Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27156 |
| ensemblid | ENSG00000100218.12 |
| hgncid | 13437 |
| symbol | RSPH14 |
| name | radial spoke head 14 homolog |
| refseq_nuc | NM_014433.3 |
| refseq_prot | NP_055248.1 |
| ensembl_nuc | ENST00000216036.9 |
| ensembl_prot | ENSP00000216036.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 23059415 |
| end | 23141990 |
| strand | - |
| ver | v1.2 |
| region | chr22:23059415-23141990 |
| region5000 | chr22:23054415-23146990 |
| regionname0 | RSPH14_chr22_23059415_23141990 |
| regionname5000 | RSPH14_chr22_23054415_23146990 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 348 | 282 | 73 | 54 | 111 | 13 | 29 | 81 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| a0002 | 0/0 | 348 | 14 | 3 | 2 | 2 | 1 | 6 | 2 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| a0003 | 0/0 | 348 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| a0004 | 0/0 | 348 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| a0005 | 0/0 | 348 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| a0006 | 0/0 | 348 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| a0007 | 0/0 | 348 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| a0008 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| a0009 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | MAHSQ others(343): Show |
chr22 | 23054415 | 23146990 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1044 | 161 | 49 | 31 | 54 | 11 | 16 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0001c0002 | 1/1 | 1044 | 119 | 23 | 23 | 56 | 2 | 13 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0001c0010 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0001c0011 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0002c0003 | 0/0 | 1044 | 14 | 3 | 2 | 2 | 1 | 6 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0003c0004 | 0/0 | 1044 | 7 | 7 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0004c0006 | 0/0 | 1044 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0004c0009 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0004c0014 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0005c0005 | 0/0 | 1044 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0005c0015 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0006c0013 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0007c0008 | 0/0 | 1044 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0008c0007 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 | ||
| a0009c0012 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | ATGGC others(1039): Show |
chr22 | 23054415 | 23146990 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1188 | 159 | 47 | 31 | 54 | 11 | 16 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0001c0001t0003 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0001c0002t0001 | 1/1 | 1188 | 110 | 15 | 22 | 56 | 2 | 13 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0001c0002t0002 | 0/0 | 1188 | 9 | 8 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0001c0010t0001 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0001c0011t0001 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0002c0003t0001 | 0/0 | 1188 | 14 | 3 | 2 | 2 | 1 | 6 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0003c0004t0001 | 0/0 | 1188 | 7 | 7 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0004c0006t0002 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0004c0009t0001 | 0/0 | 1188 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0004c0014t0001 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0005c0005t0001 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0005c0015t0002 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0006c0013t0001 | 0/0 | 1188 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0007c0008t0001 | 0/0 | 1188 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0008c0007t0001 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| a0009c0012t0001 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | AGTGG others(1183): Show |
chr22 | 23054415 | 23146990 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0010t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0001c0011t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0003c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0003c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0003c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0003c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0003c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0003c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0003c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0004c0006t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0004c0006t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0004c0009t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0004c0014t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0005c0005t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0005c0005t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0005c0015t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0006c0013t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0007c0008t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0008c0007t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| a0009c0012t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | GBR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | FIN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | CHS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0117 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01109 | hp1 | a0004 | c0009 | t0001 | g0305 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0116 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01255 | hp1 | a0006 | c0013 | t0001 | g0039 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | CLM | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0034 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01884 | hp1 | a0005 | c0005 | t0001 | g0290 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01891 | hp2 | a0004 | c0006 | t0002 | g0015 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | CDX | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02257 | hp1 | a0005 | c0015 | t0002 | g0016 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0139 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02615 | hp2 | a0001 | c0010 | t0001 | g0283 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0126 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02723 | hp1 | a0003 | c0004 | t0001 | g0295 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0122 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0133 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0123 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02896 | hp1 | a0004 | c0006 | t0002 | g0136 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0179 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03139 | hp1 | a0003 | c0004 | t0001 | g0177 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0140 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03209 | hp2 | a0005 | c0005 | t0001 | g0240 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0118 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0178 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03654 | hp1 | a0002 | c0003 | t0001 | g0121 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03654 | hp2 | a0007 | c0008 | t0001 | g0259 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03688 | hp1 | a0002 | c0003 | t0001 | g0125 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0148 | SAS | BEB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | BEB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0088 | SAS | BEB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0030 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | STU | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | CHB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0294 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18906 | hp2 | a0004 | c0014 | t0001 | g0103 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18942 | hp1 | a0001 | c0011 | t0001 | g0204 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0120 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19068 | hp2 | a0002 | c0003 | t0001 | g0119 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19081 | hp2 | a0008 | c0007 | t0001 | g0200 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | YRI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20129 | hp1 | a0009 | c0012 | t0001 | g0183 | AFR | ASW | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ASW | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0115 | EUR | TSI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0045 | EUR | TSI | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | GIH | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | GIH | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0124 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | MSL | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG06807 | hp1 | a0003 | c0004 | t0001 | g0296 | AFR | USA | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | USA | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | USA | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0127 | AFR | USA | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0033 | REF | REF | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0042 | REF | REF | RSPH14_chr22_23054415_23146990 | RSPH14 | chr22 | 23054415 | 23146990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:23059518 | C | T | 1 | a0005 | 3 | HG01884.hp1 HG02257.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.991G>A | p.Glu331Lys | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 7/7 | 1085/1188 | 991/1047 | 331/348 | chr22 | 23059518 | |||
| chr22:23059592 | C | T | 1 | a0004 | 4 | HG01109.hp1 HG01891.hp2 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.917G>A | p.Arg306His | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 7/7 | 1011/1188 | 917/1047 | 306/348 | chr22 | 23059592 | |||
| chr22:23061860 | C | T | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.739G>A | p.Val247Met | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/7 | 833/1188 | 739/1047 | 247/348 | chr22 | 23061860 | |||
| chr22:23061868 | A | G | 1 | a0007 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.731T>C | p.Val244Ala | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/7 | 825/1188 | 731/1047 | 244/348 | chr22 | 23061868 | |||
| chr22:23064002 | C | G | 1 | a0008 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.553G>C | p.Glu185Gln | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/7 | 647/1188 | 553/1047 | 185/348 | chr22 | 23064002 | |||
| chr22:23064004 | G | A | 2 | a0003 a0009 |
8 | HG02723.hp1 HG03098.hp2 HG03139.hp1 others(5): Show |
missense_variant | MODERATE | c.551C>T | p.Thr184Ile | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/7 | 645/1188 | 551/1047 | 184/348 | chr22 | 23064004 | |||
| chr22:23140258 | G | A | 1 | a0009 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.163C>T | p.His55Tyr | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/7 | 257/1188 | 163/1047 | 55/348 | chr22 | 23140258 | |||
| chr22:23140296 | G | A | 1 | a0002 | 14 | HG00738.hp2 HG01175.hp1 HG02486.hp1 others(11): Show |
missense_variant | MODERATE | c.125C>T | p.Thr42Met | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/7 | 219/1188 | 125/1047 | 42/348 | chr22 | 23140296 | |||
| chr22:23140471 | C | T | 3 | a0001 a0004 a0005 |
12 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(9): Show |
splice_region_variant | LOW | c.-51G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/7 | chr22 | 23140471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:23059506 | G | T | 1 | a0004c0014 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1003C>A | p.Arg335Arg | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 7/7 | 1097/1188 | 1003/1047 | 335/348 | chr22 | 23059506 | |||
| chr22:23063925 | G | A | 1 | a0001c0010 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.630C>T | p.Ala210Ala | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/7 | 724/1188 | 630/1047 | 210/348 | chr22 | 23063925 | |||
| chr22:23063952 | G | A | 1 | a0001c0011 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.603C>T | p.Ser201Ser | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/7 | 697/1188 | 603/1047 | 201/348 | chr22 | 23063952 | |||
| chr22:23140273 | A | G | 9 | a0001c0001 a0001c0010 a0001c0011 others(6): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
synonymous_variant | LOW | c.148T>C | p.Leu50Leu | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/7 | 242/1188 | 148/1047 | 50/348 | chr22 | 23140273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:23141955 | C | G | 1 | a0001c0001t0003 | 2 | HG02970.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/7 | 1535 | chr22 | 23141955 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:23059825 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.791-107C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23059825 | |||||||
| chr22:23060241 | G | T | 16 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(13): Show |
16 | HG01070.hp2 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.791-523C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060241 | |||||||
| chr22:23060272 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.791-554G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060272 | |||||||
| chr22:23060289 | G | A | 4 | a0001c0001t0001g0304 a0004c0006t0002g0015 a0004c0006t0002g0136 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.791-571C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060289 | |||||||
| chr22:23060325 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.791-607C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060325 | |||||||
| chr22:23060340 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
223 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.791-622C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060340 | |||||||
| chr22:23060457 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.791-739C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060457 | |||||||
| chr22:23060469 | C | CA | 11 | a0001c0001t0001g0181 a0001c0002t0001g0045 a0001c0002t0002g0017 others(8): Show |
11 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.791-752dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060469 | |||||||
| chr22:23060571 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-853G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060571 | |||||||
| chr22:23060586 | C | A | 1 | a0001c0001t0001g0269 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.791-868G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060586 | |||||||
| chr22:23060697 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0297 a0001c0002t0001g0043 |
3 | HG00741.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.791-979T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060697 | |||||||
| chr22:23060893 | C | G | 16 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(13): Show |
16 | HG01070.hp2 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.790+916G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23060893 | |||||||
| chr22:23061212 | G | A | 1 | a0002c0003t0001g0122 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.790+597C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061212 | |||||||
| chr22:23061536 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.790+273C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061536 | |||||||
| chr22:23061567 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.790+242G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061567 | |||||||
| chr22:23061568 | G | A | 2 | a0001c0002t0001g0130 a0001c0002t0001g0144 |
2 | HG00544.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.790+241C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061568 | |||||||
| chr22:23061685 | G | GT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0155 a0001c0001t0001g0156 others(18): Show |
22 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.790+123dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061685 | |||||||
| chr22:23061708 | T | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0297 a0001c0002t0001g0043 |
3 | HG00741.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.790+101A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061708 | |||||||
| chr22:23061710 | G | A | 2 | a0001c0002t0001g0085 a0001c0002t0001g0108 |
2 | NA18968.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.790+99C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061710 | |||||||
| chr22:23061734 | CCT | C | 3 | a0005c0005t0001g0240 a0005c0005t0001g0290 a0005c0015t0002g0016 |
3 | HG01884.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.790+73_790+74delAG | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061734 | |||||||
| chr22:23061769 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.790+40C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061769 | |||||||
| chr22:23061789 | G | A | 12 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(9): Show |
12 | HG00741.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.790+20C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061789 | |||||||
| chr22:23061798 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0293 a0001c0002t0001g0063 others(1): Show |
4 | HG00673.hp1 HG00741.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+11G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 6/6 | chr22 | 23061798 | |||||||
| chr22:23062136 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
13 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.654-191G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062136 | |||||||
| chr22:23062728 | C | T | 1 | a0002c0003t0001g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.654-783G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062728 | |||||||
| chr22:23062790 | G | A | 4 | a0001c0002t0001g0065 a0001c0002t0001g0089 a0001c0002t0001g0104 others(1): Show |
4 | HG00544.hp2 HG02523.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-845C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062790 | |||||||
| chr22:23062819 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.654-874G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062819 | |||||||
| chr22:23062910 | C | T | 24 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 others(21): Show |
24 | HG01070.hp2 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.654-965G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23062910 | |||||||
| chr22:23063115 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.653+787G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063115 | |||||||
| chr22:23063252 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.653+650C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063252 | |||||||
| chr22:23063296 | T | C | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.653+606A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063296 | |||||||
| chr22:23063363 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.653+539C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063363 | |||||||
| chr22:23063395 | G | A | 1 | a0001c0002t0001g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.653+507C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063395 | |||||||
| chr22:23063459 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.653+443C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063459 | |||||||
| chr22:23063693 | G | A | 2 | a0001c0001t0001g0212 a0001c0002t0001g0092 |
2 | NA18981.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.653+209C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063693 | |||||||
| chr22:23063704 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.653+198A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063704 | |||||||
| chr22:23063728 | G | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0280 |
2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.653+174C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063728 | |||||||
| chr22:23063779 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(265): Show |
275 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(272): Show |
intron_variant | MODIFIER | c.653+123T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 5/6 | chr22 | 23063779 | |||||||
| chr22:23064375 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.422-242G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064375 | |||||||
| chr22:23064441 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(265): Show |
275 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(272): Show |
intron_variant | MODIFIER | c.422-308T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064441 | |||||||
| chr22:23064480 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-347C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064480 | |||||||
| chr22:23064506 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0272 |
2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.422-373T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064506 | |||||||
| chr22:23064571 | T | C | 1 | a0001c0002t0001g0059 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.422-438A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064571 | |||||||
| chr22:23064875 | T | C | 1 | a0001c0002t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.422-742A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064875 | |||||||
| chr22:23064885 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(265): Show |
275 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(272): Show |
intron_variant | MODIFIER | c.422-752T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064885 | |||||||
| chr22:23064999 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-866G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23064999 | |||||||
| chr22:23065005 | G | A | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.422-872C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065005 | |||||||
| chr22:23065017 | G | A | 11 | a0001c0001t0001g0159 a0001c0002t0002g0017 a0001c0002t0002g0018 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-884C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065017 | |||||||
| chr22:23065063 | C | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-930G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065063 | |||||||
| chr22:23065083 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
276 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(273): Show |
intron_variant | MODIFIER | c.422-950T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065083 | |||||||
| chr22:23065123 | A | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
97 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.422-990T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065123 | |||||||
| chr22:23065334 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0239 |
