Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51493 |
| ensemblid | ENSG00000100220.12 |
| hgncid | 26935 |
| symbol | RTCB |
| name | RNA 2',3'-cyclic phosphate and 5'-OH ligase |
| refseq_nuc | NM_014306.5 |
| refseq_prot | NP_055121.1 |
| ensembl_nuc | ENST00000216038.6 |
| ensembl_prot | ENSP00000216038.5 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 32387582 |
| end | 32412247 |
| strand | - |
| ver | v1.2 |
| region | chr22:32387582-32412247 |
| region5000 | chr22:32382582-32417247 |
| regionname0 | RTCB_chr22_32387582_32412247 |
| regionname5000 | RTCB_chr22_32382582_32417247 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 505 | 436 | 94 | 79 | 197 | 14 | 50 | 159 | RTCB_chr22_32382582_32417247 | RTCB | MSRSY others(500): Show |
chr22 | 32382582 | 32417247 |
| a0002 | 0/0 | 505 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | MSRSY others(500): Show |
chr22 | 32382582 | 32417247 |
| a0003 | 0/0 | 505 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | MSRSY others(500): Show |
chr22 | 32382582 | 32417247 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1515 | 235 | 33 | 52 | 108 | 11 | 30 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 | ||
| a0001c0002 | 0/0 | 1515 | 102 | 10 | 5 | 78 | 0 | 9 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 | ||
| a0001c0003 | 0/1 | 1515 | 60 | 26 | 16 | 10 | 0 | 7 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 | ||
| a0001c0004 | 0/0 | 1515 | 23 | 11 | 4 | 1 | 3 | 4 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 | ||
| a0001c0005 | 0/0 | 1515 | 12 | 11 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 | ||
| a0001c0006 | 0/0 | 1515 | 3 | 2 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 | ||
| a0001c0009 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 | ||
| a0002c0008 | 0/0 | 1515 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 | ||
| a0003c0007 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | ATGAG others(1510): Show |
chr22 | 32382582 | 32417247 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2019 | 227 | 33 | 52 | 101 | 11 | 29 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0001t0004 | 0/0 | 2019 | 3 | 0 | 0 | 3 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0001t0005 | 0/0 | 2019 | 3 | 0 | 0 | 2 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0001t0008 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0001t0009 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0002t0001 | 0/0 | 2019 | 102 | 10 | 5 | 78 | 0 | 9 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0003t0001 | 0/1 | 2019 | 48 | 23 | 9 | 10 | 0 | 5 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0003t0003 | 0/0 | 2019 | 10 | 2 | 6 | 0 | 0 | 2 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0003t0006 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0003t0007 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0004t0001 | 0/0 | 2019 | 23 | 11 | 4 | 1 | 3 | 4 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0005t0002 | 0/0 | 2019 | 12 | 11 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0006t0001 | 0/0 | 2019 | 3 | 2 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0001c0009t0002 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0002c0008t0003 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| a0003c0007t0001 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | GTTCT others(2014): Show |
chr22 | 32382582 | 32417247 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 31 | 0 | 12 | 14 | 1 | 3 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0003 | 0/0 | 22 | 0 | 6 | 16 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0006 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 7 | 0 | 1 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0008 | 0/0 | 9 | 0 | 7 | 0 | 0 | 2 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0009 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0010 | 0/0 | 9 | 0 | 2 | 2 | 2 | 3 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0033 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0034 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0004g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0001t0009g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0001 | 0/0 | 37 | 0 | 3 | 33 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0014 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0004 | 0/0 | 16 | 1 | 5 | 7 | 0 | 3 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0003g0015 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0003g0021 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0003t0007g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0013 | 0/0 | 7 | 1 | 1 | 1 | 1 | 3 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0035 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0005t0002g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0005t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0005t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0005t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0005t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0005t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0005t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0006t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0006t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0001c0009t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0002c0008t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| a0003c0007t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0013 | EUR | FIN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0129 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00639 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00642 | hp2 | a0002 | c0008 | t0003 | g0092 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0190 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0188 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01070 | hp2 | a0001 | c0005 | t0002 | g0056 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0058 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0046 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0128 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01167 | hp2 | a0001 | c0006 | t0001 | g0132 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01256 | hp1 | a0001 | c0004 | t0001 | g0013 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01361 | hp2 | a0001 | c0003 | t0003 | g0021 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0186 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0052 | EUR | IBS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0052 | EUR | IBS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01891 | hp1 | a0001 | c0005 | t0002 | g0036 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0192 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0126 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01993 | hp1 | a0001 | c0003 | t0003 | g0091 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02004 | hp2 | a0001 | c0003 | t0007 | g0127 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02055 | hp1 | a0001 | c0005 | t0002 | g0017 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0194 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02145 | hp1 | a0001 | c0006 | t0001 | g0045 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CDX | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0045 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02258 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0051 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | KHV | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0013 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0116 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02622 | hp2 | a0001 | c0005 | t0002 | g0037 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0184 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02630 | hp2 | a0001 | c0003 | t0006 | g0117 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02647 | hp2 | a0001 | c0005 | t0002 | g0017 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0125 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02717 | hp1 | a0001 | c0009 | t0002 | g0054 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02738 | hp1 | a0001 | c0003 | t0003 | g0021 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0195 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02886 | hp1 | a0001 | c0005 | t0002 | g0057 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0191 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0187 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03041 | hp1 | a0001 | c0005 | t0002 | g0037 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03139 | hp1 | a0001 | c0005 | t0002 | g0017 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03139 | hp2 | a0001 | c0005 | t0002 | g0036 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0093 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0136 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03453 | hp1 | a0001 | c0005 | t0002 | g0017 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03491 | hp1 | a0001 | c0004 | t0001 | g0013 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0013 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0131 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03540 | hp2 | a0001 | c0005 | t0002 | g0055 | AFR | GWD | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0189 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0004 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0064 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04184 | hp1 | a0001 | c0003 | t0003 | g0015 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | BEB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0181 | SAS | STU | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | YRI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | YRI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18979 | hp2 | a0001 | c0001 | t0008 | g0103 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18988 | hp1 | a0003 | c0007 | t0001 | g0106 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19003 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0035 | AFR | LWK | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0051 | AFR | LWK | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | LWK | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19090 | hp1 | a0001 | c0001 | t0009 | g0111 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | ASW | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ASW | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | GIH | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01123 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02109 | hp2 | a0001 | c0005 | t0002 | g0053 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0035 | AFR | USA | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | USA | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | USA | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | LWK | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0185 | AFR | LWK | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0124 | REF | REF | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | RTCB_chr22_32382582_32417247 | RTCB | chr22 | 32382582 | 32417247 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:32396078 | C | T | 1 | a0003 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.986G>A | p.Arg329His | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/12 | 1077/2019 | 986/1518 | 329/505 | chr22 | 32396078 | |||
