Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22938 |
| ensemblid | ENSG00000100603.14 |
| hgncid | 16696 |
| symbol | SNW1 |
| name | SNW domain containing 1 |
| refseq_nuc | NM_012245.3 |
| refseq_prot | NP_036377.1 |
| ensembl_nuc | ENST00000261531.12 |
| ensembl_prot | ENSP00000261531.8 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 77717599 |
| end | 77761156 |
| strand | - |
| ver | v1.2 |
| region | chr14:77717599-77761156 |
| region5000 | chr14:77712599-77766156 |
| regionname0 | SNW1_chr14_77717599_77761156 |
| regionname5000 | SNW1_chr14_77712599_77766156 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 536 | 365 | 94 | 62 | 153 | 18 | 36 | 119 | SNW1_chr14_77712599_77766156 | SNW1 | MALTS others(531): Show |
chr14 | 77712599 | 77766156 |
| a0002 | 0/0 | 528 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | MALTR others(523): Show |
chr14 | 77712599 | 77766156 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1608 | 220 | 57 | 36 | 90 | 9 | 28 | SNW1_chr14_77712599_77766156 | SNW1 | ATGGC others(1603): Show |
chr14 | 77712599 | 77766156 | ||
| a0001c0002 | 1/0 | 1608 | 70 | 8 | 10 | 44 | 3 | 4 | SNW1_chr14_77712599_77766156 | SNW1 | ATGGC others(1603): Show |
chr14 | 77712599 | 77766156 | ||
| a0001c0003 | 0/1 | 1608 | 69 | 24 | 15 | 19 | 6 | 4 | SNW1_chr14_77712599_77766156 | SNW1 | ATGGC others(1603): Show |
chr14 | 77712599 | 77766156 | ||
| a0001c0004 | 0/0 | 1608 | 4 | 4 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | ATGGC others(1603): Show |
chr14 | 77712599 | 77766156 | ||
| a0001c0006 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | ATGGC others(1603): Show |
chr14 | 77712599 | 77766156 | ||
| a0001c0007 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | ATGGC others(1603): Show |
chr14 | 77712599 | 77766156 | ||
| a0002c0005 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | ATGGC others(1579): Show |
chr14 | 77712599 | 77766156 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2129 | 218 | 56 | 36 | 90 | 9 | 27 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0001c0001t0004 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0001c0001t0005 | 0/0 | 2129 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0001c0002t0001 | 1/0 | 2129 | 69 | 7 | 10 | 44 | 3 | 4 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0001c0002t0006 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0001c0003t0001 | 0/1 | 2129 | 39 | 16 | 5 | 12 | 4 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0001c0003t0002 | 0/0 | 2130 | 27 | 5 | 10 | 7 | 2 | 3 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2125): Show |
chr14 | 77712599 | 77766156 |
| a0001c0003t0003 | 0/0 | 2128 | 3 | 3 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2123): Show |
chr14 | 77712599 | 77766156 |
| a0001c0004t0001 | 0/0 | 2129 | 4 | 4 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0001c0006t0001 | 0/0 | 2129 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0001c0007t0001 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2124): Show |
chr14 | 77712599 | 77766156 |
| a0002c0005t0001 | 0/0 | 2105 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | GTCGC others(2100): Show |
chr14 | 77712599 | 77766156 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 2 | 0 | 8 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0002t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0003t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0006t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0001c0007t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| a0002c0005t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0075 | EUR | GBR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0054 | EUR | FIN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0005 | EUR | FIN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0139 | EUR | FIN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0016 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0059 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01106 | hp2 | a0001 | c0006 | t0001 | g0099 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0143 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0126 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01167 | hp2 | a0001 | c0003 | t0002 | g0141 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0016 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0123 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0134 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0053 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0140 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0058 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0117 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0127 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0311 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | CDX | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02165 | hp1 | a0001 | c0003 | t0002 | g0133 | EAS | CDX | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02280 | hp2 | a0001 | c0002 | t0006 | g0105 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02293 | hp2 | a0001 | c0003 | t0002 | g0129 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0136 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02630 | hp1 | a0001 | c0003 | t0002 | g0135 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02630 | hp2 | a0001 | c0007 | t0001 | g0312 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0313 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02809 | hp2 | a0001 | c0003 | t0003 | g0122 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03195 | hp1 | a0001 | c0003 | t0002 | g0153 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0052 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0049 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0063 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0138 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0050 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0137 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0150 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0262 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG04228 | hp2 | a0001 | c0003 | t0002 | g0142 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0120 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0130 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0131 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18986 | hp2 | a0002 | c0005 | t0001 | g0275 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0132 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18995 | hp2 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19001 | hp2 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ASW | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ASW | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0077 | EUR | TSI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0149 | EUR | TSI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | TSI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0125 | EUR | TSI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | GIH | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | GIH | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02559 | hp1 | a0001 | c0003 | t0003 | g0121 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | USA | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0051 | AFR | USA | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | USA | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0128 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0055 | REF | REF | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0070 | REF | REF | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77755096 | TAGCTGAG others(58): Show |
T | 1 | a0002 | 1 | NA18986.hp2 | splice_acceptor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.15-41_38delGAGTTTT others(58): Show |
p.Ser5_Leu13delinsAr others(1): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/14 | 67/2129 | 15/1611 | 5/536 | chr14 | 77755096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77718223 | C | A | 5 | a0001c0001 a0001c0003 a0001c0004 others(2): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
synonymous_variant | LOW | c.1476G>T | p.Val492Val | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 1505/2129 | 1476/1611 | 492/536 | chr14 | 77718223 | |||
| chr14:77718447 | G | C | 1 | a0001c0007 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1332C>G | p.Ala444Ala | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 13/14 | 1361/2129 | 1332/1611 | 444/536 | chr14 | 77718447 | |||
| chr14:77731022 | C | T | 3 | a0001c0001 a0001c0004 a0002c0005 |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
synonymous_variant | LOW | c.999G>A | p.Glu333Glu | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/14 | 1028/2129 | 999/1611 | 333/536 | chr14 | 77731022 | |||
| chr14:77751355 | A | G | 1 | a0001c0006 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.294T>C | p.Tyr98Tyr | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/14 | 323/2129 | 294/1611 | 98/536 | chr14 | 77751355 | |||
| chr14:77755021 | T | G | 1 | a0001c0004 | 4 | HG03195.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.114A>C | p.Arg38Arg | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/14 | 143/2129 | 114/1611 | 38/536 | chr14 | 77755021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77717698 | AT | A | 1 | a0001c0003t0003 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*389delA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 389 | chr14 | 77717698 | ||||||
| chr14:77717810 | C | T | 1 | a0001c0001t0005 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 278 | chr14 | 77717810 | ||||||
| chr14:77717938 | T | TC | 1 | a0001c0003t0002 | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*149dupG | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 149 | chr14 | 77717938 | ||||||
| chr14:77718038 | C | T | 1 | a0001c0001t0004 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*50G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 50 | chr14 | 77718038 | ||||||
| chr14:77718067 | T | A | 1 | a0001c0002t0006 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 21 | chr14 | 77718067 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77718318 | T | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1413-32A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 13/13 | chr14 | 77718318 | |||||||
| chr14:77718613 | T | C | 3 | a0001c0002t0001g0080 a0001c0002t0001g0081 a0001c0002t0001g0086 |
3 | NA18979.hp1 NA18985.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1249-83A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718613 | |||||||
| chr14:77718639 | A | G | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | NA18968.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1249-109T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718639 | |||||||
| chr14:77718713 | C | CT | 7 | a0001c0001t0001g0199 a0001c0001t0001g0250 a0001c0001t0001g0309 others(4): Show |
7 | HG01255.hp1 HG02071.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1249-184dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718713 | |||||||
| chr14:77718854 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1249-324C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718854 | |||||||
| chr14:77718972 | A | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1249-442T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718972 | |||||||
| chr14:77719000 | C | A | 23 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0017 others(20): Show |
27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1249-470G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719000 | |||||||
| chr14:77719074 | C | G | 1 | a0001c0003t0001g0155 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1249-544G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719074 | |||||||
| chr14:77719085 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1249-555A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719085 | |||||||
| chr14:77719118 | G | A | 5 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0126 others(2): Show |
8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-588C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719118 | |||||||
| chr14:77719167 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1249-637A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719167 | |||||||
| chr14:77719232 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
133 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1249-702A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719232 | |||||||
| chr14:77719380 | G | A | 16 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1249-850C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719380 | |||||||
| chr14:77719420 | G | A | 1 | a0001c0002t0001g0083 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1249-890C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719420 | |||||||
| chr14:77719498 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1249-968T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719498 | |||||||
| chr14:77719554 | T | A | 12 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0239 others(9): Show |
12 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1249-1024A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719554 | |||||||
| chr14:77719556 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1249-1026G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719556 | |||||||
| chr14:77719576 | G | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1249-1046C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719576 | |||||||
| chr14:77719649 | A | AAAAC | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1248+1058_1248+106 others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719649 | |||||||
| chr14:77719659 | A | AAC | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1248+1051_1248+105 others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719659 | |||||||
| chr14:77719838 | TAATA | T | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1248+869_1248+872d others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719838 | |||||||
| chr14:77719940 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1248+771A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719940 | |||||||
| chr14:77719945 | A | C | 1 | a0001c0001t0001g0299 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1248+766T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719945 | |||||||
| chr14:77719946 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1248+765A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719946 | |||||||
| chr14:77719948 | C | T | 1 | a0001c0003t0002g0132 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1248+763G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719948 | |||||||
| chr14:77719954 | C | T | 4 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0104 others(1): Show |
6 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248+757G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719954 | |||||||
| chr14:77720013 | C | G | 1 | a0001c0004t0001g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1248+698G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720013 | |||||||