2 | HG01243.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.422-1201C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065334 | |||||||
| chr22:23065357 | T | C | 3 | a0001c0001t0001g0282 a0001c0002t0001g0063 a0002c0003t0001g0118 |
3 | HG00673.hp1 HG03491.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-1224A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065357 | |||||||
| chr22:23065502 | G | A | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-1369C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065502 | |||||||
| chr22:23065534 | C | CA | 109 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0157 others(106): Show |
111 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.422-1402dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | |||||||
| chr22:23065534 | C | CAA | 55 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0154 others(52): Show |
55 | HG00741.hp1 HG01081.hp2 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.422-1403_422-1402d others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | |||||||
| chr22:23065534 | C | CAAA | 10 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0173 others(7): Show |
10 | HG00673.hp2 HG01109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.422-1404_422-1402d others(5): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | |||||||
| chr22:23065534 | CA | C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0271 a0001c0002t0001g0020 others(5): Show |
8 | HG01243.hp1 HG02015.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-1402delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | |||||||
| chr22:23065534 | CAAAAAAA others(2): Show |
C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
63 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.422-1410_422-1402d others(11): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | |||||||
| chr22:23065534 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0206 a0001c0001t0001g0231 a0001c0001t0001g0237 others(1): Show |
4 | HG00673.hp1 HG03491.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-1411_422-1402d others(12): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | |||||||
| chr22:23065534 | CAAAAAAA others(4): Show |
C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(10): Show |
14 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.422-1412_422-1402d others(13): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065534 | |||||||
| chr22:23065821 | G | A | 1 | a0001c0002t0001g0059 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.422-1688C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065821 | |||||||
| chr22:23065939 | T | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
276 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(273): Show |
intron_variant | MODIFIER | c.422-1806A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23065939 | |||||||
| chr22:23066032 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-1899G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066032 | |||||||
| chr22:23066040 | A | T | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-1907T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066040 | |||||||
| chr22:23066281 | A | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-2148T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066281 | |||||||
| chr22:23066568 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.422-2435C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066568 | |||||||
| chr22:23066661 | G | A | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-2528C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23066661 | |||||||
| chr22:23067001 | G | C | 1 | a0001c0002t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.422-2868C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067001 | |||||||
| chr22:23067065 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0225 |
2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.422-2932A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067065 | |||||||
| chr22:23067205 | T | G | 4 | a0001c0001t0001g0282 a0001c0001t0001g0293 a0001c0002t0001g0063 others(1): Show |
4 | HG00673.hp1 HG00741.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-3072A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067205 | |||||||
| chr22:23067223 | T | C | 3 | a0001c0001t0001g0282 a0001c0002t0001g0063 a0002c0003t0001g0118 |
3 | HG00673.hp1 HG03491.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-3090A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067223 | |||||||
| chr22:23067493 | C | A | 11 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0133 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-3360G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067493 | |||||||
| chr22:23067854 | A | G | 2 | a0001c0001t0001g0154 a0001c0002t0001g0147 |
2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.422-3721T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23067854 | |||||||
| chr22:23068108 | C | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0274 a0001c0001t0001g0285 |
4 | NA18946.hp2 NA18947.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-3975G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068108 | |||||||
| chr22:23068154 | G | A | 2 | a0001c0001t0001g0154 a0001c0002t0001g0147 |
2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.422-4021C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068154 | |||||||
| chr22:23068171 | T | C | 9 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(6): Show |
9 | HG02486.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-4038A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068171 | |||||||
| chr22:23068180 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.422-4047G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068180 | |||||||
| chr22:23068182 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.422-4049C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068182 | |||||||
| chr22:23068211 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-4078T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068211 | |||||||
| chr22:23068345 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-4212G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068345 | |||||||
| chr22:23068688 | G | A | 3 | a0001c0001t0001g0229 a0001c0002t0001g0105 a0008c0007t0001g0200 |
3 | HG02080.hp1 HG02155.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.422-4555C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068688 | |||||||
| chr22:23068739 | A | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
277 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(274): Show |
intron_variant | MODIFIER | c.422-4606T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068739 | |||||||
| chr22:23068878 | C | G | 1 | a0001c0001t0001g0287 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.422-4745G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068878 | |||||||
| chr22:23068904 | A | C | 2 | a0001c0001t0001g0166 a0004c0014t0001g0103 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.422-4771T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23068904 | |||||||
| chr22:23069235 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.422-5102G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069235 | |||||||
| chr22:23069237 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.422-5104C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069237 | |||||||
| chr22:23069240 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.422-5107G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069240 | |||||||
| chr22:23069269 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.422-5136G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069269 | |||||||
| chr22:23069460 | C | T | 3 | a0001c0001t0001g0282 a0001c0002t0001g0063 a0002c0003t0001g0118 |
3 | HG00673.hp1 HG03491.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-5327G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069460 | |||||||
| chr22:23069491 | T | C | 1 | a0001c0002t0001g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.422-5358A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069491 | |||||||
| chr22:23069623 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.422-5490G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069623 | |||||||
| chr22:23069654 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.422-5521G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069654 | |||||||
| chr22:23069817 | G | T | 1 | a0005c0015t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.422-5684C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069817 | |||||||
| chr22:23069838 | A | G | 147 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(144): Show |
149 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.422-5705T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069838 | |||||||
| chr22:23069879 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(253): Show |
262 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(259): Show |
intron_variant | MODIFIER | c.422-5746T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069879 | |||||||
| chr22:23069921 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-5788C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23069921 | |||||||
| chr22:23070011 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0263 |
2 | HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.422-5878C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070011 | |||||||
| chr22:23070041 | G | C | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-5908C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070041 | |||||||
| chr22:23070099 | C | T | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.422-5966G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070099 | |||||||
| chr22:23070130 | A | AC | 5 | a0001c0001t0001g0172 a0001c0002t0001g0043 a0001c0002t0001g0053 others(2): Show |
5 | HG00741.hp1 HG02056.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-5998dupG | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070130 | |||||||
| chr22:23070157 | C | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0054 a0001c0002t0001g0055 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.422-6024G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070157 | |||||||
| chr22:23070210 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.422-6077C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070210 | |||||||
| chr22:23070214 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.422-6081G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070214 | |||||||
| chr22:23070222 | A | AGGTGCCC others(7): Show |
1 | a0001c0001t0001g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-6103_422-6090d others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070222 | |||||||
| chr22:23070249 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.422-6116C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070249 | |||||||
| chr22:23070321 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.422-6188G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070321 | |||||||
| chr22:23070353 | T | TGGCGGCG | 123 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(120): Show |
125 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.422-6227_422-6221d others(9): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | |||||||
| chr22:23070353 | T | TGGCGGCG others(7): Show |
20 | a0001c0001t0001g0210 a0001c0001t0001g0229 a0001c0001t0001g0249 others(17): Show |
20 | HG00741.hp1 HG01106.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.422-6234_422-6221d others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | |||||||
| chr22:23070353 | T | TGGCGGCG others(14): Show |
2 | a0001c0001t0001g0244 a0001c0002t0001g0083 |
2 | HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.422-6241_422-6221d others(23): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | |||||||
| chr22:23070353 | TGGCGGCG | T | 5 | a0001c0001t0001g0221 a0001c0002t0001g0013 a0001c0002t0001g0054 others(2): Show |
5 | HG00597.hp2 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-6227_422-6221d others(9): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | |||||||
| chr22:23070353 | TGGCGGCG others(7): Show |
T | 1 | a0001c0001t0001g0268 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.422-6234_422-6221d others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070353 | |||||||
| chr22:23070449 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.422-6316G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070449 | |||||||
| chr22:23070483 | G | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-6350C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070483 | |||||||
| chr22:23070518 | C | CGCCCCGC others(3): Show |
1 | a0001c0002t0001g0077 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.422-6395_422-6386d others(12): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070518 | |||||||
| chr22:23070600 | C | CGCCGCTG others(1): Show |
19 | a0001c0001t0001g0244 a0001c0001t0001g0254 a0001c0001t0001g0277 others(16): Show |
19 | HG00738.hp2 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.422-6475_422-6468d others(10): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070600 | |||||||
| chr22:23070628 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-6495G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070628 | |||||||
| chr22:23070682 | C | T | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-6549G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070682 | |||||||
| chr22:23070713 | C | T | 3 | a0001c0001t0001g0282 a0001c0002t0001g0063 a0002c0003t0001g0118 |
3 | HG00673.hp1 HG03491.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-6580G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070713 | |||||||
| chr22:23070836 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-6703C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070836 | |||||||
| chr22:23070929 | G | C | 1 | a0001c0002t0001g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.422-6796C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070929 | |||||||
| chr22:23070951 | G | A | 5 | a0003c0004t0001g0011 a0003c0004t0001g0177 a0003c0004t0001g0178 others(2): Show |
5 | HG03098.hp2 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-6818C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23070951 | |||||||
| chr22:23071156 | C | T | 1 | a0002c0003t0001g0118 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.422-7023G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071156 | |||||||
| chr22:23071280 | G | C | 1 | a0001c0001t0001g0006 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.422-7147C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071280 | |||||||
| chr22:23071470 | A | G | 1 | a0001c0001t0001g0299 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.422-7337T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071470 | |||||||
| chr22:23071578 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-7445C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071578 | |||||||
| chr22:23071837 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-7704C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071837 | |||||||
| chr22:23071942 | G | A | 1 | a0001c0002t0001g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.422-7809C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23071942 | |||||||
| chr22:23072009 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-7876C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072009 | |||||||
| chr22:23072141 | G | C | 1 | a0001c0002t0001g0106 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.422-8008C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072141 | |||||||
| chr22:23072325 | G | A | 1 | a0001c0002t0001g0095 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.422-8192C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072325 | |||||||
| chr22:23072562 | T | A | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8429A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072562 | |||||||
| chr22:23072566 | C | A | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8433G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072566 | |||||||
| chr22:23072567 | T | G | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8434A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072567 | |||||||
| chr22:23072568 | T | A | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8435A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072568 | |||||||
| chr22:23072570 | G | C | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8437C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072570 | |||||||
| chr22:23072571 | T | G | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8438A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072571 | |||||||
| chr22:23072572 | A | C | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-8439T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072572 | |||||||
| chr22:23072635 | G | A | 1 | a0002c0003t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.422-8502C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072635 | |||||||
| chr22:23072656 | G | C | 1 | a0001c0001t0001g0284 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.422-8523C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072656 | |||||||
| chr22:23072897 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-8764G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072897 | |||||||
| chr22:23072960 | C | T | 70 | a0001c0001t0001g0184 a0001c0001t0001g0198 a0001c0001t0001g0210 others(67): Show |
72 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.422-8827G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23072960 | |||||||
| chr22:23073055 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.422-8922A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073055 | |||||||
| chr22:23073060 | C | A | 1 | a0001c0001t0001g0275 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.422-8927G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073060 | |||||||
| chr22:23073194 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.422-9061C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073194 | |||||||
| chr22:23073400 | C | T | 1 | a0004c0009t0001g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.422-9267G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073400 | |||||||
| chr22:23073434 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.422-9301C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073434 | |||||||
| chr22:23073475 | G | A | 2 | a0001c0001t0001g0282 a0001c0002t0001g0063 |
2 | HG00673.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.422-9342C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073475 | |||||||
| chr22:23073504 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.422-9371G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073504 | |||||||
| chr22:23073597 | T | G | 1 | a0004c0006t0002g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.422-9464A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073597 | |||||||
| chr22:23073630 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(7): Show |
11 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-9497C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073630 | |||||||
| chr22:23073819 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(129): Show |
136 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.422-9686C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073819 | |||||||
| chr22:23073840 | C | G | 1 | a0005c0005t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.422-9707G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23073840 | |||||||
| chr22:23074100 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.422-9967C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074100 | |||||||
| chr22:23074201 | A | C | 1 | a0001c0002t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.422-10068T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074201 | |||||||
| chr22:23074296 | G | A | 9 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(6): Show |
9 | HG02486.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-10163C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074296 | |||||||
| chr22:23074396 | G | A | 1 | a0001c0002t0001g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.422-10263C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074396 | |||||||
| chr22:23074653 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-10520G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074653 | |||||||
| chr22:23074666 | T | C | 1 | a0001c0002t0001g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.422-10533A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074666 | |||||||
| chr22:23074693 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0293 a0001c0002t0001g0063 |
3 | HG00673.hp1 HG00741.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.422-10560C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074693 | |||||||
| chr22:23074755 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(59): Show |
65 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.422-10622C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074755 | |||||||
| chr22:23074823 | G | A | 2 | a0001c0001t0001g0282 a0001c0002t0001g0063 |
2 | HG00673.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.422-10690C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074823 | |||||||
| chr22:23074944 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.422-10811C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23074944 | |||||||
| chr22:23075007 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.422-10874T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075007 | |||||||
| chr22:23075131 | G | A | 1 | a0003c0004t0001g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.422-10998C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075131 | |||||||
| chr22:23075275 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-11142G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075275 | |||||||
| chr22:23075298 | A | G | 1 | a0002c0003t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.422-11165T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075298 | |||||||
| chr22:23075361 | A | C | 20 | a0001c0001t0001g0159 a0001c0001t0001g0244 a0001c0002t0001g0019 others(17): Show |
20 | HG00738.hp2 HG00741.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.422-11228T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075361 | |||||||
| chr22:23075398 | G | T | 5 | a0001c0002t0001g0030 a0001c0002t0001g0045 a0001c0002t0001g0053 others(2): Show |
5 | HG02735.hp1 HG02738.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-11265C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075398 | |||||||
| chr22:23075486 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.422-11353G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075486 | |||||||
| chr22:23075491 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
107 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.422-11358T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075491 | |||||||
