846114 | G | A | 3 | a0001c0001t0010g0090 a0001c0001t0010g0091 a0001c0001t0010g0092 |
3 | HG01109.hp1 HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.673-8685C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846114 | |||||||
| chr13:43846124 | G | C | 5 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0127 others(2): Show |
7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-8695C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846124 | |||||||
| chr13:43846149 | A | G | 3 | a0001c0001t0004g0016 a0001c0001t0004g0038 a0001c0001t0004g0114 |
7 | HG01167.hp2 NA18954.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-8720T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846149 | |||||||
| chr13:43846175 | A | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8746T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846175 | |||||||
| chr13:43846176 | G | A | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8747C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846176 | |||||||
| chr13:43846193 | G | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8764C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846193 | |||||||
| chr13:43846194 | C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8765G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846194 | |||||||
| chr13:43846271 | A | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8842T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846271 | |||||||
| chr13:43846337 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(23): Show |
58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.673-8908C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846337 | |||||||
| chr13:43846369 | C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8940G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846369 | |||||||
| chr13:43846371 | G | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8942C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846371 | |||||||
| chr13:43846372 | C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8943G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846372 | |||||||
| chr13:43846669 | C | T | 16 | a0001c0002t0005g0004 a0001c0002t0005g0027 a0001c0002t0005g0058 others(13): Show |
28 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.673-9240G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846669 | |||||||
| chr13:43846875 | AAG | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.673-9448_673-9447d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846875 | |||||||
| chr13:43847009 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.673-9580T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847009 | |||||||
| chr13:43847173 | C | T | 1 | a0002c0003t0001g0182 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.673-9744G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847173 | |||||||
| chr13:43847352 | T | C | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-9923A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847352 | |||||||
| chr13:43847416 | T | A | 2 | a0001c0001t0001g0203 a0001c0001t0008g0204 |
2 | HG00642.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.673-9987A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847416 | |||||||
| chr13:43847528 | C | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.673-10099G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847528 | |||||||
| chr13:43847610 | A | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(26): Show |
77 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.673-10181T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847610 | |||||||
| chr13:43847749 | G | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10320C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847749 | |||||||
| chr13:43847750 | C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10321G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847750 | |||||||
| chr13:43847797 | C | G | 2 | a0001c0001t0003g0063 a0001c0001t0017g0246 |
3 | NA18969.hp1 NA18972.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.673-10368G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847797 | |||||||
| chr13:43847850 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.673-10421A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847850 | |||||||
| chr13:43847851 | T | C | 23 | a0001c0001t0001g0219 a0001c0002t0005g0004 a0001c0002t0005g0027 others(20): Show |
37 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.673-10422A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847851 | |||||||
| chr13:43847927 | A | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10498T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847927 | |||||||
| chr13:43847963 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.673-10534G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847963 | |||||||
| chr13:43847990 | G | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(106): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.673-10561C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847990 | |||||||
| chr13:43848059 | G | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10630C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848059 | |||||||
| chr13:43848060 | C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10631G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848060 | |||||||
| chr13:43848196 | C | T | 1 | a0001c0001t0007g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.672+10585G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848196 | |||||||
| chr13:43848235 | A | G | 79 | a0001c0001t0001g0219 a0001c0001t0002g0001 a0001c0001t0002g0014 others(76): Show |
142 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.672+10546T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848235 | |||||||
| chr13:43848392 | G | A | 5 | a0002c0003t0001g0026 a0002c0003t0001g0176 a0002c0003t0001g0190 others(2): Show |
7 | HG02071.hp1 HG02074.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+10389C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848392 | |||||||
| chr13:43848516 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.672+10265C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848516 | |||||||
| chr13:43848587 | A | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.672+10194T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848587 | |||||||
| chr13:43848828 | C | A | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+9953G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848828 | |||||||
| chr13:43848946 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.672+9835G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848946 | |||||||
| chr13:43848952 | A | G | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(23): Show |
58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.672+9829T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848952 | |||||||
| chr13:43849032 | T | A | 1 | a0001c0001t0030g0213 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.672+9749A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849032 | |||||||
| chr13:43849066 | C | T | 25 | a0001c0001t0001g0219 a0001c0002t0005g0004 a0001c0002t0005g0027 others(22): Show |
39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+9715G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849066 | |||||||
| chr13:43849134 | G | A | 1 | a0001c0001t0009g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672+9647C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849134 | |||||||
| chr13:43849162 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0015g0194 a0001c0001t0030g0213 |
4 | HG00099.hp2 HG01433.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+9619A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849162 | |||||||
| chr13:43849204 | G | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0038 |
6 | NA18954.hp2 NA18972.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.672+9577C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849204 | |||||||
| chr13:43849289 | T | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.672+9492A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849289 | |||||||
| chr13:43849376 | G | C | 4 | a0001c0002t0005g0027 a0001c0002t0005g0226 a0001c0002t0005g0232 others(1): Show |
6 | NA18941.hp1 NA18942.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.672+9405C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849376 | |||||||
| chr13:43849447 | A | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0144 others(28): Show |
39 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.672+9334T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849447 | |||||||
| chr13:43849484 | C | T | 1 | a0002c0003t0001g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.672+9297G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849484 | |||||||
| chr13:43849485 | T | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.672+9296A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849485 | |||||||
| chr13:43849531 | T | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+9250A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849531 | |||||||