| chr14:77720028 | C | T | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1248+683G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720028 | |||||||
| chr14:77720083 | T | G | 2 | a0001c0003t0001g0149 a0001c0003t0001g0150 |
2 | HG03710.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1248+628A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720083 | |||||||
| chr14:77720141 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1248+570C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720141 | |||||||
| chr14:77720146 | A | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1248+565T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720146 | |||||||
| chr14:77720233 | C | CATAAGCT others(1): Show |
257 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1248+477_1248+478i others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720233 | |||||||
| chr14:77720244 | C | T | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1248+467G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720244 | |||||||
| chr14:77720626 | C | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1248+85G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720626 | |||||||
| chr14:77720689 | T | C | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1248+22A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720689 | |||||||
| chr14:77720970 | CATA | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131-145_1131-143d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77720970 | |||||||
| chr14:77720973 | A | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1131-145T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77720973 | |||||||
| chr14:77721108 | C | A | 2 | a0001c0003t0001g0053 a0001c0003t0001g0054 |
2 | HG00280.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1131-280G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721108 | |||||||
| chr14:77721277 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1131-449C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721277 | |||||||
| chr14:77721397 | C | T | 23 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0017 others(20): Show |
27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1131-569G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721397 | |||||||
| chr14:77721509 | C | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0187 a0001c0001t0005g0262 |
3 | HG03492.hp2 HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1131-681G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721509 | |||||||
| chr14:77721654 | CTT | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0159 a0001c0001t0001g0160 others(5): Show |
10 | HG02055.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1131-828_1131-827d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721654 | |||||||
| chr14:77721742 | A | T | 9 | a0001c0002t0001g0011 a0001c0002t0001g0029 a0001c0002t0001g0030 others(6): Show |
10 | HG00408.hp1 HG01928.hp2 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.1131-914T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721742 | |||||||
| chr14:77721746 | T | A | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1131-918A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721746 | |||||||
| chr14:77721910 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1131-1082C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721910 | |||||||
| chr14:77721921 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1131-1093G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721921 | |||||||
| chr14:77721949 | T | C | 1 | a0001c0003t0002g0133 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1131-1121A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721949 | |||||||
| chr14:77721961 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1131-1133A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721961 | |||||||
| chr14:77722023 | C | A | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1130+1158G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722023 | |||||||
| chr14:77722304 | T | TA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1130+876dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722304 | |||||||
| chr14:77722535 | T | C | 38 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0210 others(35): Show |
40 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1130+646A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722535 | |||||||
| chr14:77722558 | A | G | 5 | a0001c0001t0001g0173 a0001c0001t0001g0233 a0001c0001t0001g0304 others(2): Show |
5 | HG01256.hp1 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130+623T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722558 | |||||||
| chr14:77722560 | A | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0233 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1130+621T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722560 | |||||||
| chr14:77722594 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1130+587T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722594 | |||||||
| chr14:77722769 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1130+412G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722769 | |||||||
| chr14:77722793 | G | T | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1130+388C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722793 | |||||||
| chr14:77722838 | C | CT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1130+342dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722838 | |||||||
| chr14:77722838 | C | CTT | 61 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0169 others(58): Show |
64 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1130+341_1130+342d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722838 | |||||||
| chr14:77722838 | C | CTTT | 8 | a0001c0001t0001g0278 a0001c0001t0001g0284 a0001c0001t0001g0290 others(5): Show |
8 | HG00558.hp2 HG00621.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1130+340_1130+342d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722838 | |||||||
| chr14:77722885 | C | A | 2 | a0001c0002t0001g0100 a0001c0002t0001g0102 |
2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1130+296G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722885 | |||||||
| chr14:77722893 | G | A | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1130+288C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722893 | |||||||
| chr14:77722913 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1130+268G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722913 | |||||||
| chr14:77722959 | C | T | 2 | a0001c0003t0001g0057 a0001c0003t0001g0065 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1130+222G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722959 | |||||||
| chr14:77723041 | G | A | 7 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0240 others(4): Show |
7 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1130+140C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77723041 | |||||||
| chr14:77723057 | C | G | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1130+124G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77723057 | |||||||
| chr14:77723082 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1130+99G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77723082 | |||||||
| chr14:77723354 | T | C | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-77A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723354 | |||||||
| chr14:77723559 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1034-282C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723559 | |||||||
| chr14:77723614 | T | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1034-337A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723614 | |||||||
| chr14:77723662 | T | C | 5 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0126 others(2): Show |
8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1034-385A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723662 | |||||||
| chr14:77723706 | A | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-429T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723706 | |||||||
| chr14:77723940 | T | C | 1 | a0001c0001t0004g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1034-663A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723940 | |||||||
| chr14:77723995 | TAA | T | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1034-720_1034-719d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723995 | |||||||
| chr14:77724053 | C | T | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-776G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724053 | |||||||
| chr14:77724088 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1034-811G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724088 | |||||||
| chr14:77724101 | T | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1034-824A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724101 | |||||||
| chr14:77724155 | T | C | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1034-878A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724155 | |||||||
| chr14:77724181 | A | G | 2 | a0001c0003t0001g0014 a0001c0003t0001g0060 |
3 | HG01109.hp1 HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1034-904T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724181 | |||||||
| chr14:77724222 | A | G | 1 | a0001c0002t0001g0029 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1034-945T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724222 | |||||||
| chr14:77724381 | T | A | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1034-1104A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724381 | |||||||
| chr14:77724419 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1034-1142G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724419 | |||||||
| chr14:77724529 | C | T | 1 | a0001c0001t0005g0262 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1034-1252G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724529 | |||||||
| chr14:77724568 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1034-1291G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724568 | |||||||
| chr14:77724765 | T | C | 1 | a0001c0003t0002g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1034-1488A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724765 | |||||||
| chr14:77725072 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1034-1795A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725072 | |||||||
| chr14:77725105 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1034-1828C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725105 | |||||||
| chr14:77725169 | A | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-1892T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725169 | |||||||
| chr14:77725256 | T | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1034-1979A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725256 | |||||||
| chr14:77725460 | G | A | 6 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0240 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034-2183C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725460 | |||||||
| chr14:77725600 | G | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0293 a0001c0001t0001g0300 others(2): Show |
6 | HG00558.hp2 HG00673.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034-2323C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725600 | |||||||
| chr14:77725668 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1034-2391G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725668 | |||||||
| chr14:77725738 | C | G | 1 | a0001c0002t0001g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1034-2461G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725738 | |||||||
| chr14:77725907 | C | T | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1034-2630G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725907 | |||||||
| chr14:77725935 | T | C | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-2658A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725935 | |||||||
| chr14:77725948 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1034-2671C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725948 | |||||||
| chr14:77726003 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1034-2726A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726003 | |||||||
| chr14:77726280 | T | C | 16 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1034-3003A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726280 | |||||||
| chr14:77726465 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1034-3188T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726465 | |||||||
| chr14:77726470 | T | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0181 others(6): Show |
11 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1034-3193A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726470 | |||||||
| chr14:77726470 | T | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1034-3193A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726470 | |||||||
| chr14:77726585 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1034-3308A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726585 | |||||||
| chr14:77726629 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1034-3352C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726629 | |||||||
| chr14:77726680 | G | A | 1 | a0001c0001t0004g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1034-3403C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726680 | |||||||
| chr14:77726825 | A | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0045 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1034-3548T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726825 | |||||||
| chr14:77727046 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1034-3769A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727046 | |||||||
| chr14:77727056 | G | GT | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-3780dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727056 | |||||||
| chr14:77727118 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
132 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1034-3841T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727118 | |||||||
| chr14:77727202 | C | T | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1033+3786G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727202 | |||||||
| chr14:77727555 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1033+3433A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727555 | |||||||
| chr14:77727573 | T | C | 21 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(18): Show |
25 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1033+3415A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727573 | |||||||
| chr14:77727664 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1033+3324C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727664 | |||||||
| chr14:77727748 | G | A | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1033+3240C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727748 | |||||||
| chr14:77727852 | T | C | 5 | a0001c0001t0001g0158 a0001c0001t0001g0172 a0001c0001t0001g0185 others(2): Show |
