Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57531 |
| ensemblid | ENSG00000085382.12 |
| hgncid | 21033 |
| symbol | HACE1 |
| name | HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 |
| refseq_nuc | NM_020771.4 |
| refseq_prot | NP_065822.2 |
| ensembl_nuc | ENST00000262903.9 |
| ensembl_prot | ENSP00000262903.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 104728094 |
| end | 104859919 |
| strand | - |
| ver | v1.2 |
| region | chr6:104728094-104859919 |
| region5000 | chr6:104723094-104864919 |
| regionname0 | HACE1_chr6_104728094_104859919 |
| regionname5000 | HACE1_chr6_104723094_104864919 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2727 | 281 | 45 | 48 | 150 | 8 | 29 | HACE1_chr6_104723094_104864919 | HACE1 | ATGGA others(2722): Show |
chr6 | 104723094 | 104864919 | ||
| a0001c0002 | 0/1 | 2727 | 60 | 33 | 12 | 1 | 6 | 7 | HACE1_chr6_104723094_104864919 | HACE1 | ATGGA others(2722): Show |
chr6 | 104723094 | 104864919 | ||
| a0001c0003 | 0/0 | 2727 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | ATGGA others(2722): Show |
chr6 | 104723094 | 104864919 | ||
| a0001c0004 | 0/0 | 2727 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | ATGGA others(2722): Show |
chr6 | 104723094 | 104864919 | ||
| a0001c0005 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | ATGGA others(2722): Show |
chr6 | 104723094 | 104864919 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4575 | 205 | 34 | 37 | 105 | 5 | 23 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0001t0002 | 0/0 | 4575 | 71 | 11 | 11 | 43 | 2 | 4 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0001t0003 | 0/0 | 4575 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0001t0004 | 0/0 | 4575 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0001t0005 | 0/0 | 4575 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0001t0006 | 0/0 | 4575 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0001t0007 | 0/0 | 4575 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0002t0001 | 0/1 | 4575 | 59 | 32 | 12 | 1 | 6 | 7 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0002t0008 | 0/0 | 4575 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0003t0001 | 0/0 | 4575 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0004t0001 | 0/0 | 4575 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| a0001c0005t0001 | 0/0 | 4575 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | AGAAG others(4570): Show |
chr6 | 104723094 | 104864919 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0005t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | GBR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0274 | EUR | GBR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0123 | EUR | FIN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0096 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0338 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0126 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0339 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0127 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CDX | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CDX | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0073 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0139 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0143 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0337 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CHB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18954 | hp2 | a0001 | c0005 | t0001 | g0314 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | LWK | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | ASW | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ASW | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | TSI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0129 | EUR | TSI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0326 | EUR | TSI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0128 | EUR | TSI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02109 | hp2 | a0001 | c0002 | t0008 | g0340 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | USA | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0224 | AFR | USA | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | LWK | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0130 | REF | REF | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0116 | REF | REF | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:104750392 | A | G | 1 | a0001c0002 | 59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
synonymous_variant | LOW | c.2292T>C | p.Phe764Phe | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/24 | 2569/4575 | 2292/2730 | 764/909 | chr6 | 104750392 | |||
| chr6:104750449 | A | T | 1 | a0001c0003 | 2 | HG03195.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.2235T>A | p.Thr745Thr | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/24 | 2512/4575 | 2235/2730 | 745/909 | chr6 | 104750449 | |||
| chr6:104796938 | T | C | 1 | a0001c0004 | 2 | HG03130.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.705A>G | p.Leu235Leu | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 8/24 | 982/4575 | 705/2730 | 235/909 | chr6 | 104796938 | |||
| chr6:104833054 | G | A | 1 | a0001c0005 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.522C>T | p.Asn174Asn | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/24 | 799/4575 | 522/2730 | 174/909 | chr6 | 104833054 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:104728121 | C | T | 1 | a0001c0001t0005 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 1541 | chr6 | 104728121 | ||||||
| chr6:104728134 | C | T | 1 | a0001c0001t0004 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1528G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 1528 | chr6 | 104728134 | ||||||
| chr6:104728525 | A | C | 1 | a0001c0001t0004 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1137T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 1137 | chr6 | 104728525 | ||||||
| chr6:104728653 | G | A | 3 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1009C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 1009 | chr6 | 104728653 | ||||||
| chr6:104728787 | T | A | 1 | a0001c0001t0006 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 875 | chr6 | 104728787 | ||||||
| chr6:104728900 | T | C | 1 | a0001c0001t0007 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*762A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 762 | chr6 | 104728900 | ||||||
| chr6:104729579 | C | T | 1 | a0001c0001t0003 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*83G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 83 | chr6 | 104729579 | ||||||
| chr6:104859687 | G | C | 1 | a0001c0002t0008 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-45C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/24 | 45 | chr6 | 104859687 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:104729841 | C | T | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2628-77G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 23/23 | chr6 | 104729841 | |||||||
| chr6:104730521 | A | C | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2514-105T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730521 | |||||||
| chr6:104730664 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2514-248G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730664 | |||||||
| chr6:104730773 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2514-357G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730773 | |||||||
| chr6:104730804 | A | G | 1 | a0001c0002t0001g0132 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2514-388T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730804 | |||||||
| chr6:104730825 | T | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2514-409A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730825 | |||||||
| chr6:104731198 | CA | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2514-783delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731198 | |||||||
| chr6:104731348 | G | A | 2 | a0001c0002t0001g0095 a0001c0002t0001g0096 |
2 | HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2514-932C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731348 | |||||||
| chr6:104731371 | T | C | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2514-955A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731371 | |||||||
| chr6:104731446 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2514-1030G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731446 | |||||||
| chr6:104731471 | T | A | 1 | a0001c0003t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2514-1055A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731471 | |||||||
| chr6:104731654 | G | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2514-1238C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731654 | |||||||
| chr6:104731742 | C | G | 154 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(151): Show |
157 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2514-1326G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731742 | |||||||
| chr6:104731751 | A | G | 227 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2514-1335T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731751 | |||||||
| chr6:104731794 | A | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2514-1378T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731794 | |||||||
| chr6:104731869 | G | GA | 17 | a0001c0001t0001g0277 a0001c0002t0001g0003 a0001c0002t0001g0004 others(14): Show |
19 | HG01516.hp1 HG01517.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2514-1454dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731869 | |||||||
| chr6:104731869 | G | GAA | 39 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(36): Show |
39 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2514-1455_2514-145 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731869 | |||||||
| chr6:104731869 | G | GGA | 3 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 |
4 | HG02572.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2514-1454_2514-145 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731869 | |||||||
| chr6:104731869 | GA | G | 95 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2514-1454delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731869 | |||||||
| chr6:104731883 | T | A | 6 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(3): Show |
6 | HG00735.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2514-1467A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731883 | |||||||
| chr6:104731888 | A | G | 6 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(3): Show |
6 | HG00735.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2514-1472T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731888 | |||||||
| chr6:104731973 | A | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2514-1557T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731973 | |||||||
| chr6:104731975 | A | G | 94 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(91): Show |
94 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2514-1559T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731975 | |||||||
| chr6:104732269 | C | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2514-1853G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732269 | |||||||
| chr6:104732280 | A | G | 8 | a0001c0001t0002g0012 a0001c0001t0002g0041 a0001c0001t0002g0043 others(5): Show |
8 | HG00099.hp1 HG01928.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2514-1864T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732280 | |||||||
| chr6:104732546 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2514-2130C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732546 | |||||||
| chr6:104732706 | T | TAC | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2514-2292_2514-229 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732706 | |||||||
| chr6:104732763 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2514-2347C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732763 | |||||||
| chr6:104732768 | G | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2514-2352C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732768 | |||||||
| chr6:104732771 | T | C | 2 | a0001c0002t0001g0095 a0001c0002t0001g0096 |
2 | HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2514-2355A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732771 | |||||||
| chr6:104732910 | C | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(148): Show |
154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2514-2494G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732910 | |||||||
| chr6:104732945 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2514-2529G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732945 | |||||||
| chr6:104732965 | A | G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2514-2549T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732965 | |||||||
| chr6:104733018 | G | A | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2514-2602C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733018 | |||||||
| chr6:104733134 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2514-2718C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733134 | |||||||
| chr6:104733215 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2514-2799G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733215 | |||||||
| chr6:104733245 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2514-2829A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733245 | |||||||
| chr6:104733308 | TAAC | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2514-2895_2514-289 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733308 | |||||||
| chr6:104733581 | G | A | 3 | a0001c0001t0001g0318 a0001c0003t0001g0224 a0001c0003t0001g0225 |
3 | HG03195.hp2 NA18962.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2514-3165C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733581 | |||||||
| chr6:104733712 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2514-3296T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733712 | |||||||
| chr6:104733732 | T | C | 2 | a0001c0002t0001g0081 a0001c0002t0001g0082 |
2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2514-3316A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733732 | |||||||
| chr6:104733800 | C | T | 9 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0095 others(6): Show |
9 | HG01515.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2514-3384G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733800 | |||||||
| chr6:104733827 | A | C | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2514-3411T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733827 | |||||||
| chr6:104733838 | C | CAA | 147 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(144): Show |
150 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.2514-3424_2514-342 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733838 | |||||||
| chr6:104734012 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2514-3596G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734012 | |||||||
| chr6:104734113 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2514-3697T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734113 | |||||||
| chr6:104734142 | C | CA | 216 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(213): Show |
220 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.2514-3727dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734142 | |||||||
| chr6:104734142 | C | CAA | 11 | a0001c0001t0001g0140 a0001c0001t0001g0144 a0001c0001t0001g0145 others(8): Show |
12 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2514-3728_2514-372 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734142 | |||||||
| chr6:104734315 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2514-3899T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734315 | |||||||
| chr6:104734338 | ATTATACT others(8): Show |
A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2514-3937_2514-392 others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734338 | |||||||
| chr6:104734613 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2514-4197C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734613 | |||||||
| chr6:104734769 | G | T | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2514-4353C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734769 | |||||||
| chr6:104734800 | C | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2514-4384G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734800 | |||||||
| chr6:104734842 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2514-4426G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734842 | |||||||
| chr6:104734964 | T | C | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2514-4548A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734964 | |||||||
| chr6:104734973 | G | C | 6 | a0001c0001t0001g0264 a0001c0001t0001g0310 a0001c0001t0001g0312 others(3): Show |
6 | HG00408.hp2 HG02155.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.2514-4557C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734973 | |||||||
| chr6:104735014 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(46): Show |
50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.2514-4598T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735014 | |||||||
| chr6:104735015 | T | C | 91 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(88): Show |
91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2514-4599A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735015 | |||||||
| chr6:104735100 | C | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2514-4684G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735100 | |||||||
| chr6:104735116 | G | C | 1 | a0001c0001t0002g0011 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2514-4700C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735116 | |||||||
| chr6:104735290 | G | A | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2514-4874C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735290 | |||||||
| chr6:104735367 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2514-4951C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735367 | |||||||
| chr6:104735377 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2514-4961T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735377 | |||||||
| chr6:104735398 | C | T | 91 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(88): Show |
91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2514-4982G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735398 | |||||||
| chr6:104735461 | C | T | 162 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(159): Show |
165 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.2514-5045G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735461 | |||||||
| chr6:104735499 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2514-5083G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735499 | |||||||
| chr6:104735563 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2514-5147C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735563 | |||||||
| chr6:104735608 | A | G | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2514-5192T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735608 | |||||||
| chr6:104735638 | A | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2514-5222T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735638 | |||||||
| chr6:104735689 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2514-5273G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735689 | |||||||
| chr6:104735734 | A | G | 91 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(88): Show |
91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2514-5318T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735734 | |||||||
| chr6:104735883 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0297 |
2 | HG01255.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2514-5467C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735883 | |||||||
| chr6:104736084 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2514-5668A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736084 | |||||||
| chr6:104736377 | C | A | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2514-5961G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736377 | |||||||
| chr6:104736472 | C | G | 1 | a0001c0002t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2514-6056G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736472 | |||||||
| chr6:104736492 | G | A | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2514-6076C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736492 | |||||||
| chr6:104736600 | C | G | 1 | a0001c0001t0001g0245 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2514-6184G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736600 | |||||||
| chr6:104736765 | T | G | 151 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(148): Show |
154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2514-6349A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736765 | |||||||
| chr6:104736766 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2514-6350A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736766 | |||||||
| chr6:104737041 | T | C | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2514-6625A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737041 | |||||||
| chr6:104737063 | C | T | 3 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2514-6647G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737063 | |||||||
| chr6:104737121 | TA | T | 150 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(147): Show |
153 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.2514-6706delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737121 | |||||||
| chr6:104737219 | G | C | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2514-6803C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737219 | |||||||
| chr6:104737237 | C | T | 91 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(88): Show |
91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2514-6821G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737237 | |||||||
| chr6:104737275 | T | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0289 a0001c0001t0001g0291 |
3 | HG02698.hp1 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2514-6859A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737275 | |||||||
| chr6:104737280 | C | CAA | 3 | a0001c0001t0001g0137 a0001c0003t0001g0224 a0001c0003t0001g0225 |
3 | HG03139.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2514-6865_2514-686 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737280 | |||||||
| chr6:104737280 | C | CAAAAA | 3 | a0001c0001t0001g0145 a0001c0004t0001g0139 a0001c0004t0001g0143 |
3 | HG03130.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2514-6865_2514-686 others(9): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737280 | |||||||
| chr6:104737281 | T | A | 9 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
9 | HG02055.hp1 HG02965.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.2514-6865A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737281 | |||||||
| chr6:104737282 | C | A | 9 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
9 | HG02055.hp1 HG02965.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.2514-6866G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | |||||||
| chr6:104737282 | C | CA | 27 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0234 others(24): Show |
27 | HG00438.hp1 HG00597.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.2514-6867dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | |||||||
| chr6:104737282 | C | CAA | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2514-6868_2514-686 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | |||||||
| chr6:104737282 | C | CAAA | 21 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0016 others(18): Show |
21 | HG00597.hp2 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.2514-6869_2514-686 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | |||||||
| chr6:104737282 | CA | C | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
80 | HG00609.hp2 HG00621.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.2514-6867delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | |||||||
| chr6:104737282 | CAA | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0172 a0001c0001t0001g0177 others(4): Show |
7 | HG01516.hp2 HG02056.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2514-6868_2514-686 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | |||||||
| chr6:104737282 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2513+6863_2514-686 others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | |||||||
| chr6:104737297 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2513+6863T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737297 | |||||||
| chr6:104737305 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2513+6855T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737305 | |||||||
| chr6:104737353 | G | A | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+6807C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737353 | |||||||
| chr6:104737409 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2513+6751A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737409 | |||||||
| chr6:104737476 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2513+6684C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737476 | |||||||
| chr6:104737546 | T | C | 225 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(222): Show |
230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2513+6614A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737546 | |||||||
| chr6:104737601 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2513+6559C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737601 | |||||||
| chr6:104737618 | G | A | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2513+6542C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737618 | |||||||
| chr6:104737667 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2513+6493G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737667 | |||||||
| chr6:104737675 | C | G | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2513+6485G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737675 | |||||||
| chr6:104737679 | C | CG | 3 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0057 |
3 | HG02809.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2513+6480_2513+648 others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737679 | |||||||
| chr6:104737693 | G | A | 68 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(65): Show |
70 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2513+6467C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737693 | |||||||
| chr6:104737710 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2513+6450G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737710 | |||||||
| chr6:104737716 | G | A | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2513+6444C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737716 | |||||||
| chr6:104737734 | A | G | 1 | a0001c0001t0002g0052 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2513+6426T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737734 | |||||||
| chr6:104737740 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2513+6420C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737740 | |||||||
| chr6:104737745 | T | C | 1 | a0001c0001t0002g0052 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2513+6415A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737745 | |||||||
| chr6:104737797 | G | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0281 |
2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2513+6363C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737797 | |||||||
| chr6:104737805 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0281 |
2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2513+6355G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737805 | |||||||
| chr6:104737806 | C | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0281 |
2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2513+6354G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737806 | |||||||
| chr6:104737817 | G | T | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2513+6343C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737817 | |||||||
| chr6:104737932 | C | G | 152 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(149): Show |
155 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.2513+6228G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737932 | |||||||
| chr6:104737976 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2513+6184C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737976 | |||||||
| chr6:104737981 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2513+6179C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737981 | |||||||
| chr6:104737996 | G | GCCT | 3 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0166 |
3 | HG00609.hp2 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2513+6161_2513+616 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737996 | |||||||
| chr6:104738080 | T | C | 8 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(5): Show |
10 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2513+6080A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738080 | |||||||
| chr6:104738092 | C | A | 1 | a0001c0002t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2513+6068G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738092 | |||||||
| chr6:104738153 | CA | C | 6 | a0001c0002t0001g0090 a0001c0002t0001g0104 a0001c0002t0001g0105 others(3): Show |
6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2513+6006delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738153 | |||||||
| chr6:104738194 | T | C | 2 | a0001c0001t0002g0055 a0001c0001t0004g0036 |
2 | NA18941.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2513+5966A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738194 | |||||||
| chr6:104738213 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2513+5947C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738213 | |||||||
| chr6:104738215 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2513+5945C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738215 | |||||||
| chr6:104738238 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2513+5922C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738238 | |||||||
| chr6:104738258 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2513+5902A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738258 | |||||||
| chr6:104738330 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2513+5830A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738330 | |||||||
| chr6:104738355 | C | T | 3 | a0001c0002t0001g0004 a0001c0002t0001g0077 a0001c0002t0001g0078 |
4 | HG02622.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2513+5805G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738355 | |||||||
| chr6:104738512 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2513+5648C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738512 | |||||||
| chr6:104738551 | A | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(148): Show |
154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2513+5609T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738551 | |||||||
| chr6:104738569 | C | T | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+5591G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738569 | |||||||
| chr6:104738610 | T | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2513+5550A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738610 | |||||||
| chr6:104738637 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2513+5523C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738637 | |||||||
| chr6:104738713 | G | C | 1 | a0001c0001t0001g0277 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2513+5447C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738713 | |||||||
| chr6:104738773 | G | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2513+5387C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738773 | |||||||
| chr6:104738860 | T | C | 1 | a0001c0001t0001g0304 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2513+5300A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738860 | |||||||
| chr6:104738963 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2513+5197C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738963 | |||||||
| chr6:104738995 | A | G | 227 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(224): Show |
232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2513+5165T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738995 | |||||||
| chr6:104738999 | G | C | 1 | a0001c0002t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2513+5161C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738999 | |||||||
| chr6:104739168 | G | A | 7 | a0001c0001t0001g0253 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
7 | HG03669.hp2 NA18943.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.2513+4992C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739168 | |||||||
| chr6:104739190 | T | C | 4 | a0001c0001t0001g0210 a0001c0001t0001g0276 a0001c0001t0001g0284 others(1): Show |
4 | HG00099.hp2 HG00735.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513+4970A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739190 | |||||||
| chr6:104739262 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2513+4898G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739262 | |||||||
| chr6:104739289 | C | G | 1 | a0001c0001t0005g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2513+4871G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739289 | |||||||
| chr6:104739429 | G | A | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2513+4731C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739429 | |||||||
| chr6:104739450 | C | T | 1 | a0001c0001t0002g0009 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2513+4710G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739450 | |||||||
| chr6:104739474 | C | T | 91 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(88): Show |
91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2513+4686G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739474 | |||||||
| chr6:104739531 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513+4629T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739531 | |||||||
| chr6:104739563 | A | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0245 |
2 | HG02027.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2513+4597T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739563 | |||||||
| chr6:104739586 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0313 |