| chr13:43849674 | A | G | 1 | a0001c0001t0004g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.672+9107T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849674 | |||||||
| chr13:43849737 | T | C | 1 | a0001c0002t0005g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.672+9044A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849737 | |||||||
| chr13:43849927 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(36): Show |
87 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.672+8854A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849927 | |||||||
| chr13:43849948 | G | A | 1 | a0001c0001t0004g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.672+8833C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849948 | |||||||
| chr13:43850010 | G | C | 1 | a0001c0001t0007g0101 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.672+8771C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850010 | |||||||
| chr13:43850074 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(121): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.672+8707A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850074 | |||||||
| chr13:43850208 | A | G | 10 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0090 others(7): Show |
14 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+8573T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850208 | |||||||
| chr13:43850236 | G | T | 4 | a0001c0001t0006g0011 a0001c0001t0006g0041 a0001c0001t0006g0126 others(1): Show |
10 | NA18939.hp2 NA18964.hp1 NA18978.hp1 others(7): Show |
intron_variant | MODIFIER | c.672+8545C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850236 | |||||||
| chr13:43850269 | T | A | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+8512A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850269 | |||||||
| chr13:43850578 | A | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+8203T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850578 | |||||||
| chr13:43850602 | A | G | 1 | a0001c0001t0007g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.672+8179T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850602 | |||||||
| chr13:43850630 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
217 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.672+8151T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850630 | |||||||
| chr13:43850872 | T | C | 1 | a0001c0001t0004g0038 | 2 | NA19054.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.672+7909A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850872 | |||||||
| chr13:43850921 | G | A | 3 | a0002c0003t0001g0051 a0002c0003t0001g0178 a0002c0003t0008g0179 |
4 | HG03239.hp2 HG03654.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+7860C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850921 | |||||||
| chr13:43851014 | T | C | 1 | a0001c0001t0018g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.672+7767A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851014 | |||||||
| chr13:43851091 | T | A | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+7690A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851091 | |||||||
| chr13:43851092 | C | T | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+7689G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851092 | |||||||
| chr13:43851094 | A | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+7687T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851094 | |||||||
| chr13:43851285 | T | C | 3 | a0001c0001t0002g0075 a0001c0001t0002g0079 a0001c0001t0021g0080 |
3 | HG01074.hp1 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.672+7496A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851285 | |||||||
| chr13:43851324 | C | T | 1 | a0006c0006t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.672+7457G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851324 | |||||||
| chr13:43851386 | A | G | 1 | a0001c0001t0003g0242 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.672+7395T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851386 | |||||||
| chr13:43851615 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.672+7166G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851615 | |||||||
| chr13:43851685 | C | G | 1 | a0001c0001t0008g0200 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.672+7096G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851685 | |||||||
| chr13:43851776 | C | T | 1 | a0001c0001t0009g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.672+7005G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851776 | |||||||
| chr13:43851850 | G | A | 24 | a0001c0001t0001g0219 a0001c0002t0005g0004 a0001c0002t0005g0027 others(21): Show |
38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.672+6931C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851850 | |||||||
| chr13:43851860 | G | T | 4 | a0001c0001t0010g0035 a0001c0001t0010g0090 a0001c0001t0010g0091 others(1): Show |
5 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+6921C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851860 | |||||||
| chr13:43851952 | G | GA | 9 | a0001c0002t0005g0004 a0001c0002t0005g0027 a0001c0002t0005g0058 others(6): Show |
19 | HG00673.hp2 HG01069.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.672+6828dupT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851952 | |||||||
| chr13:43851952 | GA | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(38): Show |
90 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.672+6828delT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851952 | |||||||
| chr13:43851958 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.672+6823T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851958 | |||||||
| chr13:43851968 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.672+6813T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851968 | |||||||
| chr13:43852133 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(113): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.672+6648G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852133 | |||||||
| chr13:43852178 | G | A | 1 | a0001c0001t0003g0030 | 3 | HG00621.hp2 HG02027.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.672+6603C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852178 | |||||||
| chr13:43852268 | A | T | 1 | a0001c0001t0003g0251 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.672+6513T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852268 | |||||||
| chr13:43852392 | G | A | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+6389C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852392 | |||||||
| chr13:43852668 | C | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(36): Show |
87 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.672+6113G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852668 | |||||||
| chr13:43852732 | TAGAG | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(36): Show |
87 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.672+6045_672+6048d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852732 | |||||||
| chr13:43852738 | G | T | 1 | a0001c0002t0005g0058 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.672+6043C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852738 | |||||||
| chr13:43852921 | T | A | 1 | a0001c0002t0005g0060 | 2 | HG01515.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.672+5860A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852921 | |||||||
| chr13:43852928 | A | C | 3 | a0001c0001t0002g0014 a0001c0001t0002g0081 a0001c0001t0002g0082 |
6 | NA18961.hp2 NA18964.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.672+5853T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852928 | |||||||
| chr13:43852968 | A | G | 10 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0145 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.672+5813T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852968 | |||||||
| chr13:43852971 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.672+5810T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852971 | |||||||
| chr13:43852987 | G | A | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+5794C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852987 | |||||||
| chr13:43853111 | T | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+5670A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853111 | |||||||
| chr13:43853121 | A | T | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+5660T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853121 | |||||||
| chr13:43853122 | A | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+5659T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853122 | |||||||
| chr13:43853126 | T | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+5655A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853126 | |||||||
| chr13:43853146 | T | C | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+5635A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853146 | |||||||
| chr13:43853299 | CA | C | 7 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0145 others(4): Show |
7 | HG01884.hp1 HG01981.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+5481delT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853299 | |||||||