5 | HG01256.hp2 HG01433.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033+3136A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727852 | |||||||
| chr14:77727869 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1033+3119C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727869 | |||||||
| chr14:77727903 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1033+3085A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727903 | |||||||
| chr14:77727909 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1033+3079C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727909 | |||||||
| chr14:77727949 | G | A | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1033+3039C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727949 | |||||||
| chr14:77728051 | T | TA | 171 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1033+2936dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728051 | |||||||
| chr14:77728051 | T | TAA | 25 | a0001c0001t0001g0010 a0001c0001t0001g0170 a0001c0001t0001g0309 others(22): Show |
29 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1033+2935_1033+293 others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728051 | |||||||
| chr14:77728098 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1033+2890C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728098 | |||||||
| chr14:77728134 | T | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1033+2854A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728134 | |||||||
| chr14:77728392 | A | C | 1 | a0001c0003t0002g0131 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1033+2596T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728392 | |||||||
| chr14:77728438 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
201 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1033+2550G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728438 | |||||||
| chr14:77728512 | T | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1033+2476A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728512 | |||||||
| chr14:77728559 | T | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0303 |
2 | HG00558.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1033+2429A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728559 | |||||||
| chr14:77728729 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0163 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1033+2259G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728729 | |||||||
| chr14:77728946 | G | A | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1033+2042C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728946 | |||||||
| chr14:77728975 | A | G | 1 | a0001c0003t0002g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1033+2013T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728975 | |||||||
| chr14:77728991 | C | T | 3 | a0001c0002t0001g0088 a0001c0002t0001g0098 a0001c0002t0001g0101 |
3 | HG02622.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1033+1997G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728991 | |||||||
| chr14:77729213 | C | T | 8 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0278 others(5): Show |
8 | HG00544.hp2 HG00621.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.1033+1775G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729213 | |||||||
| chr14:77729348 | C | T | 19 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(16): Show |
21 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1033+1640G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729348 | |||||||
| chr14:77729390 | T | C | 64 | a0001c0002t0001g0085 a0001c0003t0001g0013 a0001c0003t0001g0014 others(61): Show |
71 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1033+1598A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729390 | |||||||
| chr14:77729439 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(299): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1033+1549A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729439 | |||||||
| chr14:77729469 | T | C | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1033+1519A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729469 | |||||||
| chr14:77729530 | AAT | A | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1033+1456_1033+145 others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729530 | |||||||
| chr14:77729744 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1033+1244C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729744 | |||||||
| chr14:77729926 | A | G | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1033+1062T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729926 | |||||||
| chr14:77729977 | C | T | 6 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0240 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033+1011G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729977 | |||||||
| chr14:77730025 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1033+963C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730025 | |||||||
| chr14:77730111 | C | G | 6 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0240 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033+877G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730111 | |||||||
| chr14:77730410 | T | G | 2 | a0001c0004t0001g0049 a0001c0004t0001g0050 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1033+578A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730410 | |||||||
| chr14:77730430 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0181 others(6): Show |
11 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1033+558A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730430 | |||||||
| chr14:77730504 | C | G | 6 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0240 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033+484G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730504 | |||||||
| chr14:77730520 | T | C | 1 | a0001c0003t0002g0017 | 2 | NA18971.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1033+468A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730520 | |||||||
| chr14:77730521 | T | G | 1 | a0001c0003t0001g0311 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1033+467A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730521 | |||||||
| chr14:77730877 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1033+111A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730877 | |||||||
| chr14:77730940 | T | C | 23 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0017 others(20): Show |
27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1033+48A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730940 | |||||||
| chr14:77731197 | T | C | 1 | a0001c0004t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.892-68A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731197 | |||||||
| chr14:77731428 | C | G | 5 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0126 others(2): Show |
8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-299G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731428 | |||||||
| chr14:77731457 | T | C | 2 | a0001c0002t0001g0100 a0001c0002t0001g0102 |
2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.892-328A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731457 | |||||||
| chr14:77731563 | T | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
7 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-434A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731563 | |||||||
| chr14:77731613 | T | G | 2 | a0001c0003t0002g0128 a0001c0003t0002g0138 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.892-484A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731613 | |||||||
| chr14:77731653 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.892-524A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731653 | |||||||
| chr14:77731729 | A | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.892-600T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731729 | |||||||
| chr14:77731800 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
6 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-671C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731800 | |||||||
| chr14:77731844 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.891+641A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731844 | |||||||
| chr14:77731987 | T | C | 1 | a0001c0002t0001g0083 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.891+498A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731987 | |||||||
| chr14:77732041 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.891+444G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732041 | |||||||
| chr14:77732092 | C | T | 1 | a0001c0003t0002g0141 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.891+393G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732092 | |||||||
| chr14:77732106 | C | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.891+379G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732106 | |||||||
| chr14:77732217 | A | G | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+268T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732217 | |||||||
| chr14:77732443 | T | C | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.891+42A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732443 | |||||||
| chr14:77732653 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.775-52C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732653 | |||||||
| chr14:77732666 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0284 |
3 | NA18972.hp1 NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.775-65A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732666 | |||||||
| chr14:77732676 | T | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
133 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.775-75A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732676 | |||||||
| chr14:77732767 | C | T | 1 | a0001c0002t0001g0115 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.775-166G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732767 | |||||||
| chr14:77732789 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.775-188G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732789 | |||||||
| chr14:77732853 | G | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.775-252C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732853 | |||||||
| chr14:77733121 | G | A | 1 | a0001c0003t0002g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.775-520C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733121 | |||||||
| chr14:77733129 | T | G | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.775-528A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733129 | |||||||
| chr14:77733224 | T | TCAGA | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.775-624_775-623ins others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733224 | |||||||
| chr14:77733405 | T | C | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.775-804A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733405 | |||||||
| chr14:77733422 | A | G | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.775-821T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733422 | |||||||
| chr14:77733465 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.775-864G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733465 | |||||||
| chr14:77733490 | A | AT | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.775-890dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733490 | |||||||
| chr14:77733732 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.775-1131C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733732 | |||||||
| chr14:77733742 | C | CA | 14 | a0001c0002t0001g0068 a0001c0002t0001g0076 a0001c0002t0001g0083 others(11): Show |
14 | HG00544.hp1 HG01192.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.775-1142dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733742 | C | CAA | 14 | a0001c0002t0001g0074 a0001c0003t0001g0311 a0001c0003t0002g0005 others(11): Show |
16 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.775-1143_775-1142d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733742 | C | CAAA | 10 | a0001c0003t0002g0016 a0001c0003t0002g0126 a0001c0003t0002g0130 others(7): Show |
11 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.775-1144_775-1142d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733742 | C | CAAAAAA | 7 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0125 others(4): Show |
8 | HG01257.hp2 NA18946.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.775-1147_775-1142d others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733742 | C | CAAAAAAA | 9 | a0001c0003t0001g0124 a0001c0003t0001g0144 a0001c0003t0001g0145 others(6): Show |
9 | HG01258.hp1 HG03710.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-1148_775-1142d others(9): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733742 | CA | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
111 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.775-1142delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733742 | CAA | C | 76 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0020 others(73): Show |
84 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.775-1143_775-1142d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733742 | CAAA | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0229 others(13): Show |
18 | HG01515.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.775-1144_775-1142d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733742 | CAAAA | C | 8 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0239 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-1145_775-1142d others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | |||||||
| chr14:77733754 | A | C | 1 | a0001c0002t0001g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775-1153T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733754 | |||||||
| chr14:77733769 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.775-1168G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733769 | |||||||
| chr14:77733781 | G | GA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.774+1165dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733781 | |||||||
| chr14:77734049 | G | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.774+898C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734049 | |||||||
| chr14:77734056 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.774+891A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734056 | |||||||
| chr14:77734242 | C | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.774+705G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734242 | |||||||
| chr14:77734277 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.774+670C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734277 | |||||||
| chr14:77734549 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.774+398G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734549 | |||||||
| chr14:77734566 | C | T | 3 | a0001c0002t0001g0080 a0001c0002t0001g0081 a0001c0002t0001g0086 |
3 | NA18979.hp1 NA18985.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.774+381G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734566 | |||||||