2 | HG01106.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2513+4574T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739586 | |||||||
| chr6:104739644 | C | G | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513+4516G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739644 | |||||||
| chr6:104739741 | A | C | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2513+4419T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739741 | |||||||
| chr6:104739771 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2513+4389G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739771 | |||||||
| chr6:104739804 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2513+4356C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739804 | |||||||
| chr6:104739997 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2513+4163G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739997 | |||||||
| chr6:104740118 | A | G | 3 | a0001c0002t0001g0080 a0001c0002t0001g0113 a0001c0002t0001g0114 |
3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2513+4042T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740118 | |||||||
| chr6:104740119 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2513+4041A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740119 | |||||||
| chr6:104740155 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2513+4005A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740155 | |||||||
| chr6:104740185 | T | TATAGCAC | 5 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(2): Show |
7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2513+3968_2513+397 others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740185 | |||||||
| chr6:104740255 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2513+3905C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740255 | |||||||
| chr6:104740380 | G | C | 49 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(46): Show |
49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.2513+3780C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740380 | |||||||
| chr6:104740383 | G | T | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2513+3777C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740383 | |||||||
| chr6:104740416 | G | A | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+3744C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740416 | |||||||
| chr6:104740607 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2513+3553A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740607 | |||||||
| chr6:104740628 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2513+3532T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740628 | |||||||
| chr6:104740678 | A | T | 24 | a0001c0001t0001g0140 a0001c0001t0001g0148 a0001c0001t0001g0149 others(21): Show |
24 | HG00621.hp2 HG02055.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.2513+3482T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740678 | |||||||
| chr6:104740714 | C | T | 92 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(89): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+3446G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740714 | |||||||
| chr6:104740855 | A | C | 92 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(89): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+3305T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740855 | |||||||
| chr6:104740928 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2513+3232G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740928 | |||||||
| chr6:104741009 | C | T | 24 | a0001c0001t0001g0140 a0001c0001t0001g0148 a0001c0001t0001g0149 others(21): Show |
24 | HG00621.hp2 HG02055.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.2513+3151G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741009 | |||||||
| chr6:104741016 | C | A | 24 | a0001c0001t0001g0140 a0001c0001t0001g0148 a0001c0001t0001g0149 others(21): Show |
24 | HG00621.hp2 HG02055.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.2513+3144G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741016 | |||||||
| chr6:104741110 | A | AC | 225 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(222): Show |
230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2513+3049dupG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741110 | |||||||
| chr6:104741129 | C | T | 225 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(222): Show |
230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2513+3031G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741129 | |||||||
| chr6:104741222 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2513+2938A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741222 | |||||||
| chr6:104741245 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2513+2915C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741245 | |||||||
| chr6:104741260 | C | T | 224 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2513+2900G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741260 | |||||||
| chr6:104741263 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513+2897G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741263 | |||||||
| chr6:104741316 | T | C | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2513+2844A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741316 | |||||||
| chr6:104741484 | G | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2513+2676C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741484 | |||||||
| chr6:104741519 | GACAA | G | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+2637_2513+264 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741519 | |||||||
| chr6:104741588 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2513+2572C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741588 | |||||||
| chr6:104741695 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2513+2465A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741695 | |||||||
| chr6:104741780 | T | C | 92 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(89): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+2380A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741780 | |||||||
| chr6:104741807 | CTACTT | C | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+2348_2513+235 others(9): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741807 | |||||||
| chr6:104741860 | T | C | 333 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(330): Show |
339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.2513+2300A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741860 | |||||||
| chr6:104741895 | A | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2513+2265T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741895 | |||||||
| chr6:104741913 | C | T | 1 | a0001c0003t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2513+2247G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741913 | |||||||
| chr6:104741914 | G | T | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2513+2246C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741914 | |||||||
| chr6:104742002 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0300 a0001c0001t0001g0330 |
3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2513+2158G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742002 | |||||||
| chr6:104742008 | G | A | 91 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(88): Show |
91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2513+2152C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742008 | |||||||
| chr6:104742035 | A | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513+2125T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742035 | |||||||
| chr6:104742111 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2513+2049A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742111 | |||||||
| chr6:104742130 | C | G | 1 | a0001c0001t0001g0249 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2513+2030G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742130 | |||||||
| chr6:104742131 | T | C | 92 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(89): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+2029A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742131 | |||||||
| chr6:104742161 | C | G | 95 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(92): Show |
96 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.2513+1999G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742161 | |||||||
| chr6:104742207 | A | C | 152 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(149): Show |
155 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.2513+1953T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742207 | |||||||
| chr6:104742380 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2513+1780G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742380 | |||||||
| chr6:104742421 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0245 |
2 | HG02027.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2513+1739C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742421 | |||||||
| chr6:104742441 | G | C | 1 | a0001c0001t0001g0194 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2513+1719C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742441 | |||||||
| chr6:104742460 | T | G | 150 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(147): Show |
153 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.2513+1700A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742460 | |||||||
| chr6:104742617 | G | A | 152 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(149): Show |
155 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.2513+1543C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742617 | |||||||
| chr6:104742638 | C | T | 3 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2513+1522G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742638 | |||||||
| chr6:104742655 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2513+1505C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742655 | |||||||
| chr6:104742689 | C | T | 3 | a0001c0001t0001g0170 a0001c0003t0001g0224 a0001c0003t0001g0225 |
3 | HG02738.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2513+1471G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742689 | |||||||
| chr6:104742711 | G | C | 2 | a0001c0003t0001g0224 a0001c0003t0001g0225 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2513+1449C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742711 | |||||||
| chr6:104742740 | G | T | 92 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(89): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+1420C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742740 | |||||||
| chr6:104742872 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2513+1288A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742872 | |||||||
| chr6:104742980 | C | A | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2513+1180G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742980 | |||||||
| chr6:104743009 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2513+1151C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743009 | |||||||
| chr6:104743035 | C | G | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2513+1125G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743035 | |||||||
| chr6:104743052 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2513+1108A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743052 | |||||||
| chr6:104743056 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2513+1104C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743056 | |||||||
| chr6:104743098 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513+1062A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743098 | |||||||
| chr6:104743176 | G | C | 17 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(14): Show |
17 | HG00621.hp2 HG02055.hp1 HG02965.hp2 others(14): Show |
intron_variant | MODIFIER | c.2513+984C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743176 | |||||||
| chr6:104743184 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2513+976C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743184 | |||||||
| chr6:104743191 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513+969A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743191 | |||||||
| chr6:104743197 | G | T | 5 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(2): Show |
7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2513+963C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743197 | |||||||
| chr6:104743306 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2513+854C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743306 | |||||||
| chr6:104743315 | T | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2513+845A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743315 | |||||||
| chr6:104743315 | TA | T | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+844delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743315 | |||||||
| chr6:104743402 | A | G | 2 | a0001c0002t0001g0095 a0001c0002t0001g0096 |
2 | HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2513+758T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743402 | |||||||
| chr6:104743512 | C | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2513+648G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743512 | |||||||
| chr6:104743629 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0330 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2513+531T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743629 | |||||||
| chr6:104743652 | C | T | 92 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(89): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+508G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743652 | |||||||
| chr6:104743822 | CAAATATT others(1): Show |
C | 59 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(56): Show |
62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.2513+330_2513+337d others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743822 | |||||||
| chr6:104743830 | A | AAAATAAT others(4): Show |
1 | a0001c0002t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2513+329_2513+330i others(13): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743830 | |||||||
| chr6:104743836 | TTAAAA | T | 92 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(89): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+319_2513+323d others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743836 | |||||||
| chr6:104743939 | C | T | 152 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(149): Show |
155 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.2513+221G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743939 | |||||||
| chr6:104744134 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2513+26G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104744134 | |||||||
| chr6:104744140 | A | T | 1 | a0001c0003t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2513+20T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104744140 | |||||||
| chr6:104744232 | TAAC | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
splice_region_variant&intron_variant | LOW | c.2443-5_2443-3delGT others(1): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 21/23 | chr6 | 104744232 | |||||||
| chr6:104744260 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2443-30A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 21/23 | chr6 | 104744260 | |||||||
| chr6:104744365 | G | C | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2443-135C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 21/23 | chr6 | 104744365 | |||||||
| chr6:104744815 | A | G | 1 | a0001c0002t0001g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2344-205T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104744815 | |||||||
| chr6:104744942 | T | C | 1 | a0001c0002t0001g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2344-332A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104744942 | |||||||
| chr6:104745103 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2344-493G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745103 | |||||||
| chr6:104745104 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2344-494C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745104 | |||||||
| chr6:104745138 | C | A | 2 | a0001c0002t0001g0080 a0001c0002t0001g0113 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2344-528G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745138 | |||||||
| chr6:104745433 | T | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2344-823A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745433 | |||||||
| chr6:104745455 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0156 a0001c0001t0001g0190 |
2 | HG02015.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2344-846_2344-845i others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745455 | |||||||
| chr6:104745455 | C | CTTTTTTT others(4): Show |
102 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(99): Show |
105 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.2344-846_2344-845i others(13): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745455 | |||||||
| chr6:104745455 | C | CTTTTTTT others(5): Show |
106 | a0001c0001t0001g0135 a0001c0001t0001g0144 a0001c0001t0001g0145 others(103): Show |
108 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2344-846_2344-845i others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745455 | |||||||
| chr6:104745455 | C | CTTTTTTT others(6): Show |
14 | a0001c0001t0002g0014 a0001c0001t0002g0034 a0001c0001t0002g0063 others(11): Show |
14 | HG01515.hp1 HG01952.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.2344-846_2344-845i others(15): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745455 | |||||||
| chr6:104745541 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2344-931G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745541 | |||||||
| chr6:104745768 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2344-1158C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745768 | |||||||
| chr6:104745966 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2344-1356T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745966 | |||||||
| chr6:104746014 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2344-1404A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746014 | |||||||
| chr6:104746078 | A | G | 6 | a0001c0002t0001g0090 a0001c0002t0001g0104 a0001c0002t0001g0105 others(3): Show |
6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2344-1468T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746078 | |||||||
| chr6:104746158 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2344-1548A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746158 | |||||||
| chr6:104746196 | G | A | 11 | a0001c0002t0001g0090 a0001c0002t0001g0091 a0001c0002t0001g0092 others(8): Show |
11 | HG01515.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2344-1586C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746196 | |||||||
| chr6:104746303 | G | T | 57 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2344-1693C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746303 | |||||||
| chr6:104746638 | A | C | 1 | a0001c0002t0001g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2344-2028T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746638 | |||||||
| chr6:104746776 | A | G | 150 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(147): Show |
153 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.2344-2166T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746776 | |||||||
| chr6:104746905 | T | G | 47 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(44): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.2344-2295A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746905 | |||||||
| chr6:104746911 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2344-2301T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746911 | |||||||
| chr6:104747130 | T | C | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2344-2520A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747130 | |||||||
| chr6:104747369 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2344-2759G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747369 | |||||||
| chr6:104747396 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2344-2786G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747396 | |||||||
| chr6:104747516 | G | A | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | NA18962.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2343+2825C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747516 | |||||||
| chr6:104747528 | G | A | 41 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(38): Show |
41 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.2343+2813C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747528 | |||||||
| chr6:104747662 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2343+2679G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747662 | |||||||
| chr6:104747700 | T | C | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2343+2641A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747700 | |||||||
| chr6:104747716 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2343+2625T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747716 | |||||||
| chr6:104747732 | T | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2343+2609A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747732 | |||||||
| chr6:104747792 | C | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2343+2549G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747792 | |||||||
| chr6:104747838 | G | C | 1 | a0001c0001t0007g0274 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2343+2503C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747838 | |||||||
| chr6:104748248 | G | GA | 150 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(147): Show |
153 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.2343+2092dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748248 | |||||||
| chr6:104748284 | T | C | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2343+2057A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748284 | |||||||
| chr6:104748482 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2343+1859C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748482 | |||||||
| chr6:104748761 | T | C | 1 | a0001c0002t0001g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2343+1580A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748761 | |||||||
| chr6:104748908 | C | G | 91 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(88): Show |
91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2343+1433G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748908 | |||||||
| chr6:104749096 | A | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2343+1245T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749096 | |||||||
| chr6:104749119 | T | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2343+1222A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749119 | |||||||
| chr6:104749126 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2343+1215G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749126 | |||||||
| chr6:104749216 | G | T | 150 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(147): Show |
153 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.2343+1125C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749216 | |||||||
| chr6:104749349 | C | G | 1 | a0001c0001t0001g0275 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2343+992G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749349 | |||||||
| chr6:104749410 | A | G | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2343+931T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749410 | |||||||
| chr6:104749430 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2343+911T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749430 | |||||||
| chr6:104749549 | C | T | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2343+792G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749549 | |||||||
| chr6:104749866 | T | C | 1 | a0001c0001t0001g0320 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2343+475A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749866 | |||||||
| chr6:104749991 | C | T | 6 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0238 others(3): Show |
6 | HG00609.hp1 HG02027.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.2343+350G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749991 | |||||||
| chr6:104749999 | A | G | 150 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(147): Show |
153 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.2343+342T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749999 | |||||||
| chr6:104750084 | G | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(57): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2343+257C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750084 | |||||||
| chr6:104750195 | C | T | 57 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2343+146G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750195 | |||||||
| chr6:104750220 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2343+121G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750220 | |||||||
| chr6:104750238 | AC | A | 57 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2343+102delG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750238 | |||||||
| chr6:104750249 | T | G | 57 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2343+92A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750249 | |||||||
| chr6:104750290 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+51A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750290 | |||||||
| chr6:104750291 | A | T | 1 | a0001c0001t0002g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+50T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750291 | |||||||
| chr6:104750292 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+49C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750292 | |||||||
| chr6:104750303 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+38A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750303 | |||||||
| chr6:104750304 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+37C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750304 | |||||||
| chr6:104750305 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+36A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750305 | |||||||
| chr6:104750308 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+33A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750308 | |||||||
| chr6:104750309 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+32C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750309 | |||||||
| chr6:104750316 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2343+25G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750316 | |||||||
| chr6:104750535 | T | G | 1 | a0001c0001t0002g0028 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2212-63A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750535 | |||||||
| chr6:104750721 | T | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-249A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750721 | |||||||
| chr6:104750733 | C | T | 57 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2212-261G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750733 | |||||||
| chr6:104750819 | T | G | 1 | a0001c0001t0001g0288 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2212-347A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750819 | |||||||
| chr6:104750838 | C | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0212 |
2 | NA18987.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2212-366G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750838 | |||||||
| chr6:104750879 | T | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0284 a0001c0001t0007g0274 |
3 | HG00099.hp2 HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2212-407A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750879 | |||||||
| chr6:104750943 | G | A | 57 | a0001c0001t0001g0298 a0001c0002t0001g0003 a0001c0002t0001g0004 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.2212-471C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750943 | |||||||
| chr6:104750943 | G | C | 1 | a0001c0002t0001g0094 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2212-471C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750943 | |||||||
| chr6:104750963 | C | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00621.hp1 HG02015.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.2212-491G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750963 | |||||||
| chr6:104751031 | A | G | 1 | a0001c0002t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2212-559T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751031 | |||||||
| chr6:104751076 | C | A | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2212-604G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751076 | |||||||
| chr6:104751198 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2212-726G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751198 | |||||||
| chr6:104751520 | T | C | 6 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00544.hp1 HG02165.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.2212-1048A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751520 | |||||||
| chr6:104751640 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2212-1168T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751640 | |||||||
| chr6:104751743 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-1271A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751743 | |||||||
| chr6:104751809 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2212-1337A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751809 | |||||||
| chr6:104751896 | TC | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-1425delG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751896 | |||||||
| chr6:104751897 | C | T | 57 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2212-1425G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751897 | |||||||
| chr6:104751916 | G | C | 53 | a0001c0001t0001g0138 a0001c0001t0001g0158 a0001c0001t0001g0159 others(50): Show |
53 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.2212-1444C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751916 | |||||||
| chr6:104751955 | C | CA | 72 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(69): Show |
74 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2212-1484dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751955 | |||||||
| chr6:104751955 | C | CAAA | 77 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0138 others(74): Show |
77 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.2212-1486_2212-148 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751955 | |||||||
| chr6:104751955 | C | CAAAA | 14 | a0001c0001t0001g0005 a0001c0001t0001g0137 a0001c0001t0001g0144 others(11): Show |
15 | HG02896.hp2 HG02897.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.2212-1487_2212-148 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751955 | |||||||
| chr6:104752131 | G | A | 1 | a0001c0001t0003g0136 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2212-1659C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752131 | |||||||
| chr6:104752241 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2212-1769G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752241 | |||||||
| chr6:104752248 | T | C | 1 | a0001c0001t0005g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2212-1776A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752248 | |||||||
| chr6:104752272 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2212-1800A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752272 | |||||||
| chr6:104752325 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-1853C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752325 | |||||||
| chr6:104752425 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-1953A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752425 | |||||||
| chr6:104752732 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2212-2260T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752732 | |||||||
| chr6:104752785 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2212-2313G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752785 | |||||||
| chr6:104752821 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 |
3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2212-2349A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752821 | |||||||
| chr6:104753226 | C | T | 57 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2212-2754G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753226 | |||||||
| chr6:104753256 | G | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-2784C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753256 | |||||||
| chr6:104753278 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2212-2806C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753278 | |||||||
| chr6:104753372 | G | A | 73 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2212-2900C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753372 | |||||||
| chr6:104753414 | C | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-2942G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753414 | |||||||
| chr6:104753479 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2212-3007C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753479 | |||||||
| chr6:104753512 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2212-3040G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753512 | |||||||
| chr6:104753594 | T | A | 1 | a0001c0001t0001g0005 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2212-3122A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753594 | |||||||
| chr6:104753694 | C | G | 164 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(161): Show |
167 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.2212-3222G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753694 | |||||||
| chr6:104753892 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2212-3420C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753892 | |||||||
| chr6:104754153 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2212-3681G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754153 | |||||||
| chr6:104754168 | A | ACTAT | 59 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(56): Show |
61 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.2212-3697_2212-369 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754168 | |||||||
| chr6:104754316 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2212-3844A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754316 | |||||||
| chr6:104754338 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0315 |
3 | HG02132.hp2 HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2212-3866A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754338 | |||||||