| chr22:32401757 | T | C | 1 | a0002 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.487A>G | p.Met163Val | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/12 | 578/2019 | 487/1518 | 163/505 | chr22 | 32401757 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:32388064 | T | C | 1 | a0001c0002 | 102 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
synonymous_variant | LOW | c.1446A>G | p.Val482Val | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 12/12 | 1537/2019 | 1446/1518 | 482/505 | chr22 | 32388064 | |||
| chr22:32392261 | T | A | 2 | a0001c0005 a0001c0009 |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.1389A>T | p.Ser463Ser | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/12 | 1480/2019 | 1389/1518 | 463/505 | chr22 | 32392261 | |||
| chr22:32396236 | A | G | 1 | a0001c0006 | 3 | HG01167.hp2 HG02145.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.828T>C | p.Ala276Ala | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/12 | 919/2019 | 828/1518 | 276/505 | chr22 | 32396236 | |||
| chr22:32399639 | T | C | 2 | a0001c0005 a0001c0009 |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.618A>G | p.Lys206Lys | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/12 | 709/2019 | 618/1518 | 206/505 | chr22 | 32399639 | |||
| chr22:32399654 | C | T | 7 | a0001c0002 a0001c0003 a0001c0004 others(4): Show |
201 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(198): Show |
synonymous_variant | LOW | c.603G>A | p.Gln201Gln | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/12 | 694/2019 | 603/1518 | 201/505 | chr22 | 32399654 | |||
| chr22:32406693 | A | G | 2 | a0001c0005 a0001c0009 |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.309T>C | p.Asp103Asp | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/12 | 400/2019 | 309/1518 | 103/505 | chr22 | 32406693 | |||
| chr22:32408795 | T | C | 1 | a0001c0009 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.132A>G | p.Lys44Lys | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/12 | 223/2019 | 132/1518 | 44/505 | chr22 | 32408795 | |||
| chr22:32412091 | G | A | 1 | a0001c0004 | 23 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(20): Show |
synonymous_variant | LOW | c.66C>T | p.Ile22Ile | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/12 | 157/2019 | 66/1518 | 22/505 | chr22 | 32412091 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:32387629 | G | A | 2 | a0001c0005t0002 a0001c0009t0002 |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*363C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 12/12 | 363 | chr22 | 32387629 | ||||||
| chr22:32387657 | A | T | 1 | a0001c0001t0004 | 3 | NA18947.hp1 NA18969.hp1 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*335T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 12/12 | 335 | chr22 | 32387657 | ||||||
| chr22:32387668 | A | G | 1 | a0001c0001t0008 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 12/12 | 324 | chr22 | 32387668 | ||||||
| chr22:32387691 | C | T | 1 | a0001c0003t0007 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 12/12 | 301 | chr22 | 32387691 | ||||||
| chr22:32387892 | G | C | 1 | a0001c0001t0009 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 12/12 | 100 | chr22 | 32387892 | ||||||
| chr22:32387917 | T | C | 2 | a0001c0003t0003 a0002c0008t0003 |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*75A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 12/12 | 75 | chr22 | 32387917 | ||||||
| chr22:32387972 | C | T | 1 | a0001c0003t0006 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 12/12 | 20 | chr22 | 32387972 | ||||||
| chr22:32412171 | T | C | 1 | a0001c0001t0005 | 3 | HG02056.hp2 HG02129.hp1 HG02738.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-15A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/12 | chr22 | 32412171 | |||||||
| chr22:32412214 | A | T | 2 | a0001c0005t0002 a0001c0009t0002 |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-58T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/12 | 58 | chr22 | 32412214 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:32388140 | AAC | A | 3 | a0001c0003t0001g0042 a0001c0003t0001g0093 a0001c0003t0001g0094 |
4 | HG02055.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411-43_1411-42del others(2): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388140 | |||||||
| chr22:32388208 | GT | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-110delA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388208 | |||||||
| chr22:32388209 | T | G | 2 | a0001c0001t0001g0006 a0001c0003t0001g0138 |
2 | HG02109.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1411-110A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388209 | |||||||
| chr22:32388248 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-149T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388248 | |||||||
| chr22:32388293 | C | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-194G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388293 | |||||||
| chr22:32388294 | C | CTTGGT | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-196_1411-195i others(7): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388294 | |||||||
| chr22:32388401 | T | C | 1 | a0001c0009t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1411-302A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388401 | |||||||
| chr22:32388631 | A | AATTT | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-536_1411-533d others(6): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388631 | |||||||
| chr22:32388663 | A | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-564T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388663 | |||||||
| chr22:32388670 | C | T | 1 | a0001c0003t0003g0091 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1411-571G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388670 | |||||||
| chr22:32388926 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1411-827G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388926 | |||||||
| chr22:32388980 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1411-881C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32388980 | |||||||
| chr22:32389091 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0034 others(18): Show |
43 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.1411-992T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389091 | |||||||
| chr22:32389110 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0097 |
4 | HG02040.hp2 NA19070.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-1011T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389110 | |||||||
| chr22:32389233 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1411-1134C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389233 | |||||||
| chr22:32389278 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1411-1179A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389278 | |||||||
| chr22:32389320 | G | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-1221C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389320 | |||||||
| chr22:32389424 | T | C | 7 | a0001c0003t0001g0012 a0001c0003t0001g0022 a0001c0003t0001g0061 others(4): Show |
16 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1411-1325A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389424 | |||||||
| chr22:32389444 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1411-1345A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389444 | |||||||
| chr22:32389571 | C | T | 3 | a0001c0002t0001g0018 a0001c0002t0001g0059 a0001c0002t0001g0060 |
6 | HG00609.hp2 HG02080.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-1472G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389571 | |||||||
| chr22:32389610 | GCTT | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-1514_1411-151 others(7): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389610 | |||||||
| chr22:32389614 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1411-1515G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389614 | |||||||
| chr22:32389738 | C | T | 1 | a0001c0009t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1411-1639G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389738 | |||||||
| chr22:32389770 | C | G | 1 | a0001c0002t0001g0073 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1411-1671G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389770 | |||||||
| chr22:32389853 | A | C | 39 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(36): Show |
96 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1411-1754T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389853 | |||||||
| chr22:32389872 | A | G | 13 | a0001c0003t0001g0004 a0001c0003t0001g0042 a0001c0003t0001g0058 others(10): Show |
29 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1411-1773T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389872 | |||||||
| chr22:32389877 | C | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0069 a0001c0002t0001g0086 |
6 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-1778G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389877 | |||||||
| chr22:32389988 | G | A | 1 | a0001c0001t0001g0050 | 2 | HG00544.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1411-1889C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32389988 | |||||||
| chr22:32390044 | C | T | 7 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(4): Show |
12 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1411-1945G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390044 | |||||||
| chr22:32390230 | G | A | 74 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(71): Show |
171 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(168): Show |
intron_variant | MODIFIER | c.1410+2010C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390230 | |||||||