| chr22:23075526 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
139 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.422-11393C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075526 | |||||||
| chr22:23075572 | A | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0149 a0001c0001t0001g0150 others(127): Show |
133 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.422-11439T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075572 | |||||||
| chr22:23075694 | T | G | 3 | a0001c0002t0001g0035 a0001c0002t0001g0040 a0001c0002t0001g0041 |
3 | HG01106.hp2 HG01258.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.422-11561A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075694 | |||||||
| chr22:23075717 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.422-11584T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23075717 | |||||||
| chr22:23076012 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.422-11879C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076012 | |||||||
| chr22:23076023 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.422-11890C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076023 | |||||||
| chr22:23076266 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0255 |
2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.422-12133G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076266 | |||||||
| chr22:23076267 | G | C | 2 | a0001c0001t0001g0159 a0001c0002t0001g0147 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.422-12134C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076267 | |||||||
| chr22:23076306 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01346.hp1 HG02698.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.422-12173G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076306 | |||||||
| chr22:23076347 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.422-12214C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076347 | |||||||
| chr22:23076640 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-12507G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076640 | |||||||
| chr22:23076652 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
68 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.422-12519T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076652 | |||||||
| chr22:23076767 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.422-12634C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23076767 | |||||||
| chr22:23077170 | C | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02965.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.422-13037G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23077170 | |||||||
| chr22:23077323 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.422-13190G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23077323 | |||||||
| chr22:23077470 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.422-13337C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23077470 | |||||||
| chr22:23077855 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.422-13722G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23077855 | |||||||
| chr22:23078113 | G | A | 1 | a0001c0002t0001g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.422-13980C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078113 | |||||||
| chr22:23078155 | C | A | 1 | a0001c0002t0001g0100 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.422-14022G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078155 | |||||||
| chr22:23078259 | G | A | 1 | a0001c0002t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.422-14126C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078259 | |||||||
| chr22:23078322 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.422-14189C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078322 | |||||||
| chr22:23078380 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.422-14247C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078380 | |||||||
| chr22:23078438 | C | T | 2 | a0001c0002t0001g0022 a0005c0005t0001g0240 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.422-14305G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078438 | |||||||
| chr22:23078445 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.422-14312A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078445 | |||||||
| chr22:23078476 | C | T | 10 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(7): Show |
10 | HG01109.hp1 HG01884.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.422-14343G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078476 | |||||||
| chr22:23078488 | CA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(72): Show |
78 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.422-14356delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078488 | |||||||
| chr22:23078499 | T | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(7): Show |
11 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-14366A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078499 | |||||||
| chr22:23078548 | G | T | 9 | a0001c0002t0001g0067 a0001c0002t0001g0070 a0001c0002t0001g0075 others(6): Show |
9 | HG02004.hp2 HG02083.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-14415C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078548 | |||||||
| chr22:23078558 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-14425G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078558 | |||||||
| chr22:23078727 | T | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.422-14594A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078727 | |||||||
| chr22:23078791 | G | T | 2 | a0001c0002t0001g0026 a0001c0002t0001g0027 |
2 | HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.422-14658C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078791 | |||||||
| chr22:23078855 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.422-14722C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078855 | |||||||
| chr22:23078872 | C | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
200 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(197): Show |
intron_variant | MODIFIER | c.422-14739G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078872 | |||||||
| chr22:23078915 | C | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0175 a0001c0002t0001g0029 |
3 | HG02055.hp2 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.422-14782G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078915 | |||||||
| chr22:23078928 | C | T | 1 | a0002c0003t0001g0122 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.422-14795G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078928 | |||||||
| chr22:23078995 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.422-14862G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078995 | |||||||
| chr22:23078996 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.422-14863C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23078996 | |||||||
| chr22:23079031 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0231 a0002c0003t0001g0125 |
5 | HG03491.hp1 HG03492.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-14898T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079031 | |||||||
| chr22:23079078 | A | T | 249 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(246): Show |
255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.422-14945T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079078 | |||||||
| chr22:23079092 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.422-14959C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079092 | |||||||
| chr22:23079197 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.422-15064T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079197 | |||||||
| chr22:23079377 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.422-15244C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079377 | |||||||
| chr22:23079550 | T | C | 41 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(38): Show |
41 | HG00609.hp1 HG01169.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.422-15417A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079550 | |||||||
| chr22:23079565 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01192.hp2 HG01358.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-15432C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079565 | |||||||
| chr22:23079662 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG01346.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.422-15529C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079662 | |||||||
| chr22:23079731 | G | A | 1 | a0001c0002t0001g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.422-15598C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079731 | |||||||
| chr22:23079866 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
94 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.422-15733C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079866 | |||||||
| chr22:23079953 | G | A | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-15820C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079953 | |||||||
| chr22:23079999 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
96 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.422-15866T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23079999 | |||||||
| chr22:23080064 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-15931C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080064 | |||||||
| chr22:23080346 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-16213T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080346 | |||||||
| chr22:23080400 | CAGA | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0159 a0001c0001t0001g0160 others(32): Show |
36 | HG00673.hp1 HG00741.hp2 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.422-16270_422-1626 others(7): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080400 | |||||||
| chr22:23080438 | G | C | 1 | a0001c0002t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.422-16305C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080438 | |||||||
| chr22:23080570 | C | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0225 |
2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.422-16437G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080570 | |||||||
| chr22:23080573 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-16440C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080573 | |||||||
| chr22:23080578 | G | A | 19 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(16): Show |
19 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.422-16445C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080578 | |||||||
| chr22:23080619 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.422-16486T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080619 | |||||||
| chr22:23080704 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
150 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.422-16571A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080704 | |||||||
| chr22:23080824 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-16691C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080824 | |||||||
| chr22:23080915 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.422-16782G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080915 | |||||||
| chr22:23080921 | T | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
151 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.422-16788A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080921 | |||||||
| chr22:23080937 | C | T | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG02280.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.422-16804G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23080937 | |||||||
| chr22:23081056 | A | G | 1 | a0001c0002t0001g0025 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.422-16923T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081056 | |||||||
| chr22:23081061 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
132 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.422-16928C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081061 | |||||||
| chr22:23081257 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.422-17124C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081257 | |||||||
| chr22:23081261 | G | A | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-17128C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081261 | |||||||
| chr22:23081395 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-17262C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081395 | |||||||
| chr22:23081500 | A | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-17367T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081500 | |||||||
| chr22:23081506 | TGTTATAG others(9): Show |
T | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-17389_422-1737 others(20): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081506 | |||||||
| chr22:23081572 | AG | A | 15 | a0001c0001t0001g0166 a0001c0001t0001g0304 a0001c0002t0002g0017 others(12): Show |
15 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.422-17440delC | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081572 | |||||||
| chr22:23081617 | T | A | 1 | a0001c0001t0001g0208 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.422-17484A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081617 | |||||||
| chr22:23081648 | C | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-17515G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081648 | |||||||
| chr22:23081691 | G | C | 1 | a0001c0002t0001g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.422-17558C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081691 | |||||||
| chr22:23081777 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
131 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.422-17644C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081777 | |||||||
| chr22:23081786 | C | T | 3 | a0003c0004t0001g0011 a0003c0004t0001g0177 a0003c0004t0001g0179 |
3 | HG03098.hp2 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.422-17653G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081786 | |||||||
| chr22:23081808 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.422-17675A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081808 | |||||||
| chr22:23081821 | C | CA | 41 | a0001c0001t0001g0218 a0001c0001t0001g0255 a0001c0001t0001g0263 others(38): Show |
41 | HG00597.hp1 HG00639.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.422-17689dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081821 | |||||||
| chr22:23081821 | C | CAA | 8 | a0001c0001t0001g0166 a0001c0001t0001g0304 a0001c0002t0001g0036 others(5): Show |
8 | HG01106.hp2 HG01192.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-17690_422-1768 others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081821 | |||||||
| chr22:23081821 | CA | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
106 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.422-17689delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081821 | |||||||
| chr22:23081851 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.422-17718G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081851 | |||||||
| chr22:23081854 | A | G | 1 | a0002c0003t0001g0119 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.422-17721T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081854 | |||||||
| chr22:23081891 | C | T | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-17758G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081891 | |||||||
| chr22:23081922 | G | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(30): Show |
34 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(31): Show |
intron_variant | MODIFIER | c.422-17789C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23081922 | |||||||
| chr22:23082056 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(30): Show |
34 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(31): Show |
intron_variant | MODIFIER | c.422-17923G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082056 | |||||||
| chr22:23082084 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
86 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.422-17951G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082084 | |||||||
| chr22:23082104 | G | A | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0300 others(1): Show |
4 | NA18984.hp1 NA19060.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-17971C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082104 | |||||||
| chr22:23082135 | C | A | 1 | a0001c0002t0001g0102 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.422-18002G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082135 | |||||||
| chr22:23082135 | C | CA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0129 others(7): Show |
11 | HG00642.hp2 HG01192.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.422-18003dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082135 | |||||||
| chr22:23082135 | CA | C | 19 | a0001c0001t0001g0159 a0001c0001t0001g0166 a0001c0001t0001g0185 others(16): Show |
19 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.422-18003delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082135 | |||||||
| chr22:23082135 | CAA | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.422-18004_422-1800 others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082135 | |||||||
| chr22:23082137 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.422-18004T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082137 | |||||||
| chr22:23082138 | A | C | 1 | a0001c0002t0001g0037 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.422-18005T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082138 | |||||||
| chr22:23082139 | A | C | 2 | a0001c0001t0001g0266 a0001c0002t0001g0141 |
2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.422-18006T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082139 | |||||||
| chr22:23082140 | A | C | 1 | a0001c0002t0001g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.422-18007T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082140 | |||||||
| chr22:23082251 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-18118G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082251 | |||||||
| chr22:23082285 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
13 | HG02615.hp2 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.422-18152G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082285 | |||||||
| chr22:23082375 | C | T | 1 | a0005c0015t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.422-18242G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082375 | |||||||
| chr22:23082377 | A | AT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0176 a0001c0001t0001g0217 others(9): Show |
13 | HG00673.hp1 HG00673.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-18245dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082377 | |||||||
| chr22:23082377 | A | T | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-18244T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082377 | |||||||
| chr22:23082377 | AT | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
100 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.422-18245delA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082377 | |||||||
| chr22:23082466 | G | A | 7 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-18333C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082466 | |||||||
| chr22:23082938 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-18805T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082938 | |||||||
| chr22:23082982 | C | T | 1 | a0006c0013t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.422-18849G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23082982 | |||||||
| chr22:23083199 | T | C | 2 | a0001c0002t0001g0101 a0001c0002t0001g0102 |
2 | HG01257.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.422-19066A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083199 | |||||||
| chr22:23083341 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
149 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.422-19208C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083341 | |||||||
| chr22:23083430 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.422-19297C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083430 | |||||||
| chr22:23083736 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
133 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.422-19603T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083736 | |||||||
| chr22:23083744 | G | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
133 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.422-19611C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083744 | |||||||
| chr22:23083798 | C | T | 1 | a0001c0002t0001g0087 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.422-19665G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083798 | |||||||
| chr22:23083891 | A | G | 5 | a0001c0001t0001g0187 a0001c0001t0001g0206 a0001c0001t0001g0234 others(2): Show |
5 | HG00609.hp2 HG01261.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-19758T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23083891 | |||||||
| chr22:23084188 | A | G | 1 | a0001c0002t0001g0003 | 2 | NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.422-20055T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084188 | |||||||
| chr22:23084298 | C | G | 1 | a0001c0001t0001g0205 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.422-20165G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084298 | |||||||
| chr22:23084468 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-20335C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084468 | |||||||
| chr22:23084691 | T | C | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
5 | HG01070.hp2 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-20558A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084691 | |||||||
| chr22:23084746 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
133 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.422-20613T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084746 | |||||||
| chr22:23084780 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0098 |
2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.422-20647C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084780 | |||||||
| chr22:23084832 | G | A | 1 | a0001c0002t0001g0078 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.422-20699C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084832 | |||||||
| chr22:23084917 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-20784G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084917 | |||||||
| chr22:23084918 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-20785C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23084918 | |||||||
| chr22:23085486 | G | A | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-21353C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23085486 | |||||||