| chr14:77734594 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.774+353G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734594 | |||||||
| chr14:77734736 | CA | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.774+210delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734736 | |||||||
| chr14:77734811 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.774+136G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734811 | |||||||
| chr14:77734918 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.774+29T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734918 | |||||||
| chr14:77735195 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.709-183T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735195 | |||||||
| chr14:77735452 | AT | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(9): Show |
13 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.709-441delA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735452 | |||||||
| chr14:77735601 | T | G | 1 | a0001c0003t0001g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.708+336A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735601 | |||||||
| chr14:77735601 | T | TGAAAAAT others(342): Show |
1 | a0001c0001t0001g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.708+335_708+336ins others(349): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735601 | |||||||
| chr14:77735630 | A | G | 1 | a0001c0001t0001g0010 | 3 | HG03471.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.708+307T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735630 | |||||||
| chr14:77735732 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.708+205C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735732 | |||||||
| chr14:77735789 | T | C | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.708+148A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735789 | |||||||
| chr14:77736029 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0045 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.639-23C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736029 | |||||||
| chr14:77736036 | A | G | 5 | a0001c0003t0001g0056 a0001c0003t0001g0063 a0001c0003t0001g0311 others(2): Show |
5 | HG02145.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-30T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736036 | |||||||
| chr14:77736068 | A | C | 2 | a0001c0003t0001g0313 a0001c0007t0001g0312 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.639-62T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736068 | |||||||
| chr14:77736091 | T | TA | 2 | a0001c0003t0001g0014 a0001c0003t0001g0060 |
3 | HG01109.hp1 HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.639-86dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736091 | |||||||
| chr14:77736104 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.639-98G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736104 | |||||||
| chr14:77736135 | TAC | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-131_639-130del others(2): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736135 | |||||||
| chr14:77736334 | C | T | 32 | a0001c0001t0001g0026 a0001c0001t0001g0268 a0001c0001t0001g0269 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.639-328G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736334 | |||||||
| chr14:77736346 | G | A | 1 | a0001c0003t0001g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.639-340C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736346 | |||||||
| chr14:77736394 | A | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0181 others(6): Show |
11 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.639-388T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736394 | |||||||
| chr14:77736430 | A | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.639-424T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736430 | |||||||
| chr14:77736434 | A | T | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.639-428T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736434 | |||||||
| chr14:77736548 | C | CA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
169 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.638+422dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736548 | |||||||
| chr14:77736548 | C | CAAAAAAA | 36 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(33): Show |
39 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.638+422_638+423ins others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736548 | |||||||
| chr14:77736549 | A | AAAAAAAC | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0157 others(24): Show |
31 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.638+421_638+422ins others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736549 | |||||||
| chr14:77736549 | A | AAAAAAC | 8 | a0001c0002t0001g0112 a0001c0003t0002g0005 a0001c0003t0002g0016 others(5): Show |
11 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.638+416_638+421dup others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736549 | |||||||
| chr14:77736549 | A | AAAAAACA others(5): Show |
16 | a0001c0003t0002g0017 a0001c0003t0002g0028 a0001c0003t0002g0128 others(13): Show |
17 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.638+410_638+421dup others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736549 | |||||||
| chr14:77736550 | AAAAAC | A | 4 | a0001c0001t0001g0253 a0001c0001t0001g0265 a0001c0001t0001g0281 others(1): Show |
4 | HG02683.hp1 HG02698.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+416_638+420del others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736550 | |||||||
| chr14:77736555 | C | A | 1 | a0001c0004t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.638+416G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736555 | |||||||
| chr14:77736585 | A | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.638+386T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736585 | |||||||
| chr14:77736906 | A | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.638+65T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736906 | |||||||
| chr14:77737189 | T | C | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.534-114A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737189 | |||||||
| chr14:77737195 | A | C | 2 | a0001c0004t0001g0051 a0001c0004t0001g0052 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.534-120T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737195 | |||||||
| chr14:77737293 | T | C | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.534-218A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737293 | |||||||
| chr14:77737307 | C | T | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.534-232G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737307 | |||||||
| chr14:77737330 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.534-255T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737330 | |||||||
| chr14:77737334 | G | A | 2 | a0001c0004t0001g0051 a0001c0004t0001g0052 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.534-259C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737334 | |||||||
| chr14:77737370 | T | C | 16 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.534-295A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737370 | |||||||
| chr14:77737569 | C | T | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.534-494G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737569 | |||||||
| chr14:77737757 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.534-682C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737757 | |||||||
| chr14:77737986 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.533+792G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737986 | |||||||
| chr14:77737991 | C | CA | 13 | a0001c0001t0001g0173 a0001c0001t0001g0178 a0001c0001t0001g0271 others(10): Show |
13 | HG00558.hp1 HG01192.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.533+786dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737991 | |||||||
| chr14:77737991 | C | CAA | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
203 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(200): Show |
intron_variant | MODIFIER | c.533+785_533+786dup others(2): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737991 | |||||||
| chr14:77737991 | C | CAAA | 51 | a0001c0001t0001g0008 a0001c0001t0001g0186 a0001c0001t0001g0214 others(48): Show |
58 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.533+784_533+786dup others(3): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737991 | |||||||
| chr14:77737991 | C | CAAAA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.533+783_533+786dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737991 | |||||||
| chr14:77738190 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.533+588G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738190 | |||||||
| chr14:77738193 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.533+585C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738193 | |||||||
| chr14:77738252 | G | C | 1 | a0001c0002t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.533+526C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738252 | |||||||
| chr14:77738320 | A | G | 1 | a0001c0002t0001g0086 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.533+458T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738320 | |||||||
| chr14:77738429 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+349G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738429 | |||||||
| chr14:77738643 | G | A | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.533+135C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738643 | |||||||
| chr14:77739173 | C | T | 6 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0240 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-112G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739173 | |||||||
| chr14:77739351 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0256 |
2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.331-290G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739351 | |||||||
| chr14:77739357 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.331-296A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739357 | |||||||
| chr14:77739461 | T | G | 4 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0104 others(1): Show |
6 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-400A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739461 | |||||||
| chr14:77739487 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0218 |
3 | HG00408.hp2 NA18747.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.331-426A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739487 | |||||||
| chr14:77739505 | T | C | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-444A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739505 | |||||||
| chr14:77739512 | C | T | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.331-451G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739512 | |||||||
| chr14:77739612 | GAAAA | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-555_331-552del others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739612 | |||||||
| chr14:77739692 | A | G | 1 | a0001c0003t0003g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.331-631T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739692 | |||||||
| chr14:77739805 | C | A | 16 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-744G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739805 | |||||||
| chr14:77739857 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.331-796C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739857 | |||||||
| chr14:77739930 | C | T | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-869G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739930 | |||||||
| chr14:77739977 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.331-916T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739977 | |||||||
| chr14:77740026 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
7 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-965G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740026 | |||||||
| chr14:77740135 | T | TA | 7 | a0001c0002t0001g0068 a0001c0002t0001g0084 a0001c0003t0001g0152 others(4): Show |
7 | HG01496.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-1075dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740135 | |||||||
| chr14:77740135 | T | TAA | 31 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(28): Show |
33 | HG00323.hp2 HG01167.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.331-1076_331-1075d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740135 | |||||||
| chr14:77740135 | T | TAAA | 5 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0126 others(2): Show |
8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-1077_331-1075d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740135 | |||||||
| chr14:77740135 | TAAAAAAA others(4): Show |
T | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-1085_331-1075d others(13): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740135 | |||||||
| chr14:77740156 | AAAGAG | A | 12 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0239 others(9): Show |
12 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.331-1100_331-1096d others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740156 | |||||||
| chr14:77740157 | A | G | 1 | a0001c0002t0001g0011 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.331-1096T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740157 | |||||||
| chr14:77740157 | AAG | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0188 others(8): Show |
11 | HG01257.hp1 HG01981.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.331-1098_331-1097d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740157 | |||||||
| chr14:77740157 | AAGAG | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(25): Show |
30 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.331-1100_331-1097d others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740157 | |||||||
| chr14:77740158 | AGAG | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
190 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.331-1100_331-1098d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740158 | |||||||
| chr14:77740161 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0188 others(8): Show |
11 | HG01257.hp1 HG01981.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.331-1100C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740161 | |||||||
| chr14:77740287 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.331-1226A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740287 | |||||||
| chr14:77740486 | T | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-1425A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740486 | |||||||
| chr14:77740835 | G | A | 45 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(42): Show |
49 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.331-1774C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740835 | |||||||
| chr14:77740862 | C | T | 1 | a0001c0001t0005g0262 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.331-1801G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740862 | |||||||