| chr13:43853388 | A | C | 25 | a0001c0001t0001g0219 a0001c0002t0005g0004 a0001c0002t0005g0027 others(22): Show |
39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+5393T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853388 | |||||||
| chr13:43853409 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.672+5372C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853409 | |||||||
| chr13:43853436 | C | T | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+5345G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853436 | |||||||
| chr13:43853599 | A | G | 7 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0145 others(4): Show |
7 | HG01884.hp1 HG01981.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+5182T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853599 | |||||||
| chr13:43853852 | T | A | 1 | a0001c0001t0003g0257 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.672+4929A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853852 | |||||||
| chr13:43853862 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.672+4919A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853862 | |||||||
| chr13:43853983 | A | C | 6 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0090 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.672+4798T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853983 | |||||||
| chr13:43854067 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.672+4714G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854067 | |||||||
| chr13:43854085 | A | G | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+4696T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854085 | |||||||
| chr13:43854156 | CA | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(214): Show |
378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.672+4624delT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854156 | |||||||
| chr13:43854169 | C | T | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(23): Show |
58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.672+4612G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854169 | |||||||
| chr13:43854291 | G | A | 1 | a0002c0003t0001g0012 | 5 | NA18971.hp1 NA18988.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+4490C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854291 | |||||||
| chr13:43854592 | T | C | 1 | a0001c0002t0005g0228 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.672+4189A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854592 | |||||||
| chr13:43854601 | A | G | 25 | a0001c0001t0001g0219 a0001c0002t0005g0004 a0001c0002t0005g0027 others(22): Show |
39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+4180T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854601 | |||||||
| chr13:43854611 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672+4170G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854611 | |||||||
| chr13:43854657 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
217 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.672+4124C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854657 | |||||||
| chr13:43854697 | T | C | 3 | a0001c0001t0007g0099 a0001c0001t0007g0101 a0001c0001t0012g0100 |
3 | HG01928.hp2 HG01993.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.672+4084A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854697 | |||||||
| chr13:43854911 | G | T | 1 | a0001c0001t0002g0033 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.672+3870C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854911 | |||||||
| chr13:43855036 | A | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.672+3745T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855036 | |||||||
| chr13:43855040 | G | A | 1 | a0001c0001t0003g0249 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.672+3741C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855040 | |||||||
| chr13:43855067 | A | T | 1 | a0001c0001t0006g0122 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.672+3714T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855067 | |||||||
| chr13:43855213 | A | C | 1 | a0001c0001t0003g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.672+3568T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855213 | |||||||
| chr13:43855237 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.672+3544C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855237 | |||||||
| chr13:43855256 | C | G | 1 | a0001c0002t0005g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.672+3525G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855256 | |||||||
| chr13:43855331 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.672+3450T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855331 | |||||||
| chr13:43855362 | G | GACACACA others(1): Show |
4 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0091 others(1): Show |
7 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+3418_672+3419i others(10): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855362 | |||||||
| chr13:43855363 | C | A | 6 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0090 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.672+3418G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | |||||||
| chr13:43855363 | C | CCA | 57 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0141 others(54): Show |
77 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.672+3416_672+3417d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | |||||||
| chr13:43855363 | C | CCACA | 22 | a0001c0001t0001g0184 a0001c0001t0001g0188 a0001c0001t0001g0217 others(19): Show |
27 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.672+3414_672+3417d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | |||||||
| chr13:43855363 | CCA | C | 80 | a0001c0001t0001g0197 a0001c0001t0001g0219 a0001c0001t0002g0001 others(77): Show |
150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.672+3416_672+3417d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | |||||||
| chr13:43855363 | CCACA | C | 9 | a0001c0001t0001g0164 a0001c0001t0001g0167 a0001c0001t0003g0028 others(6): Show |
13 | HG01891.hp1 HG02486.hp1 NA18969.hp1 others(10): Show |
intron_variant | MODIFIER | c.672+3414_672+3417d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | |||||||
| chr13:43855363 | CCACACA | C | 16 | a0001c0002t0005g0004 a0001c0002t0005g0027 a0001c0002t0005g0058 others(13): Show |
28 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.672+3412_672+3417d others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | |||||||
| chr13:43855363 | CCACACAC others(7): Show |
C | 1 | a0001c0001t0006g0123 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.672+3404_672+3417d others(16): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | |||||||
| chr13:43855393 | A | C | 18 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(15): Show |
31 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.672+3388T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855393 | |||||||
| chr13:43855395 | C | A | 1 | a0001c0001t0007g0102 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.672+3386G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855395 | |||||||
| chr13:43855417 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.672+3364C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855417 | |||||||
| chr13:43855418 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.672+3363T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855418 | |||||||
| chr13:43855537 | G | T | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+3244C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855537 | |||||||
| chr13:43855580 | T | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.672+3201A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855580 | |||||||
| chr13:43855681 | AT | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(109): Show |
194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.672+3099delA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855681 | |||||||
| chr13:43855682 | T | A | 21 | a0001c0001t0001g0199 a0001c0001t0004g0016 a0001c0001t0004g0017 others(18): Show |
34 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.672+3099A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855682 | |||||||
| chr13:43855688 | AAAAC | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0144 others(41): Show |
65 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.672+3089_672+3092d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855688 | |||||||
| chr13:43856178 | G | A | 1 | a0001c0002t0016g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.672+2603C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856178 | |||||||
| chr13:43856358 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672+2423G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856358 | |||||||
| chr13:43856397 | G | A | 10 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0022 others(7): Show |
23 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(20): Show |
intron_variant | MODIFIER | c.672+2384C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856397 | |||||||