| chr22:32390254 | T | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG01255.hp2 HG02080.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1410+1986A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390254 | |||||||
| chr22:32390267 | G | C | 13 | a0001c0004t0001g0013 a0001c0004t0001g0035 a0001c0004t0001g0051 others(10): Show |
23 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1410+1973C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390267 | |||||||
| chr22:32390299 | C | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+1941G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390299 | |||||||
| chr22:32390311 | G | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+1929C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390311 | |||||||
| chr22:32390453 | CT | C | 8 | a0001c0004t0001g0186 a0001c0005t0002g0017 a0001c0005t0002g0036 others(5): Show |
13 | HG01070.hp2 HG01496.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+1786delA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390453 | |||||||
| chr22:32390507 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+1733T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390507 | |||||||
| chr22:32390543 | C | T | 1 | a0001c0001t0001g0031 | 3 | HG03486.hp2 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1410+1697G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390543 | |||||||
| chr22:32390553 | G | A | 72 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(69): Show |
166 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.1410+1687C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390553 | |||||||
| chr22:32390563 | C | G | 3 | a0001c0003t0001g0042 a0001c0003t0001g0093 a0001c0003t0001g0094 |
4 | HG02055.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1410+1677G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390563 | |||||||
| chr22:32390582 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+1658T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390582 | |||||||
| chr22:32390605 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1410+1635G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390605 | |||||||
| chr22:32390642 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(22): Show |
55 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.1410+1598C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390642 | |||||||
| chr22:32390740 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+1500T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390740 | |||||||
| chr22:32390774 | C | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+1466G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390774 | |||||||
| chr22:32390812 | T | C | 2 | a0001c0002t0001g0041 a0001c0002t0001g0121 |
3 | NA18971.hp2 NA18972.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1410+1428A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32390812 | |||||||
| chr22:32391110 | G | A | 4 | a0001c0003t0001g0012 a0001c0003t0001g0061 a0001c0003t0001g0116 others(1): Show |
10 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1410+1130C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391110 | |||||||
| chr22:32391212 | G | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+1028C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391212 | |||||||
| chr22:32391395 | A | AT | 6 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
8 | HG00738.hp1 HG01255.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1410+844dupA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391395 | |||||||
| chr22:32391395 | AT | A | 22 | a0001c0001t0001g0049 a0001c0001t0001g0142 a0001c0001t0001g0147 others(19): Show |
42 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1410+844delA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391395 | |||||||
| chr22:32391438 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+802A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391438 | |||||||
| chr22:32391671 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1410+569C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391671 | |||||||
| chr22:32391719 | G | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG01255.hp2 HG02080.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1410+521C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391719 | |||||||
| chr22:32391794 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1410+446C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391794 | |||||||
| chr22:32391815 | A | G | 3 | a0001c0002t0001g0076 a0001c0002t0001g0083 a0001c0002t0001g0088 |
3 | HG00558.hp2 NA19070.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1410+425T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391815 | |||||||
| chr22:32391951 | A | G | 92 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(89): Show |
201 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.1410+289T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32391951 | |||||||
| chr22:32392041 | C | T | 18 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0042 others(15): Show |
40 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1410+199G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32392041 | |||||||
| chr22:32392042 | G | A | 1 | a0001c0001t0001g0033 | 3 | HG01496.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1410+198C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32392042 | |||||||
| chr22:32392089 | T | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
261 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(258): Show |
intron_variant | MODIFIER | c.1410+151A>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32392089 | |||||||
| chr22:32392119 | T | TA | 2 | a0001c0001t0001g0006 a0001c0001t0001g0145 |
10 | HG01243.hp1 HG02109.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1410+120dupT | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32392119 | |||||||
| chr22:32392143 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1410+97A>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32392143 | |||||||
| chr22:32392164 | T | C | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1410+76A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32392164 | |||||||
| chr22:32392210 | T | C | 3 | a0001c0003t0001g0042 a0001c0003t0001g0093 a0001c0003t0001g0094 |
4 | HG02055.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1410+30A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 11/11 | chr22 | 32392210 | |||||||
| chr22:32392428 | C | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291-69G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32392428 | |||||||
| chr22:32392578 | G | A | 3 | a0001c0003t0001g0042 a0001c0003t0001g0093 a0001c0003t0001g0094 |
4 | HG02055.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291-219C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32392578 | |||||||
| chr22:32392644 | T | G | 3 | a0001c0002t0001g0011 a0001c0002t0001g0078 a0001c0002t0001g0080 |
9 | HG02027.hp1 NA18946.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.1291-285A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32392644 | |||||||
| chr22:32392895 | C | T | 1 | a0001c0005t0002g0017 | 4 | HG02055.hp1 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291-536G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32392895 | |||||||
| chr22:32393005 | T | C | 1 | a0001c0003t0001g0181 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1291-646A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393005 | |||||||
| chr22:32393040 | A | C | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291-681T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393040 | |||||||
| chr22:32393095 | C | T | 18 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0042 others(15): Show |
40 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1291-736G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393095 | |||||||
| chr22:32393104 | T | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291-745A>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393104 | |||||||
| chr22:32393133 | C | T | 2 | a0001c0002t0001g0040 a0001c0002t0001g0072 |
3 | NA18950.hp2 NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1290+759G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393133 | |||||||
| chr22:32393323 | G | C | 1 | a0001c0002t0001g0059 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1290+569C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393323 | |||||||
| chr22:32393341 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1290+551G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393341 | |||||||
| chr22:32393433 | G | C | 1 | a0001c0002t0001g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1290+459C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393433 | |||||||
| chr22:32393472 | T | C | 1 | a0001c0003t0001g0129 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1290+420A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393472 | |||||||
| chr22:32393492 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1290+400A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393492 | |||||||
| chr22:32393496 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1290+396C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393496 | |||||||
| chr22:32393533 | G | T | 89 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(86): Show |
196 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.1290+359C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393533 | |||||||
| chr22:32393540 | G | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0167 others(3): Show |
14 | HG00099.hp2 HG00735.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1290+352C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393540 | |||||||
| chr22:32393549 | G | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1290+343C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393549 | |||||||
| chr22:32393609 | A | G | 1 | a0001c0003t0001g0136 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1290+283T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393609 | |||||||
| chr22:32393781 | G | A | 1 | a0001c0004t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1290+111C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 10/11 | chr22 | 32393781 | |||||||
| chr22:32394112 | T | A | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-110A>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394112 | |||||||
| chr22:32394114 | C | CT | 69 | a0001c0001t0001g0169 a0001c0001t0001g0180 a0001c0002t0001g0001 others(66): Show |
159 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.1180-113dupA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394114 | |||||||
| chr22:32394114 | C | CTT | 6 | a0001c0003t0001g0094 a0001c0003t0003g0015 a0001c0003t0003g0021 others(3): Show |