| chr22:23085805 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-21672C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23085805 | |||||||
| chr22:23085982 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(7): Show |
11 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-21849C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23085982 | |||||||
| chr22:23086247 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
133 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.422-22114A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086247 | |||||||
| chr22:23086384 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0098 |
2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.422-22251C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086384 | |||||||
| chr22:23086437 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-22304C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086437 | |||||||
| chr22:23086509 | C | T | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-22376G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086509 | |||||||
| chr22:23086511 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0255 |
2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.422-22378G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086511 | |||||||
| chr22:23086623 | A | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
134 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.422-22490T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086623 | |||||||
| chr22:23086883 | C | T | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-22750G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086883 | |||||||
| chr22:23086897 | C | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(29): Show |
33 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-22764G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086897 | |||||||
| chr22:23086994 | G | A | 2 | a0001c0002t0001g0080 a0001c0002t0001g0104 |
2 | NA18946.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.422-22861C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23086994 | |||||||
| chr22:23087037 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
91 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.422-22904G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087037 | |||||||
| chr22:23087343 | G | A | 1 | a0005c0005t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.422-23210C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087343 | |||||||
| chr22:23087358 | C | T | 1 | a0002c0003t0001g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.422-23225G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087358 | |||||||
| chr22:23087365 | C | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
100 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.422-23232G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087365 | |||||||
| chr22:23087377 | T | C | 8 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
8 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-23244A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087377 | |||||||
| chr22:23087395 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-23262A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087395 | |||||||
| chr22:23087501 | C | T | 1 | a0002c0003t0001g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.422-23368G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087501 | |||||||
| chr22:23087569 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
132 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.422-23436A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087569 | |||||||
| chr22:23087601 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.422-23468G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087601 | |||||||
| chr22:23087966 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
131 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.422-23833T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23087966 | |||||||
| chr22:23088223 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
132 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.422-24090T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088223 | |||||||
| chr22:23088506 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
131 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.422-24373T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088506 | |||||||
| chr22:23088540 | C | T | 1 | a0001c0002t0002g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.422-24407G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088540 | |||||||
| chr22:23088681 | T | C | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-24548A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088681 | |||||||
| chr22:23088695 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.422-24562G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088695 | |||||||
| chr22:23088702 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0264 |
3 | HG00642.hp1 HG01358.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.422-24569T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088702 | |||||||
| chr22:23088729 | G | A | 1 | a0001c0002t0001g0112 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.422-24596C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088729 | |||||||
| chr22:23088903 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.422-24770A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088903 | |||||||
| chr22:23088967 | G | T | 1 | a0005c0005t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.422-24834C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23088967 | |||||||
| chr22:23089160 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
86 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.422-25027C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089160 | |||||||
| chr22:23089193 | A | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-25060T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089193 | |||||||
| chr22:23089205 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.422-25072C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089205 | |||||||
| chr22:23089400 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.422-25267C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089400 | |||||||
| chr22:23089550 | G | A | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-25417C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089550 | |||||||
| chr22:23089576 | A | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.422-25443T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089576 | |||||||
| chr22:23089669 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(28): Show |
32 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(29): Show |
intron_variant | MODIFIER | c.422-25536C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089669 | |||||||
| chr22:23089776 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.422-25643A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23089776 | |||||||
| chr22:23090019 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-25886G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090019 | |||||||
| chr22:23090020 | C | G | 1 | a0001c0002t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.422-25887G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090020 | |||||||
| chr22:23090047 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
128 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.422-25914G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090047 | |||||||
| chr22:23090457 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
85 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.422-26324C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090457 | |||||||
| chr22:23090562 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.422-26429G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090562 | |||||||
| chr22:23090850 | C | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-26717G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23090850 | |||||||
| chr22:23091056 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
91 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.422-26923G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091056 | |||||||
| chr22:23091069 | C | T | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-26936G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091069 | |||||||
| chr22:23091079 | C | G | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-26946G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091079 | |||||||
| chr22:23091208 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-27075C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091208 | |||||||
| chr22:23091229 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.422-27096G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091229 | |||||||
| chr22:23091461 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.422-27328G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091461 | |||||||
| chr22:23091476 | A | G | 2 | a0001c0002t0001g0024 a0001c0010t0001g0283 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.422-27343T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091476 | |||||||
| chr22:23091561 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-27428A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091561 | |||||||
| chr22:23091567 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-27434G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091567 | |||||||
| chr22:23091611 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0165 a0001c0001t0001g0167 others(2): Show |
6 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-27478G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091611 | |||||||
| chr22:23091612 | G | A | 2 | a0002c0003t0001g0119 a0002c0003t0001g0120 |
2 | NA19010.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.422-27479C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091612 | |||||||
| chr22:23091617 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-27484A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091617 | |||||||
| chr22:23091636 | A | G | 1 | a0004c0006t0002g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.422-27503T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091636 | |||||||
| chr22:23091642 | A | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0302 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.422-27509T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091642 | |||||||
| chr22:23091676 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
132 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.422-27543C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091676 | |||||||
| chr22:23091703 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(41): Show |
45 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(42): Show |
intron_variant | MODIFIER | c.422-27570C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091703 | |||||||
| chr22:23091910 | T | G | 2 | a0001c0001t0001g0150 a0001c0002t0001g0029 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.422-27777A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091910 | |||||||
| chr22:23091959 | C | T | 14 | a0001c0001t0001g0304 a0001c0002t0002g0017 a0001c0002t0002g0018 others(11): Show |
14 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.422-27826G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23091959 | |||||||
| chr22:23092124 | T | TC | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-27992dupG | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092124 | |||||||
| chr22:23092140 | G | A | 72 | a0001c0001t0001g0218 a0001c0001t0001g0284 a0001c0002t0001g0002 others(69): Show |
74 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.422-28007C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092140 | |||||||
| chr22:23092392 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-28259G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092392 | |||||||
| chr22:23092406 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
151 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.422-28273G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092406 | |||||||
| chr22:23092421 | G | A | 1 | a0003c0004t0001g0178 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.422-28288C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092421 | |||||||
| chr22:23092557 | T | C | 1 | a0004c0006t0002g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.422-28424A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092557 | |||||||
| chr22:23092618 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-28485C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092618 | |||||||
| chr22:23092854 | C | T | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.422-28721G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092854 | |||||||
| chr22:23092855 | G | A | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-28722C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092855 | |||||||
| chr22:23092964 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(40): Show |
44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.422-28831C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23092964 | |||||||
| chr22:23093208 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.422-29075G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093208 | |||||||
| chr22:23093219 | T | A | 1 | a0001c0002t0001g0112 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.422-29086A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093219 | |||||||
| chr22:23093293 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.422-29160G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093293 | |||||||
| chr22:23093426 | C | T | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-29293G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093426 | |||||||
| chr22:23093439 | G | T | 1 | a0001c0002t0001g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.422-29306C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093439 | |||||||
| chr22:23093468 | G | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(18): Show |
22 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-29335C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23093468 | |||||||
| chr22:23094098 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(40): Show |
44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.422-29965G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094098 | |||||||
| chr22:23094157 | G | A | 14 | a0001c0001t0001g0304 a0001c0002t0002g0017 a0001c0002t0002g0018 others(11): Show |
14 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.422-30024C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094157 | |||||||
| chr22:23094158 | C | G | 14 | a0001c0001t0001g0304 a0001c0002t0002g0017 a0001c0002t0002g0018 others(11): Show |
14 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.422-30025G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094158 | |||||||
| chr22:23094180 | G | T | 1 | a0004c0009t0001g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.422-30047C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094180 | |||||||
| chr22:23094237 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
151 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.422-30104A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094237 | |||||||
| chr22:23094308 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-30175G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094308 | |||||||
| chr22:23094400 | GC | G | 3 | a0001c0002t0001g0053 a0002c0003t0001g0122 a0002c0003t0001g0126 |
3 | HG02698.hp1 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.422-30268delG | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094400 | |||||||
| chr22:23094437 | G | A | 1 | a0006c0013t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.422-30304C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094437 | |||||||
| chr22:23094708 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-30575G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094708 | |||||||
| chr22:23094819 | C | T | 1 | a0001c0011t0001g0204 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.422-30686G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094819 | |||||||
| chr22:23094854 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-30721G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23094854 | |||||||
| chr22:23095065 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-30932C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095065 | |||||||
| chr22:23095075 | A | G | 11 | a0001c0001t0001g0304 a0001c0002t0002g0017 a0001c0002t0002g0018 others(8): Show |
11 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-30942T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095075 | |||||||
| chr22:23095084 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
128 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.422-30951C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095084 | |||||||
| chr22:23095109 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-30976C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095109 | |||||||
| chr22:23095170 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.422-31037T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095170 | |||||||
| chr22:23095197 | T | G | 1 | a0001c0002t0001g0130 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.422-31064A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095197 | |||||||
| chr22:23095280 | C | T | 1 | a0001c0002t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.422-31147G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095280 | |||||||
| chr22:23095289 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.422-31156C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095289 | |||||||
| chr22:23095312 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.422-31179G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095312 | |||||||
| chr22:23095611 | G | A | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-31478C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095611 | |||||||
| chr22:23095705 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.422-31572G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095705 | |||||||
| chr22:23095929 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG00642.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.422-31796G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23095929 | |||||||
| chr22:23096004 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
87 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.422-31871G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096004 | |||||||
| chr22:23096010 | G | A | 1 | a0001c0002t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.422-31877C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096010 | |||||||
| chr22:23096094 | C | T | 2 | a0001c0002t0001g0026 a0001c0002t0001g0027 |
2 | HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.422-31961G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096094 | |||||||
| chr22:23096154 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.422-32021C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096154 | |||||||
| chr22:23096244 | G | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0280 |
2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.422-32111C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096244 | |||||||
| chr22:23096319 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-32186C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096319 | |||||||
| chr22:23096382 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.422-32249G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096382 | |||||||
| chr22:23096549 | G | A | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-32416C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096549 | |||||||
| chr22:23096600 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.422-32467C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096600 | |||||||
| chr22:23096675 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.422-32542C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096675 | |||||||
| chr22:23096841 | A | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-32708T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096841 | |||||||
| chr22:23096909 | C | T | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-32776G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23096909 | |||||||
| chr22:23097198 | G | T | 5 | a0001c0002t0001g0070 a0001c0002t0001g0081 a0001c0002t0001g0099 others(2): Show |
5 | NA18942.hp2 NA18944.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-33065C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097198 | |||||||
| chr22:23097343 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
86 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.422-33210G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097343 | |||||||
| chr22:23097408 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422-33275G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097408 | |||||||
| chr22:23097569 | C | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(38): Show |
42 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(39): Show |
intron_variant | MODIFIER | c.422-33436G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097569 | |||||||
| chr22:23097573 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.422-33440G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097573 | |||||||
| chr22:23097580 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.422-33447C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097580 | |||||||
| chr22:23097749 | C | T | 1 | a0001c0002t0002g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.422-33616G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097749 | |||||||
| chr22:23097782 | G | T | 1 | a0001c0002t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.422-33649C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097782 | |||||||
| chr22:23097834 | T | C | 2 | a0001c0002t0001g0024 a0001c0010t0001g0283 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.422-33701A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097834 | |||||||
| chr22:23097850 | A | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
13 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.422-33717T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097850 | |||||||
| chr22:23097851 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0165 a0001c0001t0001g0167 others(2): Show |
6 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-33718G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097851 | |||||||
| chr22:23097912 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-33779T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23097912 | |||||||
| chr22:23098146 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.422-34013C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098146 | |||||||