| chr14:77740925 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.331-1864G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740925 | |||||||
| chr14:77741005 | G | A | 7 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0240 others(4): Show |
7 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-1944C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741005 | |||||||
| chr14:77741029 | G | A | 5 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0216 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.331-1968C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741029 | |||||||
| chr14:77741096 | C | CA | 6 | a0001c0002t0001g0068 a0001c0002t0001g0074 a0001c0002t0001g0088 others(3): Show |
6 | HG02027.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-2036dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741096 | |||||||
| chr14:77741096 | CA | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.331-2036delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741096 | |||||||
| chr14:77741096 | CAA | C | 42 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0242 others(39): Show |
47 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.331-2037_331-2036d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741096 | |||||||
| chr14:77741096 | CAAAAAAA others(5): Show |
C | 3 | a0001c0003t0001g0154 a0001c0003t0001g0155 a0001c0003t0001g0156 |
3 | NA18943.hp2 NA18947.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.331-2047_331-2036d others(14): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741096 | |||||||
| chr14:77741137 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.331-2076T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741137 | |||||||
| chr14:77741155 | T | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-2094A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741155 | |||||||
| chr14:77741312 | G | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-2251C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741312 | |||||||
| chr14:77741365 | G | A | 2 | a0001c0003t0002g0128 a0001c0003t0002g0138 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.331-2304C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741365 | |||||||
| chr14:77741382 | A | G | 1 | a0001c0003t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.331-2321T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741382 | |||||||
| chr14:77741486 | G | A | 1 | a0001c0002t0001g0190 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.331-2425C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741486 | |||||||
| chr14:77741550 | T | TA | 2 | a0001c0001t0001g0022 a0001c0001t0001g0218 |
3 | HG00408.hp2 NA18747.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.331-2490dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741550 | |||||||
| chr14:77741736 | A | C | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-2675T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741736 | |||||||
| chr14:77741742 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.331-2681C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741742 | |||||||
| chr14:77741742 | GA | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0170 a0001c0001t0001g0178 others(5): Show |
9 | HG00642.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-2682delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741742 | |||||||
| chr14:77741778 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.331-2717C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741778 | |||||||
| chr14:77741951 | A | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-2890T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741951 | |||||||
| chr14:77741962 | G | A | 5 | a0001c0001t0001g0274 a0001c0001t0001g0278 a0001c0001t0001g0296 others(2): Show |
5 | HG00544.hp2 HG00621.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-2901C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741962 | |||||||
| chr14:77742035 | A | AT | 7 | a0001c0001t0001g0252 a0001c0001t0001g0299 a0001c0003t0002g0005 others(4): Show |
10 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.331-2975dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742035 | |||||||
| chr14:77742085 | G | C | 7 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0056 others(4): Show |
9 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-3024C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742085 | |||||||
| chr14:77742093 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.331-3032C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742093 | |||||||
| chr14:77742125 | G | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-3064C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742125 | |||||||
| chr14:77742225 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.331-3164C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742225 | |||||||
| chr14:77742413 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.331-3352G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742413 | |||||||
| chr14:77742571 | C | T | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.331-3510G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742571 | |||||||
| chr14:77742723 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.331-3662G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742723 | |||||||
| chr14:77742761 | A | G | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-3700T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742761 | |||||||
| chr14:77742793 | G | A | 1 | a0001c0002t0001g0190 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.331-3732C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742793 | |||||||
| chr14:77742862 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0279 |
3 | HG01175.hp1 HG01978.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.331-3801C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742862 | |||||||
| chr14:77742991 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
134 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.331-3930G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742991 | |||||||
| chr14:77743014 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-3953A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743014 | |||||||
| chr14:77743218 | T | C | 8 | a0001c0003t0002g0129 a0001c0003t0002g0134 a0001c0003t0002g0135 others(5): Show |
8 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-4157A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743218 | |||||||
| chr14:77743261 | GA | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-4201delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743261 | |||||||
| chr14:77743307 | T | C | 1 | a0001c0003t0001g0155 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.331-4246A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743307 | |||||||
| chr14:77743500 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.331-4439G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743500 | |||||||
| chr14:77743525 | C | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-4464G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743525 | |||||||
| chr14:77743526 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-4465C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743526 | |||||||
| chr14:77743842 | C | A | 1 | a0001c0003t0001g0156 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.331-4781G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743842 | |||||||
| chr14:77743910 | T | A | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-4849A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743910 | |||||||
| chr14:77744095 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331-5034G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744095 | |||||||
| chr14:77744135 | CA | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.331-5075delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744135 | |||||||
| chr14:77744135 | CAA | C | 13 | a0001c0001t0001g0169 a0001c0001t0001g0271 a0001c0003t0001g0060 others(10): Show |
14 | HG01069.hp2 HG01167.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.331-5076_331-5075d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744135 | |||||||
| chr14:77744191 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.331-5130C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744191 | |||||||
| chr14:77744446 | C | CA | 7 | a0001c0001t0001g0239 a0001c0001t0001g0252 a0001c0002t0001g0003 others(4): Show |
9 | HG00099.hp1 HG01099.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-5386dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744446 | |||||||
| chr14:77744446 | CA | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
194 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.331-5386delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744446 | |||||||
| chr14:77744446 | CAA | C | 43 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0191 others(40): Show |
48 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.331-5387_331-5386d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744446 | |||||||
| chr14:77744615 | C | T | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.331-5554G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744615 | |||||||
| chr14:77744644 | A | G | 16 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-5583T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744644 | |||||||
| chr14:77744691 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.331-5630G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744691 | |||||||
| chr14:77744882 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.331-5821T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744882 | |||||||
| chr14:77744934 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.331-5873G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744934 | |||||||
| chr14:77744947 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.331-5886G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744947 | |||||||
| chr14:77745242 | T | C | 4 | a0001c0004t0001g0049 a0001c0004t0001g0050 a0001c0004t0001g0051 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+6077A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745242 | |||||||
| chr14:77745320 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.330+5999C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745320 | |||||||
| chr14:77745404 | T | A | 2 | a0001c0004t0001g0051 a0001c0004t0001g0052 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.330+5915A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745404 | |||||||
| chr14:77745435 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.330+5884G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745435 | |||||||
| chr14:77745568 | A | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.330+5751T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745568 | |||||||
| chr14:77745681 | T | G | 2 | a0001c0003t0001g0149 a0001c0003t0001g0150 |
2 | HG03710.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.330+5638A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745681 | |||||||
| chr14:77745891 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.330+5428C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745891 | |||||||
| chr14:77745904 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.330+5415C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745904 | |||||||
| chr14:77746000 | G | T | 1 | a0001c0006t0001g0099 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.330+5319C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746000 | |||||||
| chr14:77746119 | G | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.330+5200C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746119 | |||||||
| chr14:77746173 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.330+5146A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746173 | |||||||
| chr14:77746176 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0040 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.330+5143G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746176 | |||||||
| chr14:77746201 | A | G | 1 | a0001c0004t0001g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.330+5118T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746201 | |||||||
| chr14:77746234 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+5085G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746234 | |||||||
| chr14:77746314 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.330+5005C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746314 | |||||||
| chr14:77746423 | G | A | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+4896C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746423 | |||||||
| chr14:77746429 | TCA | T | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+4888_330+4889d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746429 | |||||||
| chr14:77746519 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.330+4800A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746519 | |||||||
| chr14:77746757 | T | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.330+4562A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746757 | |||||||
| chr14:77746901 | C | T | 1 | a0001c0003t0002g0137 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.330+4418G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746901 | |||||||
| chr14:77746922 | GTCTCCCT others(5): Show |
G | 1 | a0001c0001t0001g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.330+4385_330+4396d others(14): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746922 | |||||||
| chr14:77747004 | T | G | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+4315A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747004 | |||||||
| chr14:77747041 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.330+4278G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747041 | |||||||
| chr14:77747065 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0289 |
2 | HG02293.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.330+4254G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747065 | |||||||
| chr14:77747073 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0045 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.330+4246G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747073 | |||||||
| chr14:77747179 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.330+4140C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747179 | |||||||
| chr14:77747315 | C | T | 78 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(75): Show |
86 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.330+4004G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747315 | |||||||
| chr14:77747514 | C | T | 2 | a0001c0001t0001g0264 a0001c0004t0001g0049 |
2 | HG00609.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.330+3805G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747514 | |||||||
| chr14:77747525 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3794G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747525 | |||||||
| chr14:77747533 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330+3786C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747533 | |||||||