13 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-114_1180-113d others(4): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394114 | |||||||
| chr22:32394114 | CT | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
18 | HG01099.hp1 HG01167.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1180-113delA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394114 | |||||||
| chr22:32394133 | TG | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1180-132delC | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394133 | |||||||
| chr22:32394172 | C | T | 1 | a0001c0001t0001g0032 | 3 | HG02818.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1180-170G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394172 | |||||||
| chr22:32394173 | G | A | 2 | a0001c0001t0001g0109 a0001c0003t0001g0046 |
3 | HG01099.hp1 HG02647.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1180-171C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394173 | |||||||
| chr22:32394255 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0167 others(3): Show |
14 | HG00099.hp2 HG00735.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1180-253C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394255 | |||||||
| chr22:32394313 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1180-311T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394313 | |||||||
| chr22:32394341 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1180-339C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394341 | |||||||
| chr22:32394349 | G | C | 3 | a0001c0002t0001g0020 a0001c0002t0001g0069 a0001c0002t0001g0086 |
6 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-347C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394349 | |||||||
| chr22:32394372 | A | G | 1 | a0001c0004t0001g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180-370T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394372 | |||||||
| chr22:32394393 | A | G | 6 | a0001c0001t0001g0102 a0001c0002t0001g0014 a0001c0002t0001g0019 others(3): Show |
14 | HG01099.hp1 HG02155.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180-391T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394393 | |||||||
| chr22:32394398 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0101 |
2 | HG02155.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1180-396T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394398 | |||||||
| chr22:32394411 | G | T | 45 | a0001c0001t0001g0155 a0001c0002t0001g0001 a0001c0002t0001g0011 others(42): Show |
112 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1180-409C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394411 | |||||||
| chr22:32394419 | C | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1180-417G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394419 | |||||||
| chr22:32394506 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0167 others(3): Show |
14 | HG00099.hp2 HG00735.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1180-504C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394506 | |||||||
| chr22:32394534 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1179+492T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394534 | |||||||
| chr22:32394657 | A | C | 42 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(39): Show |
102 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1179+369T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394657 | |||||||
| chr22:32394659 | A | G | 1 | a0001c0001t0001g0006 | 9 | HG01243.hp1 HG02109.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+367T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394659 | |||||||
| chr22:32394701 | G | A | 1 | a0001c0002t0001g0019 | 4 | NA18949.hp1 NA18991.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+325C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394701 | |||||||
| chr22:32394823 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(22): Show |
53 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1179+203A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394823 | |||||||
| chr22:32394827 | A | AGT | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1179+198_1179+199i others(4): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394827 | |||||||
| chr22:32394844 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1179+182G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394844 | |||||||
| chr22:32394985 | G | A | 10 | a0001c0003t0001g0004 a0001c0003t0001g0058 a0001c0003t0001g0125 others(7): Show |
25 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1179+41C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394985 | |||||||
| chr22:32394994 | C | G | 26 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0042 others(23): Show |
53 | HG00597.hp1 HG01070.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.1179+32G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32394994 | |||||||
| chr22:32395016 | A | C | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
261 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(258): Show |
intron_variant | MODIFIER | c.1179+10T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 9/11 | chr22 | 32395016 | |||||||
| chr22:32395299 | T | C | 1 | a0001c0002t0001g0137 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.991-85A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395299 | |||||||
| chr22:32395358 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.991-144A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395358 | |||||||
| chr22:32395368 | G | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0167 others(3): Show |
14 | HG00099.hp2 HG00735.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.991-154C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395368 | |||||||
| chr22:32395457 | C | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.991-243G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395457 | |||||||
| chr22:32395460 | T | C | 42 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(39): Show |
102 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.991-246A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395460 | |||||||
| chr22:32395467 | T | C | 1 | a0001c0002t0001g0081 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.991-253A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395467 | |||||||
| chr22:32395508 | T | C | 93 | a0001c0001t0001g0160 a0001c0002t0001g0001 a0001c0002t0001g0011 others(90): Show |
202 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(199): Show |
intron_variant | MODIFIER | c.991-294A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395508 | |||||||
| chr22:32395521 | T | C | 18 | a0001c0003t0001g0046 a0001c0003t0001g0133 a0001c0003t0001g0134 others(15): Show |
30 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.991-307A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395521 | |||||||
| chr22:32395577 | G | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.991-363C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395577 | |||||||
| chr22:32395694 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0100 |
2 | HG00673.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.990+380G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395694 | |||||||
| chr22:32395819 | C | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.990+255G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395819 | |||||||
| chr22:32395934 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.990+140A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395934 | |||||||
| chr22:32395942 | GC | G | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
261 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(258): Show |
intron_variant | MODIFIER | c.990+131delG | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395942 | |||||||
| chr22:32395944 | C | T | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+130G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395944 | |||||||
| chr22:32395991 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.990+83A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32395991 | |||||||
| chr22:32396002 | G | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.990+72C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32396002 | |||||||
| chr22:32396033 | A | G | 1 | a0001c0003t0001g0046 | 2 | HG01099.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.990+41T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32396033 | |||||||
| chr22:32396069 | T | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0137 |
4 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.990+5A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 8/11 | chr22 | 32396069 | |||||||
| chr22:32396295 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.815-46T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32396295 | |||||||
| chr22:32396455 | T | G | 18 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0042 others(15): Show |
40 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.815-206A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32396455 | |||||||
| chr22:32396573 | T | C | 1 | a0001c0009t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.815-324A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32396573 | |||||||
| chr22:32396677 | C | T | 18 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0042 others(15): Show |
40 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.815-428G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32396677 | |||||||
| chr22:32396686 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0147 |
3 | HG02622.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.815-437C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32396686 | |||||||
| chr22:32396840 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.815-591C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32396840 | |||||||
| chr22:32396845 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.815-596T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32396845 | |||||||
| chr22:32396942 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.815-693A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32396942 | |||||||
| chr22:32397114 | A | AGCTCAAG others(6): Show |
8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.814+826_814+827ins others(13): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397114 | |||||||
| chr22:32397193 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.814+748G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397193 | |||||||
| chr22:32397245 | C | G | 5 | a0001c0003t0001g0012 a0001c0003t0001g0061 a0001c0003t0001g0116 others(2): Show |