| chr22:23098191 | T | G | 1 | a0001c0002t0001g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.422-34058A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098191 | |||||||
| chr22:23098339 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
91 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.422-34206G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098339 | |||||||
| chr22:23098545 | C | A | 2 | a0001c0002t0001g0024 a0001c0010t0001g0283 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.422-34412G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098545 | |||||||
| chr22:23098571 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.422-34438G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098571 | |||||||
| chr22:23098775 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.422-34642C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098775 | |||||||
| chr22:23098800 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.422-34667C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098800 | |||||||
| chr22:23098860 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-34727G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098860 | |||||||
| chr22:23098888 | C | T | 1 | a0001c0002t0001g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.422-34755G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23098888 | |||||||
| chr22:23099045 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0201 |
2 | NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.422-34912C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099045 | |||||||
| chr22:23099151 | C | T | 1 | a0001c0002t0001g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421+34875G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099151 | |||||||
| chr22:23099261 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.421+34765C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099261 | |||||||
| chr22:23099328 | G | C | 119 | a0001c0001t0001g0218 a0001c0001t0001g0230 a0001c0001t0001g0284 others(116): Show |
121 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.421+34698C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099328 | |||||||
| chr22:23099371 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.421+34655G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099371 | |||||||
| chr22:23099503 | G | A | 2 | a0001c0002t0001g0071 a0001c0002t0001g0082 |
2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.421+34523C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099503 | |||||||
| chr22:23099693 | A | C | 1 | a0001c0002t0001g0080 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.421+34333T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23099693 | |||||||
| chr22:23100015 | T | C | 2 | a0001c0002t0001g0024 a0001c0010t0001g0283 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+34011A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100015 | |||||||
| chr22:23100076 | C | G | 1 | a0007c0008t0001g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.421+33950G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100076 | |||||||
| chr22:23100097 | C | CCTG | 4 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG01884.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+33926_421+3392 others(7): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100097 | |||||||
| chr22:23100145 | T | C | 2 | a0001c0002t0001g0024 a0001c0010t0001g0283 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+33881A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100145 | |||||||
| chr22:23100301 | A | G | 1 | a0001c0002t0001g0094 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.421+33725T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100301 | |||||||
| chr22:23100482 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.421+33544A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100482 | |||||||
| chr22:23100504 | G | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+33522C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100504 | |||||||
| chr22:23100565 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.421+33461G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100565 | |||||||
| chr22:23100729 | G | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
90 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.421+33297C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100729 | |||||||
| chr22:23100799 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+33227T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100799 | |||||||
| chr22:23100865 | G | T | 7 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+33161C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100865 | |||||||
| chr22:23100902 | G | A | 13 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(10): Show |
13 | HG01175.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.421+33124C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23100902 | |||||||
| chr22:23101101 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.421+32925C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101101 | |||||||
| chr22:23101216 | G | A | 1 | a0001c0002t0001g0059 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.421+32810C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101216 | |||||||
| chr22:23101323 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.421+32703G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101323 | |||||||
| chr22:23101423 | A | G | 1 | a0001c0002t0001g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.421+32603T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101423 | |||||||
| chr22:23101722 | G | A | 6 | a0001c0002t0001g0031 a0002c0003t0001g0115 a0002c0003t0001g0116 others(3): Show |
6 | HG01175.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+32304C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101722 | |||||||
| chr22:23101865 | C | A | 3 | a0001c0002t0001g0012 a0001c0002t0001g0050 a0001c0002t0001g0051 |
3 | NA18973.hp2 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.421+32161G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101865 | |||||||
| chr22:23101880 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
90 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.421+32146C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23101880 | |||||||
| chr22:23102003 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.421+32023G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102003 | |||||||
| chr22:23102029 | G | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(40): Show |
44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+31997C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102029 | |||||||
| chr22:23102063 | G | C | 1 | a0001c0002t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.421+31963C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102063 | |||||||
| chr22:23102120 | C | T | 1 | a0001c0011t0001g0204 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.421+31906G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102120 | |||||||
| chr22:23102149 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
135 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.421+31877C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102149 | |||||||
| chr22:23102214 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG00642.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.421+31812C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102214 | |||||||
| chr22:23102392 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421+31634A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102392 | |||||||
| chr22:23102567 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+31459C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102567 | |||||||
| chr22:23102605 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(40): Show |
44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+31421G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102605 | |||||||
| chr22:23102609 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
91 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.421+31417T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102609 | |||||||
| chr22:23102896 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
152 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.421+31130A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23102896 | |||||||
| chr22:23103296 | G | A | 1 | a0001c0002t0001g0032 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.421+30730C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103296 | |||||||
| chr22:23103472 | C | T | 2 | a0002c0003t0001g0121 a0002c0003t0001g0124 |
2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.421+30554G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103472 | |||||||
| chr22:23103505 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.421+30521G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103505 | |||||||
| chr22:23103639 | A | AT | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+30386dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103639 | |||||||
| chr22:23103931 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421+30095G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23103931 | |||||||
| chr22:23104119 | G | A | 7 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+29907C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104119 | |||||||
| chr22:23104199 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
147 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.421+29827C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104199 | |||||||
| chr22:23104231 | A | G | 3 | a0001c0002t0001g0012 a0001c0002t0001g0050 a0001c0002t0001g0051 |
3 | NA18973.hp2 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.421+29795T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104231 | |||||||
| chr22:23104369 | T | C | 1 | a0005c0005t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.421+29657A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104369 | |||||||
| chr22:23104858 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+29168C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23104858 | |||||||
| chr22:23105160 | C | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(262): Show |
272 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(269): Show |
intron_variant | MODIFIER | c.421+28866G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105160 | |||||||
| chr22:23105224 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+28802A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105224 | |||||||
| chr22:23105282 | G | A | 1 | a0001c0002t0001g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.421+28744C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105282 | |||||||
| chr22:23105327 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.421+28699G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105327 | |||||||
| chr22:23105726 | A | G | 44 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(41): Show |
45 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(42): Show |
intron_variant | MODIFIER | c.421+28300T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105726 | |||||||
| chr22:23105782 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.421+28244C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105782 | |||||||
| chr22:23105904 | T | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(41): Show |
45 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(42): Show |
intron_variant | MODIFIER | c.421+28122A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105904 | |||||||
| chr22:23105983 | G | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(55): Show |
59 | HG00673.hp1 HG00741.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.421+28043C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23105983 | |||||||
| chr22:23106037 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.421+27989T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106037 | |||||||
| chr22:23106044 | A | T | 2 | a0001c0001t0001g0150 a0001c0002t0001g0029 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.421+27982T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106044 | |||||||
| chr22:23106109 | C | CCCGCCAC others(35): Show |
1 | a0001c0002t0001g0064 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+27916_421+2791 others(46): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106109 | |||||||
| chr22:23106280 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.421+27746G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106280 | |||||||
| chr22:23106402 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.421+27624C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106402 | |||||||
| chr22:23106460 | A | ACTGTGGG others(13): Show |
3 | a0001c0002t0001g0071 a0001c0002t0001g0082 a0001c0002t0001g0107 |
3 | HG01975.hp1 HG02056.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.421+27546_421+2756 others(24): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106460 | |||||||
| chr22:23106509 | C | A | 1 | a0007c0008t0001g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.421+27517G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106509 | |||||||
| chr22:23106568 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.421+27458G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106568 | |||||||
| chr22:23106696 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(16): Show |
20 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+27330G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106696 | |||||||
| chr22:23106796 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421+27230G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106796 | |||||||
| chr22:23106814 | G | C | 1 | a0004c0009t0001g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+27212C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106814 | |||||||
| chr22:23106854 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0231 |
4 | HG03491.hp1 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+27172G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23106854 | |||||||
| chr22:23107180 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0255 |
2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.421+26846G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107180 | |||||||
| chr22:23107291 | C | T | 2 | a0001c0002t0001g0024 a0001c0010t0001g0283 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+26735G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107291 | |||||||
| chr22:23107350 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(40): Show |
44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+26676A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107350 | |||||||
| chr22:23107372 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+26654T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107372 | |||||||
| chr22:23107768 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
152 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.421+26258T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107768 | |||||||
| chr22:23107870 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.421+26156G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107870 | |||||||
| chr22:23107918 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.421+26108G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23107918 | |||||||
| chr22:23108152 | A | G | 1 | a0001c0002t0001g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.421+25874T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108152 | |||||||
| chr22:23108258 | G | A | 2 | a0001c0001t0001g0159 a0001c0002t0001g0041 |
2 | HG01981.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.421+25768C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108258 | |||||||
| chr22:23108454 | C | T | 2 | a0001c0002t0002g0134 a0001c0002t0002g0135 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.421+25572G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108454 | |||||||
| chr22:23108462 | C | T | 2 | a0001c0002t0001g0024 a0001c0010t0001g0283 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+25564G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108462 | |||||||
| chr22:23108577 | TGGATCCT others(6): Show |
T | 1 | a0001c0002t0001g0064 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+25436_421+2544 others(17): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108577 | |||||||
| chr22:23108695 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(40): Show |
44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+25331C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108695 | |||||||
| chr22:23108716 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(40): Show |
44 | HG00673.hp1 HG00741.hp2 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.421+25310T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108716 | |||||||
| chr22:23108928 | C | T | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+25098G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23108928 | |||||||
| chr22:23109049 | G | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0155 others(38): Show |
42 | HG00673.hp1 HG00741.hp2 HG02257.hp2 others(39): Show |
intron_variant | MODIFIER | c.421+24977C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109049 | |||||||
| chr22:23109169 | A | G | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+24857T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109169 | |||||||
| chr22:23109236 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.421+24790G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109236 | |||||||
| chr22:23109264 | G | A | 2 | a0001c0002t0001g0024 a0001c0010t0001g0283 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+24762C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109264 | |||||||
| chr22:23109287 | G | A | 1 | a0001c0002t0001g0020 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.421+24739C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109287 | |||||||
| chr22:23109588 | G | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
96 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.421+24438C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109588 | |||||||
| chr22:23109639 | T | A | 1 | a0001c0002t0001g0064 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+24387A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109639 | |||||||
| chr22:23109650 | C | T | 3 | a0001c0002t0001g0022 a0001c0002t0001g0048 a0001c0002t0001g0049 |
3 | HG02809.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.421+24376G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109650 | |||||||
| chr22:23109655 | G | A | 8 | a0003c0004t0001g0011 a0003c0004t0001g0177 a0003c0004t0001g0178 others(5): Show |
8 | HG02723.hp1 HG03098.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+24371C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109655 | |||||||
| chr22:23109876 | C | A | 7 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+24150G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109876 | |||||||
| chr22:23109878 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.421+24148G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109878 | |||||||
| chr22:23109901 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0154 others(16): Show |
20 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+24125C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109901 | |||||||
| chr22:23109929 | C | T | 7 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+24097G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23109929 | |||||||
| chr22:23110244 | C | G | 15 | a0001c0001t0001g0159 a0001c0001t0001g0180 a0001c0001t0001g0304 others(12): Show |
15 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.421+23782G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23110244 | |||||||
| chr22:23110579 | G | A | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0163 others(1): Show |
4 | HG02258.hp2 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+23447C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23110579 | |||||||
| chr22:23110656 | A | T | 1 | a0001c0002t0001g0064 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+23370T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23110656 | |||||||
| chr22:23110868 | C | A | 1 | a0001c0001t0001g0232 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.421+23158G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23110868 | |||||||
| chr22:23111027 | G | GGGGGTAG others(3): Show |
1 | a0001c0002t0001g0064 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+22989_421+2299 others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111027 | |||||||
| chr22:23111101 | G | A | 1 | a0001c0002t0001g0059 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.421+22925C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111101 | |||||||
| chr22:23111153 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.421+22873G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111153 | |||||||
| chr22:23111206 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.421+22820G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111206 | |||||||
| chr22:23111321 | C | T | 9 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(6): Show |
9 | HG00558.hp1 NA18957.hp1 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.421+22705G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111321 | |||||||
| chr22:23111380 | C | T | 21 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(18): Show |
21 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+22646G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111380 | |||||||
| chr22:23111389 | G | A | 1 | a0001c0002t0001g0003 | 2 | NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.421+22637C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111389 | |||||||
| chr22:23111610 | A | C | 1 | a0001c0002t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.421+22416T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111610 | |||||||
| chr22:23111768 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18952.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.421+22258C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111768 | |||||||
| chr22:23111844 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.421+22182G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111844 | |||||||
| chr22:23111857 | G | C | 1 | a0001c0002t0001g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.421+22169C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23111857 | |||||||
| chr22:23112260 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.421+21766G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112260 | |||||||
| chr22:23112298 | C | T | 5 | a0001c0002t0001g0070 a0001c0002t0001g0081 a0001c0002t0001g0099 others(2): Show |
5 | NA18942.hp2 NA18944.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+21728G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112298 | |||||||
| chr22:23112302 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.421+21724G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112302 | |||||||