| chr14:77747601 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.330+3718G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747601 | |||||||
| chr14:77747607 | C | A | 2 | a0001c0004t0001g0049 a0001c0004t0001g0050 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.330+3712G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747607 | |||||||
| chr14:77747638 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.330+3681G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747638 | |||||||
| chr14:77747651 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.330+3668T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747651 | |||||||
| chr14:77747669 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.330+3650C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747669 | |||||||
| chr14:77747675 | GCCCGGCA others(39): Show |
G | 1 | a0001c0002t0001g0088 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.330+3598_330+3643d others(48): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747675 | |||||||
| chr14:77747678 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.330+3641G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747678 | |||||||
| chr14:77747695 | AGGAGGGA others(39): Show |
A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0159 a0001c0001t0001g0309 others(1): Show |
6 | HG02818.hp2 HG02922.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+3578_330+3623d others(48): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747695 | |||||||
| chr14:77747725 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0188 |
2 | NA19082.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.330+3594C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747725 | |||||||
| chr14:77747736 | CGTCT | C | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+3579_330+3582d others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747736 | |||||||
| chr14:77747740 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.330+3579A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747740 | |||||||
| chr14:77747767 | C | G | 2 | a0001c0004t0001g0051 a0001c0004t0001g0052 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.330+3552G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747767 | |||||||
| chr14:77747786 | C | T | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+3533G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747786 | |||||||
| chr14:77747818 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.330+3501C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747818 | |||||||
| chr14:77747826 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.330+3493G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747826 | |||||||
| chr14:77747854 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.330+3465G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747854 | |||||||
| chr14:77747912 | T | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+3407A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747912 | |||||||
| chr14:77747946 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.330+3373G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747946 | |||||||
| chr14:77747947 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
132 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.330+3372C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747947 | |||||||
| chr14:77747962 | G | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+3357C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747962 | |||||||
| chr14:77748239 | CCTAATCT | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG02451.hp1 HG02572.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+3073_330+3079d others(9): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748239 | |||||||
| chr14:77748382 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.330+2937G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748382 | |||||||
| chr14:77748447 | GA | G | 18 | a0001c0003t0002g0017 a0001c0003t0002g0028 a0001c0003t0002g0128 others(15): Show |
19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.330+2871delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748447 | |||||||
| chr14:77748532 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.330+2787T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748532 | |||||||
| chr14:77748900 | T | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.330+2419A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748900 | |||||||
| chr14:77748905 | T | A | 45 | a0001c0002t0001g0085 a0001c0003t0001g0018 a0001c0003t0001g0123 others(42): Show |
50 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.330+2414A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748905 | |||||||
| chr14:77748956 | A | G | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+2363T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748956 | |||||||
| chr14:77748971 | T | C | 2 | a0001c0002t0001g0108 a0001c0002t0001g0109 |
2 | HG02683.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.330+2348A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748971 | |||||||
| chr14:77749184 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+2135G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749184 | |||||||
| chr14:77749262 | G | A | 16 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.330+2057C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749262 | |||||||
| chr14:77749305 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.330+2014G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749305 | |||||||
| chr14:77749444 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330+1875G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749444 | |||||||
| chr14:77749537 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.330+1782A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749537 | |||||||
| chr14:77749628 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.330+1691T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749628 | |||||||
| chr14:77749663 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.330+1656C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749663 | |||||||
| chr14:77749671 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.330+1648T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749671 | |||||||
| chr14:77749704 | T | C | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+1615A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749704 | |||||||
| chr14:77749763 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.330+1556A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749763 | |||||||
| chr14:77749948 | C | A | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0302 |
3 | HG02486.hp1 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.330+1371G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749948 | |||||||
| chr14:77750044 | A | G | 2 | a0001c0004t0001g0049 a0001c0004t0001g0050 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.330+1275T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750044 | |||||||
| chr14:77750176 | G | A | 9 | a0001c0003t0001g0053 a0001c0003t0001g0054 a0001c0003t0001g0057 others(6): Show |
9 | HG00280.hp1 HG01516.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.330+1143C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750176 | |||||||
| chr14:77750260 | C | T | 23 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0017 others(20): Show |
27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.330+1059G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750260 | |||||||
| chr14:77750261 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.330+1058C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750261 | |||||||
| chr14:77750502 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.330+817C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750502 | |||||||
| chr14:77750510 | A | G | 1 | a0001c0002t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.330+809T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750510 | |||||||
| chr14:77750629 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.330+690C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750629 | |||||||
| chr14:77750667 | GA | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.330+651delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750667 | |||||||
| chr14:77750674 | A | G | 5 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0126 others(2): Show |
8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+645T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750674 | |||||||
| chr14:77750949 | T | C | 2 | a0001c0004t0001g0051 a0001c0004t0001g0052 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.330+370A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750949 | |||||||
| chr14:77751254 | G | A | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.330+65C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77751254 | |||||||
| chr14:77751532 | A | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-52T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751532 | |||||||
| chr14:77751567 | TCCTTAGT others(3): Show |
T | 1 | a0001c0004t0001g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.169-97_169-88delCA others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751567 | |||||||
| chr14:77751733 | G | C | 1 | a0001c0002t0001g0086 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.169-253C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751733 | |||||||
| chr14:77751805 | G | GAC | 9 | a0001c0001t0001g0038 a0001c0002t0001g0015 a0001c0002t0001g0087 others(6): Show |
10 | HG01167.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-327_169-326dup others(2): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751805 | G | GACAC | 6 | a0001c0002t0001g0030 a0001c0002t0001g0077 a0001c0002t0001g0088 others(3): Show |
6 | HG01109.hp2 HG01928.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-329_169-326dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751805 | G | GACACAC | 25 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0011 others(22): Show |
34 | HG00099.hp1 HG00423.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.169-331_169-326dup others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751805 | G | GACACACA others(1): Show |
6 | a0001c0002t0001g0096 a0001c0002t0001g0097 a0001c0002t0001g0098 others(3): Show |
6 | HG01891.hp2 HG02809.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-333_169-326dup others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751805 | G | GACACACA others(3): Show |
4 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0001g0102 others(1): Show |
4 | HG00544.hp1 HG01106.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-335_169-326dup others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751805 | GAC | G | 46 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0040 others(43): Show |
48 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.169-327_169-326del others(2): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751805 | GACACACA others(3): Show |
G | 28 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0018 others(25): Show |
31 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.169-335_169-326del others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751805 | GACACACA others(9): Show |
G | 2 | a0001c0001t0001g0298 a0001c0003t0001g0058 |
2 | HG01891.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.169-341_169-326del others(16): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751805 | GACACACA others(13): Show |
G | 3 | a0001c0003t0001g0057 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG02572.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.169-345_169-326del others(20): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | |||||||
| chr14:77751807 | C | G | 1 | a0001c0003t0002g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.169-327G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751807 | |||||||
| chr14:77751814 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.169-334T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751814 | |||||||
| chr14:77751821 | C | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(9): Show |
13 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.169-341G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751821 | |||||||
| chr14:77751837 | CACACA | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0159 a0001c0001t0001g0309 others(1): Show |
6 | HG02818.hp2 HG02922.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-362_169-358del others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751837 | |||||||
| chr14:77751838 | A | ACACACAC | 3 | a0001c0002t0001g0004 a0001c0002t0001g0104 a0001c0002t0006g0105 |
5 | HG00099.hp2 HG00733.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-365_169-359dup others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751838 | |||||||
| chr14:77751839 | CACA | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0161 others(4): Show |
9 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-362_169-360del others(3): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751839 | |||||||
| chr14:77751841 | CA | C | 3 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0004g0231 |
3 | HG02486.hp2 HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.169-362delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751841 | |||||||
| chr14:77751843 | CACCACA | C | 10 | a0001c0001t0001g0023 a0001c0001t0001g0165 a0001c0001t0001g0175 others(7): Show |
11 | HG00673.hp2 HG02165.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-369_169-364del others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751843 | |||||||
| chr14:77751844 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.169-364T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751844 | |||||||
| chr14:77751844 | AC | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.169-365delG | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751844 | |||||||
| chr14:77751845 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.169-365G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | |||||||
| chr14:77751845 | C | CA | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01106.hp1 HG03492.hp2 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(1): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | |||||||
| chr14:77751845 | C | CACACACA others(3): Show |
6 | a0001c0001t0001g0241 a0001c0001t0001g0254 a0001c0002t0001g0071 others(3): Show |
6 | HG02615.hp1 NA18945.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | |||||||
| chr14:77751845 | C | CACACACC others(1): Show |
4 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0240 others(1): Show |
4 | HG02280.hp1 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | |||||||
| chr14:77751845 | C | CACACCA | 4 | a0001c0001t0001g0239 a0001c0001t0001g0263 a0001c0002t0001g0118 others(1): Show |
4 | HG02258.hp1 NA18906.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | |||||||
| chr14:77751845 | C | CACCA | 4 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0260 others(1): Show |
4 | HG03654.hp2 HG04199.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | |||||||
| chr14:77751845 | CCACA | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0173 others(8): Show |