| chr13:43856528 | G | A | 20 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(17): Show |
33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.672+2253C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856528 | |||||||
| chr13:43856570 | C | T | 1 | a0001c0001t0004g0191 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.672+2211G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856570 | |||||||
| chr13:43856579 | G | A | 10 | a0001c0001t0002g0078 a0001c0001t0007g0005 a0001c0001t0007g0103 others(7): Show |
17 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.672+2202C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856579 | |||||||
| chr13:43856642 | A | G | 20 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(17): Show |
33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.672+2139T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856642 | |||||||
| chr13:43856659 | CT | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
217 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.672+2121delA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856659 | |||||||
| chr13:43856808 | C | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0164 a0001c0001t0001g0166 others(1): Show |
6 | HG00408.hp2 NA18952.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.672+1973G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856808 | |||||||
| chr13:43856887 | C | G | 1 | a0001c0001t0002g0069 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.672+1894G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856887 | |||||||
| chr13:43856943 | AAT | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.672+1836_672+1837d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856943 | |||||||
| chr13:43857059 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0030g0213 |
3 | HG00099.hp2 HG01433.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.672+1722A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857059 | |||||||
| chr13:43857174 | C | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+1607G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857174 | |||||||
| chr13:43857449 | A | AGT | 6 | a0001c0001t0003g0239 a0001c0001t0003g0240 a0001c0001t0010g0035 others(3): Show |
7 | HG01109.hp1 HG02135.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+1330_672+1331d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857449 | A | AGTGT | 3 | a0001c0001t0003g0061 a0001c0001t0003g0238 a0001c0001t0013g0088 |
4 | HG01496.hp1 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+1328_672+1331d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857449 | A | AGTGTGT | 3 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0089 |
4 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+1326_672+1331d others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857449 | AGT | A | 13 | a0001c0001t0003g0031 a0001c0001t0003g0245 a0001c0001t0003g0251 others(10): Show |
18 | HG00558.hp2 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.672+1330_672+1331d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857449 | AGTGT | A | 8 | a0001c0001t0006g0022 a0001c0001t0006g0040 a0001c0001t0006g0125 others(5): Show |
12 | HG02257.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.672+1328_672+1331d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857449 | AGTGTGT | A | 32 | a0001c0001t0001g0153 a0001c0001t0001g0165 a0001c0001t0001g0197 others(29): Show |
56 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.672+1326_672+1331d others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857449 | AGTGTGTG others(1): Show |
A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(106): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.672+1324_672+1331d others(10): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857449 | AGTGTGTG others(3): Show |
A | 26 | a0001c0001t0001g0152 a0001c0001t0001g0184 a0001c0001t0002g0014 others(23): Show |
39 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+1322_672+1331d others(12): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857449 | AGTGTGTG others(5): Show |
A | 26 | a0001c0001t0001g0219 a0001c0001t0006g0122 a0001c0002t0005g0004 others(23): Show |
40 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.672+1320_672+1331d others(14): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | |||||||
| chr13:43857524 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(173): Show |
289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.672+1257T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857524 | |||||||
| chr13:43857602 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(106): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.672+1179A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857602 | |||||||
| chr13:43857605 | T | G | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+1176A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857605 | |||||||
| chr13:43857765 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.672+1016A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857765 | |||||||
| chr13:43857774 | G | A | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+1007C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857774 | |||||||
| chr13:43857808 | T | A | 1 | a0006c0006t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.672+973A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857808 | |||||||
| chr13:43857828 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.672+953C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857828 | |||||||
| chr13:43857895 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(173): Show |
289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.672+886A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857895 | |||||||
| chr13:43857932 | A | T | 1 | a0001c0001t0006g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.672+849T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857932 | |||||||
| chr13:43858047 | A | C | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+734T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858047 | |||||||
| chr13:43858089 | G | T | 1 | a0001c0001t0008g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.672+692C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858089 | |||||||
| chr13:43858261 | G | T | 1 | a0001c0001t0009g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.672+520C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858261 | |||||||
| chr13:43858504 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672+277A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858504 | |||||||
| chr13:43858662 | GTTCT | G | 2 | a0001c0001t0003g0063 a0001c0001t0017g0246 |
3 | NA18969.hp1 NA18972.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.672+115_672+118del others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858662 | |||||||
| chr13:43858747 | A | G | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+34T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858747 | |||||||
| chr13:43859227 | G | A | 36 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(33): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.556-330C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859227 | |||||||
| chr13:43859429 | A | G | 36 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(33): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.555+243T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859429 | |||||||
| chr13:43859431 | G | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.555+241C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859431 | |||||||
| chr13:43859494 | C | A | 70 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0055 others(67): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.555+178G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859494 | |||||||
| chr13:43859564 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.555+108C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859564 | |||||||
| chr13:43859598 | A | T | 1 | a0007c0007t0002g0068 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.555+74T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859598 | |||||||
| chr13:43859644 | A | T | 1 | a0001c0002t0005g0225 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.555+28T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859644 | |||||||
| chr13:43860145 | TAATG | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
217 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.157-79_157-76delCA others(2): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860145 | |||||||
| chr13:43860159 | A | T | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01993.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.157-89T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860159 | |||||||
| chr13:43860224 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-154A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860224 | |||||||
| chr13:43860231 | AATT | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(23): Show |
58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.157-164_157-162del others(3): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860231 | |||||||