11 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.814+696G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397245 | |||||||
| chr22:32397282 | G | A | 46 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(43): Show |
113 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.814+659C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397282 | |||||||
| chr22:32397319 | A | AAT | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.814+621_814+622ins others(2): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397319 | |||||||
| chr22:32397324 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.814+617A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397324 | |||||||
| chr22:32397397 | T | C | 72 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(69): Show |
166 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.814+544A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397397 | |||||||
| chr22:32397472 | A | G | 1 | a0001c0003t0001g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.814+469T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397472 | |||||||
| chr22:32397521 | C | G | 1 | a0001c0002t0001g0075 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.814+420G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397521 | |||||||
| chr22:32397547 | C | A | 92 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(89): Show |
201 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.814+394G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397547 | |||||||
| chr22:32397618 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.814+323G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397618 | |||||||
| chr22:32397654 | A | C | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.814+287T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397654 | |||||||
| chr22:32397662 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18981.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.814+279T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397662 | |||||||
| chr22:32397665 | T | C | 4 | a0001c0003t0001g0012 a0001c0003t0001g0061 a0001c0003t0001g0116 others(1): Show |
10 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.814+276A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397665 | |||||||
| chr22:32397828 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.814+113T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 7/11 | chr22 | 32397828 | |||||||
| chr22:32398373 | G | A | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-273C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398373 | |||||||
| chr22:32398396 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.655-296G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398396 | |||||||
| chr22:32398452 | C | T | 46 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(43): Show |
113 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.655-352G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398452 | |||||||
| chr22:32398487 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.655-387C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398487 | |||||||
| chr22:32398505 | G | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.655-405C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398505 | |||||||
| chr22:32398506 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.655-406A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398506 | |||||||
| chr22:32398520 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.655-420A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398520 | |||||||
| chr22:32398527 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.655-427A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398527 | |||||||
| chr22:32398565 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.655-465A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398565 | |||||||
| chr22:32398586 | C | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0048 others(6): Show |
20 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.655-486G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398586 | |||||||
| chr22:32398600 | C | T | 18 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0042 others(15): Show |
40 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.655-500G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398600 | |||||||
| chr22:32398615 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655-515A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398615 | |||||||
| chr22:32398616 | T | A | 48 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(45): Show |
118 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.655-516A>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398616 | |||||||
| chr22:32398624 | T | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.655-524A>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398624 | |||||||
| chr22:32398840 | T | C | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-740A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398840 | |||||||
| chr22:32398874 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.654+729C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398874 | |||||||
| chr22:32398889 | G | C | 18 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0042 others(15): Show |
40 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.654+714C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398889 | |||||||
| chr22:32398895 | C | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.654+708G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32398895 | |||||||
| chr22:32399064 | A | G | 39 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(36): Show |
96 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.654+539T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399064 | |||||||
| chr22:32399119 | C | T | 4 | a0001c0003t0001g0012 a0001c0003t0001g0061 a0001c0003t0001g0116 others(1): Show |
10 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.654+484G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399119 | |||||||
| chr22:32399187 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0141 |
4 | HG02717.hp2 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+416T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399187 | |||||||
| chr22:32399298 | G | C | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.654+305C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399298 | |||||||
| chr22:32399303 | AT | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0001g0169 others(3): Show |
6 | HG00639.hp2 HG02896.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+299delA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399303 | |||||||
| chr22:32399355 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.654+248C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399355 | |||||||
| chr22:32399431 | C | A | 1 | a0001c0001t0001g0043 | 2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.654+172G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399431 | |||||||
| chr22:32399440 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.654+163A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399440 | |||||||
| chr22:32399457 | T | C | 4 | a0001c0003t0001g0012 a0001c0003t0001g0061 a0001c0003t0001g0116 others(1): Show |
10 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.654+146A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399457 | |||||||
| chr22:32399536 | T | C | 3 | a0001c0003t0001g0042 a0001c0003t0001g0093 a0001c0003t0001g0094 |
4 | HG02055.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+67A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 6/11 | chr22 | 32399536 | |||||||
| chr22:32399764 | A | G | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.498-5T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32399764 | |||||||
| chr22:32399850 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG01255.hp2 HG02080.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-91G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32399850 | |||||||
| chr22:32399968 | C | T | 1 | a0001c0003t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.498-209G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32399968 | |||||||
| chr22:32400111 | AAAC | A | 9 | a0001c0001t0001g0148 a0001c0005t0002g0017 a0001c0005t0002g0036 others(6): Show |
14 | HG01070.hp2 HG01891.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.498-355_498-353del others(3): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400111 | |||||||
| chr22:32400168 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-409T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400168 | |||||||
| chr22:32400187 | T | C | 20 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0022 others(17): Show |
45 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.498-428A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400187 | |||||||
| chr22:32400242 | C | G | 1 | a0001c0003t0001g0126 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.498-483G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400242 | |||||||
| chr22:32400260 | G | C | 73 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(70): Show |
170 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.498-501C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400260 | |||||||
| chr22:32400260 | G | T | 1 | a0001c0002t0001g0073 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.498-501C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400260 | |||||||
| chr22:32400262 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0004g0024 others(1): Show |
9 | HG02735.hp2 NA18947.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-503A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400262 | |||||||
| chr22:32400285 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.498-526C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400285 | |||||||
| chr22:32400296 | G | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-537C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400296 | |||||||
| chr22:32400307 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0156 others(1): Show |
15 | HG00544.hp2 NA18948.hp2 NA18951.hp1 others(12): Show |
intron_variant | MODIFIER | c.498-548A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400307 | |||||||
| chr22:32400317 | A | AGGTACAC | 3 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG01255.hp2 HG02080.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-565_498-559dup others(7): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400317 | |||||||
| chr22:32400358 | T | C | 20 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0022 others(17): Show |
45 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.498-599A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400358 | |||||||