| chr6:104754392 | A | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-3920T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754392 | |||||||
| chr6:104754851 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2212-4379T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754851 | |||||||
| chr6:104754994 | A | G | 40 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(37): Show |
42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.2212-4522T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754994 | |||||||
| chr6:104755067 | G | T | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2212-4595C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755067 | |||||||
| chr6:104755258 | T | C | 59 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(56): Show |
61 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.2212-4786A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755258 | |||||||
| chr6:104755290 | G | C | 51 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(48): Show |
51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2212-4818C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755290 | |||||||
| chr6:104755312 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2212-4840G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755312 | |||||||
| chr6:104755899 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-5427T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755899 | |||||||
| chr6:104756140 | C | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-5668G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756140 | |||||||
| chr6:104756150 | T | C | 7 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0001g0124 others(4): Show |
7 | HG01167.hp2 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.2212-5678A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756150 | |||||||
| chr6:104756237 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-5765C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756237 | |||||||
| chr6:104756246 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2212-5774T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756246 | |||||||
| chr6:104756384 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2212-5912G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756384 | |||||||
| chr6:104756397 | G | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-5925C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756397 | |||||||
| chr6:104756398 | C | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2212-5926G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756398 | |||||||
| chr6:104756404 | T | G | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2212-5932A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756404 | |||||||
| chr6:104756411 | C | CA | 43 | a0001c0001t0001g0184 a0001c0001t0001g0195 a0001c0001t0001g0309 others(40): Show |
43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.2212-5940dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756411 | |||||||
| chr6:104756411 | CA | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0001g0141 others(38): Show |
42 | HG00621.hp2 HG02055.hp1 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.2212-5940delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756411 | |||||||
| chr6:104756421 | AAAAAAAT | A | 9 | a0001c0001t0002g0011 a0001c0001t0002g0031 a0001c0001t0002g0044 others(6): Show |
9 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.2212-5956_2212-595 others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756421 | |||||||
| chr6:104756422 | AAAAAATA others(1): Show |
A | 8 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0014 others(5): Show |
8 | HG01243.hp2 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2212-5958_2212-595 others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756422 | |||||||
| chr6:104756423 | AAAAATAT | A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0032 others(31): Show |
36 | HG00735.hp2 HG01106.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.2212-5958_2212-595 others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756423 | |||||||
| chr6:104756424 | AAAATATA others(1): Show |
A | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0012 others(16): Show |
19 | HG00099.hp1 HG00597.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2212-5960_2212-595 others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756424 | |||||||
| chr6:104756426 | A | AT | 8 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0270 others(5): Show |
8 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2212-5955_2212-595 others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756426 | |||||||
| chr6:104756426 | A | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(18): Show |
22 | HG01168.hp1 HG01891.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.2212-5954T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756426 | |||||||
| chr6:104756427 | AT | A | 51 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0138 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.2212-5956delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756427 | |||||||
| chr6:104756428 | T | A | 47 | a0001c0001t0001g0117 a0001c0001t0001g0193 a0001c0001t0001g0269 others(44): Show |
47 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.2212-5956A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756428 | |||||||
| chr6:104756430 | T | A | 8 | a0001c0001t0001g0147 a0001c0001t0001g0174 a0001c0001t0001g0178 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2212-5958A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756430 | |||||||
| chr6:104756446 | T | C | 58 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0002t0001g0003 others(55): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2212-5974A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756446 | |||||||
| chr6:104756448 | C | T | 1 | a0001c0002t0001g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2212-5976G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756448 | |||||||
| chr6:104756564 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-6092G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756564 | |||||||
| chr6:104756588 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2212-6116C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756588 | |||||||
| chr6:104756623 | G | C | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 |
3 | HG00735.hp2 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2212-6151C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756623 | |||||||
| chr6:104756746 | T | C | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2212-6274A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756746 | |||||||
| chr6:104756897 | G | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-6425C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756897 | |||||||
| chr6:104756998 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2212-6526C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756998 | |||||||
| chr6:104757188 | C | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-6716G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757188 | |||||||
| chr6:104757312 | G | A | 45 | a0001c0001t0001g0137 a0001c0002t0001g0079 a0001c0002t0001g0081 others(42): Show |
45 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.2212-6840C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757312 | |||||||
| chr6:104757637 | A | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0300 a0001c0001t0001g0330 |
3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2212-7165T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757637 | |||||||
| chr6:104757687 | A | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2212-7215T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757687 | |||||||
| chr6:104757804 | G | C | 3 | a0001c0002t0001g0080 a0001c0002t0001g0113 a0001c0002t0001g0114 |
3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2212-7332C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757804 | |||||||
| chr6:104757951 | C | T | 210 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(207): Show |
215 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.2212-7479G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757951 | |||||||
| chr6:104758049 | G | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-7577C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758049 | |||||||
| chr6:104758200 | C | T | 1 | a0001c0002t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2212-7728G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758200 | |||||||
| chr6:104758289 | C | A | 1 | a0001c0001t0001g0253 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2212-7817G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758289 | |||||||
| chr6:104758293 | CAGAG | C | 51 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(48): Show |
51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2212-7825_2212-782 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758293 | |||||||
| chr6:104758314 | C | T | 41 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(38): Show |
41 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.2212-7842G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758314 | |||||||
| chr6:104758445 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2212-7973T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758445 | |||||||
| chr6:104758454 | T | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0015 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2212-7982A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758454 | |||||||
| chr6:104758500 | G | A | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2212-8028C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758500 | |||||||
| chr6:104758544 | A | AG | 51 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(48): Show |
51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2212-8073dupC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758544 | |||||||
| chr6:104758574 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0015 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2212-8102C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758574 | |||||||
| chr6:104758619 | C | T | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2212-8147G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758619 | |||||||
| chr6:104758645 | T | C | 59 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(56): Show |
61 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.2212-8173A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758645 | |||||||
| chr6:104759109 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02027.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2212-8637T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759109 | |||||||
| chr6:104759252 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0137 a0001c0001t0001g0141 others(5): Show |
9 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2212-8780G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759252 | |||||||
| chr6:104759263 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2212-8791T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759263 | |||||||
| chr6:104759433 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-8961C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759433 | |||||||
| chr6:104759568 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2212-9096A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759568 | |||||||
| chr6:104759633 | G | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2212-9161C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759633 | |||||||
| chr6:104759640 | C | A | 4 | a0001c0002t0001g0093 a0001c0002t0001g0094 a0001c0002t0001g0097 others(1): Show |
4 | HG01257.hp1 HG01433.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.2212-9168G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759640 | |||||||
| chr6:104759704 | C | A | 1 | a0001c0001t0001g0005 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2212-9232G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759704 | |||||||
| chr6:104759710 | T | A | 51 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(48): Show |
51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2212-9238A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759710 | |||||||
| chr6:104759798 | A | G | 59 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(56): Show |
61 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.2212-9326T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759798 | |||||||
| chr6:104759818 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2212-9346T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759818 | |||||||
| chr6:104759827 | GAGA | G | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2212-9358_2212-935 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759827 | |||||||
| chr6:104759874 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2212-9402G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759874 | |||||||
| chr6:104759919 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2212-9447T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759919 | |||||||
| chr6:104759956 | G | A | 12 | a0001c0001t0001g0227 a0001c0001t0001g0242 a0001c0001t0001g0246 others(9): Show |
12 | HG00438.hp1 HG00558.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.2212-9484C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759956 | |||||||
| chr6:104759973 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2212-9501G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759973 | |||||||
| chr6:104760074 | A | G | 165 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(162): Show |
168 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2212-9602T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760074 | |||||||
| chr6:104760084 | G | A | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2212-9612C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760084 | |||||||
| chr6:104760101 | C | T | 49 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(46): Show |
49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.2212-9629G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760101 | |||||||
| chr6:104760130 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-9658G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760130 | |||||||
| chr6:104760142 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2212-9670G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760142 | |||||||
| chr6:104760206 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-9734T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760206 | |||||||
| chr6:104760264 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2212-9792T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760264 | |||||||
| chr6:104760275 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2212-9803A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760275 | |||||||
| chr6:104760309 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-9837C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760309 | |||||||
| chr6:104760360 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-9888C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760360 | |||||||
| chr6:104760370 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2212-9898G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760370 | |||||||
| chr6:104760504 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2212-10032G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760504 | |||||||
| chr6:104760524 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2212-10052T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760524 | |||||||
| chr6:104760574 | C | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2212-10102G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760574 | |||||||
| chr6:104760608 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2212-10136G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760608 | |||||||
| chr6:104760613 | A | G | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2212-10141T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760613 | |||||||
| chr6:104760705 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2212-10233C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760705 | |||||||
| chr6:104760828 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2212-10356A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760828 | |||||||
| chr6:104760866 | A | T | 1 | a0001c0002t0001g0096 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2211+10327T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760866 | |||||||
| chr6:104760938 | A | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+10255T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760938 | |||||||
| chr6:104760939 | A | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+10254T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760939 | |||||||
| chr6:104761055 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2211+10138C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761055 | |||||||
| chr6:104761204 | T | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+9989A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761204 | |||||||
| chr6:104761290 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2211+9903A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761290 | |||||||
| chr6:104761553 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0218 |
2 | HG00544.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2211+9640G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761553 | |||||||
| chr6:104761760 | C | T | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2211+9433G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761760 | |||||||
| chr6:104761828 | C | A | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | NA18962.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2211+9365G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761828 | |||||||
| chr6:104761837 | TAAAC | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+9352_2211+935 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761837 | |||||||
| chr6:104762003 | T | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+9190A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762003 | |||||||
| chr6:104762004 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+9189C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762004 | |||||||
| chr6:104762151 | A | G | 1 | a0001c0002t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2211+9042T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762151 | |||||||
| chr6:104762226 | G | A | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2211+8967C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762226 | |||||||
| chr6:104762388 | T | C | 51 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(48): Show |
51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2211+8805A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762388 | |||||||
| chr6:104762491 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2211+8702A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762491 | |||||||
| chr6:104762510 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2211+8683A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762510 | |||||||
| chr6:104762567 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2211+8626C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762567 | |||||||
| chr6:104762584 | G | A | 73 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2211+8609C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762584 | |||||||
| chr6:104762620 | A | G | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+8573T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762620 | |||||||
| chr6:104762637 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0279 a0001c0001t0001g0331 |
3 | HG00733.hp2 HG01175.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2211+8556C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762637 | |||||||
| chr6:104762729 | A | G | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+8464T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762729 | |||||||
| chr6:104762807 | A | G | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+8386T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762807 | |||||||
| chr6:104762888 | G | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0137 a0001c0001t0001g0141 others(5): Show |
9 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2211+8305C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762888 | |||||||
| chr6:104762906 | T | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+8287A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762906 | |||||||
| chr6:104762989 | C | CA | 19 | a0001c0001t0001g0148 a0001c0001t0001g0171 a0001c0001t0001g0276 others(16): Show |
19 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2211+8203dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762989 | |||||||
| chr6:104762989 | CA | C | 8 | a0001c0001t0001g0117 a0001c0001t0001g0241 a0001c0001t0001g0244 others(5): Show |
8 | HG01255.hp1 HG01934.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.2211+8203delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762989 | |||||||
| chr6:104763183 | C | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+8010G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763183 | |||||||
| chr6:104763278 | T | C | 1 | a0001c0002t0001g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2211+7915A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763278 | |||||||
| chr6:104763286 | A | C | 2 | a0001c0001t0001g0282 a0001c0001t0001g0322 |
2 | NA18747.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2211+7907T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763286 | |||||||
| chr6:104763485 | G | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2211+7708C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763485 | |||||||
| chr6:104763706 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211+7487G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763706 | |||||||
| chr6:104763725 | T | C | 59 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(56): Show |
61 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.2211+7468A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763725 | |||||||
| chr6:104763836 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0284 a0001c0001t0007g0274 |
3 | HG00099.hp2 HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2211+7357C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763836 | |||||||
| chr6:104763856 | C | T | 2 | a0001c0002t0001g0102 a0001c0002t0001g0115 |
2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2211+7337G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763856 | |||||||
| chr6:104764062 | A | C | 9 | a0001c0001t0001g0229 a0001c0001t0001g0250 a0001c0001t0001g0304 others(6): Show |
9 | NA18969.hp1 NA19000.hp1 NA19056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2211+7131T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764062 | |||||||
| chr6:104764250 | G | A | 49 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(46): Show |
49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.2211+6943C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764250 | |||||||
| chr6:104764607 | ACTT | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(162): Show |
168 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2211+6583_2211+658 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764607 | |||||||
| chr6:104764706 | T | C | 1 | a0001c0001t0002g0009 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2211+6487A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764706 | |||||||
| chr6:104764941 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2211+6252C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764941 | |||||||
| chr6:104765048 | A | G | 7 | a0001c0001t0001g0153 a0001c0001t0001g0168 a0001c0001t0001g0176 others(4): Show |
7 | HG00621.hp2 NA18947.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.2211+6145T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765048 | |||||||
| chr6:104765053 | T | A | 1 | a0001c0002t0001g0082 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2211+6140A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765053 | |||||||
| chr6:104765389 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2211+5804G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765389 | |||||||
| chr6:104765428 | C | G | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2211+5765G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765428 | |||||||
| chr6:104765450 | T | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0211 |
3 | NA18957.hp1 NA18973.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2211+5743A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765450 | |||||||
| chr6:104765736 | A | C | 61 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0141 others(58): Show |
63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2211+5457T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765736 | |||||||
| chr6:104765802 | T | C | 1 | a0001c0005t0001g0314 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2211+5391A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765802 | |||||||
| chr6:104765893 | T | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0334 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.2211+5300A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765893 | |||||||
| chr6:104765973 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+5220G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765973 | |||||||
| chr6:104766176 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2211+5017G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766176 | |||||||
| chr6:104766253 | G | A | 2 | a0001c0001t0001g0328 a0001c0001t0001g0329 |
2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2211+4940C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766253 | |||||||
| chr6:104766408 | G | A | 2 | a0001c0001t0001g0144 a0001c0002t0008g0340 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2211+4785C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766408 | |||||||
| chr6:104766703 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0334 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.2211+4490C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766703 | |||||||
| chr6:104766910 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2211+4283T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766910 | |||||||
| chr6:104767084 | A | T | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2211+4109T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767084 | |||||||
| chr6:104767148 | G | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2211+4045C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767148 | |||||||
| chr6:104767216 | G | T | 13 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0156 others(10): Show |
13 | HG00621.hp2 NA18947.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.2211+3977C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767216 | |||||||
| chr6:104767268 | C | T | 6 | a0001c0001t0002g0031 a0001c0001t0002g0038 a0001c0001t0002g0045 others(3): Show |
6 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.2211+3925G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767268 | |||||||
| chr6:104767351 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2211+3842G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767351 | |||||||
| chr6:104767414 | T | C | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2211+3779A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767414 | |||||||
| chr6:104767478 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2211+3715C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767478 | |||||||
| chr6:104767481 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2211+3712G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767481 | |||||||
| chr6:104767490 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2211+3703G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767490 | |||||||
| chr6:104767540 | A | T | 2 | a0001c0002t0001g0102 a0001c0002t0001g0115 |
2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2211+3653T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767540 | |||||||
| chr6:104768143 | G | A | 6 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(3): Show |
6 | HG00735.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2211+3050C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768143 | |||||||
| chr6:104768271 | T | G | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2211+2922A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768271 | |||||||
| chr6:104768273 | A | G | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2211+2920T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768273 | |||||||
| chr6:104768359 | G | C | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2211+2834C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768359 | |||||||
| chr6:104768530 | T | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+2663A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768530 | |||||||
| chr6:104768576 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2211+2617G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768576 | |||||||
| chr6:104768625 | G | GA | 167 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(164): Show |
170 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.2211+2567dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768625 | |||||||
| chr6:104768820 | T | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2211+2373A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768820 | |||||||
| chr6:104768890 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2211+2303A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768890 | |||||||
| chr6:104768895 | T | A | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2211+2298A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768895 | |||||||
| chr6:104769016 | T | C | 1 | a0001c0002t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2211+2177A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769016 | |||||||
| chr6:104769054 | T | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2211+2139A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769054 | |||||||
| chr6:104769075 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2211+2118G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769075 | |||||||
| chr6:104769094 | A | G | 226 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(223): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2211+2099T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769094 | |||||||
| chr6:104769240 | G | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+1953C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769240 | |||||||
| chr6:104769313 | T | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+1880A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769313 | |||||||
| chr6:104769319 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2211+1874A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769319 | |||||||
| chr6:104769334 | T | C | 1 | a0001c0002t0001g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2211+1859A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769334 | |||||||
| chr6:104769341 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2211+1852A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769341 | |||||||
| chr6:104769766 | G | A | 49 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(46): Show |
49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.2211+1427C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769766 | |||||||
| chr6:104769813 | A | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2211+1380T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769813 | |||||||
| chr6:104769895 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2211+1298C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769895 | |||||||
| chr6:104769989 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+1204G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769989 | |||||||
| chr6:104770017 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2211+1176T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770017 | |||||||
| chr6:104770043 | C | T | 2 | a0001c0002t0001g0097 a0001c0002t0001g0098 |
2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2211+1150G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770043 | |||||||
| chr6:104770051 | C | G | 2 | a0001c0001t0001g0323 a0001c0001t0001g0332 |
2 | NA19000.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2211+1142G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770051 | |||||||
| chr6:104770156 | T | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 |
3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2211+1037A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770156 | |||||||
| chr6:104770214 | G | T | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2211+979C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770214 | |||||||
| chr6:104770556 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2211+637A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770556 | |||||||
| chr6:104770750 | C | T | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2211+443G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770750 | |||||||
| chr6:104770845 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2211+348G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770845 | |||||||
| chr6:104770856 | C | T | 30 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(27): Show |
30 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2211+337G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770856 | |||||||
| chr6:104770970 | C | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+223G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770970 | |||||||
| chr6:104771085 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2211+108G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104771085 | |||||||
| chr6:104771107 | A | G | 51 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(48): Show |
51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2211+86T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104771107 | |||||||
| chr6:104771662 | C | T | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2014+263G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771662 | |||||||
| chr6:104771697 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2014+228G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771697 | |||||||
| chr6:104771698 | A | T | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2014+227T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771698 | |||||||
| chr6:104771705 | G | GA | 87 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0138 others(84): Show |