| chr13:43860279 | T | C | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-209A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860279 | |||||||
| chr13:43860527 | T | C | 43 | a0001c0001t0001g0219 a0001c0001t0006g0122 a0001c0001t0009g0043 others(40): Show |
61 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.157-457A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860527 | |||||||
| chr13:43860552 | G | GATATTTA others(3): Show |
26 | a0001c0001t0001g0219 a0001c0001t0006g0122 a0001c0002t0005g0004 others(23): Show |
40 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.157-492_157-483dup others(10): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860552 | |||||||
| chr13:43860599 | C | T | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.157-529G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860599 | |||||||
| chr13:43860612 | C | T | 43 | a0001c0001t0001g0219 a0001c0001t0006g0122 a0001c0001t0009g0043 others(40): Show |
61 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.157-542G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860612 | |||||||
| chr13:43860632 | T | C | 1 | a0001c0001t0002g0081 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.157-562A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860632 | |||||||
| chr13:43860700 | C | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(36): Show |
87 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.157-630G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860700 | |||||||
| chr13:43861204 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0148 a0001c0001t0008g0150 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-1134A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861204 | |||||||
| chr13:43861259 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0167 a0001c0001t0008g0147 |
4 | HG02109.hp2 HG02486.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-1189A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861259 | |||||||
| chr13:43861267 | T | C | 10 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0145 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-1197A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861267 | |||||||
| chr13:43861374 | C | T | 1 | a0001c0001t0022g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.157-1304G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861374 | |||||||
| chr13:43861396 | G | A | 4 | a0002c0003t0001g0112 a0002c0003t0001g0121 a0002c0003t0001g0172 others(1): Show |
4 | HG00438.hp1 HG00673.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-1326C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861396 | |||||||
| chr13:43861406 | C | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(248): Show |
433 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(430): Show |
intron_variant | MODIFIER | c.157-1336G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861406 | |||||||
| chr13:43861453 | G | C | 1 | a0001c0001t0008g0168 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.157-1383C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861453 | |||||||
| chr13:43861672 | A | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-1602T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861672 | |||||||
| chr13:43861826 | CAT | C | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-1758_157-1757d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861826 | |||||||
| chr13:43861852 | T | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.157-1782A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861852 | |||||||
| chr13:43861933 | C | A | 1 | a0001c0001t0003g0248 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.157-1863G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861933 | |||||||
| chr13:43862250 | C | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-2180G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862250 | |||||||
| chr13:43862300 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.157-2230G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862300 | |||||||
| chr13:43862308 | C | T | 13 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(10): Show |
24 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.157-2238G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862308 | |||||||
| chr13:43862350 | C | T | 1 | a0001c0001t0017g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157-2280G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862350 | |||||||
| chr13:43862817 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.157-2747G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862817 | |||||||
| chr13:43862876 | C | A | 1 | a0001c0001t0003g0251 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.157-2806G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862876 | |||||||
| chr13:43862916 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.157-2846G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862916 | |||||||
| chr13:43862936 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(173): Show |
289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.157-2866A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862936 | |||||||
| chr13:43862968 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.157-2898G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862968 | |||||||
| chr13:43863029 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.157-2959C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863029 | |||||||
| chr13:43863035 | AAATT | A | 17 | a0001c0001t0006g0122 a0001c0002t0005g0004 a0001c0002t0005g0027 others(14): Show |
29 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-2969_157-2966d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863035 | |||||||
| chr13:43863488 | A | G | 2 | a0002c0003t0001g0121 a0002c0003t0001g0172 |
2 | NA19005.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.157-3418T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863488 | |||||||
| chr13:43863596 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.157-3526C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863596 | |||||||
| chr13:43863675 | T | TTG | 7 | a0001c0001t0003g0013 a0001c0001t0003g0061 a0001c0001t0003g0249 others(4): Show |
12 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-3607_157-3606d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863675 | |||||||
| chr13:43863675 | T | TTGTGTG | 3 | a0001c0001t0010g0090 a0001c0001t0010g0091 a0001c0001t0010g0092 |
3 | HG01109.hp1 HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.157-3611_157-3606d others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863675 | |||||||
| chr13:43863675 | TTG | T | 64 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0001 others(61): Show |
129 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.157-3607_157-3606d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863675 | |||||||
| chr13:43863675 | TTGTG | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(144): Show |
240 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.157-3609_157-3606d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863675 | |||||||
| chr13:43863768 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.157-3698G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863768 | |||||||
| chr13:43863854 | A | G | 26 | a0001c0001t0001g0219 a0001c0001t0006g0122 a0001c0002t0005g0004 others(23): Show |
40 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.157-3784T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863854 | |||||||
| chr13:43863957 | G | C | 1 | a0001c0001t0002g0019 | 3 | NA18988.hp2 NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.157-3887C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863957 | |||||||
| chr13:43864046 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.157-3976T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864046 | |||||||
| chr13:43864130 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.157-4060G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864130 | |||||||
| chr13:43864142 | T | C | 2 | a0001c0001t0003g0254 a0001c0001t0017g0253 |
2 | HG00639.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.157-4072A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864142 | |||||||
| chr13:43864391 | G | A | 9 | a0001c0001t0009g0045 a0001c0001t0009g0046 a0001c0001t0009g0132 others(6): Show |
11 | HG01361.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+4303C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864391 | |||||||
| chr13:43864420 | G | C | 17 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0045 others(14): Show |
21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.156+4274C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864420 | |||||||
| chr13:43864821 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(173): Show |
289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.156+3873A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864821 | |||||||
| chr13:43864867 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.156+3827A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864867 | |||||||
| chr13:43865014 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(36): Show |
87 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.156+3680A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865014 | |||||||