| chr22:23112387 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0233 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.421+21639T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112387 | |||||||
| chr22:23112535 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
83 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.421+21491G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112535 | |||||||
| chr22:23112694 | A | G | 165 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0154 others(162): Show |
167 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.421+21332T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112694 | |||||||
| chr22:23112699 | C | T | 1 | a0003c0004t0001g0177 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.421+21327G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112699 | |||||||
| chr22:23112741 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421+21285C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112741 | |||||||
| chr22:23112932 | C | T | 1 | a0001c0002t0001g0022 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.421+21094G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112932 | |||||||
| chr22:23112950 | G | A | 2 | a0001c0001t0001g0159 a0004c0009t0001g0305 |
2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.421+21076C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23112950 | |||||||
| chr22:23113095 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0010 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.421+20931C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113095 | |||||||
| chr22:23113179 | C | T | 154 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0154 others(151): Show |
156 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.421+20847G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113179 | |||||||
| chr22:23113680 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.421+20346G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113680 | |||||||
| chr22:23113696 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421+20330G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113696 | |||||||
| chr22:23113793 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+20233G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113793 | |||||||
| chr22:23113974 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.421+20052G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113974 | |||||||
| chr22:23113988 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.421+20038T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23113988 | |||||||
| chr22:23114017 | G | A | 25 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0154 others(22): Show |
25 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.421+20009C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114017 | |||||||
| chr22:23114206 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0098 |
2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.421+19820C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114206 | |||||||
| chr22:23114266 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0054 a0001c0002t0001g0055 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.421+19760G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114266 | |||||||
| chr22:23114286 | A | G | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.421+19740T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114286 | |||||||
| chr22:23114413 | C | T | 6 | a0001c0001t0001g0180 a0003c0004t0001g0011 a0003c0004t0001g0177 others(3): Show |
6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+19613G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114413 | |||||||
| chr22:23114509 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.421+19517A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114509 | |||||||
| chr22:23114515 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.421+19511A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114515 | |||||||
| chr22:23114621 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.421+19405A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114621 | |||||||
| chr22:23114835 | G | C | 1 | a0001c0002t0001g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.421+19191C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114835 | |||||||
| chr22:23114911 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.421+19115T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114911 | |||||||
| chr22:23114991 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.421+19035C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23114991 | |||||||
| chr22:23115002 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+19024C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115002 | |||||||
| chr22:23115233 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.421+18793A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115233 | |||||||
| chr22:23115299 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+18727G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115299 | |||||||
| chr22:23115607 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.421+18419G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115607 | |||||||
| chr22:23115630 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421+18396C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115630 | |||||||
| chr22:23115802 | A | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0293 |
3 | HG00673.hp1 HG00741.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.421+18224T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23115802 | |||||||
| chr22:23116104 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.421+17922G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116104 | |||||||
| chr22:23116301 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | NA18957.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.421+17725C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116301 | |||||||
| chr22:23116382 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.421+17644C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116382 | |||||||
| chr22:23116390 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.421+17636C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116390 | |||||||
| chr22:23116548 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.421+17478G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116548 | |||||||
| chr22:23116597 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+17429T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116597 | |||||||
| chr22:23116611 | G | T | 2 | a0001c0002t0001g0066 a0001c0002t0001g0098 |
2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.421+17415C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116611 | |||||||
| chr22:23116766 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0232 |
2 | HG01515.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.421+17260C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23116766 | |||||||
| chr22:23117003 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421+17023C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117003 | |||||||
| chr22:23117228 | T | C | 2 | a0002c0003t0001g0119 a0002c0003t0001g0120 |
2 | NA19010.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.421+16798A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117228 | |||||||
| chr22:23117243 | T | TGA | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.421+16781_421+1678 others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117243 | |||||||
| chr22:23117257 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0181 |
3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.421+16769G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117257 | |||||||
| chr22:23117268 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.421+16758C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117268 | |||||||
| chr22:23117356 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.421+16670C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117356 | |||||||
| chr22:23117397 | C | A | 1 | a0001c0001t0001g0225 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.421+16629G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117397 | |||||||
| chr22:23117676 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.421+16350C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117676 | |||||||
| chr22:23117771 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.421+16255C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117771 | |||||||
| chr22:23117850 | C | G | 7 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
7 | HG02080.hp1 NA18952.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+16176G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117850 | |||||||
| chr22:23117887 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.421+16139G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23117887 | |||||||
| chr22:23118022 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0293 |
2 | HG00673.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.421+16004G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118022 | |||||||
| chr22:23118256 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
5 | HG00642.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+15770C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118256 | |||||||
| chr22:23118413 | G | A | 1 | a0001c0002t0002g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.421+15613C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118413 | |||||||
| chr22:23118467 | T | TCCCCG | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+15554_421+1555 others(9): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118467 | |||||||
| chr22:23118482 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.421+15544T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118482 | |||||||
| chr22:23118482 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+15544T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118482 | |||||||
| chr22:23118497 | C | CT | 41 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(38): Show |
43 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.421+15528dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118497 | |||||||
| chr22:23118539 | G | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+15487C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118539 | |||||||
| chr22:23118575 | C | G | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.421+15451G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118575 | |||||||
| chr22:23118589 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+15437C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118589 | |||||||
| chr22:23118730 | A | G | 1 | a0001c0002t0001g0020 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.421+15296T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118730 | |||||||
| chr22:23118752 | G | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.421+15274C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118752 | |||||||
| chr22:23118816 | G | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.421+15210C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118816 | |||||||
| chr22:23118907 | A | G | 4 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG01884.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+15119T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23118907 | |||||||
| chr22:23119000 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.421+15026C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119000 | |||||||
| chr22:23119011 | A | G | 6 | a0001c0001t0001g0180 a0003c0004t0001g0011 a0003c0004t0001g0177 others(3): Show |
6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+15015T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119011 | |||||||
| chr22:23119113 | G | A | 4 | a0001c0001t0001g0216 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+14913C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119113 | |||||||
| chr22:23119174 | C | A | 1 | a0004c0009t0001g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+14852G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119174 | |||||||
| chr22:23119209 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.421+14817G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119209 | |||||||
| chr22:23119238 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.421+14788T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119238 | |||||||
| chr22:23119409 | G | A | 1 | a0005c0005t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.421+14617C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119409 | |||||||
| chr22:23119536 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.421+14490T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119536 | |||||||
| chr22:23119727 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.421+14299G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23119727 | |||||||
| chr22:23120067 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.421+13959G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120067 | |||||||
| chr22:23120141 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.421+13885G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120141 | |||||||
| chr22:23120260 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.421+13766T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120260 | |||||||
| chr22:23120711 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.421+13315C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120711 | |||||||
| chr22:23120838 | T | C | 1 | a0001c0002t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.421+13188A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120838 | |||||||
| chr22:23120866 | A | G | 8 | a0001c0002t0002g0018 a0001c0002t0002g0134 a0001c0002t0002g0135 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+13160T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120866 | |||||||
| chr22:23120882 | G | A | 1 | a0002c0003t0001g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.421+13144C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120882 | |||||||
| chr22:23120886 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+13140A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120886 | |||||||
| chr22:23120897 | T | C | 25 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0154 others(22): Show |
25 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.421+13129A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120897 | |||||||
| chr22:23120996 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+13030T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23120996 | |||||||
| chr22:23121066 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+12960T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121066 | |||||||
| chr22:23121105 | C | T | 6 | a0001c0001t0001g0180 a0003c0004t0001g0011 a0003c0004t0001g0177 others(3): Show |
6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+12921G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121105 | |||||||
| chr22:23121417 | G | T | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG02280.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.421+12609C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121417 | |||||||
| chr22:23121720 | CT | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0154 others(39): Show |
43 | HG01192.hp2 HG01517.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.421+12305delA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121720 | |||||||
| chr22:23121720 | CTT | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.421+12304_421+1230 others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121720 | |||||||
| chr22:23121720 | CTTT | C | 8 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0262 others(5): Show |
8 | HG01433.hp1 HG01515.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+12303_421+1230 others(7): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121720 | |||||||
| chr22:23121783 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421+12243T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121783 | |||||||
| chr22:23121890 | TTTG | T | 13 | a0001c0001t0001g0304 a0001c0002t0002g0017 a0001c0002t0002g0018 others(10): Show |
13 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+12133_421+1213 others(7): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121890 | |||||||
| chr22:23121933 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.421+12093C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23121933 | |||||||
| chr22:23122270 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.421+11756T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122270 | |||||||
| chr22:23122277 | G | T | 1 | a0001c0002t0001g0043 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.421+11749C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122277 | |||||||
| chr22:23122422 | C | T | 1 | a0002c0003t0001g0117 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.421+11604G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122422 | |||||||
| chr22:23122567 | G | A | 9 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 others(6): Show |
9 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.421+11459C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122567 | |||||||
| chr22:23122578 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.421+11448T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122578 | |||||||
| chr22:23122620 | T | C | 3 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02965.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.421+11406A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122620 | |||||||
| chr22:23122623 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.421+11403C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122623 | |||||||
| chr22:23122759 | G | T | 1 | a0001c0002t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.421+11267C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122759 | |||||||
| chr22:23122778 | G | C | 5 | a0001c0001t0001g0170 a0001c0001t0001g0228 a0001c0001t0001g0292 others(2): Show |
5 | HG02486.hp2 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+11248C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122778 | |||||||
| chr22:23122811 | T | G | 2 | a0001c0002t0001g0083 a0001c0002t0001g0084 |
2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.421+11215A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122811 | |||||||
| chr22:23122891 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
89 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.421+11135T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23122891 | |||||||
| chr22:23123254 | C | T | 1 | a0003c0004t0001g0294 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.421+10772G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123254 | |||||||
| chr22:23123377 | C | T | 1 | a0001c0002t0002g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.421+10649G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123377 | |||||||
| chr22:23123444 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0293 others(1): Show |
4 | HG00673.hp1 HG00741.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+10582C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123444 | |||||||
| chr22:23123489 | A | G | 1 | a0001c0002t0001g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.421+10537T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123489 | |||||||
| chr22:23123595 | A | C | 1 | a0001c0002t0001g0067 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.421+10431T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123595 | |||||||
| chr22:23123641 | A | G | 4 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG01884.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+10385T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123641 | |||||||
| chr22:23123844 | G | A | 133 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.421+10182C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123844 | |||||||
| chr22:23123870 | C | T | 2 | a0001c0002t0001g0066 a0001c0002t0001g0098 |
2 | NA18952.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.421+10156G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23123870 | |||||||
| chr22:23124089 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.421+9937G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124089 | |||||||
| chr22:23124099 | G | A | 1 | a0001c0002t0001g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421+9927C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124099 | |||||||
| chr22:23124190 | A | AT | 14 | a0001c0002t0001g0111 a0001c0002t0001g0147 a0001c0002t0002g0017 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+9835dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124190 | |||||||
| chr22:23124199 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.421+9827A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124199 | |||||||
| chr22:23124199 | T | TG | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.421+9826_421+9827i others(3): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124199 | |||||||
| chr22:23124201 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.421+9825C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124201 | |||||||
| chr22:23124214 | G | GT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(32): Show |
36 | HG00673.hp1 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.421+9811dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124214 | |||||||
| chr22:23124214 | GT | G | 10 | a0001c0001t0001g0180 a0001c0001t0001g0297 a0001c0002t0001g0060 others(7): Show |
10 | HG02258.hp1 HG02970.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.421+9811delA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124214 | |||||||
| chr22:23124314 | A | G | 1 | a0001c0002t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.421+9712T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124314 | |||||||
| chr22:23124442 | G | A | 1 | a0001c0002t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.421+9584C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124442 | |||||||
| chr22:23124722 | G | A | 1 | a0002c0003t0001g0123 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.421+9304C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124722 | |||||||
| chr22:23124782 | A | G | 1 | a0001c0002t0001g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.421+9244T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124782 | |||||||
| chr22:23124880 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.421+9146G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124880 | |||||||
| chr22:23124893 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+9133G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23124893 | |||||||
| chr22:23125302 | G | A | 1 | a0004c0009t0001g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+8724C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125302 | |||||||
| chr22:23125302 | G | C | 2 | a0001c0002t0001g0048 a0001c0002t0001g0049 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.421+8724C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125302 | |||||||