87 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.2014+219dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771705 | |||||||
| chr6:104771845 | C | T | 1 | a0001c0001t0002g0028 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2014+80G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771845 | |||||||
| chr6:104771873 | G | GA | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2014+51dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771873 | |||||||
| chr6:104771898 | T | C | 44 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(41): Show |
44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.2014+27A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771898 | |||||||
| chr6:104772198 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1865-124G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104772198 | |||||||
| chr6:104772383 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1865-309C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104772383 | |||||||
| chr6:104773044 | C | CA | 7 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0179 others(4): Show |
7 | HG02055.hp1 HG02055.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1865-971dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773044 | |||||||
| chr6:104773245 | T | G | 1 | a0001c0001t0001g0288 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1865-1171A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773245 | |||||||
| chr6:104773359 | C | T | 2 | a0001c0002t0001g0080 a0001c0002t0001g0113 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1865-1285G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773359 | |||||||
| chr6:104773550 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1865-1476C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773550 | |||||||
| chr6:104773580 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1865-1506G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773580 | |||||||
| chr6:104773647 | A | G | 5 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(2): Show |
7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1865-1573T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773647 | |||||||
| chr6:104773765 | CT | C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0217 a0001c0001t0002g0052 others(1): Show |
4 | HG01943.hp2 HG02040.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1865-1692delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773765 | |||||||
| chr6:104773770 | T | TA | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0192 |
3 | HG02895.hp1 HG02897.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1865-1697_1865-169 others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773770 | |||||||
| chr6:104773771 | T | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(163): Show |
169 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1865-1697A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773771 | |||||||
| chr6:104773771 | T | TA | 52 | a0001c0001t0001g0230 a0001c0001t0001g0327 a0001c0001t0001g0330 others(49): Show |
52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1865-1698dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773771 | |||||||
| chr6:104774024 | C | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0288 |
2 | HG00323.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1865-1950G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774024 | |||||||
| chr6:104774076 | TTCTCTTT others(306): Show |
T | 51 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(48): Show |
51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1865-2315_1865-200 others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774076 | |||||||
| chr6:104774080 | C | CT | 17 | a0001c0001t0001g0228 a0001c0001t0001g0235 a0001c0001t0001g0239 others(14): Show |
17 | HG00423.hp2 HG00741.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1865-2007dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | |||||||
| chr6:104774080 | CTTT | C | 10 | a0001c0001t0001g0141 a0001c0001t0001g0163 a0001c0001t0001g0176 others(7): Show |
10 | HG01109.hp1 HG02027.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1865-2009_1865-200 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | |||||||
| chr6:104774080 | CTTTT | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(83): Show |
87 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1865-2010_1865-200 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | |||||||
| chr6:104774080 | CTTTTT | C | 67 | a0001c0001t0001g0165 a0001c0001t0001g0209 a0001c0001t0002g0001 others(64): Show |
68 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1865-2011_1865-200 others(9): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | |||||||
| chr6:104774080 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0002g0012 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1865-2021_1865-200 others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | |||||||
| chr6:104774081 | TTTTTTTT others(305): Show |
T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1865-2319_1865-200 others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774081 | |||||||
| chr6:104774113 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1865-2039C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774113 | |||||||
| chr6:104774122 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1865-2048G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774122 | |||||||
| chr6:104774151 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1865-2077C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774151 | |||||||
| chr6:104774217 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1865-2143C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774217 | |||||||
| chr6:104774381 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1865-2307G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774381 | |||||||
| chr6:104774382 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1865-2308C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774382 | |||||||
| chr6:104774388 | CCTCT | C | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.1865-2318_1865-231 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774388 | |||||||
| chr6:104774446 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1864+2295T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774446 | |||||||
| chr6:104774663 | C | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0288 |
2 | HG00323.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1864+2078G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774663 | |||||||
| chr6:104774673 | C | T | 2 | a0001c0002t0001g0102 a0001c0002t0001g0115 |
2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1864+2068G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774673 | |||||||
| chr6:104774715 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0321 |
2 | NA18747.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1864+2026C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774715 | |||||||
| chr6:104774740 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1864+2001G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774740 | |||||||
| chr6:104774852 | A | C | 1 | a0001c0001t0001g0319 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1864+1889T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774852 | |||||||
| chr6:104774874 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1864+1867A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774874 | |||||||
| chr6:104775049 | T | C | 1 | a0001c0002t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1864+1692A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775049 | |||||||
| chr6:104775068 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1864+1673C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775068 | |||||||
| chr6:104775112 | C | A | 6 | a0001c0002t0001g0090 a0001c0002t0001g0104 a0001c0002t0001g0105 others(3): Show |
6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1864+1629G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775112 | |||||||
| chr6:104775353 | T | C | 326 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(323): Show |
332 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(329): Show |
intron_variant | MODIFIER | c.1864+1388A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775353 | |||||||
| chr6:104775380 | T | C | 40 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(37): Show |
42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1864+1361A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775380 | |||||||
| chr6:104775413 | G | A | 50 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(47): Show |
50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1864+1328C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775413 | |||||||
| chr6:104775601 | T | A | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1140A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775601 | |||||||
| chr6:104775602 | T | C | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1139A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775602 | |||||||
| chr6:104775605 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1136T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775605 | |||||||
| chr6:104775606 | C | A | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1135G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775606 | |||||||
| chr6:104775609 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1132T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775609 | |||||||
| chr6:104775610 | T | C | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1131A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775610 | |||||||
| chr6:104775612 | A | T | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1129T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775612 | |||||||
| chr6:104775613 | C | G | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1128G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775613 | |||||||
| chr6:104775788 | T | C | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1864+953A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775788 | |||||||
| chr6:104775916 | G | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1864+825C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775916 | |||||||
| chr6:104775989 | G | A | 5 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG00738.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1864+752C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775989 | |||||||
| chr6:104776249 | G | A | 6 | a0001c0001t0001g0153 a0001c0001t0001g0168 a0001c0001t0001g0176 others(3): Show |
6 | NA18947.hp2 NA18984.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.1864+492C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104776249 | |||||||
| chr6:104776361 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1864+380G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104776361 | |||||||
| chr6:104776512 | C | T | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1864+229G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104776512 | |||||||
| chr6:104777337 | T | C | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1567-20A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777337 | |||||||
| chr6:104777372 | T | G | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1567-55A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777372 | |||||||
| chr6:104777406 | A | G | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-89T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777406 | |||||||
| chr6:104777525 | T | C | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1567-208A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777525 | |||||||
| chr6:104777537 | A | T | 12 | a0001c0001t0001g0282 a0001c0001t0001g0306 a0001c0001t0001g0310 others(9): Show |
12 | HG00408.hp2 HG01943.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.1567-220T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777537 | |||||||
| chr6:104777628 | A | AT | 225 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(222): Show |
230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1567-312dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777628 | |||||||
| chr6:104777907 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1567-590C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777907 | |||||||
| chr6:104777979 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1567-662C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777979 | |||||||
| chr6:104778116 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1567-799G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778116 | |||||||
| chr6:104778375 | A | AAT | 14 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0007 others(11): Show |
14 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1567-1060_1567-105 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778375 | |||||||
| chr6:104778375 | A | AATAT | 12 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(9): Show |
12 | HG00597.hp2 HG02135.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.1567-1062_1567-105 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778375 | |||||||
| chr6:104778375 | A | T | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1567-1058T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778375 | |||||||
| chr6:104778601 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1567-1284G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778601 | |||||||
| chr6:104778630 | C | CA | 73 | a0001c0001t0001g0255 a0001c0001t0001g0268 a0001c0001t0001g0275 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1567-1314dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778630 | |||||||
| chr6:104778647 | T | A | 81 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(78): Show |
85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-1330A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778647 | |||||||
| chr6:104778719 | T | G | 81 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(78): Show |
85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-1402A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778719 | |||||||
| chr6:104778794 | C | G | 81 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(78): Show |
85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-1477G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778794 | |||||||
| chr6:104778844 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1567-1527A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778844 | |||||||
| chr6:104779068 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1567-1751C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779068 | |||||||
| chr6:104779441 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1567-2124T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779441 | |||||||
| chr6:104779546 | A | G | 81 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(78): Show |
85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-2229T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779546 | |||||||
| chr6:104779734 | C | G | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1567-2417G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779734 | |||||||
| chr6:104779857 | T | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567-2540A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779857 | |||||||
| chr6:104779874 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567-2557T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779874 | |||||||
| chr6:104779911 | A | G | 73 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1567-2594T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779911 | |||||||
| chr6:104780098 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1567-2781G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780098 | |||||||
| chr6:104780135 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1567-2818C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780135 | |||||||
| chr6:104780216 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1567-2899G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780216 | |||||||
| chr6:104780608 | C | G | 81 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(78): Show |
85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-3291G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780608 | |||||||
| chr6:104780673 | T | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-3356A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780673 | |||||||
| chr6:104780776 | C | T | 29 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(26): Show |
29 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1566+3310G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780776 | |||||||
| chr6:104780804 | C | A | 1 | a0001c0001t0001g0325 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1566+3282G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780804 | |||||||
| chr6:104780887 | A | G | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566+3199T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780887 | |||||||
| chr6:104781233 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1566+2853G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781233 | |||||||
| chr6:104781258 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1566+2828T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781258 | |||||||
| chr6:104781302 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1566+2784G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781302 | |||||||
| chr6:104781330 | CT | C | 4 | a0001c0001t0001g0138 a0001c0001t0001g0158 a0001c0001t0001g0160 others(1): Show |
4 | HG00741.hp2 HG01516.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566+2755delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781330 | |||||||
| chr6:104781431 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1566+2655A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781431 | |||||||
| chr6:104781635 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1566+2451G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781635 | |||||||
| chr6:104781646 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1566+2440A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781646 | |||||||
| chr6:104781733 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1566+2353T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781733 | |||||||
| chr6:104781734 | T | C | 3 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1566+2352A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781734 | |||||||
| chr6:104781771 | C | G | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1566+2315G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781771 | |||||||
| chr6:104781932 | T | C | 227 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(224): Show |
232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1566+2154A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781932 | |||||||
| chr6:104781953 | G | C | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1566+2133C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781953 | |||||||
| chr6:104782013 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1566+2073A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782013 | |||||||
| chr6:104782209 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1566+1877G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782209 | |||||||
| chr6:104782299 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1566+1787C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782299 | |||||||
| chr6:104782437 | C | G | 223 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(220): Show |
228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1566+1649G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782437 | |||||||
| chr6:104782457 | C | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG02132.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1566+1629G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782457 | |||||||
| chr6:104782482 | C | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1566+1604G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782482 | |||||||
| chr6:104782487 | A | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0281 |
2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1566+1599T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782487 | |||||||
| chr6:104782761 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1566+1325G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782761 | |||||||
| chr6:104782805 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1566+1281A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782805 | |||||||
| chr6:104782854 | C | A | 223 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(220): Show |
228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1566+1232G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782854 | |||||||
| chr6:104782937 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1566+1149G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782937 | |||||||
| chr6:104782965 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1566+1121C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782965 | |||||||
| chr6:104783135 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1566+951G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783135 | |||||||
| chr6:104783349 | C | A | 1 | a0001c0001t0001g0283 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1566+737G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783349 | |||||||
| chr6:104783380 | A | C | 163 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(160): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1566+706T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783380 | |||||||
| chr6:104783382 | G | A | 223 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(220): Show |
228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1566+704C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783382 | |||||||
| chr6:104783656 | G | A | 43 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(40): Show |
43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.1566+430C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783656 | |||||||
| chr6:104783855 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1566+231G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783855 | |||||||
| chr6:104784055 | A | C | 50 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(47): Show |
50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1566+31T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104784055 | |||||||
| chr6:104784329 | C | T | 223 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(220): Show |
228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1478+88G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 13/23 | chr6 | 104784329 | |||||||
| chr6:104784330 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1478+87C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 13/23 | chr6 | 104784330 | |||||||
| chr6:104784358 | A | C | 144 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(141): Show |
145 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1478+59T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 13/23 | chr6 | 104784358 | |||||||
| chr6:104784562 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1410-77G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 12/23 | chr6 | 104784562 | |||||||
| chr6:104784585 | C | CA | 144 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(141): Show |
145 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1410-101dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 12/23 | chr6 | 104784585 | |||||||
| chr6:104784710 | A | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1410-225T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 12/23 | chr6 | 104784710 | |||||||
| chr6:104784952 | GA | G | 11 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0035 others(8): Show |
12 | HG00099.hp1 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1409+32delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 12/23 | chr6 | 104784952 | |||||||
| chr6:104785369 | T | TA | 6 | a0001c0001t0001g0193 a0001c0001t0001g0255 a0001c0001t0001g0306 others(3): Show |
6 | HG02004.hp2 HG02056.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075-51dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785369 | |||||||
| chr6:104785369 | TA | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-51delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785369 | |||||||
| chr6:104785382 | AC | A | 10 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 others(7): Show |
10 | HG01168.hp2 HG01256.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-64delG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785382 | |||||||
| chr6:104785383 | C | A | 41 | a0001c0001t0001g0217 a0001c0002t0001g0079 a0001c0002t0001g0084 others(38): Show |
41 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.1075-64G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785383 | |||||||
| chr6:104785610 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1075-291A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785610 | |||||||
| chr6:104785626 | A | C | 1 | a0001c0002t0001g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1075-307T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785626 | |||||||
| chr6:104785822 | T | C | 5 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0015 others(2): Show |
5 | HG01891.hp1 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-503A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785822 | |||||||
| chr6:104785955 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1075-636A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785955 | |||||||
| chr6:104786294 | T | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0315 |
2 | HG02155.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1075-975A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786294 | |||||||
| chr6:104786340 | C | CA | 24 | a0001c0001t0001g0154 a0001c0001t0001g0172 a0001c0001t0001g0257 others(21): Show |
24 | HG01515.hp1 HG02040.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1075-1022dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786340 | |||||||
| chr6:104786407 | T | TA | 267 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0118 others(264): Show |
270 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1075-1089dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786407 | |||||||
| chr6:104786407 | T | TAA | 10 | a0001c0001t0001g0278 a0001c0001t0001g0283 a0001c0001t0001g0304 others(7): Show |
10 | HG01433.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075-1090_1075-108 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786407 | |||||||
| chr6:104786468 | C | G | 60 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(57): Show |
62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.1075-1149G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786468 | |||||||
| chr6:104786530 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1075-1211C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786530 | |||||||
| chr6:104786566 | T | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1075-1247A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786566 | |||||||
| chr6:104786600 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1075-1281A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786600 | |||||||
| chr6:104786604 | C | CA | 17 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0201 others(14): Show |
19 | HG00735.hp1 HG01433.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.1075-1286dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786604 | |||||||
| chr6:104786613 | A | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1075-1294T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786613 | |||||||
| chr6:104786617 | A | C | 86 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0156 others(83): Show |
88 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1075-1298T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786617 | |||||||
| chr6:104786621 | C | A | 7 | a0001c0002t0001g0085 a0001c0002t0001g0096 a0001c0002t0001g0111 others(4): Show |
7 | HG01515.hp1 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-1302G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786621 | |||||||
| chr6:104786625 | C | A | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1075-1306G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786625 | |||||||
| chr6:104786633 | C | CA | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0322 others(4): Show |
7 | HG02055.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-1315dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786633 | |||||||
| chr6:104786633 | C | CAA | 5 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(2): Show |
7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-1316_1075-131 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786633 | |||||||
| chr6:104786637 | A | C | 54 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0232 others(51): Show |
54 | HG00099.hp2 HG00323.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1075-1318T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786637 | |||||||
| chr6:104786922 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1075-1603G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786922 | |||||||
| chr6:104786930 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1075-1611A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786930 | |||||||
| chr6:104786962 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1075-1643C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786962 | |||||||
| chr6:104787699 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1075-2380C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104787699 | |||||||
| chr6:104787715 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1075-2396A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104787715 | |||||||
| chr6:104787882 | A | G | 144 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(141): Show |
145 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1075-2563T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104787882 | |||||||
| chr6:104787946 | T | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1075-2627A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104787946 | |||||||
| chr6:104788022 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1075-2703A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788022 | |||||||
| chr6:104788027 | A | G | 50 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(47): Show |
50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1075-2708T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788027 | |||||||
| chr6:104788100 | A | G | 165 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(162): Show |
168 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1075-2781T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788100 | |||||||
| chr6:104788112 | C | T | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-2793G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788112 | |||||||
| chr6:104788295 | T | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-2976A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788295 | |||||||
| chr6:104788413 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+3091T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788413 | |||||||
| chr6:104788427 | T | G | 73 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+3077A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788427 | |||||||
| chr6:104788577 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1074+2927T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788577 | |||||||
| chr6:104788597 | T | C | 73 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+2907A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788597 | |||||||
| chr6:104788730 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1074+2774C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788730 | |||||||
| chr6:104788844 | A | G | 13 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0156 others(10): Show |
13 | HG00621.hp2 NA18947.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.1074+2660T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788844 | |||||||
| chr6:104789214 | C | T | 43 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(40): Show |
43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.1074+2290G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789214 | |||||||
| chr6:104789270 | A | T | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1074+2234T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789270 | |||||||
| chr6:104789281 | T | C | 3 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0057 |
3 | HG02809.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1074+2223A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789281 | |||||||
| chr6:104789452 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+2052T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789452 | |||||||
| chr6:104789826 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1074+1678C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789826 | |||||||
| chr6:104790068 | G | GA | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1074+1435dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790068 | |||||||
| chr6:104790216 | C | T | 1 | a0001c0001t0002g0009 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1074+1288G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790216 | |||||||
| chr6:104790352 | A | T | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1074+1152T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790352 | |||||||
| chr6:104790359 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+1145G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790359 | |||||||
| chr6:104790577 | G | A | 60 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(57): Show |
62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.1074+927C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790577 | |||||||
| chr6:104790750 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1074+754C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790750 | |||||||
| chr6:104790900 | A | AATTTAAC others(2): Show |
52 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(49): Show |
52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1074+595_1074+603d others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790900 | |||||||
| chr6:104791172 | A | G | 73 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(70): Show |
75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+332T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104791172 | |||||||
| chr6:104791477 | C | T | 27 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0007 others(24): Show |
27 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+27G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104791477 | |||||||