| chr13:43865033 | T | C | 35 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(32): Show |
80 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.156+3661A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865033 | |||||||
| chr13:43865083 | A | G | 20 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(17): Show |
33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.156+3611T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865083 | |||||||
| chr13:43865129 | T | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(26): Show |
77 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.156+3565A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865129 | |||||||
| chr13:43865211 | C | T | 11 | a0001c0001t0001g0156 a0001c0001t0006g0010 a0001c0001t0006g0011 others(8): Show |
24 | HG01981.hp1 HG02738.hp2 HG03239.hp1 others(21): Show |
intron_variant | MODIFIER | c.156+3483G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865211 | |||||||
| chr13:43865321 | T | C | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+3373A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865321 | |||||||
| chr13:43865452 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.156+3242A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865452 | |||||||
| chr13:43865462 | G | GT | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+3231dupA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865462 | |||||||
| chr13:43865475 | A | G | 19 | a0001c0001t0007g0005 a0001c0001t0007g0015 a0001c0001t0007g0094 others(16): Show |
29 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.156+3219T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865475 | |||||||
| chr13:43865484 | T | C | 10 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0022 others(7): Show |
23 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(20): Show |
intron_variant | MODIFIER | c.156+3210A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865484 | |||||||
| chr13:43865524 | G | C | 43 | a0001c0001t0001g0219 a0001c0001t0006g0122 a0001c0001t0009g0043 others(40): Show |
61 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.156+3170C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865524 | |||||||
| chr13:43865742 | C | T | 6 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0090 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+2952G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865742 | |||||||
| chr13:43865821 | A | G | 2 | a0001c0001t0006g0122 a0001c0002t0034g0222 |
2 | NA19059.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.156+2873T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865821 | |||||||
| chr13:43865912 | G | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(173): Show |
289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.156+2782C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865912 | |||||||
| chr13:43866012 | A | T | 1 | a0001c0001t0003g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.156+2682T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866012 | |||||||
| chr13:43866085 | A | G | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+2609T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866085 | |||||||
| chr13:43866305 | C | G | 36 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(33): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.156+2389G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866305 | |||||||
| chr13:43866380 | A | C | 1 | a0001c0001t0010g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.156+2314T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866380 | |||||||
| chr13:43866391 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(173): Show |
289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.156+2303A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866391 | |||||||
| chr13:43866435 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.156+2259T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866435 | |||||||
| chr13:43866457 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.156+2237C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866457 | |||||||
| chr13:43866605 | C | T | 3 | a0001c0001t0006g0010 a0001c0001t0006g0123 a0001c0001t0006g0124 |
7 | NA18953.hp2 NA18955.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+2089G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866605 | |||||||
| chr13:43866684 | C | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+2010G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866684 | |||||||
| chr13:43866879 | C | T | 1 | a0001c0001t0018g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.156+1815G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866879 | |||||||
| chr13:43866888 | T | G | 1 | a0001c0002t0005g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.156+1806A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866888 | |||||||
| chr13:43866956 | G | A | 1 | a0002c0003t0001g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.156+1738C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866956 | |||||||
| chr13:43867072 | T | G | 10 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0022 others(7): Show |
23 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(20): Show |
intron_variant | MODIFIER | c.156+1622A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867072 | |||||||
| chr13:43867085 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.156+1609G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867085 | |||||||
| chr13:43867238 | A | G | 20 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(17): Show |
33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.156+1456T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867238 | |||||||
| chr13:43867327 | G | C | 1 | a0001c0001t0004g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.156+1367C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867327 | |||||||
| chr13:43867510 | T | C | 3 | a0001c0001t0003g0009 a0001c0001t0003g0255 a0001c0001t0017g0256 |
8 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+1184A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867510 | |||||||
| chr13:43867698 | G | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(26): Show |
77 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.156+996C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867698 | |||||||
| chr13:43867897 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(221): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.156+797T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867897 | |||||||
| chr13:43867901 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.156+793C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867901 | |||||||
| chr13:43867982 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.156+712T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867982 | |||||||
| chr13:43868057 | T | TTCAA | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.156+636_156+637ins others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868057 | |||||||
| chr13:43868102 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.156+592A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868102 | |||||||
| chr13:43868154 | G | A | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+540C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868154 | |||||||
| chr13:43868199 | T | G | 1 | a0001c0001t0006g0126 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.156+495A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868199 | |||||||
| chr13:43868220 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.156+474A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868220 | |||||||
| chr13:43868238 | G | A | 2 | a0001c0001t0002g0032 a0001c0001t0002g0083 |
3 | HG01952.hp1 HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.156+456C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868238 | |||||||
| chr13:43868271 | T | G | 1 | a0001c0001t0013g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.156+423A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868271 | |||||||
| chr13:43868459 | A | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+235T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868459 | |||||||
| chr13:43868508 | T | C | 2 | a0001c0002t0005g0232 a0001c0002t0033g0231 |
2 | NA18941.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.156+186A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868508 | |||||||
| chr13:43868619 | G | A | 1 | a0001c0001t0020g0084 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.156+75C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868619 | |||||||
| chr13:43868903 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.47-100G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/6 | chr13 | 43868903 | |||||||
| chr13:43869087 | T | C | 1 | a0002c0003t0001g0182 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.46+244A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/6 | chr13 | 43869087 | |||||||
| chr13:43869201 | T | C | 2 | a0001c0001t0004g0017 a0001c0001t0022g0120 |