11 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-369_169-366del others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | |||||||
| chr14:77751848 | CA | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.169-369delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751848 | |||||||
| chr14:77751865 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0265 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.169-385T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751865 | |||||||
| chr14:77752065 | T | C | 18 | a0001c0003t0002g0017 a0001c0003t0002g0028 a0001c0003t0002g0128 others(15): Show |
19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-585A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752065 | |||||||
| chr14:77752096 | C | G | 2 | a0001c0004t0001g0049 a0001c0004t0001g0050 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.169-616G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752096 | |||||||
| chr14:77752413 | G | A | 4 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0104 others(1): Show |
6 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-933C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752413 | |||||||
| chr14:77752499 | C | G | 2 | a0001c0004t0001g0051 a0001c0004t0001g0052 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.169-1019G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752499 | |||||||
| chr14:77752800 | C | T | 16 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.169-1320G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752800 | |||||||
| chr14:77752801 | G | A | 5 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0126 others(2): Show |
8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-1321C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752801 | |||||||
| chr14:77752817 | A | T | 1 | a0001c0001t0001g0261 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.169-1337T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752817 | |||||||
| chr14:77752841 | T | C | 1 | a0001c0003t0001g0311 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.169-1361A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752841 | |||||||
| chr14:77752942 | T | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
202 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.169-1462A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752942 | |||||||
| chr14:77752988 | TAG | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.169-1510_169-1509d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752988 | |||||||
| chr14:77753066 | T | C | 46 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(43): Show |
50 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.169-1586A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753066 | |||||||
| chr14:77753112 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.169-1632G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753112 | |||||||
| chr14:77753207 | A | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0191 |
2 | NA19065.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.169-1727T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753207 | |||||||
| chr14:77753464 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.168+1503A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753464 | |||||||
| chr14:77753469 | A | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.168+1498T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753469 | |||||||
| chr14:77753812 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.168+1155T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753812 | |||||||
| chr14:77753823 | C | T | 2 | a0001c0004t0001g0049 a0001c0004t0001g0050 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.168+1144G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753823 | |||||||
| chr14:77753825 | T | C | 4 | a0001c0004t0001g0049 a0001c0004t0001g0050 a0001c0004t0001g0051 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+1142A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753825 | |||||||
| chr14:77754040 | A | C | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.168+927T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754040 | |||||||
| chr14:77754046 | A | C | 1 | a0001c0003t0002g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.168+921T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754046 | |||||||
| chr14:77754194 | G | A | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.168+773C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754194 | |||||||
| chr14:77754232 | C | T | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.168+735G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754232 | |||||||
| chr14:77754271 | T | G | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168+696A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754271 | |||||||
| chr14:77754529 | C | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.168+438G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754529 | |||||||
| chr14:77754597 | C | T | 1 | a0001c0004t0001g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.168+370G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754597 | |||||||
| chr14:77754635 | A | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.168+332T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754635 | |||||||
| chr14:77754683 | T | A | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.168+284A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754683 | |||||||
| chr14:77755159 | C | CAA | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-40_15-39insTT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755159 | |||||||
| chr14:77755160 | T | G | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-40A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755160 | |||||||
| chr14:77755161 | C | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-41G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755161 | |||||||
| chr14:77755166 | G | C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-46C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755166 | |||||||
| chr14:77755167 | T | TTCTTTCT others(90): Show |
1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-48_15-47insGAAA others(93): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755167 | |||||||
| chr14:77755170 | A | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-50T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755170 | |||||||
| chr14:77755171 | A | C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-51T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755171 | |||||||
| chr14:77755175 | G | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-55C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755175 | |||||||
| chr14:77755179 | A | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-59T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755179 | |||||||
| chr14:77755180 | C | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-60G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755180 | |||||||
| chr14:77755182 | G | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-62C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755182 | |||||||
| chr14:77755184 | A | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-64T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755184 | |||||||
| chr14:77755186 | C | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-66G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755186 | |||||||
| chr14:77755188 | TGGCCACA others(4): Show |
T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-79_15-69delTCTC others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755188 | |||||||
| chr14:77755201 | A | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-81T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755201 | |||||||
| chr14:77755202 | A | C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-82T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755202 | |||||||
| chr14:77755211 | A | C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-91T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755211 | |||||||
| chr14:77755213 | G | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-93C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755213 | |||||||
| chr14:77755214 | A | C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-94T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755214 | |||||||
| chr14:77755216 | G | A | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-96C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755216 | |||||||
| chr14:77755222 | A | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-102T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755222 | |||||||
| chr14:77755225 | T | C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-105A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755225 | |||||||
| chr14:77755228 | CAGAAAAA others(7): Show |
C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-122_15-109delTC others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755228 | |||||||
| chr14:77755244 | T | C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-124A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755244 | |||||||
| chr14:77755257 | A | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-137T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755257 | |||||||
| chr14:77755260 | G | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-140C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755260 | |||||||
| chr14:77755261 | T | C | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-141A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755261 | |||||||
| chr14:77755262 | A | T | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-142T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755262 | |||||||
| chr14:77755272 | A | G | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-152T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755272 | |||||||
| chr14:77755273 | C | A | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-153G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755273 | |||||||
| chr14:77755274 | T | G | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-154A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755274 | |||||||
| chr14:77755277 | C | A | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-157G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755277 | |||||||
| chr14:77755278 | C | G | 1 | a0002c0005t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-158G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755278 | |||||||
| chr14:77755386 | A | G | 5 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0126 others(2): Show |
8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-266T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755386 | |||||||
| chr14:77755487 | C | T | 5 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0126 others(2): Show |
8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-367G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755487 | |||||||
| chr14:77755725 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.15-605C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755725 | |||||||
| chr14:77755744 | C | CT | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.15-625dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755744 | |||||||
| chr14:77755808 | A | G | 2 | a0001c0004t0001g0051 a0001c0004t0001g0052 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.15-688T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755808 | |||||||
| chr14:77755893 | C | T | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG02155.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.15-773G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755893 | |||||||
| chr14:77755958 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.15-838G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755958 | |||||||
| chr14:77756131 | T | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-1011A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756131 | |||||||
| chr14:77756455 | T | C | 16 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(13): Show |
17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.15-1335A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756455 | |||||||
| chr14:77756563 | T | C | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-1443A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756563 | |||||||
| chr14:77756613 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.15-1493C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756613 | |||||||
| chr14:77756653 | G | A | 2 | a0001c0004t0001g0049 a0001c0004t0001g0050 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.15-1533C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756653 | |||||||
| chr14:77756804 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.15-1684C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756804 | |||||||
| chr14:77756840 | T | C | 1 | a0001c0003t0002g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.15-1720A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756840 | |||||||
| chr14:77756939 | G | A | 2 | a0001c0004t0001g0051 a0001c0004t0001g0052 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.15-1819C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756939 | |||||||
| chr14:77757224 | C | CA | 8 | a0001c0001t0001g0250 a0001c0001t0001g0305 a0001c0002t0001g0077 others(5): Show |
11 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-2105dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757224 | |||||||
| chr14:77757224 | CA | C | 68 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0270 others(65): Show |
72 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.15-2105delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757224 | |||||||
| chr14:77757307 | A | C | 2 | a0001c0003t0001g0056 a0001c0003t0001g0063 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.15-2187T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757307 | |||||||
| chr14:77757862 | C | T | 23 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0017 others(20): Show |
27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.15-2742G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757862 | |||||||
| chr14:77757890 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.15-2770A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757890 | |||||||
| chr14:77757919 | C | CATCT | 53 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(50): Show |
61 | HG00642.hp1 HG00735.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.15-2803_15-2800dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | |||||||
| chr14:77757919 | C | CATCTATC others(1): Show |
21 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0045 others(18): Show |
21 | HG00558.hp1 HG00621.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-2807_15-2800dup others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | |||||||
| chr14:77757919 | C | CATCTATC others(5): Show |
6 | a0001c0001t0001g0033 a0001c0001t0001g0159 a0001c0001t0001g0268 others(3): Show |
6 | HG00544.hp2 HG02559.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-2811_15-2800dup others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | |||||||