| chr6:104792165 | T | C | 5 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 others(2): Show |
5 | HG02809.hp2 HG02895.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.924-511A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792165 | |||||||
| chr6:104792229 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.924-575G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792229 | |||||||
| chr6:104792435 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-781G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792435 | |||||||
| chr6:104792525 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.924-871T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792525 | |||||||
| chr6:104792554 | G | A | 3 | a0001c0002t0001g0004 a0001c0002t0001g0077 a0001c0002t0001g0078 |
4 | HG02622.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-900C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792554 | |||||||
| chr6:104792653 | A | AC | 3 | a0001c0002t0001g0080 a0001c0002t0001g0113 a0001c0002t0001g0114 |
3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.924-1000dupG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792653 | |||||||
| chr6:104792706 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-1052G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792706 | |||||||
| chr6:104792717 | A | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(89): Show |
93 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.924-1063T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792717 | |||||||
| chr6:104792846 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.924-1192G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792846 | |||||||
| chr6:104792960 | G | C | 9 | a0001c0001t0002g0041 a0001c0002t0001g0003 a0001c0002t0001g0004 others(6): Show |
11 | HG01928.hp1 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.924-1306C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792960 | |||||||
| chr6:104793192 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0044 a0001c0001t0002g0048 |
3 | HG02132.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.924-1538C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793192 | |||||||
| chr6:104793222 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.924-1568C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793222 | |||||||
| chr6:104793232 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.924-1578T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793232 | |||||||
| chr6:104793233 | C | CGAACCCC others(16): Show |
2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.924-1580_924-1579i others(25): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793233 | |||||||
| chr6:104793254 | G | A | 2 | a0001c0002t0001g0003 a0001c0002t0001g0076 |
3 | HG02257.hp2 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.924-1600C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793254 | |||||||
| chr6:104793262 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-1608T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793262 | |||||||
| chr6:104793266 | C | CA | 124 | a0001c0001t0001g0135 a0001c0001t0001g0162 a0001c0001t0001g0169 others(121): Show |
128 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.924-1613dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793266 | |||||||
| chr6:104793266 | C | CAA | 13 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0010 others(10): Show |
13 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.924-1614_924-1613d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793266 | |||||||
| chr6:104793449 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.924-1795C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793449 | |||||||
| chr6:104793477 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-1823C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793477 | |||||||
| chr6:104793522 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.924-1868T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793522 | |||||||
| chr6:104793933 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.923+1646T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793933 | |||||||
| chr6:104794064 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.923+1515G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794064 | |||||||
| chr6:104794286 | A | C | 225 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(222): Show |
230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.923+1293T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794286 | |||||||
| chr6:104794309 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.923+1270T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794309 | |||||||
| chr6:104794638 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.923+941C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794638 | |||||||
| chr6:104794670 | G | A | 92 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(89): Show |
93 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.923+909C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794670 | |||||||
| chr6:104794716 | C | A | 1 | a0001c0001t0002g0021 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.923+863G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794716 | |||||||
| chr6:104794870 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.923+709C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794870 | |||||||
| chr6:104794910 | A | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0322 |
2 | NA18747.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.923+669T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794910 | |||||||
| chr6:104794926 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.923+653C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794926 | |||||||
| chr6:104795070 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.923+509A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104795070 | |||||||
| chr6:104795158 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.923+421A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104795158 | |||||||
| chr6:104795346 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.923+233G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104795346 | |||||||
| chr6:104795531 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.923+48G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104795531 | |||||||
| chr6:104795962 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-277C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 9/23 | chr6 | 104795962 | |||||||
| chr6:104796068 | C | A | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.817-383G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 9/23 | chr6 | 104796068 | |||||||
| chr6:104796263 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.816+392T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 9/23 | chr6 | 104796263 | |||||||
| chr6:104796651 | A | T | 223 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(220): Show |
228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
splice_region_variant&intron_variant | LOW | c.816+4T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 9/23 | chr6 | 104796651 | |||||||
| chr6:104797174 | C | CT | 222 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(219): Show |
227 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.618-150dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797174 | |||||||
| chr6:104797193 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.618-168A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797193 | |||||||
| chr6:104797489 | T | TA | 8 | a0001c0001t0001g0288 a0001c0002t0001g0003 a0001c0002t0001g0004 others(5): Show |
10 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-465dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797489 | |||||||
| chr6:104797489 | TA | T | 6 | a0001c0001t0001g0140 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG02040.hp1 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-465delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797489 | |||||||
| chr6:104797496 | A | AG | 52 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(49): Show |
52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.618-472_618-471ins others(1): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797496 | |||||||
| chr6:104797546 | T | C | 52 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(49): Show |
52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.618-521A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797546 | |||||||
| chr6:104797724 | G | C | 1 | a0001c0001t0002g0048 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.618-699C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797724 | |||||||
| chr6:104797763 | A | G | 60 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(57): Show |
62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.618-738T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797763 | |||||||
| chr6:104798064 | G | A | 11 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(8): Show |
11 | HG00597.hp2 HG02135.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-1039C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798064 | |||||||
| chr6:104798069 | GA | G | 222 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(219): Show |
227 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.618-1045delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798069 | |||||||
| chr6:104798103 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-1078C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798103 | |||||||
| chr6:104798245 | C | T | 24 | a0001c0001t0001g0140 a0001c0001t0001g0148 a0001c0001t0001g0149 others(21): Show |
24 | HG00621.hp2 HG02055.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.618-1220G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798245 | |||||||
| chr6:104798248 | A | G | 7 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0104 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-1223T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798248 | |||||||
| chr6:104798286 | A | T | 1 | a0001c0002t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.618-1261T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798286 | |||||||
| chr6:104798346 | A | G | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.618-1321T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798346 | |||||||
| chr6:104798399 | T | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-1374A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798399 | |||||||
| chr6:104798414 | A | G | 45 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(42): Show |
45 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.618-1389T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798414 | |||||||
| chr6:104798479 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.618-1454C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798479 | |||||||
| chr6:104798559 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-1534T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798559 | |||||||
| chr6:104799064 | C | T | 50 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(47): Show |
50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.618-2039G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799064 | |||||||
| chr6:104799166 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-2141G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799166 | |||||||
| chr6:104799167 | G | T | 1 | a0001c0001t0002g0024 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-2142C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799167 | |||||||
| chr6:104799172 | C | A | 1 | a0001c0001t0001g0316 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.618-2147G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799172 | |||||||
| chr6:104799249 | T | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0311 |
2 | NA18969.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.618-2224A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799249 | |||||||
| chr6:104799404 | C | A | 27 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0007 others(24): Show |
27 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.618-2379G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799404 | |||||||
| chr6:104799405 | A | G | 27 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0007 others(24): Show |
27 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.618-2380T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799405 | |||||||
| chr6:104799432 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618-2407A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799432 | |||||||
| chr6:104799484 | A | G | 52 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(49): Show |
52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.618-2459T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799484 | |||||||
| chr6:104799559 | T | G | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.618-2534A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799559 | |||||||
| chr6:104799616 | T | C | 1 | a0001c0002t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.618-2591A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799616 | |||||||
| chr6:104799824 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.618-2799G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799824 | |||||||
| chr6:104799909 | G | GCCAAAGT others(12): Show |
224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.618-2885_618-2884i others(21): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799909 | |||||||
| chr6:104800146 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.618-3121G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800146 | |||||||
| chr6:104800177 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.618-3152T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800177 | |||||||
| chr6:104800178 | C | A | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.618-3153G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800178 | |||||||
| chr6:104800221 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.618-3196A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800221 | |||||||
| chr6:104800309 | G | C | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.618-3284C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800309 | |||||||
| chr6:104800324 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.618-3299G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800324 | |||||||
| chr6:104800699 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.618-3674G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800699 | |||||||
| chr6:104800981 | C | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.618-3956G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800981 | |||||||
| chr6:104800981 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-3956G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800981 | |||||||
| chr6:104801071 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.618-4046G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801071 | |||||||
| chr6:104801072 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0044 a0001c0001t0002g0048 |
3 | HG02132.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.618-4047T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801072 | |||||||
| chr6:104801111 | A | C | 3 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0057 |
3 | HG02809.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.618-4086T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801111 | |||||||
| chr6:104801275 | C | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-4250G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801275 | |||||||
| chr6:104801297 | G | T | 43 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(40): Show |
43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.618-4272C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801297 | |||||||
| chr6:104801366 | A | G | 72 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0001 others(69): Show |
74 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.618-4341T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801366 | |||||||
| chr6:104801558 | T | C | 2 | a0001c0002t0001g0081 a0001c0002t0001g0082 |
2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.618-4533A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801558 | |||||||
| chr6:104801561 | T | C | 25 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(22): Show |
25 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.618-4536A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801561 | |||||||
| chr6:104801632 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.618-4607C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801632 | |||||||
| chr6:104801667 | G | A | 7 | a0001c0001t0001g0153 a0001c0001t0001g0168 a0001c0001t0001g0176 others(4): Show |
7 | HG00621.hp2 NA18947.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-4642C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801667 | |||||||
| chr6:104801934 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.618-4909G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801934 | |||||||
| chr6:104802033 | C | CA | 8 | a0001c0001t0001g0148 a0001c0001t0001g0213 a0001c0001t0001g0237 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.618-5009dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802033 | |||||||
| chr6:104802033 | C | CAA | 45 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(42): Show |
47 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.618-5010_618-5009d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802033 | |||||||
| chr6:104802033 | C | CAAA | 26 | a0001c0001t0001g0268 a0001c0001t0001g0275 a0001c0001t0002g0007 others(23): Show |
26 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.618-5011_618-5009d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802033 | |||||||
| chr6:104802033 | CAA | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-5010_618-5009d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802033 | |||||||
| chr6:104802095 | G | C | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.618-5070C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802095 | |||||||
| chr6:104802187 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-5162G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802187 | |||||||
| chr6:104802254 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.618-5229T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802254 | |||||||
| chr6:104802327 | G | T | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.618-5302C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802327 | |||||||
| chr6:104802463 | C | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-5438G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802463 | |||||||
| chr6:104802649 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.618-5624T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802649 | |||||||
| chr6:104802699 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618-5674C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802699 | |||||||
| chr6:104802734 | T | C | 1 | a0001c0001t0002g0056 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.618-5709A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802734 | |||||||
| chr6:104802776 | C | T | 3 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.618-5751G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802776 | |||||||
| chr6:104802915 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.618-5890C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802915 | |||||||
| chr6:104803034 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.618-6009G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803034 | |||||||
| chr6:104803080 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.618-6055T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803080 | |||||||
| chr6:104803159 | G | A | 54 | a0001c0001t0001g0138 a0001c0001t0001g0158 a0001c0001t0001g0159 others(51): Show |
54 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.618-6134C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803159 | |||||||
| chr6:104803166 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.618-6141G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803166 | |||||||
| chr6:104803194 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.618-6169A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803194 | |||||||
| chr6:104803233 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.618-6208T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803233 | |||||||
| chr6:104803235 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.618-6210C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803235 | |||||||
| chr6:104803381 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.618-6356A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803381 | |||||||
| chr6:104803448 | T | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6423A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803448 | |||||||
| chr6:104803514 | C | A | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.618-6489G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803514 | |||||||
| chr6:104803554 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6529G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803554 | |||||||
| chr6:104803635 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6610C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803635 | |||||||
| chr6:104803649 | C | T | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.618-6624G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803649 | |||||||
| chr6:104803653 | A | G | 1 | a0001c0002t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.618-6628T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803653 | |||||||
| chr6:104803766 | T | G | 1 | a0001c0001t0002g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.618-6741A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803766 | |||||||
| chr6:104803799 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.618-6774G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803799 | |||||||
| chr6:104803831 | T | C | 1 | a0001c0002t0001g0083 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.618-6806A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803831 | |||||||
| chr6:104803875 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.618-6850G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803875 | |||||||
| chr6:104803977 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.618-6952G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803977 | |||||||
| chr6:104803980 | A | C | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.618-6955T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803980 | |||||||
| chr6:104804005 | C | T | 3 | a0001c0002t0001g0080 a0001c0002t0001g0113 a0001c0002t0001g0114 |
3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.618-6980G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804005 | |||||||
| chr6:104804039 | C | CA | 14 | a0001c0001t0002g0002 a0001c0001t0002g0037 a0001c0001t0002g0047 others(11): Show |
15 | HG02080.hp1 NA18939.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.618-7015dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804039 | |||||||
| chr6:104804290 | C | G | 337 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.617+7021G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804290 | |||||||
| chr6:104804436 | G | T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+6875C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804436 | |||||||
| chr6:104804447 | C | G | 1 | a0001c0001t0002g0012 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.617+6864G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804447 | |||||||
| chr6:104804631 | G | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02055.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.617+6680C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804631 | |||||||
| chr6:104804784 | A | G | 224 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(221): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.617+6527T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804784 | |||||||
| chr6:104804877 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.617+6434C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804877 | |||||||
| chr6:104804883 | C | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(67): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.617+6428G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804883 | |||||||
| chr6:104805278 | A | T | 13 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(10): Show |
13 | HG00323.hp2 HG01074.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.617+6033T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805278 | |||||||
| chr6:104805279 | T | C | 1 | a0001c0002t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.617+6032A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805279 | |||||||
| chr6:104805372 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.617+5939T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805372 | |||||||
| chr6:104805414 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.617+5897A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805414 | |||||||
| chr6:104805466 | C | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+5845G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805466 | |||||||
| chr6:104805623 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.617+5688T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805623 | |||||||
| chr6:104805866 | C | CA | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+5444dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805866 | |||||||
| chr6:104806125 | C | T | 222 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(219): Show |
227 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.617+5186G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104806125 | |||||||
| chr6:104806951 | T | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.617+4360A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104806951 | |||||||
| chr6:104806958 | G | A | 44 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(41): Show |
44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.617+4353C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104806958 | |||||||
| chr6:104807052 | C | T | 43 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(40): Show |
43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.617+4259G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807052 | |||||||
| chr6:104807168 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.617+4143G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807168 | |||||||
| chr6:104807231 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0300 a0001c0001t0001g0330 |
3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.617+4080G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807231 | |||||||
| chr6:104807236 | A | T | 3 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG02132.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.617+4075T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807236 | |||||||
| chr6:104807304 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.617+4007C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807304 | |||||||
| chr6:104807880 | CACT | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+3428_617+3430d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807880 | |||||||
| chr6:104807914 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.617+3397G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807914 | |||||||
| chr6:104807977 | G | A | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.617+3334C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807977 | |||||||
| chr6:104808175 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.617+3136C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808175 | |||||||
| chr6:104808227 | A | G | 3 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.617+3084T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808227 | |||||||
| chr6:104808319 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.617+2992C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808319 | |||||||
| chr6:104808362 | T | A | 1 | a0001c0001t0002g0051 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.617+2949A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808362 | |||||||
| chr6:104808382 | T | C | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.617+2929A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808382 | |||||||
| chr6:104808443 | C | T | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.617+2868G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808443 | |||||||
| chr6:104808577 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.617+2734T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808577 | |||||||
| chr6:104808615 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.617+2696T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808615 | |||||||
| chr6:104808618 | T | C | 86 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(83): Show |
88 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.617+2693A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808618 | |||||||
| chr6:104808669 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.617+2642G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808669 | |||||||
| chr6:104808679 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.617+2632C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808679 | |||||||
| chr6:104809109 | T | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+2202A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809109 | |||||||
| chr6:104809122 | T | G | 1 | a0001c0001t0001g0289 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.617+2189A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809122 | |||||||
| chr6:104809135 | A | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+2176T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809135 | |||||||
| chr6:104809655 | C | CT | 115 | a0001c0001t0001g0117 a0001c0001t0001g0173 a0001c0001t0001g0186 others(112): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.617+1655dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809655 | |||||||
| chr6:104809655 | C | CTT | 9 | a0001c0001t0004g0036 a0001c0002t0001g0003 a0001c0002t0001g0004 others(6): Show |
11 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+1654_617+1655d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809655 | |||||||
| chr6:104809655 | CT | C | 9 | a0001c0001t0001g0200 a0001c0001t0001g0206 a0001c0001t0001g0212 others(6): Show |
9 | HG00609.hp1 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+1655delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809655 | |||||||
| chr6:104809700 | G | C | 1 | a0001c0001t0002g0016 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.617+1611C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809700 | |||||||
| chr6:104809756 | C | A | 29 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(26): Show |
29 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.617+1555G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809756 | |||||||
| chr6:104809815 | G | A | 222 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(219): Show |
227 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.617+1496C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809815 | |||||||
| chr6:104809886 | A | T | 1 | a0001c0001t0001g0256 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.617+1425T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809886 | |||||||
| chr6:104810072 | A | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(67): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.617+1239T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810072 | |||||||
| chr6:104810250 | C | A | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.617+1061G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810250 | |||||||
| chr6:104810302 | T | G | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.617+1009A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810302 | |||||||
| chr6:104810461 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+850G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810461 | |||||||
| chr6:104810694 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.617+617G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810694 | |||||||
| chr6:104810862 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.617+449T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810862 | |||||||
| chr6:104810911 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.617+400G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810911 | |||||||
| chr6:104811019 | A | T | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.617+292T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811019 | |||||||
| chr6:104811112 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+199T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811112 | |||||||
| chr6:104811207 | AT | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+103delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811207 | |||||||
| chr6:104811238 | T | TTATACAT others(1): Show |
3 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0003t0001g0225 |
3 | HG03195.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.617+72_617+73insTA others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(3): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0144 others(4): Show |
8 | HG02055.hp1 HG02165.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(5): Show |
9 | a0001c0001t0001g0142 a0001c0001t0001g0148 a0001c0001t0001g0151 others(6): Show |
9 | HG00738.hp1 HG01361.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(7): Show |
13 | a0001c0001t0001g0135 a0001c0001t0001g0156 a0001c0001t0001g0159 others(10): Show |
13 | HG00544.hp1 HG00621.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(9): Show |
12 | a0001c0001t0001g0134 a0001c0001t0001g0146 a0001c0001t0001g0150 others(9): Show |
12 | HG01993.hp2 HG02027.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(11): Show |
11 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0158 others(8): Show |
11 | HG00621.hp1 HG01516.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(16): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(13): Show |
13 | a0001c0001t0001g0138 a0001c0001t0001g0154 a0001c0001t0001g0155 others(10): Show |
13 | HG00733.hp1 HG00741.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(18): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(15): Show |
5 | a0001c0001t0001g0167 a0001c0001t0001g0194 a0001c0001t0001g0213 others(2): Show |
5 | HG00408.hp1 HG02004.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(20): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(17): Show |