5 | NA18952.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+130A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/6 | chr13 | 43869201 | |||||||
| chr13:43869587 | A | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(36): Show |
87 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.-113-98T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43869587 | |||||||
| chr13:43869717 | A | AAAGT | 10 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0145 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.-113-232_-113-229d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43869717 | |||||||
| chr13:43869841 | T | C | 37 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(34): Show |
82 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-352A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43869841 | |||||||
| chr13:43870153 | G | A | 1 | a0002c0003t0008g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-113-664C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870153 | |||||||
| chr13:43870233 | T | G | 1 | a0001c0002t0016g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-113-744A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870233 | |||||||
| chr13:43870272 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-113-783G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870272 | |||||||
| chr13:43870344 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-113-855A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870344 | |||||||
| chr13:43870438 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-113-949A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870438 | |||||||
| chr13:43870570 | C | T | 25 | a0001c0001t0001g0219 a0001c0002t0005g0004 a0001c0002t0005g0027 others(22): Show |
39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-113-1081G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870570 | |||||||
| chr13:43870680 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-113-1191T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870680 | |||||||
| chr13:43870682 | G | A | 1 | a0002c0003t0001g0051 | 2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-113-1193C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870682 | |||||||
| chr13:43870766 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0148 a0001c0001t0008g0150 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113-1277G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870766 | |||||||
| chr13:43870854 | T | C | 42 | a0001c0001t0001g0219 a0001c0001t0009g0043 a0001c0001t0009g0044 others(39): Show |
60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-113-1365A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870854 | |||||||
| chr13:43870934 | G | C | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-1445C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870934 | |||||||
| chr13:43870965 | T | C | 1 | a0001c0001t0003g0257 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-113-1476A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870965 | |||||||
| chr13:43871017 | G | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-113-1528C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871017 | |||||||
| chr13:43871048 | G | A | 1 | a0001c0002t0005g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-113-1559C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871048 | |||||||
| chr13:43871062 | C | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-1573G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871062 | |||||||
| chr13:43871184 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0008g0147 |
3 | HG02109.hp2 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-113-1695G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871184 | |||||||
| chr13:43871285 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-113-1796A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871285 | |||||||
| chr13:43871293 | G | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-1804C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871293 | |||||||
| chr13:43871373 | A | T | 42 | a0001c0001t0001g0219 a0001c0001t0009g0043 a0001c0001t0009g0044 others(39): Show |
60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-113-1884T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871373 | |||||||
| chr13:43871402 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-113-1913G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871402 | |||||||
| chr13:43871731 | A | G | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-2242T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871731 | |||||||
| chr13:43871879 | T | C | 1 | a0003c0004t0011g0143 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-113-2390A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871879 | |||||||
| chr13:43872025 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(23): Show |
58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113-2536C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872025 | |||||||
| chr13:43872031 | T | A | 1 | a0001c0001t0001g0025 | 3 | NA18950.hp2 NA19070.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-113-2542A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872031 | |||||||
| chr13:43872174 | G | A | 1 | a0002c0003t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-114+2668C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872174 | |||||||
| chr13:43872337 | G | T | 42 | a0001c0001t0001g0219 a0001c0001t0009g0043 a0001c0001t0009g0044 others(39): Show |
60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-114+2505C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872337 | |||||||
| chr13:43872476 | T | C | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-114+2366A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872476 | |||||||
| chr13:43872681 | A | G | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(23): Show |
58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-114+2161T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872681 | |||||||
| chr13:43872878 | A | G | 1 | a0001c0001t0008g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-114+1964T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872878 | |||||||
| chr13:43873047 | C | T | 21 | a0001c0001t0001g0184 a0002c0003t0001g0012 a0002c0003t0001g0018 others(18): Show |
31 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.-114+1795G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873047 | |||||||
| chr13:43873107 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(174): Show |
290 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.-114+1735A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873107 | |||||||
| chr13:43873144 | C | T | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-114+1698G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873144 | |||||||
| chr13:43873362 | A | T | 1 | a0001c0001t0002g0032 | 2 | HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-114+1480T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873362 | |||||||
| chr13:43873630 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-114+1212C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873630 | |||||||
| chr13:43873713 | T | C | 1 | a0001c0002t0005g0027 | 3 | NA18942.hp2 NA18960.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-114+1129A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873713 | |||||||
| chr13:43873726 | A | G | 1 | a0001c0002t0005g0221 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-114+1116T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873726 | |||||||
| chr13:43873749 | T | C | 1 | a0001c0001t0018g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-114+1093A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873749 | |||||||
| chr13:43873996 | C | A | 77 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0055 others(74): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-114+846G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873996 | |||||||
| chr13:43874035 | T | C | 1 | a0001c0001t0004g0039 | 2 | NA18945.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-114+807A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874035 | |||||||
| chr13:43874386 | T | C | 42 | a0001c0001t0001g0219 a0001c0001t0009g0043 a0001c0001t0009g0044 others(39): Show |
60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-114+456A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874386 | |||||||
| chr13:43874644 | T | C | 3 | a0001c0001t0010g0035 a0001c0001t0010g0091 a0001c0001t0010g0092 |
4 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-114+198A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874644 | |||||||
| chr13:43874798 | C | T | 42 | a0001c0001t0001g0219 a0001c0001t0009g0043 a0001c0001t0009g0044 others(39): Show |
60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-114+44G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874798 | |||||||
| chr13:43874825 | A | G | 2 | a0001c0001t0009g0045 a0001c0001t0009g0132 |
3 | HG02257.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-114+17T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874825 | |||||||
| chr13:43875136 | G | A | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-209C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875136 | |||||||