| chr22:32400657 | C | T | 7 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(4): Show |
12 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.498-898G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400657 | |||||||
| chr22:32400665 | G | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-906C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400665 | |||||||
| chr22:32400681 | T | C | 20 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0022 others(17): Show |
45 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.498-922A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400681 | |||||||
| chr22:32400731 | C | T | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-972G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400731 | |||||||
| chr22:32400892 | C | T | 1 | a0001c0003t0001g0136 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497+855G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400892 | |||||||
| chr22:32400926 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+821A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400926 | |||||||
| chr22:32400952 | C | A | 2 | a0001c0001t0001g0044 a0003c0007t0001g0106 |
3 | NA18949.hp2 NA18984.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.497+795G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32400952 | |||||||
| chr22:32401002 | T | C | 4 | a0001c0003t0001g0012 a0001c0003t0001g0061 a0001c0003t0001g0116 others(1): Show |
10 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.497+745A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401002 | |||||||
| chr22:32401005 | G | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0110 |
2 | NA19075.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.497+742C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401005 | |||||||
| chr22:32401090 | G | GT | 47 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(44): Show |
108 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.497+656dupA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401090 | |||||||
| chr22:32401090 | G | GTTTT | 6 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(3): Show |
11 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.497+653_497+656dup others(4): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401090 | |||||||
| chr22:32401090 | GT | G | 9 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
10 | HG01256.hp2 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.497+656delA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401090 | |||||||
| chr22:32401228 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.497+519A>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401228 | |||||||
| chr22:32401262 | A | AT | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+484dupA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401262 | |||||||
| chr22:32401316 | G | A | 4 | a0001c0003t0001g0012 a0001c0003t0001g0061 a0001c0003t0001g0116 others(1): Show |
10 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.497+431C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401316 | |||||||
| chr22:32401369 | C | T | 1 | a0001c0003t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497+378G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401369 | |||||||
| chr22:32401488 | A | G | 10 | a0001c0003t0001g0004 a0001c0003t0001g0058 a0001c0003t0001g0125 others(7): Show |
25 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.497+259T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401488 | |||||||
| chr22:32401493 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.497+254C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 5/11 | chr22 | 32401493 | |||||||
| chr22:32401972 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-69T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32401972 | |||||||
| chr22:32402183 | C | T | 1 | a0001c0004t0001g0190 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.341-280G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402183 | |||||||
| chr22:32402395 | A | G | 2 | a0001c0006t0001g0045 a0001c0006t0001g0132 |
3 | HG01167.hp2 HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.341-492T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402395 | |||||||
| chr22:32402445 | A | T | 1 | a0001c0002t0001g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.341-542T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402445 | |||||||
| chr22:32402536 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.341-633C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402536 | |||||||
| chr22:32402561 | TGCCTCAG others(133): Show |
T | 39 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(36): Show |
96 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.341-798_341-659del | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402561 | |||||||
| chr22:32402578 | T | C | 13 | a0001c0004t0001g0013 a0001c0004t0001g0035 a0001c0004t0001g0051 others(10): Show |
23 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.341-675A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402578 | |||||||
| chr22:32402661 | G | C | 1 | a0001c0001t0001g0003 | 9 | HG02071.hp2 NA18962.hp1 NA18974.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-758C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402661 | |||||||
| chr22:32402681 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-778A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402681 | |||||||
| chr22:32402702 | G | A | 2 | a0001c0002t0001g0065 a0001c0002t0001g0087 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.341-799C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402702 | |||||||
| chr22:32402751 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.341-848G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402751 | |||||||
| chr22:32402772 | T | G | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
261 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(258): Show |
intron_variant | MODIFIER | c.341-869A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402772 | |||||||
| chr22:32402841 | C | G | 1 | a0001c0003t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.341-938G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402841 | |||||||
| chr22:32402844 | C | G | 95 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0001g0123 others(92): Show |
206 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(203): Show |
intron_variant | MODIFIER | c.341-941G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402844 | |||||||
| chr22:32402845 | A | C | 42 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(39): Show |
102 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.341-942T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402845 | |||||||
| chr22:32402923 | T | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0176 |
2 | HG01243.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.341-1020A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32402923 | |||||||
| chr22:32403009 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.341-1106A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403009 | |||||||
| chr22:32403047 | TA | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-1145delT | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403047 | |||||||
| chr22:32403090 | C | T | 13 | a0001c0004t0001g0013 a0001c0004t0001g0035 a0001c0004t0001g0051 others(10): Show |
23 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.341-1187G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403090 | |||||||
| chr22:32403116 | G | A | 1 | a0001c0003t0001g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.341-1213C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403116 | |||||||
| chr22:32403178 | G | A | 1 | a0001c0001t0005g0195 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.341-1275C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403178 | |||||||
| chr22:32403181 | C | T | 9 | a0001c0001t0001g0096 a0001c0005t0002g0017 a0001c0005t0002g0036 others(6): Show |
14 | HG00673.hp1 HG01070.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-1278G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403181 | |||||||
| chr22:32403202 | C | G | 1 | a0001c0002t0001g0071 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.341-1299G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403202 | |||||||
| chr22:32403202 | C | T | 3 | a0001c0005t0002g0036 a0001c0005t0002g0055 a0001c0005t0002g0056 |
4 | HG01070.hp2 HG01891.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-1299G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403202 | |||||||
| chr22:32403207 | A | C | 1 | a0001c0002t0001g0071 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.341-1304T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403207 | |||||||
| chr22:32403302 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.341-1399C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403302 | |||||||
| chr22:32403319 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.341-1416T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403319 | |||||||
| chr22:32403381 | C | T | 51 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(48): Show |
120 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.341-1478G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403381 | |||||||
| chr22:32403386 | A | T | 1 | a0001c0004t0001g0190 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.341-1483T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403386 | |||||||
| chr22:32403452 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0112 others(3): Show |
27 | HG00597.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.341-1549A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403452 | |||||||
| chr22:32403608 | C | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-1705G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403608 | |||||||
| chr22:32403634 | T | C | 43 | a0001c0001t0001g0031 a0001c0002t0001g0001 a0001c0002t0001g0011 others(40): Show |
105 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.341-1731A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403634 | |||||||
| chr22:32403690 | G | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-1787C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403690 | |||||||
| chr22:32403709 | G | A | 46 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(43): Show |
113 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.341-1806C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403709 | |||||||
| chr22:32403718 | T | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0048 others(6): Show |
20 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.341-1815A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403718 | |||||||