4 | a0001c0001t0001g0152 a0001c0001t0001g0176 a0001c0001t0001g0200 others(1): Show |
4 | HG01167.hp1 NA19010.hp1 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811238 | T | TTATACAT others(19): Show |
1 | a0001c0001t0001g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.617+72_617+73insTA others(24): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | |||||||
| chr6:104811240 | ATT | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0186 a0001c0001t0002g0065 |
3 | NA18972.hp1 NA18972.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.617+69_617+70delAA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811240 | |||||||
| chr6:104811241 | T | TAC | 3 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0175 |
3 | NA18961.hp2 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.617+69_617+70insGT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811241 | |||||||
| chr6:104811242 | T | A | 91 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(88): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.617+69A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811242 | |||||||
| chr6:104811243 | T | C | 7 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0170 others(4): Show |
7 | HG00609.hp2 HG01109.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+68A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811243 | |||||||
| chr6:104811245 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0186 a0001c0001t0002g0065 |
3 | NA18972.hp1 NA18972.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.617+66A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811245 | |||||||
| chr6:104811247 | C | CAT | 16 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0001g0244 others(13): Show |
16 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.617+62_617+63dupAT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | C | CATAT | 5 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0288 others(2): Show |
5 | HG00323.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+60_617+63dupAT others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | C | CATATAT | 5 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0068 others(2): Show |
5 | HG02647.hp2 HG03540.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+58_617+63dupAT others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | C | CATATATA others(1): Show |
10 | a0001c0001t0001g0279 a0001c0001t0002g0007 a0001c0001t0002g0010 others(7): Show |
10 | HG00733.hp2 HG01175.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+56_617+63dupAT others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | C | CATATATA others(3): Show |
11 | a0001c0001t0001g0248 a0001c0001t0002g0008 a0001c0001t0002g0009 others(8): Show |
11 | HG00597.hp2 HG02572.hp2 HG03688.hp2 others(8): Show |
intron_variant | MODIFIER | c.617+54_617+63dupAT others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | C | CATATATA others(5): Show |
1 | a0001c0001t0002g0027 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.617+52_617+63dupAT others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | C | CATATATA others(7): Show |
1 | a0001c0001t0002g0028 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.617+50_617+63dupAT others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | C | CATATATA others(9): Show |
1 | a0001c0001t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.617+48_617+63dupAT others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.617+64G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | CAT | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0251 a0001c0001t0001g0252 others(9): Show |
13 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.617+62_617+63delAT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | CATAT | C | 41 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(38): Show |
43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.617+60_617+63delAT others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811247 | CATATAT | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+58_617+63delAT others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | |||||||
| chr6:104811277 | C | T | 222 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(219): Show |
227 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.617+34G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811277 | |||||||
| chr6:104811513 | T | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-120A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811513 | |||||||
| chr6:104811573 | G | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-180C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811573 | |||||||
| chr6:104811588 | C | T | 9 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0001g0124 others(6): Show |
9 | HG01167.hp2 HG01168.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.535-195G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811588 | |||||||
| chr6:104811793 | A | T | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.535-400T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811793 | |||||||
| chr6:104811977 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0030 |
2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.535-584A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811977 | |||||||
| chr6:104812065 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.535-672G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812065 | |||||||
| chr6:104812092 | G | A | 2 | a0001c0003t0001g0224 a0001c0003t0001g0225 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.535-699C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812092 | |||||||
| chr6:104812100 | A | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.535-707T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812100 | |||||||
| chr6:104812120 | TA | T | 214 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(211): Show |
217 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.535-728delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812120 | |||||||
| chr6:104812229 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.535-836C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812229 | |||||||
| chr6:104812375 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.535-982C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812375 | |||||||
| chr6:104812476 | C | A | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.535-1083G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812476 | |||||||
| chr6:104812830 | G | C | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.535-1437C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812830 | |||||||
| chr6:104812837 | T | C | 3 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.535-1444A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812837 | |||||||
| chr6:104812908 | T | C | 2 | a0001c0002t0001g0102 a0001c0002t0001g0115 |
2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.535-1515A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812908 | |||||||
| chr6:104812951 | TGCACAAA others(2924): Show |
T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.535-4489_535-1559d others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812951 | |||||||
| chr6:104813017 | G | A | 4 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-1624C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813017 | |||||||
| chr6:104813048 | C | T | 43 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(40): Show |
43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.535-1655G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813048 | |||||||
| chr6:104813060 | A | G | 4 | a0001c0001t0001g0249 a0001c0001t0001g0268 a0001c0001t0001g0275 others(1): Show |
4 | NA18747.hp2 NA18984.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-1667T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813060 | |||||||
| chr6:104813207 | T | G | 231 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0118 others(228): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.535-1814A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813207 | |||||||
| chr6:104813304 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0281 |
2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.535-1911A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813304 | |||||||
| chr6:104813465 | C | T | 40 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(37): Show |
40 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.535-2072G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813465 | |||||||
| chr6:104813785 | G | A | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.535-2392C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813785 | |||||||
| chr6:104813835 | A | G | 29 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(26): Show |
29 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.535-2442T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813835 | |||||||
| chr6:104814121 | A | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0044 a0001c0001t0002g0048 |
3 | HG02132.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.535-2728T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814121 | |||||||
| chr6:104814249 | C | T | 58 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(55): Show |
60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.535-2856G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814249 | |||||||
| chr6:104814306 | G | A | 128 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(125): Show |
132 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.535-2913C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814306 | |||||||
| chr6:104814668 | T | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-3275A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814668 | |||||||
| chr6:104814735 | T | A | 1 | a0001c0001t0001g0316 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.535-3342A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814735 | |||||||
| chr6:104814790 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.535-3397G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814790 | |||||||
| chr6:104815008 | A | G | 129 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(126): Show |
133 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.535-3615T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815008 | |||||||
| chr6:104815404 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.535-4011C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815404 | |||||||
| chr6:104815528 | A | G | 3 | a0001c0002t0001g0080 a0001c0002t0001g0113 a0001c0002t0001g0114 |
3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.535-4135T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815528 | |||||||
| chr6:104815586 | G | A | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.535-4193C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815586 | |||||||
| chr6:104815704 | T | G | 1 | a0001c0001t0001g0280 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.535-4311A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815704 | |||||||
| chr6:104815869 | T | C | 129 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0001 others(126): Show |
133 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.535-4476A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815869 | |||||||
| chr6:104815918 | T | C | 337 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.535-4525A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815918 | |||||||
| chr6:104816005 | G | A | 1 | a0001c0001t0005g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.535-4612C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816005 | |||||||
| chr6:104816027 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.535-4634G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816027 | |||||||
| chr6:104816050 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-4657C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816050 | |||||||
| chr6:104816073 | CA | C | 60 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0175 others(57): Show |
62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.535-4681delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816073 | |||||||
| chr6:104816203 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.535-4810C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816203 | |||||||
| chr6:104816328 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-4935G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816328 | |||||||
| chr6:104816331 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.535-4938T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816331 | |||||||
| chr6:104816410 | A | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-5017T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816410 | |||||||
| chr6:104816592 | G | T | 3 | a0001c0002t0001g0004 a0001c0002t0001g0077 a0001c0002t0001g0078 |
4 | HG02622.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-5199C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816592 | |||||||
| chr6:104816593 | AG | A | 44 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(41): Show |
44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.535-5201delC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816593 | |||||||
| chr6:104816666 | C | T | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.535-5273G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816666 | |||||||
| chr6:104816765 | G | A | 1 | a0001c0001t0002g0052 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.535-5372C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816765 | |||||||
| chr6:104816773 | T | C | 4 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-5380A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816773 | |||||||
| chr6:104816887 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.535-5494C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816887 | |||||||
| chr6:104816966 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-5573G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816966 | |||||||
| chr6:104817172 | T | C | 1 | a0001c0002t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.535-5779A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104817172 | |||||||
| chr6:104817187 | C | T | 1 | a0001c0001t0002g0023 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.535-5794G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104817187 | |||||||
| chr6:104818118 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | HG01167.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.535-6725A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818118 | |||||||
| chr6:104818171 | T | C | 1 | a0001c0003t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.535-6778A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818171 | |||||||
| chr6:104818243 | A | G | 222 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(219): Show |
227 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.535-6850T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818243 | |||||||
| chr6:104818274 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-6881C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818274 | |||||||
| chr6:104818314 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.535-6921T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818314 | |||||||
| chr6:104818322 | C | T | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.535-6929G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818322 | |||||||
| chr6:104818363 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0015 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-6970C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818363 | |||||||
| chr6:104818455 | A | C | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.535-7062T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818455 | |||||||
| chr6:104818494 | T | C | 8 | a0001c0001t0001g0229 a0001c0001t0001g0304 a0001c0001t0001g0307 others(5): Show |
8 | NA18969.hp1 NA19000.hp1 NA19056.hp1 others(5): Show |
intron_variant | MODIFIER | c.535-7101A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818494 | |||||||
| chr6:104818565 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.535-7172A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818565 | |||||||
| chr6:104818754 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.535-7361C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818754 | |||||||
| chr6:104818829 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0051 |
3 | NA18947.hp1 NA18970.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.535-7436T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818829 | |||||||
| chr6:104818939 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.535-7546T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818939 | |||||||
| chr6:104819070 | C | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0017 others(1): Show |
4 | HG01891.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-7677G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819070 | |||||||
| chr6:104819087 | A | T | 1 | a0001c0001t0002g0027 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.535-7694T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819087 | |||||||
| chr6:104819314 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.535-7921C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819314 | |||||||
| chr6:104819337 | G | A | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.535-7944C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819337 | |||||||
| chr6:104819513 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.535-8120C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819513 | |||||||
| chr6:104819581 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-8188G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819581 | |||||||
| chr6:104819883 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-8490T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819883 | |||||||
| chr6:104819934 | C | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.535-8541G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819934 | |||||||
| chr6:104820126 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.535-8733A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820126 | |||||||
| chr6:104820187 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0166 |
3 | HG00609.hp2 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.535-8794A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820187 | |||||||
| chr6:104820194 | C | CA | 13 | a0001c0001t0001g0161 a0001c0001t0001g0234 a0001c0001t0001g0243 others(10): Show |
15 | HG00609.hp2 HG01981.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-8802dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820194 | |||||||
| chr6:104820194 | CA | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0158 a0001c0001t0001g0200 others(8): Show |
11 | HG01167.hp1 HG01516.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.535-8802delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820194 | |||||||
| chr6:104820326 | T | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-8933A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820326 | |||||||
| chr6:104820371 | T | C | 2 | a0001c0001t0001g0288 a0001c0002t0001g0095 |
2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.535-8978A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820371 | |||||||
| chr6:104820705 | T | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-9312A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820705 | |||||||
| chr6:104820742 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.535-9349C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820742 | |||||||
| chr6:104820982 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.535-9589A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820982 | |||||||
| chr6:104821005 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.535-9612C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821005 | |||||||
| chr6:104821006 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.535-9613G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821006 | |||||||
| chr6:104821296 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.535-9903G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821296 | |||||||
| chr6:104821336 | T | C | 1 | a0001c0005t0001g0314 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.535-9943A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821336 | |||||||
| chr6:104821392 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG01978.hp2 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.535-9999T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821392 | |||||||
| chr6:104821532 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.535-10139G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821532 | |||||||
| chr6:104821561 | G | C | 1 | a0001c0001t0003g0136 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.535-10168C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821561 | |||||||
| chr6:104821610 | G | T | 50 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0079 others(47): Show |
50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.535-10217C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821610 | |||||||
| chr6:104822060 | A | AT | 5 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(2): Show |
7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.535-10668dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822060 | |||||||
| chr6:104822071 | A | T | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.535-10678T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822071 | |||||||
| chr6:104822084 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.535-10691C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822084 | |||||||
| chr6:104822203 | T | TA | 134 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(131): Show |
135 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.535-10811dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822203 | |||||||
| chr6:104822203 | T | TAA | 14 | a0001c0001t0001g0137 a0001c0001t0001g0161 a0001c0001t0001g0193 others(11): Show |
16 | HG00609.hp2 HG02056.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.535-10812_535-1081 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822203 | |||||||
| chr6:104822203 | TA | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(108): Show |
112 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.535-10811delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822203 | |||||||
| chr6:104822264 | T | C | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.534+10778A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822264 | |||||||
| chr6:104822314 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534+10728G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822314 | |||||||
| chr6:104822384 | G | GA | 14 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
15 | HG01175.hp2 HG02027.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.534+10657dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822384 | |||||||
| chr6:104822384 | GA | G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0209 a0001c0001t0001g0217 others(3): Show |
6 | HG00323.hp1 HG01167.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+10657delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822384 | |||||||
| chr6:104822402 | A | T | 1 | a0001c0001t0001g0316 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.534+10640T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822402 | |||||||
| chr6:104822420 | G | A | 1 | a0001c0002t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.534+10622C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822420 | |||||||
| chr6:104822518 | G | A | 1 | a0001c0001t0002g0043 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.534+10524C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822518 | |||||||
| chr6:104822578 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.534+10464G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822578 | |||||||
| chr6:104822718 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.534+10324C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822718 | |||||||
| chr6:104822751 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.534+10291C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822751 | |||||||
| chr6:104822938 | A | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.534+10104T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822938 | |||||||
| chr6:104822983 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+10059C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822983 | |||||||
| chr6:104823015 | A | G | 268 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(265): Show |
272 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.534+10027T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823015 | |||||||
| chr6:104823231 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.534+9811G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823231 | |||||||
| chr6:104823254 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.534+9788A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823254 | |||||||
| chr6:104823295 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.534+9747T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823295 | |||||||
| chr6:104823398 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.534+9644G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823398 | |||||||
| chr6:104823431 | CA | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0151 a0001c0001t0001g0194 others(3): Show |
6 | HG01993.hp1 HG03490.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+9610delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823431 | |||||||
| chr6:104823504 | A | AT | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.534+9537dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823504 | |||||||
| chr6:104823511 | T | A | 6 | a0001c0002t0001g0090 a0001c0002t0001g0104 a0001c0002t0001g0105 others(3): Show |
6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+9531A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823511 | |||||||
| chr6:104823512 | A | T | 7 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 others(4): Show |
7 | HG01516.hp1 HG01517.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+9530T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823512 | |||||||
| chr6:104823558 | A | AGAAACAT others(6102): Show |
1 | a0001c0001t0001g0164 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.534+9483_534+9484i others(6111): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823558 | |||||||
| chr6:104823758 | TA | T | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(4): Show |
7 | HG01978.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+9283delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823758 | |||||||
| chr6:104823914 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.534+9128C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823914 | |||||||
| chr6:104824158 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.534+8884A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824158 | |||||||
| chr6:104824197 | G | A | 2 | a0001c0001t0001g0328 a0001c0001t0001g0329 |
2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.534+8845C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824197 | |||||||
| chr6:104824298 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.534+8744G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824298 | |||||||
| chr6:104824397 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.534+8645C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824397 | |||||||
| chr6:104824795 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.534+8247G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824795 | |||||||
| chr6:104824909 | T | TA | 15 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0145 others(12): Show |
18 | HG01081.hp1 HG02257.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.534+8132dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824909 | |||||||
| chr6:104824945 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.534+8097A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824945 | |||||||
| chr6:104825076 | CG | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.534+7965delC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825076 | |||||||
| chr6:104825081 | C | CA | 75 | a0001c0001t0001g0163 a0001c0001t0002g0001 a0001c0001t0002g0002 others(72): Show |
77 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.534+7960dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825081 | |||||||
| chr6:104825081 | C | CAA | 11 | a0001c0001t0002g0018 a0001c0001t0002g0051 a0001c0002t0001g0003 others(8): Show |
13 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.534+7959_534+7960d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825081 | |||||||
| chr6:104825130 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+7912T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825130 | |||||||
| chr6:104825283 | G | A | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+7759C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825283 | |||||||
| chr6:104825310 | G | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0001g0244 |
3 | HG01934.hp1 HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.534+7732C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825310 | |||||||
| chr6:104825325 | T | C | 1 | a0001c0001t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.534+7717A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825325 | |||||||
| chr6:104825327 | G | A | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+7715C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825327 | |||||||
| chr6:104825341 | T | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00621.hp1 HG02015.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.534+7701A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825341 | |||||||
| chr6:104825483 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.534+7559A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825483 | |||||||
| chr6:104825496 | G | A | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+7546C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825496 | |||||||
| chr6:104825529 | T | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | NA18994.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.534+7513A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825529 | |||||||
| chr6:104825667 | C | A | 3 | a0001c0002t0001g0080 a0001c0002t0001g0113 a0001c0002t0001g0114 |
3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+7375G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825667 | |||||||
| chr6:104825790 | T | C | 1 | a0001c0002t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.534+7252A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825790 | |||||||
| chr6:104825849 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.534+7193G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825849 | |||||||
| chr6:104826063 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 |
3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.534+6979T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826063 | |||||||
| chr6:104826222 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.534+6820G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826222 | |||||||
| chr6:104826316 | G | A | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.534+6726C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826316 | |||||||
| chr6:104826464 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.534+6578A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826464 | |||||||
| chr6:104826471 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.534+6571G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826471 | |||||||
| chr6:104826543 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.534+6499A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826543 | |||||||
| chr6:104826641 | T | C | 2 | a0001c0002t0001g0003 a0001c0002t0001g0076 |
3 | HG02257.hp2 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.534+6401A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826641 | |||||||
| chr6:104826671 | T | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.534+6371A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826671 | |||||||
| chr6:104826696 | T | C | 56 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(53): Show |
58 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.534+6346A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826696 | |||||||
| chr6:104826986 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.534+6056G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826986 | |||||||
| chr6:104827399 | C | G | 25 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(22): Show |
25 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.534+5643G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104827399 | |||||||
| chr6:104827723 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.534+5319G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104827723 | |||||||
| chr6:104827795 | T | C | 14 | a0001c0001t0002g0002 a0001c0001t0002g0037 a0001c0001t0002g0047 others(11): Show |
15 | HG02080.hp1 NA18939.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.534+5247A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104827795 | |||||||
| chr6:104827866 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.534+5176C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104827866 | |||||||
| chr6:104828044 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.534+4998G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828044 | |||||||
| chr6:104828069 | A | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.534+4973T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828069 | |||||||
| chr6:104828517 | A | C | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.534+4525T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828517 | |||||||
| chr6:104828517 | A | G | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.534+4525T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828517 | |||||||
| chr6:104828549 | A | G | 1 | a0001c0001t0007g0274 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.534+4493T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828549 | |||||||
| chr6:104828609 | T | C | 40 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(37): Show |
40 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.534+4433A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828609 | |||||||
| chr6:104828971 | G | A | 40 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(37): Show |
42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.534+4071C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828971 | |||||||
| chr6:104829059 | T | A | 3 | a0001c0001t0001g0230 a0001c0001t0001g0300 a0001c0001t0001g0330 |