| chr14:77757919 | CATCT | C | 86 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0048 others(83): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.15-2803_15-2800del others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | |||||||
| chr14:77757919 | CATCTATC others(1): Show |
C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0227 a0001c0001t0001g0228 others(8): Show |
13 | HG01168.hp2 HG02109.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-2807_15-2800del others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | |||||||
| chr14:77757919 | CATCTATC others(5): Show |
C | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
6 | HG02055.hp2 HG02647.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-2811_15-2800del others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | |||||||
| chr14:77757942 | CTATCTAT others(9): Show |
C | 1 | a0001c0003t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.15-2838_15-2823del others(16): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757942 | |||||||
| chr14:77757946 | CTATCTAT others(5): Show |
C | 19 | a0001c0003t0001g0018 a0001c0003t0001g0144 a0001c0003t0001g0145 others(16): Show |
21 | HG02630.hp1 HG03710.hp1 NA18943.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-2838_15-2827del others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757946 | |||||||
| chr14:77757950 | CTATCGCA others(1): Show |
C | 9 | a0001c0003t0001g0125 a0001c0003t0002g0133 a0001c0003t0002g0134 others(6): Show |
9 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-2838_15-2831del others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757950 | |||||||
| chr14:77757954 | C | T | 12 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0001c0001t0001g0239 others(9): Show |
12 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.15-2834G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757954 | |||||||
| chr14:77757955 | G | T | 2 | a0001c0003t0002g0127 a0001c0003t0002g0136 |
2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.15-2835C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757955 | |||||||
| chr14:77757955 | GCAAT | G | 8 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0002g0005 others(5): Show |
11 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-2839_15-2836del others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757955 | |||||||
| chr14:77757956 | C | A | 2 | a0001c0003t0002g0127 a0001c0003t0002g0136 |
2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.15-2836G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757956 | |||||||
| chr14:77757957 | A | T | 2 | a0001c0003t0002g0127 a0001c0003t0002g0136 |
2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.15-2837T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757957 | |||||||
| chr14:77757958 | A | C | 2 | a0001c0003t0002g0127 a0001c0003t0002g0136 |
2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.15-2838T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757958 | |||||||
| chr14:77757959 | T | G | 31 | a0001c0003t0001g0018 a0001c0003t0001g0125 a0001c0003t0001g0144 others(28): Show |
33 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.15-2839A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757959 | |||||||
| chr14:77757978 | C | CTCTA | 258 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.15-2862_15-2859dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757978 | |||||||
| chr14:77758021 | T | C | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.15-2901A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758021 | |||||||
| chr14:77758027 | G | GCAAT | 251 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.15-2911_15-2908dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758027 | |||||||
| chr14:77758059 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-2939C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758059 | |||||||
| chr14:77758098 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.15-2978C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758098 | |||||||
| chr14:77758189 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.14+2925C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758189 | |||||||
| chr14:77758193 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.14+2921C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758193 | |||||||
| chr14:77758203 | G | A | 18 | a0001c0003t0002g0017 a0001c0003t0002g0028 a0001c0003t0002g0128 others(15): Show |
19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.14+2911C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758203 | |||||||
| chr14:77758295 | G | A | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.14+2819C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758295 | |||||||
| chr14:77758315 | C | CA | 7 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(4): Show |
7 | HG02055.hp1 NA18948.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+2798dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAA | 100 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.14+2795_14+2798dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAAA | 58 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0039 others(55): Show |
61 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.14+2794_14+2798dup others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAAAA | 38 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(35): Show |
42 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.14+2793_14+2798dup others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAAAAA | 13 | a0001c0001t0001g0264 a0001c0001t0001g0295 a0001c0001t0001g0296 others(10): Show |
13 | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+2792_14+2798dup others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAAAAA others(3): Show |
2 | a0001c0003t0001g0311 a0001c0007t0001g0312 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.14+2789_14+2798dup others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAAAAA others(4): Show |
1 | a0001c0003t0001g0313 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.14+2788_14+2798dup others(11): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAAAAA others(7): Show |
5 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0125 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+2785_14+2798dup others(14): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAAAAA others(8): Show |
6 | a0001c0003t0001g0018 a0001c0003t0001g0146 a0001c0003t0001g0147 others(3): Show |
7 | HG03710.hp1 NA18960.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+2784_14+2798dup others(15): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | C | CAAAAAAA others(9): Show |
5 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0154 others(2): Show |
5 | NA18943.hp2 NA18946.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+2783_14+2798dup others(16): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758315 | CAAA | C | 22 | a0001c0003t0002g0005 a0001c0003t0002g0016 a0001c0003t0002g0017 others(19): Show |
26 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.14+2796_14+2798del others(3): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | |||||||
| chr14:77758562 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.14+2552G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758562 | |||||||
| chr14:77758610 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0159 a0001c0001t0001g0160 others(5): Show |
10 | HG02055.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.14+2504G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758610 | |||||||
| chr14:77758790 | C | T | 3 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0122 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.14+2324G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758790 | |||||||
| chr14:77758868 | A | AAGTGT | 3 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0125 |
3 | HG01257.hp2 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.14+2241_14+2245dup others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758868 | |||||||
| chr14:77758888 | C | G | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.14+2226G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758888 | |||||||
| chr14:77758914 | T | C | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.14+2200A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758914 | |||||||
| chr14:77759156 | TC | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
202 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.14+1957delG | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759156 | |||||||
| chr14:77759226 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.14+1888G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759226 | |||||||
| chr14:77759385 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.14+1729C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759385 | |||||||
| chr14:77759405 | T | G | 1 | a0001c0001t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.14+1709A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759405 | |||||||
| chr14:77759413 | T | C | 1 | a0001c0003t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.14+1701A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759413 | |||||||
| chr14:77759414 | G | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.14+1700C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759414 | |||||||
| chr14:77759515 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.14+1599T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759515 | |||||||
| chr14:77759566 | T | C | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | NA18968.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.14+1548A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759566 | |||||||
| chr14:77759768 | G | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.14+1346C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759768 | |||||||
| chr14:77759820 | T | A | 36 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0270 others(33): Show |
38 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.14+1294A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759820 | |||||||
| chr14:77759820 | T | TA | 16 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+1293_14+1294ins others(1): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759820 | |||||||
| chr14:77759821 | T | A | 98 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0266 others(95): Show |
107 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.14+1293A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759821 | |||||||
| chr14:77759822 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14+1292T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759822 | |||||||
| chr14:77759827 | A | AG | 6 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
7 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+1286_14+1287ins others(1): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759827 | |||||||
| chr14:77759827 | A | G | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
13 | HG02257.hp1 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+1287T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759827 | |||||||
| chr14:77759846 | G | A | 3 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 |
3 | HG02738.hp2 HG04228.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.14+1268C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759846 | |||||||
| chr14:77759963 | T | C | 3 | a0001c0003t0001g0154 a0001c0003t0001g0155 a0001c0003t0001g0156 |
3 | NA18943.hp2 NA18947.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.14+1151A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759963 | |||||||
| chr14:77759996 | G | C | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0053 others(17): Show |
22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.14+1118C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759996 | |||||||
| chr14:77760173 | G | A | 1 | a0001c0001t0001g0027 | 2 | NA18959.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.14+941C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760173 | |||||||
| chr14:77760310 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.14+804C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760310 | |||||||
| chr14:77760349 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.14+765G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760349 | |||||||
| chr14:77760369 | T | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG00597.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.14+745A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760369 | |||||||
| chr14:77760371 | G | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.14+743C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760371 | |||||||
| chr14:77760384 | C | A | 39 | a0001c0003t0001g0018 a0001c0003t0001g0123 a0001c0003t0001g0124 others(36): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.14+730G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760384 | |||||||
| chr14:77760507 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
202 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.14+607C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760507 | |||||||
| chr14:77760616 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0309 a0001c0001t0001g0310 |
5 | HG02818.hp2 HG02922.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+498A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760616 | |||||||
| chr14:77760631 | A | C | 3 | a0001c0002t0001g0011 a0001c0002t0001g0029 a0001c0002t0001g0030 |
4 | HG01928.hp2 NA18747.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+483T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760631 | |||||||
| chr14:77760668 | G | A | 3 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0007t0001g0312 |
3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.14+446C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760668 | |||||||
| chr14:77760702 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.14+412G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760702 | |||||||
| chr14:77760718 | G | C | 1 | a0001c0001t0001g0315 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.14+396C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760718 | |||||||
| chr14:77760804 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.14+310G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760804 | |||||||
| chr14:77760875 | C | T | 1 | a0001c0003t0002g0028 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.14+239G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760875 | |||||||
| chr14:77760917 | C | A | 1 | a0001c0001t0001g0315 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.14+197G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760917 | |||||||
| chr14:77760999 | CCCACGTC others(8): Show |
C | 1 | a0001c0001t0001g0316 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.14+100_14+114delCA others(13): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760999 | |||||||
| chr14:77761093 | G | GGACCCCA others(6): Show |
1 | a0001c0001t0001g0317 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.14+8_14+20dupGTTGA others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77761093 |