| chr22:32403896 | C | T | 1 | a0001c0001t0005g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.341-1993G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403896 | |||||||
| chr22:32403965 | C | T | 1 | a0001c0002t0001g0070 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.341-2062G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32403965 | |||||||
| chr22:32404084 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.341-2181G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404084 | |||||||
| chr22:32404113 | A | C | 18 | a0001c0003t0001g0046 a0001c0003t0001g0133 a0001c0003t0001g0134 others(15): Show |
30 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.341-2210T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404113 | |||||||
| chr22:32404354 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.340+2308A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404354 | |||||||
| chr22:32404365 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.340+2297T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404365 | |||||||
| chr22:32404422 | T | C | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+2240A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404422 | |||||||
| chr22:32404438 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.340+2224A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404438 | |||||||
| chr22:32404448 | C | A | 20 | a0001c0003t0001g0004 a0001c0003t0001g0012 a0001c0003t0001g0022 others(17): Show |
45 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.340+2214G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404448 | |||||||
| chr22:32404524 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.340+2138C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404524 | |||||||
| chr22:32404607 | A | C | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+2055T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404607 | |||||||
| chr22:32404718 | G | A | 2 | a0001c0002t0001g0065 a0001c0002t0001g0087 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.340+1944C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404718 | |||||||
| chr22:32404723 | T | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0137 |
4 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+1939A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404723 | |||||||
| chr22:32404739 | C | T | 1 | a0001c0003t0001g0136 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.340+1923G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404739 | |||||||
| chr22:32404840 | C | T | 2 | a0001c0005t0002g0055 a0001c0005t0002g0056 |
2 | HG01070.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.340+1822G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404840 | |||||||
| chr22:32404855 | AT | A | 15 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0002t0001g0088 others(12): Show |
26 | HG01070.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.340+1806delA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404855 | |||||||
| chr22:32404872 | G | C | 1 | a0001c0004t0001g0188 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.340+1790C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32404872 | |||||||
| chr22:32405059 | G | T | 1 | a0001c0004t0001g0189 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.340+1603C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32405059 | |||||||
| chr22:32405113 | G | A | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+1549C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32405113 | |||||||
| chr22:32405268 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+1394T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32405268 | |||||||
| chr22:32405345 | G | A | 46 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(43): Show |
113 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.340+1317C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32405345 | |||||||
| chr22:32405517 | C | T | 1 | a0001c0002t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.340+1145G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32405517 | |||||||
| chr22:32405907 | C | T | 1 | a0001c0003t0001g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.340+755G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32405907 | |||||||
| chr22:32406168 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.340+494T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32406168 | |||||||
| chr22:32406386 | G | A | 42 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(39): Show |
102 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.340+276C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32406386 | |||||||
| chr22:32406471 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.340+191G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32406471 | |||||||
| chr22:32406568 | G | A | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+94C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32406568 | |||||||
| chr22:32406616 | C | G | 10 | a0001c0003t0001g0004 a0001c0003t0001g0058 a0001c0003t0001g0125 others(7): Show |
25 | HG00597.hp1 HG01074.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.340+46G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 4/11 | chr22 | 32406616 | |||||||
| chr22:32406879 | CTG | C | 2 | a0001c0002t0001g0041 a0001c0002t0001g0121 |
3 | NA18971.hp2 NA18972.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.241-120_241-119del others(2): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32406879 | |||||||
| chr22:32406975 | G | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-214C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32406975 | |||||||
| chr22:32407055 | CTAT | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-297_241-295del others(3): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407055 | |||||||
| chr22:32407214 | G | A | 1 | a0001c0006t0001g0045 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.241-453C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407214 | |||||||
| chr22:32407302 | A | C | 43 | a0001c0001t0001g0031 a0001c0002t0001g0001 a0001c0002t0001g0011 others(40): Show |
105 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.241-541T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407302 | |||||||
| chr22:32407463 | C | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-702G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407463 | |||||||
| chr22:32407466 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.241-705G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407466 | |||||||
| chr22:32407543 | C | T | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+632G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407543 | |||||||
| chr22:32407566 | T | C | 3 | a0001c0001t0001g0026 a0001c0003t0001g0022 a0001c0003t0001g0131 |
8 | HG02071.hp1 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.240+609A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407566 | |||||||
| chr22:32407604 | T | C | 13 | a0001c0004t0001g0013 a0001c0004t0001g0035 a0001c0004t0001g0051 others(10): Show |
23 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.240+571A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407604 | |||||||
| chr22:32407629 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.240+546A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407629 | |||||||
| chr22:32407667 | G | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.240+508C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407667 | |||||||
| chr22:32407824 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0048 others(7): Show |
21 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.240+351C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407824 | |||||||
| chr22:32407956 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.240+219A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407956 | |||||||
| chr22:32407965 | G | A | 42 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0014 others(39): Show |
102 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.240+210C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407965 | |||||||
| chr22:32407966 | A | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.240+209T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407966 | |||||||
| chr22:32407989 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.240+186T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32407989 | |||||||
| chr22:32408135 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.240+40A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 3/11 | chr22 | 32408135 | |||||||
| chr22:32408326 | G | A | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.173-84C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/11 | chr22 | 32408326 | |||||||
| chr22:32408464 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.173-222A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/11 | chr22 | 32408464 | |||||||
| chr22:32408489 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.173-247A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/11 | chr22 | 32408489 | |||||||
| chr22:32408583 | C | T | 1 | a0001c0003t0001g0046 | 2 | HG01099.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.172+172G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/11 | chr22 | 32408583 | |||||||
| chr22:32408638 | T | C | 5 | a0001c0004t0001g0013 a0001c0004t0001g0052 a0001c0004t0001g0189 others(2): Show |
12 | HG00280.hp1 HG00733.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+117A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/11 | chr22 | 32408638 | |||||||
| chr22:32408669 | G | A | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.172+86C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/11 | chr22 | 32408669 | |||||||
| chr22:32408678 | T | C | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.172+77A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/11 | chr22 | 32408678 | |||||||
| chr22:32408730 | A | T | 1 | a0001c0002t0001g0067 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.172+25T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 2/11 | chr22 | 32408730 | |||||||
| chr22:32408901 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.94-68A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32408901 | |||||||
| chr22:32408918 | T | C | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.94-85A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32408918 | |||||||
| chr22:32408951 | C | T | 5 | a0001c0003t0001g0046 a0001c0003t0001g0133 a0001c0003t0001g0134 others(2): Show |
7 | HG01099.hp1 HG01167.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-118G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32408951 | |||||||