| chr13:43875195 | A | G | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-268T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875195 | |||||||
| chr13:43875232 | G | C | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(23): Show |
58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-199-305C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875232 | |||||||
| chr13:43875256 | G | T | 1 | a0001c0001t0003g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-199-329C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875256 | |||||||
| chr13:43875369 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-199-442G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875369 | |||||||
| chr13:43875421 | T | C | 1 | a0002c0003t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-199-494A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875421 | |||||||
| chr13:43875425 | G | T | 6 | a0001c0001t0004g0053 a0001c0001t0004g0191 a0001c0001t0004g0193 others(3): Show |
8 | HG02027.hp2 HG02083.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.-199-498C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875425 | |||||||
| chr13:43875690 | G | T | 2 | a0001c0001t0010g0020 a0001c0001t0010g0111 |
4 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-763C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875690 | |||||||
| chr13:43875986 | G | T | 7 | a0001c0001t0009g0043 a0001c0001t0009g0044 a0001c0001t0009g0127 others(4): Show |
9 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-199-1059C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875986 | |||||||
| chr13:43876068 | T | A | 1 | a0001c0001t0002g0085 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-199-1141A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876068 | |||||||
| chr13:43876086 | G | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
217 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-199-1159C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876086 | |||||||
| chr13:43876110 | T | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.-199-1183A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876110 | |||||||
| chr13:43876153 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-199-1226G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876153 | |||||||
| chr13:43876210 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-199-1283C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876210 | |||||||
| chr13:43876355 | T | C | 6 | a0001c0001t0010g0020 a0001c0001t0010g0035 a0001c0001t0010g0090 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-199-1428A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876355 | |||||||
| chr13:43876458 | A | T | 42 | a0001c0001t0001g0219 a0001c0001t0009g0043 a0001c0001t0009g0044 others(39): Show |
60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-199-1531T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876458 | |||||||
| chr13:43876485 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-199-1558C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876485 | |||||||
| chr13:43876591 | C | G | 1 | a0001c0001t0003g0236 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-199-1664G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876591 | |||||||
| chr13:43876658 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0144 others(28): Show |
39 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.-199-1731C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876658 | |||||||
| chr13:43876833 | T | TATAGCGG others(47): Show |
1 | a0001c0001t0001g0216 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-199-1960_-199-190 others(58): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876833 | |||||||
| chr13:43876853 | G | A | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-1926C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876853 | |||||||
| chr13:43876908 | C | T | 13 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(10): Show |
24 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-199-1981G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876908 | |||||||
| chr13:43876971 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-199-2044G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876971 | |||||||
| chr13:43876983 | C | T | 5 | a0001c0001t0001g0219 a0001c0001t0010g0020 a0001c0001t0010g0111 others(2): Show |
8 | HG01243.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199-2056G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876983 | |||||||
| chr13:43876985 | C | T | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-2058G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876985 | |||||||
| chr13:43877044 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-199-2117G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877044 | |||||||
| chr13:43877097 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-199-2170G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877097 | |||||||
| chr13:43877160 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-199-2233G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877160 | |||||||
| chr13:43877276 | A | G | 4 | a0001c0001t0013g0034 a0001c0001t0013g0087 a0001c0001t0013g0088 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-199-2349T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877276 | |||||||
| chr13:43877341 | T | C | 25 | a0001c0001t0001g0219 a0001c0002t0005g0004 a0001c0002t0005g0027 others(22): Show |
39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-200+2290A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877341 | |||||||
| chr13:43877403 | A | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.-200+2228T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877403 | |||||||
| chr13:43877440 | C | A | 1 | a0002c0003t0001g0234 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-200+2191G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877440 | |||||||
| chr13:43877684 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-200+1947G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877684 | |||||||
| chr13:43877708 | T | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(172): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-200+1923A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877708 | |||||||
| chr13:43877784 | A | G | 4 | a0003c0004t0011g0006 a0003c0004t0011g0142 a0003c0004t0011g0143 others(1): Show |
11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-200+1847T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877784 | |||||||
| chr13:43878091 | TTC | T | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0009g0043 others(16): Show |
23 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-200+1538_-200+153 others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878091 | |||||||
| chr13:43878241 | GTCTT | G | 11 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0022 others(8): Show |
24 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(21): Show |
intron_variant | MODIFIER | c.-200+1386_-200+138 others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878241 | |||||||
| chr13:43878456 | T | G | 1 | a0001c0002t0016g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-200+1175A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878456 | |||||||
| chr13:43878648 | C | T | 11 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0022 others(8): Show |
24 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(21): Show |
intron_variant | MODIFIER | c.-200+983G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878648 | |||||||
| chr13:43878959 | G | A | 2 | a0001c0001t0010g0020 a0001c0001t0010g0111 |
4 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+672C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878959 | |||||||
| chr13:43878978 | T | C | 1 | a0002c0003t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-200+653A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878978 | |||||||
| chr13:43878979 | G | C | 1 | a0002c0003t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-200+652C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878979 | |||||||
| chr13:43879040 | A | AAAAAAAG others(21): Show |
1 | a0002c0003t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-200+590_-200+591i others(30): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879040 | |||||||
| chr13:43879099 | C | G | 13 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0021 others(10): Show |
24 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-200+532G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879099 | |||||||
| chr13:43879324 | C | G | 1 | a0001c0002t0014g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-200+307G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879324 | |||||||
| chr13:43879344 | C | T | 27 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0019 others(24): Show |
59 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-200+287G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879344 | |||||||
| chr13:43879616 | G | T | 1 | a0002c0003t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-200+15C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879616 |