| chr22:23125559 | G | A | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+8467C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125559 | |||||||
| chr22:23125617 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+8409C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125617 | |||||||
| chr22:23125759 | G | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+8267C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125759 | |||||||
| chr22:23125763 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+8263T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125763 | |||||||
| chr22:23125837 | G | C | 19 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(16): Show |
19 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.421+8189C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125837 | |||||||
| chr22:23125902 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.421+8124C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125902 | |||||||
| chr22:23125913 | A | G | 1 | a0001c0002t0001g0043 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.421+8113T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125913 | |||||||
| chr22:23125937 | A | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0181 |
3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.421+8089T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125937 | |||||||
| chr22:23125955 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.421+8071T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23125955 | |||||||
| chr22:23126005 | C | T | 1 | a0004c0009t0001g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+8021G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126005 | |||||||
| chr22:23126069 | T | G | 1 | a0004c0014t0001g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.421+7957A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126069 | |||||||
| chr22:23126153 | C | CTGTGAGC others(45): Show |
1 | a0001c0002t0001g0064 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+7872_421+7873i others(54): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126153 | |||||||
| chr22:23126281 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.421+7745G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126281 | |||||||
| chr22:23126345 | C | T | 21 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0168 others(18): Show |
21 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+7681G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126345 | |||||||
| chr22:23126351 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+7675A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126351 | |||||||
| chr22:23126434 | G | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02965.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.421+7592C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126434 | |||||||
| chr22:23126573 | G | A | 7 | a0001c0001t0001g0180 a0001c0001t0001g0297 a0003c0004t0001g0011 others(4): Show |
7 | HG02258.hp1 HG02970.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+7453C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126573 | |||||||
| chr22:23126603 | T | C | 2 | a0002c0003t0001g0121 a0002c0003t0001g0124 |
2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.421+7423A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126603 | |||||||
| chr22:23126637 | G | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0193 |
3 | NA19010.hp1 NA19079.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.421+7389C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126637 | |||||||
| chr22:23126772 | G | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0284 |
2 | HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.421+7254C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126772 | |||||||
| chr22:23126981 | T | C | 1 | a0001c0002t0001g0043 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.421+7045A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126981 | |||||||
| chr22:23126994 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+7032A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23126994 | |||||||
| chr22:23127071 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.421+6955G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127071 | |||||||
| chr22:23127080 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.421+6946G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127080 | |||||||
| chr22:23127152 | C | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+6874G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127152 | |||||||
| chr22:23127228 | A | C | 1 | a0001c0002t0001g0063 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.421+6798T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127228 | |||||||
| chr22:23127246 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.421+6780T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127246 | |||||||
| chr22:23127251 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+6775C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127251 | |||||||
| chr22:23127523 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+6503T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127523 | |||||||
| chr22:23127593 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.421+6433C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127593 | |||||||
| chr22:23127731 | C | T | 17 | a0001c0002t0001g0024 a0001c0002t0001g0031 a0001c0002t0001g0043 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.421+6295G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127731 | |||||||
| chr22:23127903 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+6123C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127903 | |||||||
| chr22:23127978 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+6048G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23127978 | |||||||
| chr22:23128172 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.421+5854G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128172 | |||||||
| chr22:23128220 | T | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+5806A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128220 | |||||||
| chr22:23128301 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.421+5725A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128301 | |||||||
| chr22:23128473 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+5553C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128473 | |||||||
| chr22:23128524 | C | T | 14 | a0001c0002t0001g0111 a0001c0002t0001g0147 a0001c0002t0002g0017 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+5502G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128524 | |||||||
| chr22:23128599 | G | T | 1 | a0001c0002t0002g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.421+5427C>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128599 | |||||||
| chr22:23128712 | C | T | 4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG01070.hp2 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+5314G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23128712 | |||||||
| chr22:23129067 | C | T | 10 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(7): Show |
10 | HG00558.hp1 NA18957.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.421+4959G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129067 | |||||||
| chr22:23129104 | G | C | 1 | a0001c0002t0001g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.421+4922C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129104 | |||||||
| chr22:23129233 | G | C | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+4793C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129233 | |||||||
| chr22:23129346 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+4680G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129346 | |||||||
| chr22:23129437 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+4589C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129437 | |||||||
| chr22:23129706 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0293 |
3 | HG00673.hp1 HG00741.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.421+4320C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129706 | |||||||
| chr22:23129813 | G | A | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG02280.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.421+4213C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129813 | |||||||
| chr22:23129824 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.421+4202A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23129824 | |||||||
| chr22:23130053 | GAAAGAAA others(18): Show |
G | 1 | a0001c0001t0001g0251 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.421+3948_421+3972d others(27): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130053 | |||||||
| chr22:23130059 | A | AAAAG | 10 | a0001c0002t0001g0013 a0001c0002t0001g0054 a0001c0002t0001g0055 others(7): Show |
10 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.421+3963_421+3966d others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(21): Show |
A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0156 a0001c0001t0001g0160 others(15): Show |
19 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.421+3939_421+3966d others(30): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(25): Show |
A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0150 a0001c0001t0001g0162 others(14): Show |
18 | HG00280.hp1 HG00673.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.421+3935_421+3966d others(34): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(29): Show |
A | 7 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0173 others(4): Show |
7 | HG00639.hp1 HG01169.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+3931_421+3966d others(38): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(33): Show |
A | 8 | a0001c0001t0001g0153 a0001c0001t0001g0175 a0001c0001t0001g0227 others(5): Show |
8 | HG01071.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+3927_421+3966d others(42): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(37): Show |
A | 11 | a0001c0001t0001g0152 a0001c0001t0001g0168 a0001c0001t0001g0212 others(8): Show |
11 | HG01081.hp1 HG01175.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.421+3923_421+3966d others(46): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(41): Show |
A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0205 others(2): Show |
5 | HG01975.hp2 HG02080.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+3919_421+3966d others(50): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(45): Show |
A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0151 others(12): Show |
15 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.421+3915_421+3966d others(54): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(49): Show |
A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0185 others(18): Show |
22 | HG00280.hp2 HG00735.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.421+3911_421+3966d others(58): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(53): Show |
A | 24 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0191 others(21): Show |
24 | HG00609.hp1 HG01261.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.421+3907_421+3966d others(62): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(57): Show |
A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0014 others(10): Show |
14 | HG00558.hp1 HG01192.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+3903_421+3966d others(66): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130059 | AAAAGAAA others(61): Show |
A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | NA18944.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.421+3899_421+3966d others(70): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130059 | |||||||
| chr22:23130060 | AAAGAAAG others(17): Show |
A | 12 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0001g0164 others(9): Show |
12 | HG00741.hp2 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+3942_421+3965d others(26): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130060 | |||||||
| chr22:23130064 | AAAGAAAG others(13): Show |
A | 12 | a0001c0001t0001g0129 a0001c0001t0001g0157 a0001c0001t0001g0165 others(9): Show |
12 | HG00642.hp1 HG00642.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+3942_421+3961d others(22): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130064 | |||||||
| chr22:23130068 | AAAGAAAG others(9): Show |
A | 6 | a0001c0001t0001g0154 a0001c0002t0001g0062 a0001c0002t0001g0096 others(3): Show |
6 | HG00673.hp2 HG01109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+3942_421+3957d others(18): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130068 | |||||||
| chr22:23130072 | AAAGAAAG others(5): Show |
A | 1 | a0009c0012t0001g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.421+3942_421+3953d others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130072 | |||||||
| chr22:23130084 | G | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0278 others(2): Show |
5 | HG01346.hp2 HG02027.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+3942C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130084 | G | GAAGA | 5 | a0001c0002t0001g0002 a0001c0002t0001g0031 a0001c0002t0001g0052 others(2): Show |
5 | HG01175.hp1 HG02129.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+3938_421+3941d others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130084 | GAAGA | G | 32 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0012 others(29): Show |
32 | HG00558.hp2 HG01081.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.421+3938_421+3941d others(6): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130084 | GAAGAAAG others(1): Show |
G | 32 | a0001c0002t0001g0003 a0001c0002t0001g0019 a0001c0002t0001g0020 others(29): Show |
32 | HG00544.hp1 HG00597.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.421+3934_421+3941d others(10): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130084 | GAAGAAAG others(5): Show |
G | 13 | a0001c0002t0001g0013 a0001c0002t0001g0028 a0001c0002t0001g0035 others(10): Show |
13 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+3930_421+3941d others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130084 | GAAGAAAG others(9): Show |
G | 11 | a0001c0002t0001g0027 a0001c0002t0001g0037 a0001c0002t0001g0073 others(8): Show |
11 | HG01243.hp1 HG01361.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.421+3926_421+3941d others(18): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130084 | GAAGAAAG others(13): Show |
G | 5 | a0001c0001t0001g0155 a0001c0002t0001g0024 a0001c0002t0001g0026 others(2): Show |
5 | HG00741.hp1 HG02818.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+3922_421+3941d others(22): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130084 | GAAGAAAG others(17): Show |
G | 3 | a0001c0002t0001g0029 a0001c0002t0001g0131 a0001c0002t0001g0147 |
3 | HG00544.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.421+3918_421+3941d others(26): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130084 | GAAGAAAG others(21): Show |
G | 1 | a0001c0002t0001g0106 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.421+3914_421+3941d others(30): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130084 | |||||||
| chr22:23130096 | A | G | 3 | a0001c0002t0001g0062 a0001c0002t0001g0096 a0001c0002t0001g0111 |
3 | HG00673.hp2 HG03453.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.421+3930T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130096 | |||||||
| chr22:23130096 | AAAGAAAG others(24): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.421+3899_421+3929d others(33): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130096 | |||||||
| chr22:23130100 | A | G | 2 | a0001c0002t0001g0074 a0001c0002t0001g0110 |
2 | HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.421+3926T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130100 | |||||||
| chr22:23130115 | GAAAGAAA others(39): Show |
G | 1 | a0001c0001t0001g0278 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.421+3865_421+3910d others(48): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130115 | |||||||
| chr22:23130138 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421+3888T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130138 | |||||||
| chr22:23130139 | GAAAGAAA others(15): Show |
G | 1 | a0001c0001t0001g0284 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.421+3865_421+3886d others(24): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130139 | |||||||
| chr22:23130161 | A | G | 1 | a0001c0002t0001g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.421+3865T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130161 | |||||||
| chr22:23130197 | T | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(31): Show |
36 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.421+3829A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130197 | |||||||
| chr22:23130222 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0233 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.421+3804C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130222 | |||||||
| chr22:23130393 | T | C | 1 | a0001c0002t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.421+3633A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130393 | |||||||
| chr22:23130412 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.421+3614T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130412 | |||||||
| chr22:23130476 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.421+3550C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130476 | |||||||
| chr22:23130485 | A | G | 1 | a0004c0009t0001g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+3541T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130485 | |||||||
| chr22:23130489 | G | A | 1 | a0004c0009t0001g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421+3537C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130489 | |||||||
| chr22:23130489 | G | GAAGAAAG others(23): Show |
1 | a0009c0012t0001g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.421+3536_421+3537i others(32): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130489 | |||||||
| chr22:23130489 | G | GGAGAAAG others(15): Show |
1 | a0001c0002t0001g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.421+3536_421+3537i others(24): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130489 | |||||||
| chr22:23130489 | GGAAAGAA others(7): Show |
G | 1 | a0001c0002t0001g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.421+3523_421+3536d others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130489 | |||||||
| chr22:23130490 | GAAAGAA | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0165 a0001c0001t0001g0167 others(2): Show |
6 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+3530_421+3535d others(8): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130490 | |||||||
| chr22:23130493 | A | G | 1 | a0001c0002t0001g0077 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.421+3533T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130493 | |||||||
| chr22:23130494 | GAA | G | 3 | a0001c0001t0001g0162 a0001c0002t0001g0031 a0001c0002t0001g0034 |
3 | HG01516.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.421+3530_421+3531d others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130494 | |||||||
| chr22:23130496 | A | AAG | 8 | a0001c0001t0001g0155 a0001c0001t0001g0164 a0001c0002t0001g0030 others(5): Show |
8 | HG01258.hp1 HG01981.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAG | 28 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0163 others(25): Show |
29 | HG00609.hp2 HG01081.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(8): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(3): Show |
28 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(25): Show |
28 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(12): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(7): Show |
24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(21): Show |
25 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(16): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(11): Show |
36 | a0001c0001t0001g0014 a0001c0001t0001g0152 a0001c0001t0001g0153 others(33): Show |
36 | HG00558.hp2 HG01071.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(20): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(15): Show |
38 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(35): Show |
38 | HG00639.hp1 HG00735.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(24): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(19): Show |
43 | a0001c0001t0001g0149 a0001c0001t0001g0168 a0001c0001t0001g0169 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(28): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(23): Show |
32 | a0001c0001t0001g0129 a0001c0001t0001g0150 a0001c0001t0001g0170 others(29): Show |
32 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(32): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(27): Show |
20 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0176 others(17): Show |
21 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(36): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(31): Show |
15 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0282 others(12): Show |
15 | HG00544.hp1 HG00673.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(40): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(35): Show |
8 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0001t0001g0269 others(5): Show |
8 | HG01255.hp2 HG01358.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(44): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(39): Show |
6 | a0001c0001t0001g0227 a0001c0002t0001g0013 a0001c0002t0001g0054 others(3): Show |
6 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+3529_421+3530i others(48): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(43): Show |
2 | a0001c0001t0001g0264 a0001c0002t0001g0002 |
2 | HG02129.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.421+3529_421+3530i others(52): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(47): Show |
2 | a0001c0002t0001g0098 a0001c0002t0001g0106 |
2 | NA19074.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.421+3529_421+3530i others(56): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(51): Show |
1 | a0001c0002t0001g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.421+3529_421+3530i others(60): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(59): Show |
1 | a0001c0001t0001g0285 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.421+3529_421+3530i others(68): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(63): Show |
1 | a0001c0001t0001g0219 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.421+3529_421+3530i others(72): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(67): Show |
1 | a0001c0002t0001g0063 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.421+3529_421+3530i others(76): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130496 | A | AAGAAAGA others(46): Show |