3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.534+3983A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829059 | |||||||
| chr6:104829076 | AATAT | A | 3 | a0001c0002t0001g0080 a0001c0002t0001g0113 a0001c0002t0001g0114 |
3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+3962_534+3965d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829076 | |||||||
| chr6:104829260 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.534+3782A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829260 | |||||||
| chr6:104829423 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.534+3619G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829423 | |||||||
| chr6:104829574 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.534+3468C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829574 | |||||||
| chr6:104829627 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0149 a0001c0001t0001g0179 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+3415G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829627 | |||||||
| chr6:104829720 | A | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.534+3322T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829720 | |||||||
| chr6:104829899 | A | T | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.534+3143T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829899 | |||||||
| chr6:104829918 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.534+3124A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829918 | |||||||
| chr6:104830134 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+2908A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830134 | |||||||
| chr6:104830321 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.534+2721A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830321 | |||||||
| chr6:104830551 | C | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(67): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.534+2491G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830551 | |||||||
| chr6:104830758 | C | CT | 155 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(152): Show |
157 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.534+2283dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | |||||||
| chr6:104830758 | C | CTT | 11 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
12 | HG01934.hp2 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.534+2282_534+2283d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | |||||||
| chr6:104830758 | C | CTTT | 50 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0002t0001g0003 others(47): Show |
52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.534+2281_534+2283d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | |||||||
| chr6:104830758 | C | CTTTT | 7 | a0001c0002t0001g0080 a0001c0002t0001g0085 a0001c0002t0001g0091 others(4): Show |
7 | HG02809.hp2 HG02895.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+2280_534+2283d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | |||||||
| chr6:104830758 | CT | C | 7 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0257 others(4): Show |
7 | HG00558.hp2 HG01074.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+2283delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | |||||||
| chr6:104830913 | C | A | 1 | a0001c0001t0002g0070 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.534+2129G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830913 | |||||||
| chr6:104831049 | G | T | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.534+1993C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831049 | |||||||
| chr6:104831312 | C | T | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.534+1730G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831312 | |||||||
| chr6:104831465 | A | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0191 |
2 | HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.534+1577T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831465 | |||||||
| chr6:104831484 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.534+1558G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831484 | |||||||
| chr6:104831496 | G | A | 45 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(42): Show |
45 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.534+1546C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831496 | |||||||
| chr6:104831584 | C | CA | 7 | a0001c0001t0001g0240 a0001c0001t0001g0307 a0001c0002t0001g0003 others(4): Show |
9 | HG00609.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1457dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831584 | |||||||
| chr6:104831591 | A | AG | 3 | a0001c0002t0001g0080 a0001c0002t0001g0113 a0001c0002t0001g0114 |
3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+1450_534+1451i others(3): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831591 | |||||||
| chr6:104831591 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.534+1451T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831591 | |||||||
| chr6:104831622 | G | A | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.534+1420C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831622 | |||||||
| chr6:104831635 | T | C | 6 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG00621.hp2 NA18947.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+1407A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831635 | |||||||
| chr6:104831708 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.534+1334C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831708 | |||||||
| chr6:104831750 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.534+1292C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831750 | |||||||
| chr6:104831754 | G | A | 1 | a0001c0002t0001g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.534+1288C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831754 | |||||||
| chr6:104831918 | A | AAGAAG | 43 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0149 others(40): Show |
43 | HG00408.hp1 HG00597.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.534+1119_534+1123d others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(3): Show |
46 | a0001c0001t0001g0138 a0001c0001t0001g0147 a0001c0001t0001g0150 others(43): Show |
46 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.534+1114_534+1123d others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(8): Show |
50 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0238 others(47): Show |
52 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.534+1109_534+1123d others(17): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(13): Show |
41 | a0001c0001t0001g0157 a0001c0001t0001g0178 a0001c0001t0001g0227 others(38): Show |
41 | HG00558.hp1 HG00609.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.534+1104_534+1123d others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(18): Show |
23 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0001t0001g0226 others(20): Show |
24 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.534+1099_534+1123d others(27): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(23): Show |
9 | a0001c0001t0001g0241 a0001c0001t0001g0264 a0001c0001t0001g0290 others(6): Show |
9 | HG00323.hp2 HG01255.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1094_534+1123d others(32): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(28): Show |
3 | a0001c0002t0001g0093 a0001c0002t0001g0109 a0001c0002t0001g0120 |
3 | HG01243.hp1 HG01256.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.534+1089_534+1123d others(37): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(33): Show |
5 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(2): Show |
5 | HG04115.hp1 NA18965.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+1084_534+1123d others(42): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(38): Show |
1 | a0001c0001t0001g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.534+1079_534+1123d others(47): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | A | AAGAAGAG others(43): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0263 |
2 | HG00738.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.534+1074_534+1123d others(52): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | AAGAAG | A | 34 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0140 others(31): Show |
34 | HG00738.hp1 HG01256.hp2 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.534+1119_534+1123d others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | AAGAAGAG others(3): Show |
A | 21 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0163 others(18): Show |
21 | HG00621.hp2 HG00733.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.534+1114_534+1123d others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | AAGAAGAG others(8): Show |
A | 1 | a0001c0002t0001g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.534+1109_534+1123d others(17): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831918 | AAGAAGAG others(23): Show |
A | 1 | a0001c0001t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534+1094_534+1123d others(32): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | |||||||
| chr6:104831945 | GAAGAGAA others(32): Show |
G | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.534+1058_534+1096d others(41): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831945 | |||||||
| chr6:104831946 | AAGAGAAG others(10): Show |
A | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.534+1079_534+1095d others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831946 | |||||||
| chr6:104831946 | AAGAGAAG others(15): Show |
A | 2 | a0001c0002t0001g0003 a0001c0002t0001g0004 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.534+1074_534+1095d others(24): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831946 | |||||||
| chr6:104831946 | AAGAGAAG others(20): Show |
A | 4 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1069_534+1095d others(29): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831946 | |||||||
| chr6:104831947 | A | G | 2 | a0001c0002t0001g0113 a0001c0002t0001g0114 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+1095T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831947 | |||||||
| chr6:104831949 | AGAAGAGA others(24): Show |
A | 2 | a0001c0002t0001g0113 a0001c0002t0001g0114 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+1062_534+1092d others(33): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831949 | |||||||
| chr6:104831950 | GAAGAGAA others(31): Show |
G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0215 a0001c0003t0001g0224 |
4 | HG02970.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1054_534+1091d others(40): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831950 | |||||||
| chr6:104831950 | GAAGAGAA others(35): Show |
G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0003t0001g0225 |
3 | HG02055.hp1 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.534+1050_534+1091d others(44): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831950 | |||||||
| chr6:104831950 | GAAGAGAA others(39): Show |
G | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.534+1046_534+1091d others(48): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831950 | |||||||
| chr6:104831960 | GAAGAGAA others(21): Show |
G | 1 | a0001c0001t0001g0161 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.534+1054_534+1081d others(30): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831960 | |||||||
| chr6:104831960 | GAAGAGAA others(29): Show |
G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534+1046_534+1081d others(38): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831960 | |||||||
| chr6:104831962 | A | G | 1 | a0001c0002t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.534+1080T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831962 | |||||||
| chr6:104831964 | A | G | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.534+1078T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831964 | |||||||
| chr6:104831965 | GAAGAGAA others(16): Show |
G | 1 | a0001c0001t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.534+1054_534+1076d others(25): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831965 | |||||||
| chr6:104831965 | GAAGAGAA others(28): Show |
G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.534+1042_534+1076d others(37): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831965 | |||||||
| chr6:104831968 | G | GAGAAGAG others(13): Show |
1 | a0001c0001t0001g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.534+1073_534+1074i others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831968 | |||||||
| chr6:104831969 | A | G | 2 | a0001c0002t0001g0003 a0001c0002t0001g0004 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.534+1073T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831969 | |||||||
| chr6:104831971 | A | G | 1 | a0001c0002t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.534+1071T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831971 | |||||||
| chr6:104831973 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.534+1069C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831973 | |||||||
| chr6:104831973 | GA | G | 4 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0077 others(1): Show |
4 | HG02615.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+1068delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831973 | |||||||
| chr6:104831974 | A | G | 5 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+1068T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831974 | |||||||
| chr6:104831977 | A | AGAGAGGA others(3): Show |
1 | a0001c0001t0001g0237 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.534+1064_534+1065i others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831977 | |||||||
| chr6:104831979 | A | AGAAGAGA others(9): Show |
1 | a0001c0001t0001g0276 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.534+1062_534+1063i others(18): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831979 | |||||||
| chr6:104831979 | A | G | 7 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(4): Show |
9 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1063T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831979 | |||||||
| chr6:104831980 | G | A | 7 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(4): Show |
9 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1062C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | G | GAAGAGAA others(12): Show |
1 | a0001c0001t0002g0056 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.534+1061_534+1062i others(21): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | G | GAGGA | 36 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0280 others(33): Show |
36 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.534+1058_534+1061d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | G | GAGGAAGG others(1): Show |
10 | a0001c0001t0001g0281 a0001c0001t0001g0291 a0001c0001t0002g0031 others(7): Show |
10 | HG00423.hp1 HG01257.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.534+1054_534+1061d others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | G | GAGGAAGG others(5): Show |
3 | a0001c0001t0001g0285 a0001c0001t0002g0061 a0001c0001t0002g0062 |
3 | HG01074.hp1 NA18994.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.534+1050_534+1061d others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | G | GAGGAAGG others(13): Show |
1 | a0001c0002t0001g0083 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.534+1042_534+1061d others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | GAGGA | G | 95 | a0001c0001t0001g0006 a0001c0001t0001g0152 a0001c0001t0001g0154 others(92): Show |
96 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.534+1058_534+1061d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | GAGGAAGG others(1): Show |
G | 69 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0150 others(66): Show |
69 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.534+1054_534+1061d others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | GAGGAAGG others(5): Show |
G | 27 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0146 others(24): Show |
27 | HG00099.hp1 HG00621.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.534+1050_534+1061d others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | GAGGAAGG others(9): Show |
G | 1 | a0001c0001t0001g0176 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.534+1046_534+1061d others(18): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831980 | GAGGAAGG others(13): Show |
G | 3 | a0001c0001t0001g0324 a0001c0004t0001g0139 a0001c0004t0001g0143 |
3 | HG03130.hp1 HG03139.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.534+1042_534+1061d others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | |||||||
| chr6:104831981 | A | AAGAGAAG others(10): Show |
1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+1060_534+1061i others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831981 | |||||||
| chr6:104831982 | G | A | 5 | a0001c0001t0001g0284 a0001c0001t0001g0315 a0001c0001t0001g0327 others(2): Show |
5 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+1060C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831982 | |||||||
| chr6:104831984 | A | AGAAGAGA others(9): Show |
1 | a0001c0001t0002g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.534+1057_534+1058i others(18): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831984 | |||||||
| chr6:104831984 | A | AGAAGAGA others(5): Show |
1 | a0001c0001t0007g0274 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.534+1057_534+1058i others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831984 | |||||||
| chr6:104831991 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+1051C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831991 | |||||||
| chr6:104831992 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+1050T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831992 | |||||||
| chr6:104832168 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.534+874A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832168 | |||||||
| chr6:104832357 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.534+685A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832357 | |||||||
| chr6:104832381 | TTTG | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.534+658_534+660del others(3): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832381 | |||||||
| chr6:104832384 | G | T | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.534+658C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832384 | |||||||
| chr6:104832387 | G | T | 13 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(10): Show |
13 | HG00323.hp2 HG01074.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.534+655C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832387 | |||||||
| chr6:104832474 | A | C | 7 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0104 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+568T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832474 | |||||||
| chr6:104832517 | C | T | 1 | a0001c0001t0002g0020 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.534+525G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832517 | |||||||
| chr6:104832760 | G | A | 43 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(40): Show |
43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.534+282C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832760 | |||||||
| chr6:104832844 | A | T | 1 | a0001c0002t0001g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.534+198T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832844 | |||||||
| chr6:104832870 | G | C | 2 | a0001c0001t0001g0220 a0001c0001t0003g0136 |
2 | HG00408.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.534+172C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832870 | |||||||
| chr6:104833193 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.403-20G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833193 | |||||||
| chr6:104833233 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 |
3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.403-60T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833233 | |||||||
| chr6:104833259 | C | T | 7 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00544.hp1 HG02165.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.403-86G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833259 | |||||||
| chr6:104833337 | C | T | 20 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0232 others(17): Show |
20 | HG00609.hp1 HG00738.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.403-164G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833337 | |||||||
| chr6:104833448 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.403-275A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833448 | |||||||
| chr6:104833616 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-443T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833616 | |||||||
| chr6:104833622 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.403-449A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833622 | |||||||
| chr6:104833624 | G | A | 1 | a0001c0002t0001g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-451C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833624 | |||||||
| chr6:104833854 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.403-681C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833854 | |||||||
| chr6:104834147 | C | CA | 9 | a0001c0001t0001g0157 a0001c0001t0001g0170 a0001c0001t0001g0277 others(6): Show |
9 | HG01109.hp2 HG02738.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-975dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834147 | |||||||
| chr6:104834303 | G | A | 82 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0138 others(79): Show |
82 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.403-1130C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834303 | |||||||
| chr6:104834388 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.403-1215G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834388 | |||||||
| chr6:104834437 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.403-1264G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834437 | |||||||
| chr6:104834588 | G | A | 2 | a0001c0002t0001g0102 a0001c0002t0001g0115 |
2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.403-1415C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834588 | |||||||
| chr6:104834679 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.403-1506A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834679 | |||||||
| chr6:104834839 | T | A | 1 | a0001c0002t0001g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.403-1666A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834839 | |||||||
| chr6:104834933 | C | A | 1 | a0001c0001t0001g0195 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.403-1760G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834933 | |||||||
| chr6:104834971 | T | A | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.403-1798A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834971 | |||||||
| chr6:104835152 | T | C | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.403-1979A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835152 | |||||||
| chr6:104835278 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.403-2105C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835278 | |||||||
| chr6:104835410 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.403-2237A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835410 | |||||||
| chr6:104835542 | GAAAAGAA others(8): Show |
G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.403-2384_403-2370d others(17): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835542 | |||||||
| chr6:104835661 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.403-2488C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835661 | |||||||
| chr6:104836126 | G | C | 48 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(45): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.403-2953C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836126 | |||||||
| chr6:104836243 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.403-3070C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836243 | |||||||
| chr6:104836397 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.403-3224G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836397 | |||||||
| chr6:104836432 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.403-3259C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836432 | |||||||
| chr6:104836439 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.403-3266C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836439 | |||||||
| chr6:104836487 | T | C | 1 | a0001c0002t0001g0096 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.403-3314A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836487 | |||||||
| chr6:104836496 | G | A | 78 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0148 others(75): Show |
78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.403-3323C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836496 | |||||||
| chr6:104836700 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.403-3527C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836700 | |||||||
| chr6:104836911 | A | G | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-3738T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836911 | |||||||
| chr6:104836956 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.403-3783G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836956 | |||||||
| chr6:104836986 | T | A | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-3813A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836986 | |||||||
| chr6:104837066 | A | G | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-3893T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837066 | |||||||
| chr6:104837263 | T | A | 1 | a0001c0002t0001g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.403-4090A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837263 | |||||||
| chr6:104837356 | T | G | 1 | a0001c0001t0001g0320 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.403-4183A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837356 | |||||||
| chr6:104837433 | T | C | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-4260A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837433 | |||||||
| chr6:104837677 | C | G | 1 | a0001c0001t0001g0336 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.403-4504G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837677 | |||||||
| chr6:104837740 | G | T | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.403-4567C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837740 | |||||||
| chr6:104837875 | T | C | 124 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(121): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.403-4702A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837875 | |||||||
| chr6:104837884 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.403-4711G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837884 | |||||||
| chr6:104838020 | C | G | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-4847G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838020 | |||||||
| chr6:104838022 | A | G | 3 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.403-4849T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838022 | |||||||
| chr6:104838128 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.403-4955G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838128 | |||||||
| chr6:104838238 | T | C | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+4985A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838238 | |||||||
| chr6:104838249 | A | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.402+4974T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838249 | |||||||
| chr6:104838352 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.402+4871T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838352 | |||||||
| chr6:104838671 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.402+4552G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838671 | |||||||
| chr6:104838890 | T | TA | 91 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0001t0001g0226 others(88): Show |
92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.402+4332dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | |||||||
| chr6:104838890 | T | TAA | 19 | a0001c0001t0001g0248 a0001c0001t0001g0278 a0001c0001t0001g0279 others(16): Show |
19 | HG00323.hp1 HG00733.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.402+4331_402+4332d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | |||||||
| chr6:104838890 | TA | T | 82 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0140 others(79): Show |
82 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.402+4332delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | |||||||
| chr6:104838890 | TAA | T | 31 | a0001c0001t0001g0184 a0001c0001t0001g0200 a0001c0001t0002g0008 others(28): Show |
31 | HG00597.hp2 HG00735.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.402+4331_402+4332d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | |||||||
| chr6:104838890 | TAAA | T | 41 | a0001c0001t0001g0117 a0001c0001t0002g0001 a0001c0001t0002g0002 others(38): Show |
43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.402+4330_402+4332d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | |||||||
| chr6:104838890 | TAAAAAAA others(2): Show |
T | 42 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(39): Show |
42 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.402+4324_402+4332d others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | |||||||
| chr6:104838890 | TAAAAAAA others(3): Show |
T | 1 | a0001c0002t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.402+4323_402+4332d others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | |||||||
| chr6:104838916 | A | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0038 |
3 | HG01256.hp2 HG01258.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.402+4307T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838916 | |||||||
| chr6:104839145 | G | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.402+4078C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839145 | |||||||
| chr6:104839263 | A | G | 9 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(6): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+3960T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839263 | |||||||
| chr6:104839699 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0300 a0001c0001t0001g0330 |
3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.402+3524G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839699 | |||||||
| chr6:104839748 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3475C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839748 | |||||||
| chr6:104839776 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0004t0001g0139 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+3447G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839776 | |||||||
| chr6:104840250 | A | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(67): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.402+2973T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840250 | |||||||
| chr6:104840301 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.402+2922C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840301 | |||||||
| chr6:104840551 | C | G | 4 | a0001c0001t0001g0138 a0001c0001t0001g0158 a0001c0001t0001g0160 others(1): Show |
4 | HG00741.hp2 HG01516.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+2672G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840551 | |||||||
| chr6:104840600 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.402+2623C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840600 | |||||||
| chr6:104840711 | C | T | 43 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(40): Show |
43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.402+2512G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840711 | |||||||
| chr6:104840722 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.402+2501C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840722 | |||||||
| chr6:104840792 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.402+2431G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840792 | |||||||
| chr6:104840824 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.402+2399C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840824 | |||||||
| chr6:104840926 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.402+2297C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840926 | |||||||
| chr6:104840955 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.402+2268G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840955 | |||||||
| chr6:104841052 | T | C | 111 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(108): Show |
112 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.402+2171A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841052 | |||||||
| chr6:104841053 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.402+2170C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841053 | |||||||
| chr6:104841118 | C | CA | 10 | a0001c0001t0001g0166 a0001c0001t0001g0306 a0001c0001t0001g0323 others(7): Show |
10 | HG01952.hp1 HG02004.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.402+2104dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841118 | |||||||
| chr6:104841476 | C | T | 1 | a0001c0002t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.402+1747G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841476 | |||||||
| chr6:104841744 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.402+1479A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841744 | |||||||
| chr6:104841797 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.402+1426C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841797 | |||||||
| chr6:104841886 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402+1337C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841886 | |||||||
| chr6:104842008 | TATATAAA | T | 11 | a0001c0002t0001g0090 a0001c0002t0001g0091 a0001c0002t0001g0092 others(8): Show |
11 | HG01515.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+1208_402+1214d others(9): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842008 | |||||||
| chr6:104842139 | T | C | 53 | a0001c0001t0001g0138 a0001c0001t0001g0158 a0001c0001t0001g0159 others(50): Show |
53 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.402+1084A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842139 | |||||||
| chr6:104842316 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.402+907C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842316 | |||||||
| chr6:104842348 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.402+875C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842348 | |||||||