| chr22:32409022 | G | A | 1 | a0001c0002t0001g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.94-189C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409022 | |||||||
| chr22:32409028 | T | C | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.94-195A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409028 | |||||||
| chr22:32409075 | C | T | 1 | a0001c0002t0001g0066 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.94-242G>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409075 | |||||||
| chr22:32409201 | T | TA | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.94-369dupT | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409201 | |||||||
| chr22:32409201 | T | TAA | 49 | a0001c0001t0001g0039 a0001c0002t0001g0001 a0001c0002t0001g0011 others(46): Show |
115 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.94-370_94-369dupTT | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409201 | |||||||
| chr22:32409381 | G | GTAGT | 2 | a0001c0006t0001g0045 a0001c0006t0001g0132 |
3 | HG01167.hp2 HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.94-552_94-549dupAC others(2): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409381 | |||||||
| chr22:32409420 | A | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.94-587T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409420 | |||||||
| chr22:32409487 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.94-654A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409487 | |||||||
| chr22:32409525 | AAT | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.94-694_94-693delAT | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409525 | |||||||
| chr22:32409530 | T | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.94-697A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409530 | |||||||
| chr22:32409532 | T | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.94-699A>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409532 | |||||||
| chr22:32409535 | AAGAGCTG others(1): Show |
A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.94-710_94-703delAC others(6): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409535 | |||||||
| chr22:32409546 | AGT | A | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.94-715_94-714delAC | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409546 | |||||||
| chr22:32409694 | A | C | 1 | a0001c0003t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94-861T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409694 | |||||||
| chr22:32409744 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.94-911C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409744 | |||||||
| chr22:32409818 | C | CT | 10 | a0001c0003t0001g0042 a0001c0003t0001g0093 a0001c0003t0001g0094 others(7): Show |
15 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-986dupA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409818 | |||||||
| chr22:32409818 | C | CTT | 2 | a0001c0005t0002g0037 a0001c0009t0002g0054 |
3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.94-987_94-986dupAA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409818 | |||||||
| chr22:32409820 | TTTG | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.94-990_94-988delCA others(1): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409820 | |||||||
| chr22:32409821 | TTG | T | 19 | a0001c0002t0001g0020 a0001c0003t0001g0046 a0001c0003t0001g0133 others(16): Show |
31 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.94-990_94-989delCA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409821 | |||||||
| chr22:32409822 | TG | T | 49 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0140 others(46): Show |
114 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.94-990delC | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409822 | |||||||
| chr22:32409823 | G | T | 25 | a0001c0002t0001g0001 a0001c0002t0001g0041 a0001c0003t0001g0004 others(22): Show |
51 | HG00597.hp1 HG01070.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.94-990C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409823 | |||||||
| chr22:32409842 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.94-1009C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32409842 | |||||||
| chr22:32410038 | G | A | 1 | a0001c0005t0002g0037 | 2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.94-1205C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410038 | |||||||
| chr22:32410093 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0120 |
4 | NA18945.hp2 NA18959.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-1260C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410093 | |||||||
| chr22:32410110 | C | G | 4 | a0001c0003t0003g0015 a0001c0003t0003g0021 a0001c0003t0003g0091 others(1): Show |
11 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.94-1277G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410110 | |||||||
| chr22:32410142 | A | G | 3 | a0001c0005t0002g0017 a0001c0005t0002g0053 a0001c0005t0002g0057 |
6 | HG02055.hp1 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-1309T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410142 | |||||||
| chr22:32410143 | T | C | 2 | a0001c0003t0001g0022 a0001c0003t0001g0131 |
5 | HG02809.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-1310A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410143 | |||||||
| chr22:32410306 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.94-1473T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410306 | |||||||
| chr22:32410316 | T | C | 3 | a0001c0003t0001g0042 a0001c0003t0001g0093 a0001c0003t0001g0094 |
4 | HG02055.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-1483A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410316 | |||||||
| chr22:32410344 | A | G | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.94-1511T>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410344 | |||||||
| chr22:32410455 | T | TAAGG | 53 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0140 others(50): Show |
121 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.93+1608_93+1609ins others(4): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410455 | |||||||
| chr22:32410516 | C | G | 4 | a0001c0002t0001g0038 a0001c0002t0001g0063 a0001c0002t0001g0064 others(1): Show |
5 | HG03834.hp1 HG03927.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+1548G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410516 | |||||||
| chr22:32410608 | A | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.93+1456T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410608 | |||||||
| chr22:32410722 | C | CTTT | 43 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0140 others(40): Show |
106 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.93+1339_93+1341dup others(3): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410722 | |||||||
| chr22:32410722 | CT | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.93+1341delA | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410722 | |||||||
| chr22:32410722 | CTT | C | 20 | a0001c0001t0001g0135 a0001c0001t0001g0179 a0001c0003t0001g0046 others(17): Show |
32 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.93+1340_93+1341del others(2): Show |
RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410722 | |||||||
| chr22:32410815 | A | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0137 |
4 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1249T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410815 | |||||||
| chr22:32410876 | T | G | 1 | a0001c0005t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.93+1188A>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32410876 | |||||||
| chr22:32411045 | G | C | 1 | a0001c0003t0001g0136 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.93+1019C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411045 | |||||||
| chr22:32411273 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.93+791T>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411273 | |||||||
| chr22:32411328 | T | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0137 |
4 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+736A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411328 | |||||||
| chr22:32411388 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.93+676C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411388 | |||||||
| chr22:32411419 | G | A | 1 | a0001c0003t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.93+645C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411419 | |||||||
| chr22:32411470 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.93+594C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411470 | |||||||
| chr22:32411477 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.93+587C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411477 | |||||||
| chr22:32411535 | A | C | 1 | a0001c0003t0001g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.93+529T>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411535 | |||||||
| chr22:32411675 | G | A | 1 | a0001c0004t0001g0192 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.93+389C>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411675 | |||||||
| chr22:32411775 | A | AAT | 3 | a0001c0002t0001g0018 a0001c0002t0001g0059 a0001c0002t0001g0060 |
6 | HG00609.hp2 HG02080.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+288_93+289insAT | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411775 | |||||||
| chr22:32411782 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(57): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.93+282A>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411782 | |||||||
| chr22:32411974 | G | C | 2 | a0001c0003t0001g0058 a0001c0003t0001g0181 |
2 | HG01074.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.93+90C>G | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32411974 | |||||||
| chr22:32412009 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.93+55G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32412009 | |||||||
| chr22:32412013 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.93+51G>T | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32412013 | |||||||
| chr22:32412024 | C | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0036 a0001c0005t0002g0037 others(5): Show |
13 | HG01070.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.93+40G>C | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32412024 | |||||||
| chr22:32412025 | G | T | 1 | a0001c0003t0001g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.93+39C>A | RTCB | ENSG00000100220.12 | transcript | ENST00000216038.6 | protein_coding | 1/11 | chr22 | 32412025 |