1 | a0001c0002t0001g0064 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421+3529_421+3530i others(55): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130496 | |||||||
| chr22:23130529 | A | AAAGAAAG others(24): Show |
1 | a0001c0002t0001g0061 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.421+3496_421+3497i others(33): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130529 | |||||||
| chr22:23130534 | G | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+3492C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130534 | |||||||
| chr22:23130627 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.421+3399A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130627 | |||||||
| chr22:23130767 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.421+3259A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130767 | |||||||
| chr22:23130812 | G | A | 3 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0144 |
3 | HG00544.hp1 HG02523.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.421+3214C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130812 | |||||||
| chr22:23130873 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0181 |
3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.421+3153C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130873 | |||||||
| chr22:23130936 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+3090T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130936 | |||||||
| chr22:23130958 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+3068C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23130958 | |||||||
| chr22:23131044 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.421+2982A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131044 | |||||||
| chr22:23131063 | A | C | 3 | a0001c0002t0001g0022 a0001c0002t0001g0048 a0001c0002t0001g0049 |
3 | HG02809.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.421+2963T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131063 | |||||||
| chr22:23131072 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+2954T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131072 | |||||||
| chr22:23131389 | AG | A | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.421+2636delC | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131389 | |||||||
| chr22:23131611 | G | A | 1 | a0001c0002t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.421+2415C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131611 | |||||||
| chr22:23131646 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.421+2380C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131646 | |||||||
| chr22:23131652 | T | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+2374A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131652 | |||||||
| chr22:23131675 | T | A | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+2351A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131675 | |||||||
| chr22:23131687 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.421+2339C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131687 | |||||||
| chr22:23131898 | G | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(37): Show |
42 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.421+2128C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23131898 | |||||||
| chr22:23132243 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0165 a0001c0001t0001g0167 others(2): Show |
6 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+1783C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132243 | |||||||
| chr22:23132281 | C | T | 1 | a0001c0002t0001g0032 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.421+1745G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132281 | |||||||
| chr22:23132392 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.421+1634G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132392 | |||||||
| chr22:23132565 | A | AAT | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.421+1459_421+1460d others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132565 | |||||||
| chr22:23132569 | T | C | 15 | a0001c0002t0001g0031 a0002c0003t0001g0115 a0002c0003t0001g0116 others(12): Show |
15 | HG00738.hp2 HG01175.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.421+1457A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132569 | |||||||
| chr22:23132608 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+1418T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132608 | |||||||
| chr22:23132637 | A | ACCC | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+1388_421+1389i others(5): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132637 | |||||||
| chr22:23132638 | A | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.421+1388T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132638 | |||||||
| chr22:23132721 | A | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+1305T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132721 | |||||||
| chr22:23132785 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.421+1241T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132785 | |||||||
| chr22:23132880 | T | A | 21 | a0001c0001t0001g0152 a0001c0001t0001g0184 a0001c0001t0001g0215 others(18): Show |
21 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+1146A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132880 | |||||||
| chr22:23132915 | G | A | 8 | a0001c0002t0001g0056 a0001c0002t0001g0060 a0001c0002t0001g0091 others(5): Show |
8 | HG01928.hp2 HG01943.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+1111C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132915 | |||||||
| chr22:23132930 | G | A | 20 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.421+1096C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23132930 | |||||||
| chr22:23133140 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.421+886A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133140 | |||||||
| chr22:23133451 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.421+575G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133451 | |||||||
| chr22:23133563 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+463C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133563 | |||||||
| chr22:23133575 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.421+451G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133575 | |||||||
| chr22:23133576 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.421+450C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133576 | |||||||
| chr22:23133675 | C | T | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.421+351G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133675 | |||||||
| chr22:23133781 | G | C | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.421+245C>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133781 | |||||||
| chr22:23133878 | A | T | 4 | a0001c0001t0001g0159 a0003c0004t0001g0294 a0003c0004t0001g0295 others(1): Show |
4 | HG02723.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+148T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23133878 | |||||||
| chr22:23134015 | C | T | 1 | a0001c0002t0002g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.421+11G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 4/6 | chr22 | 23134015 | |||||||
| chr22:23134237 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0281 |
3 | HG00609.hp2 HG02056.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.303-93T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134237 | |||||||
| chr22:23134548 | CA | C | 186 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(183): Show |
191 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.303-405delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134548 | |||||||
| chr22:23134548 | CAA | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0128 others(43): Show |
48 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.303-406_303-405del others(2): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134548 | |||||||
| chr22:23134548 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0181 |
3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.303-418_303-405del others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134548 | |||||||
| chr22:23134808 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.303-664A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134808 | |||||||
| chr22:23134852 | G | A | 4 | a0001c0001t0001g0159 a0003c0004t0001g0294 a0003c0004t0001g0295 others(1): Show |
4 | HG02723.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-708C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23134852 | |||||||
| chr22:23135007 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.303-863G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135007 | |||||||
| chr22:23135182 | A | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-1038T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135182 | |||||||
| chr22:23135212 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.303-1068C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135212 | |||||||
| chr22:23135287 | C | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
85 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.303-1143G>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135287 | |||||||
| chr22:23135290 | A | G | 1 | a0002c0003t0001g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.303-1146T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135290 | |||||||
| chr22:23135315 | T | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(35): Show |
40 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.303-1171A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135315 | |||||||
| chr22:23135317 | C | CA | 34 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(31): Show |
34 | HG00544.hp2 HG00741.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.303-1174dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135317 | |||||||
| chr22:23135317 | CA | C | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(32): Show |
37 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.303-1174delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135317 | |||||||
| chr22:23135317 | CAA | C | 16 | a0001c0001t0001g0154 a0001c0001t0001g0159 a0001c0001t0001g0167 others(13): Show |
16 | HG01243.hp2 HG01261.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.303-1175_303-1174d others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135317 | |||||||
| chr22:23135317 | CAAA | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
86 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.303-1176_303-1174d others(5): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135317 | |||||||
| chr22:23135319 | A | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0274 |
2 | HG03471.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.303-1175T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135319 | |||||||
| chr22:23135364 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.303-1220G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135364 | |||||||
| chr22:23135422 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.303-1278C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135422 | |||||||
| chr22:23135446 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0181 |
3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.303-1302G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135446 | |||||||
| chr22:23135457 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.303-1313C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135457 | |||||||
| chr22:23135498 | G | GTAAATAA others(5): Show |
126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(123): Show |
131 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.303-1366_303-1355d others(14): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135498 | |||||||
| chr22:23135498 | G | GTAAATAA others(9): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0153 a0001c0001t0001g0244 others(6): Show |
10 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.303-1370_303-1355d others(18): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135498 | |||||||
| chr22:23135516 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0054 a0001c0002t0001g0055 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.303-1372T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135516 | |||||||
| chr22:23135623 | C | T | 2 | a0001c0002t0001g0052 a0001c0002t0001g0053 |
2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.303-1479G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135623 | |||||||
| chr22:23135711 | A | G | 1 | a0001c0002t0002g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.303-1567T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135711 | |||||||
| chr22:23135783 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.303-1639T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135783 | |||||||
| chr22:23135840 | G | A | 1 | a0001c0002t0001g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.303-1696C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135840 | |||||||
| chr22:23135952 | T | C | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-1808A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135952 | |||||||
| chr22:23135963 | G | A | 6 | a0001c0002t0002g0018 a0001c0002t0002g0137 a0001c0002t0002g0138 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-1819C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135963 | |||||||
| chr22:23135996 | A | AT | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0181 |
3 | HG02055.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.303-1853dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23135996 | |||||||
| chr22:23136081 | G | A | 6 | a0001c0001t0001g0180 a0003c0004t0001g0011 a0003c0004t0001g0177 others(3): Show |
6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-1937C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136081 | |||||||
| chr22:23136241 | ATGTCATG others(1124): Show |
A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
92 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.302+1468_303-2098d others(2): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136241 | |||||||
| chr22:23136508 | C | T | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(46): Show |
51 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.302+2332G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136508 | |||||||
| chr22:23136630 | G | A | 1 | a0001c0002t0001g0099 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.302+2210C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136630 | |||||||
| chr22:23136650 | C | T | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(46): Show |
51 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.302+2190G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136650 | |||||||
| chr22:23136893 | G | A | 1 | a0001c0002t0001g0073 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.302+1947C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23136893 | |||||||
| chr22:23137372 | G | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(46): Show |
51 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.302+1468C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137372 | |||||||
| chr22:23137431 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.302+1409T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137431 | |||||||
| chr22:23137476 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+1364T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137476 | |||||||
| chr22:23137503 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.302+1337G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137503 | |||||||
| chr22:23137569 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.302+1271G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137569 | |||||||
| chr22:23137571 | G | GT | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(37): Show |
42 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.302+1268dupA | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137571 | |||||||
| chr22:23137578 | T | A | 1 | a0001c0001t0001g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.302+1262A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137578 | |||||||
| chr22:23137696 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+1144C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137696 | |||||||
| chr22:23137928 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01192.hp2 HG01358.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+912A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23137928 | |||||||
| chr22:23138327 | C | T | 3 | a0001c0002t0001g0012 a0001c0002t0001g0050 a0001c0002t0001g0051 |
3 | NA18973.hp2 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.302+513G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138327 | |||||||
| chr22:23138454 | A | G | 6 | a0001c0001t0001g0180 a0003c0004t0001g0011 a0003c0004t0001g0177 others(3): Show |
6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+386T>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138454 | |||||||
| chr22:23138473 | A | T | 6 | a0001c0001t0001g0180 a0003c0004t0001g0011 a0003c0004t0001g0177 others(3): Show |
6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+367T>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138473 | |||||||
| chr22:23138561 | C | CA | 6 | a0001c0001t0001g0180 a0003c0004t0001g0011 a0003c0004t0001g0177 others(3): Show |
6 | HG02258.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+278dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138561 | |||||||
| chr22:23138597 | G | A | 1 | a0001c0002t0001g0049 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302+243C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138597 | |||||||
| chr22:23138651 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.302+189G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138651 | |||||||
| chr22:23138738 | G | A | 76 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0012 others(73): Show |
78 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.302+102C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138738 | |||||||
| chr22:23138775 | T | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.302+65A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 3/6 | chr22 | 23138775 | |||||||
| chr22:23138946 | G | GA | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0181 others(3): Show |
6 | HG02055.hp2 HG02135.hp1 HG02145.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.200-5dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23138946 | |||||||
| chr22:23138946 | GA | G | 73 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(70): Show |
75 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(72): Show |
splice_region_variant&intron_variant | LOW | c.200-5delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23138946 | |||||||
| chr22:23138946 | GAA | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
79 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(76): Show |
splice_region_variant&intron_variant | LOW | c.200-6_200-5delTT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23138946 | |||||||
| chr22:23139085 | T | A | 2 | a0001c0002t0001g0113 a0001c0002t0001g0114 |
2 | HG02083.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.200-143A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139085 | |||||||
| chr22:23139396 | G | A | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.200-454C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139396 | |||||||
| chr22:23139623 | AAAAT | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.199+595_199+598del others(4): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139623 | |||||||
| chr22:23139684 | G | A | 4 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG01884.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+538C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139684 | |||||||
| chr22:23139903 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199+319A>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139903 | |||||||
| chr22:23139909 | T | G | 1 | a0001c0001t0001g0293 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.199+313A>C | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 2/6 | chr22 | 23139909 | |||||||
| chr22:23140531 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52-59G>A | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23140531 | |||||||
| chr22:23140557 | C | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52-85G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23140557 | |||||||
| chr22:23140775 | A | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
12 | HG02258.hp2 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-303T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23140775 | |||||||
| chr22:23141068 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-52-596C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141068 | |||||||
| chr22:23141081 | G | A | 2 | a0001c0002t0001g0130 a0001c0002t0001g0131 |
2 | HG00544.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-52-609C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141081 | |||||||
| chr22:23141242 | T | C | 3 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0296 |
3 | HG02723.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53+707A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141242 | |||||||
| chr22:23141244 | G | A | 4 | a0001c0001t0001g0159 a0003c0004t0001g0294 a0003c0004t0001g0295 others(1): Show |
4 | HG02723.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53+705C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141244 | |||||||
| chr22:23141324 | T | C | 1 | a0001c0002t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+625A>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141324 | |||||||
| chr22:23141327 | C | CA | 16 | a0001c0002t0001g0141 a0001c0002t0001g0142 a0001c0002t0001g0143 others(13): Show |
16 | HG00544.hp1 HG00597.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53+621dupT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141327 | |||||||
| chr22:23141327 | CA | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-53+621delT | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141327 | |||||||
| chr22:23141327 | CAA | C | 11 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(8): Show |
11 | HG01515.hp1 HG01516.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-53+620_-53+621del others(2): Show |
RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141327 | |||||||
| chr22:23141582 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-53+367G>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141582 | |||||||
| chr22:23141846 | G | A | 2 | a0001c0001t0001g0304 a0004c0009t0001g0305 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-53+103C>T | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141846 | |||||||
| chr22:23141883 | A | C | 1 | a0003c0004t0001g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-53+66T>G | RSPH14 | ENSG00000100218.12 | transcript | ENST00000216036.9 | protein_coding | 1/6 | chr22 | 23141883 |