| chr6:104842356 | A | T | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.402+867T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842356 | |||||||
| chr6:104842374 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.402+849G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842374 | |||||||
| chr6:104842500 | AG | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 |
3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.402+722delC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842500 | |||||||
| chr6:104842551 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.402+672A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842551 | |||||||
| chr6:104842686 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402+537C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842686 | |||||||
| chr6:104842878 | G | C | 1 | a0001c0001t0001g0282 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.402+345C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842878 | |||||||
| chr6:104843537 | A | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.327-239T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104843537 | |||||||
| chr6:104844002 | G | A | 80 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0144 others(77): Show |
80 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.327-704C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844002 | |||||||
| chr6:104844034 | G | GT | 28 | a0001c0001t0001g0141 a0001c0001t0001g0175 a0001c0001t0001g0178 others(25): Show |
28 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.327-737dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844034 | |||||||
| chr6:104844049 | T | C | 27 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(24): Show |
27 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.327-751A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844049 | |||||||
| chr6:104844212 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.327-914A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844212 | |||||||
| chr6:104844310 | C | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-1012G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844310 | |||||||
| chr6:104844314 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.327-1016G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844314 | |||||||
| chr6:104844344 | A | AT | 7 | a0001c0001t0001g0170 a0001c0001t0001g0220 a0001c0001t0001g0244 others(4): Show |
7 | HG00408.hp1 HG01934.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.327-1047dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844344 | |||||||
| chr6:104844344 | ATTT | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(67): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.327-1049_327-1047d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844344 | |||||||
| chr6:104844365 | G | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(67): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.327-1067C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844365 | |||||||
| chr6:104844469 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0146 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-1171C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844469 | |||||||
| chr6:104844504 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.327-1206T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844504 | |||||||
| chr6:104844567 | A | G | 1 | a0001c0002t0001g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.327-1269T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844567 | |||||||
| chr6:104844599 | C | A | 1 | a0001c0002t0001g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.327-1301G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844599 | |||||||
| chr6:104844662 | C | CT | 18 | a0001c0001t0001g0161 a0001c0001t0001g0201 a0001c0001t0002g0014 others(15): Show |
18 | HG00609.hp2 HG01175.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.327-1365dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844662 | |||||||
| chr6:104844672 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.327-1374A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844672 | |||||||
| chr6:104844821 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.327-1523G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844821 | |||||||
| chr6:104844856 | G | T | 1 | a0001c0001t0001g0336 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.327-1558C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844856 | |||||||
| chr6:104844925 | A | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-1627T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844925 | |||||||
| chr6:104844934 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.327-1636C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844934 | |||||||
| chr6:104845227 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.327-1929A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845227 | |||||||
| chr6:104845273 | T | C | 2 | a0001c0002t0001g0088 a0001c0002t0001g0089 |
2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.327-1975A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845273 | |||||||
| chr6:104845476 | C | CT | 176 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0001g0138 others(173): Show |
177 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.327-2179dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845476 | |||||||
| chr6:104845476 | C | CTT | 15 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0176 others(12): Show |
15 | HG00408.hp1 HG01981.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.327-2180_327-2179d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845476 | |||||||
| chr6:104845546 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.327-2248G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845546 | |||||||
| chr6:104845654 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.327-2356A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845654 | |||||||
| chr6:104845707 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0006g0337 |
2 | HG02145.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.327-2409T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845707 | |||||||
| chr6:104845728 | C | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.327-2430G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845728 | |||||||
| chr6:104846269 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.326+2873T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846269 | |||||||
| chr6:104846296 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.326+2846A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846296 | |||||||
| chr6:104846304 | T | G | 5 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(2): Show |
5 | NA18962.hp2 NA18993.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+2838A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846304 | |||||||
| chr6:104846625 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.326+2517G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846625 | |||||||
| chr6:104846955 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0245 |
2 | HG02027.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.326+2187A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846955 | |||||||
| chr6:104846981 | T | C | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.326+2161A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846981 | |||||||
| chr6:104847087 | CTTTA | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+2051_326+2054d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847087 | |||||||
| chr6:104847660 | C | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(67): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.326+1482G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847660 | |||||||
| chr6:104847755 | TA | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+1386delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847755 | |||||||
| chr6:104847772 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.326+1370G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847772 | |||||||
| chr6:104847810 | G | GT | 6 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0239 others(3): Show |
6 | HG03942.hp2 HG04199.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+1331dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847810 | |||||||
| chr6:104848059 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.326+1083A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848059 | |||||||
| chr6:104848094 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0015 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+1048G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848094 | |||||||
| chr6:104848098 | C | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.326+1044G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848098 | |||||||
| chr6:104848191 | C | T | 45 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(42): Show |
47 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.326+951G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848191 | |||||||
| chr6:104848275 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.326+867C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848275 | |||||||
| chr6:104848387 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.326+755A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848387 | |||||||
| chr6:104848400 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.326+742C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848400 | |||||||
| chr6:104848411 | G | A | 3 | a0001c0002t0001g0085 a0001c0002t0001g0111 a0001c0002t0001g0112 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.326+731C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848411 | |||||||
| chr6:104848515 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | NA18943.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.326+627T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848515 | |||||||
| chr6:104848553 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+589C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848553 | |||||||
| chr6:104848977 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.326+165T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848977 | |||||||
| chr6:104849007 | A | G | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.326+135T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104849007 | |||||||
| chr6:104849021 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.326+121G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104849021 | |||||||
| chr6:104849504 | A | AT | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.222-259dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849504 | |||||||
| chr6:104849504 | A | ATT | 7 | a0001c0001t0001g0148 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG00735.hp2 HG02135.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-260_222-259dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849504 | |||||||
| chr6:104849604 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-358T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849604 | |||||||
| chr6:104849641 | C | T | 2 | a0001c0004t0001g0139 a0001c0004t0001g0143 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.222-395G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849641 | |||||||
| chr6:104849651 | A | ATT | 327 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(324): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.222-407_222-406dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849651 | |||||||
| chr6:104849767 | G | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.222-521C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849767 | |||||||
| chr6:104849773 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.222-527G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849773 | |||||||
| chr6:104849852 | A | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-606T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849852 | |||||||
| chr6:104849893 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.222-647C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849893 | |||||||
| chr6:104849908 | C | T | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.222-662G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849908 | |||||||
| chr6:104849942 | G | A | 1 | a0001c0002t0001g0119 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.222-696C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849942 | |||||||
| chr6:104849949 | C | CT | 11 | a0001c0001t0001g0140 a0001c0001t0001g0160 a0001c0001t0002g0031 others(8): Show |
13 | HG00423.hp1 HG00741.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.222-704dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849949 | |||||||
| chr6:104849949 | CT | C | 114 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0171 others(111): Show |
115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.222-704delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849949 | |||||||
| chr6:104850014 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.222-768T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850014 | |||||||
| chr6:104850123 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.221+784A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850123 | |||||||
| chr6:104850568 | C | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+339G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850568 | |||||||
| chr6:104850599 | A | C | 1 | a0001c0001t0002g0018 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.221+308T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850599 | |||||||
| chr6:104850697 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.221+210T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850697 | |||||||
| chr6:104850852 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | NA18943.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.221+55C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850852 | |||||||
| chr6:104851056 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.132-60A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851056 | |||||||
| chr6:104851471 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.132-475A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851471 | |||||||
| chr6:104851508 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.132-512C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851508 | |||||||
| chr6:104851649 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.132-653C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851649 | |||||||
| chr6:104851719 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 |
4 | HG02572.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+598C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851719 | |||||||
| chr6:104851730 | CA | C | 184 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(181): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.131+586delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851730 | |||||||
| chr6:104851741 | A | T | 12 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0246 others(9): Show |
14 | HG02080.hp2 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.131+576T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851741 | |||||||
| chr6:104851960 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131+357G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851960 | |||||||
| chr6:104852055 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.131+262C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852055 | |||||||
| chr6:104852086 | T | C | 2 | a0001c0002t0001g0095 a0001c0002t0001g0096 |
2 | HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.131+231A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852086 | |||||||
| chr6:104852195 | C | CTG | 61 | a0001c0001t0001g0006 a0001c0001t0001g0227 a0001c0001t0001g0229 others(58): Show |
62 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.131+120_131+121dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852195 | |||||||
| chr6:104852195 | C | CTGTG | 17 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0239 others(14): Show |
17 | HG00609.hp1 HG01175.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.131+121_131+122ins others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852195 | |||||||
| chr6:104852195 | C | CTGTGTG | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
6 | HG01981.hp1 HG03130.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+121_131+122ins others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852195 | |||||||
| chr6:104852195 | CTGTCTG | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0300 a0001c0001t0001g0330 |
3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.131+116_131+121del others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852195 | |||||||
| chr6:104852199 | C | CTG | 19 | a0001c0001t0001g0135 a0001c0001t0001g0147 a0001c0001t0002g0007 others(16): Show |
19 | HG00597.hp2 HG01175.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.131+116_131+117dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | |||||||
| chr6:104852199 | C | CTGTG | 9 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0001g0145 others(6): Show |
9 | HG01243.hp2 HG01891.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.131+114_131+117dup others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | |||||||
| chr6:104852199 | C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0013 |
3 | HG02055.hp1 HG02965.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.131+110_131+117dup others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | |||||||
| chr6:104852199 | C | CTGTGTGT others(3): Show |
4 | a0001c0001t0001g0137 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02572.hp1 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+108_131+117dup others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | |||||||
| chr6:104852199 | C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 |
4 | HG02895.hp1 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+106_131+117dup others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | |||||||
| chr6:104852199 | C | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(111): Show |
115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.131+118G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | |||||||
| chr6:104852199 | CTG | C | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.131+116_131+117del others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | |||||||
| chr6:104852209 | G | GTT | 5 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG00738.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+107_131+108ins others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852209 | |||||||
| chr6:104852210 | T | TGC | 4 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(1): Show |
4 | NA18965.hp1 NA18967.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+106_131+107ins others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852210 | |||||||
| chr6:104852228 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.131+89A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852228 | T | TGC | 12 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(9): Show |
12 | HG01167.hp1 HG02896.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.131+87_131+88dupGC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852228 | T | TGTGC | 48 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(45): Show |
48 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852228 | T | TGTGCGC | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852228 | T | TGTGTGC | 45 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0160 others(42): Show |
46 | HG00323.hp2 HG00609.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852228 | T | TGTGTGTG others(1): Show |
17 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(14): Show |
17 | HG01515.hp1 HG01516.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852228 | T | TGTGTGTG others(3): Show |
6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0002t0001g0003 others(3): Show |
7 | HG02280.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852228 | T | TGTGTGTG others(5): Show |
2 | a0001c0002t0001g0082 a0001c0002t0001g0083 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131+88_131+89insGC others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852228 | T | TGTGTGTG others(7): Show |
2 | a0001c0002t0001g0076 a0001c0003t0001g0225 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.131+88_131+89insGC others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | |||||||
| chr6:104852230 | C | T | 147 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0226 others(144): Show |
150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.131+87G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852230 | |||||||
| chr6:104852232 | C | T | 2 | a0001c0002t0001g0111 a0001c0002t0001g0112 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.131+85G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852232 | |||||||
| chr6:104852234 | C | T | 4 | a0001c0002t0001g0085 a0001c0002t0001g0090 a0001c0002t0001g0111 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+83G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852234 | |||||||
| chr6:104852246 | C | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.131+71G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852246 | |||||||
| chr6:104852375 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
splice_region_variant&intron_variant | LOW | c.77-4T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852375 | |||||||
| chr6:104852387 | C | CAG | 174 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0118 others(171): Show |
177 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77-17_77-16insCT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852387 | |||||||
| chr6:104852445 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.77-74T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852445 | |||||||
| chr6:104852531 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.77-160G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852531 | |||||||
| chr6:104852695 | C | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.77-324G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852695 | |||||||
| chr6:104852723 | G | C | 1 | a0001c0001t0002g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.77-352C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852723 | |||||||
| chr6:104852733 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.77-362A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852733 | |||||||
| chr6:104852854 | T | A | 1 | a0001c0001t0001g0333 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.77-483A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852854 | |||||||
| chr6:104853302 | T | C | 1 | a0001c0002t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.77-931A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853302 | |||||||
| chr6:104853375 | A | C | 4 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.77-1004T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853375 | |||||||
| chr6:104853609 | C | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.77-1238G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853609 | |||||||
| chr6:104853708 | G | T | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77-1337C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853708 | |||||||
| chr6:104853723 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.77-1352T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853723 | |||||||
| chr6:104853780 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.77-1409A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853780 | |||||||
| chr6:104853803 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(5): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.77-1432G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853803 | |||||||
| chr6:104853837 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.77-1466C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853837 | |||||||
| chr6:104853902 | A | G | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.77-1531T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853902 | |||||||
| chr6:104854075 | G | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.77-1704C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854075 | |||||||
| chr6:104854206 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.77-1835C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854206 | |||||||
| chr6:104854347 | T | C | 44 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(41): Show |
44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.77-1976A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854347 | |||||||
| chr6:104854575 | A | AT | 44 | a0001c0002t0001g0079 a0001c0002t0001g0081 a0001c0002t0001g0082 others(41): Show |
44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.77-2205dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854575 | |||||||
| chr6:104854595 | T | C | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77-2224A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854595 | |||||||
| chr6:104854785 | C | A | 1 | a0001c0003t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.77-2414G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854785 | |||||||
| chr6:104854856 | G | A | 1 | a0001c0001t0001g0326 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.77-2485C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854856 | |||||||
| chr6:104854888 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.77-2517G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854888 | |||||||
| chr6:104855009 | T | C | 1 | a0001c0002t0001g0132 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.77-2638A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855009 | |||||||
| chr6:104855057 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.77-2686A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855057 | |||||||
| chr6:104855254 | C | T | 1 | a0001c0002t0001g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.77-2883G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855254 | |||||||
| chr6:104855429 | C | G | 1 | a0001c0002t0001g0119 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77-3058G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855429 | |||||||
| chr6:104855430 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.77-3059C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855430 | |||||||
| chr6:104855749 | C | T | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77-3378G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855749 | |||||||
| chr6:104855777 | T | C | 2 | a0001c0001t0001g0328 a0001c0001t0001g0329 |
2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.77-3406A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855777 | |||||||
| chr6:104855868 | G | A | 47 | a0001c0001t0001g0330 a0001c0002t0001g0079 a0001c0002t0001g0081 others(44): Show |
47 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.77-3497C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855868 | |||||||
| chr6:104856245 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.76+3322T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856245 | |||||||
| chr6:104856362 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.76+3205A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856362 | |||||||
| chr6:104856441 | G | GT | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0002t0001g0003 others(15): Show |
20 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.76+3125dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856441 | |||||||
| chr6:104856441 | G | GTT | 41 | a0001c0002t0001g0079 a0001c0002t0001g0086 a0001c0002t0001g0087 others(38): Show |
41 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.76+3124_76+3125dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856441 | |||||||
| chr6:104856494 | G | C | 2 | a0001c0003t0001g0224 a0001c0003t0001g0225 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.76+3073C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856494 | |||||||
| chr6:104856532 | T | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(67): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.76+3035A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856532 | |||||||
| chr6:104856803 | C | T | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.76+2764G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856803 | |||||||
| chr6:104857164 | T | C | 2 | a0001c0002t0001g0085 a0001c0002t0001g0112 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.76+2403A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857164 | |||||||
| chr6:104857169 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.76+2398T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857169 | |||||||
| chr6:104857178 | C | A | 1 | a0001c0001t0001g0213 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.76+2389G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857178 | |||||||
| chr6:104857202 | C | CAT | 6 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(3): Show |
8 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+2363_76+2364dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857202 | |||||||
| chr6:104857202 | CAT | C | 40 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 others(37): Show |
40 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.76+2363_76+2364del others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857202 | |||||||
| chr6:104857275 | A | G | 57 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0076 others(54): Show |
59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.76+2292T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857275 | |||||||
| chr6:104857343 | T | C | 1 | a0001c0001t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.76+2224A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857343 | |||||||
| chr6:104857627 | G | C | 1 | a0001c0002t0008g0340 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76+1940C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857627 | |||||||
| chr6:104857653 | C | CA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0214 a0001c0001t0001g0215 others(5): Show |
9 | HG02074.hp1 HG02074.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.76+1913dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857653 | |||||||
| chr6:104857747 | G | C | 1 | a0001c0002t0001g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.76+1820C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857747 | |||||||
| chr6:104857774 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.76+1793C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857774 | |||||||
| chr6:104857774 | G | T | 1 | a0001c0001t0001g0229 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.76+1793C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857774 | |||||||
| chr6:104857874 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.76+1693C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857874 | |||||||
| chr6:104857956 | C | CA | 10 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(7): Show |
10 | HG00733.hp1 HG01943.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.76+1610dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857956 | |||||||
| chr6:104857956 | CA | C | 169 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0118 others(166): Show |
172 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.76+1610delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857956 | |||||||
| chr6:104858027 | G | T | 1 | a0001c0001t0002g0008 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.76+1540C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858027 | |||||||
| chr6:104858091 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.76+1476A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858091 | |||||||
| chr6:104858269 | C | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.76+1298G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858269 | |||||||
| chr6:104858384 | G | A | 2 | a0001c0001t0001g0336 a0001c0001t0006g0337 |
2 | HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.76+1183C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858384 | |||||||
| chr6:104858460 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG01978.hp2 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.76+1107C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858460 | |||||||
| chr6:104858460 | G | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0338 others(1): Show |
4 | HG01515.hp2 HG01517.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.76+1107C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858460 | |||||||
| chr6:104858460 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76+1107C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858460 | |||||||
| chr6:104858527 | T | A | 14 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(11): Show |
14 | HG00323.hp2 HG01074.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.76+1040A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858527 | |||||||
| chr6:104858531 | C | T | 1 | a0001c0001t0003g0136 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.76+1036G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858531 | |||||||
| chr6:104858547 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.76+1020T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858547 | |||||||
| chr6:104858659 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.76+908T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858659 | |||||||
| chr6:104858983 | T | C | 1 | a0001c0001t0002g0075 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.76+584A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858983 | |||||||
| chr6:104859039 | A | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.76+528T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859039 | |||||||
| chr6:104859311 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.76+256T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859311 | |||||||
| chr6:104859349 | C | A | 2 | a0001c0003t0001g0224 a0001c0003t0001g0225 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.76+218G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859349 | |||||||
| chr6:104859486 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.76+81G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859486 | |||||||
| chr6:104859486 | C | T | 1 | a0001c0001t0002g0007 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.76+81G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859486 | |||||||
| chr6:104859503 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.76+64C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859503 | |||||||
| chr6:104859560 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0227 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
splice_region_variant&intron_variant | LOW | c.76+7C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859560 |